2017 Group Project 6

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The cerebellum is a large portion of the brain that functions in coordination, balance and control, and its development occurs both prenatally and postnatally. The cerebellum underlies the occipital and temporal lobes of the cerebral cortex and constitutes to about 10% of the brain's weight but contains around 50% of the neurons. This page will highlight the anatomy of the cerebellum, its developmental process, current research on the structure, animal models and abnormalities associated with it. The anatomy will discuss the distinguishable lobes and zones of the cerebellum. The anatomy of the cerebellum cannot be completely discussed without explaining the vasculature of the structure and hence this page will provide a brief overview of it. The development of the cerebellum discusses the neural development and where the cerebellum forms on the neural tube. The development will highlight how the circuitry of the post-natal cerebellum came to be from neurons. Hence purkinje cells, granule cells, deep nuclei cells, glia cells and cerebellar nuclei will be highlighted to discuss the developmental process. A developmental timeline of the formation of the cerebellum is also included on this page. The cerebellum is a topic of continuous research and past findings would not have been done without the use of animal models, hence key historical discoveries, current research and animal models will be discussed. Towards the end of the page there are future questions listed on future investigations involving the cerebellum and the abnormalities from an affected cerebellum are also highlighted. Terms that may be difficult to understand have also been identified and defined.

The following video provides a brief overview on the cerebellum which will be further discussed on this page: <html5media height="315" width="560">https://www.youtube.com/watch?v=Fir-v6EoZNE</html5media> [1]

Basic Anatomy of the Cerebellum

The cerebellum has 3 distinguishable lobes; flocculonodular lobe, anterior lobe and the posterior lobe. The anterior and posterior lobe can be further divided in a midline cerebellar vermis and lateral cerebellar hemispheres (Figure 1) [2]. In a superior cerebellar view, the cerebellum contains a vermis that runs through the middle of the organ and 2 intermediate zones located laterally from the vermis (Figure 2).


Figure 1: Anatomical lobes observed in the cerebellum; anterior lobe, posterior lobe and flocculonodular lobe, which is divided by two fissures – the primary fissure and posterolateral fissure [3]

Cerebellum anatomical subdivisions.png

Figure 2: Superior view of the 3 cerebellar zones. The middle is the vermis. Either side of the vermis is the intermediate zone. Lateral to the intermediate zone is the lateral hemispheres. There is no difference in gross structure between the lateral hemispheres and intermediate zones. [4]

Figure 3: Diagram of the main arteries of the cerebellum [3]


The cerebellum contains 3 bilateral paired arteries which supplies this organ with oxygenated blood. These arteries all originate from the vertebrobasilar system: Superior Cerebellar Artery (SCA), Anterior Inferior Cerebellar Artery (AICA) and Posterior inferior cerebellar artery (PICA). The SCA and AICA are branches of the basilar artery, which wraps around the anterior aspect of the pons before reaching the cerebellum. The PICA arises from the left and right vertebral artery, which form the basilar artery [5]. The PICA and AICA combine to supply the inferior half of the cerebellum, while the SCA supplies the majority of the superior half. The PICA and SCA combine to supply the vermis[6]. Blood is then drained by superior and inferior cerebellar veins into the superior petrosal and then straight dural venous sinuses. (Figure 3)[7]


Cortical Layers

Figure 4: (A). Cell types and where they are found in the cerebellar cortical layers. (B) Shows how the different layers of the cerebellum can be easily determined. P - the Purkinje layer; G - the granular layer; M - the molecular layer; W - the white matter.[8]

There are 3 major cortical layers of the cerebellum: the molecular layer, the purkinje cell layer, and the granule cell layer. The molecular layer contains basket cells, stellate cells and the purkinje cell and Golgi cell dendrites. The purkinje cell layer contains purkinje cell bodies and Bergmann glia. The granule cell layer contains granule cells, mossy fibers, and Golgi cell bodies. [9]

Purkinje/Pyramidal Cells

Discovered by Jan Evangelista Purkinje in 1837, purkinje cells are inhibitory neurons found in the outside layer of the cerebellum. They receive signals from the granule cell parallel fibers and the superior olive and send inhibitory signals to the deep nuclei in the white matter region via GABA signaling. Purkinje cells have a large branching network of dendrites which allows them to be identified by their morphology.

Granule Cells

Named for their small cell body, cerebellar granule cells of were discovered by Camillo Golgi and Ramon y Cajal in 1899. Cerebellar granule cells are the most numerous cell type in the human brain. They receive signals from mossy fibers of the pons and synapse on the fast network of dendrites of the pyramidal cells. Cerebellar granule cells are glutamatergic and the only excitatory neurons found in the cerebellum. [10]

Deep Nuclei

There are four different deep nuclei of the cerebellum: the dentate, interpositus, fastigial, and vestibular nuclei. The dentate nucleus receives signals from the lateral purkinje cells, the interpositus nucleus receives signals from the intermediate purkinje cells, the fastigial nucleus receives signals from the medial purkinje cells, and the vestibular nucleus receives signals from the flocculonodular purkinje cells. The deep nuclei integrate the inhibitory signals from the purkinje cells and the excitatory signals from the mossy and climbing fibers to determine their output signals. [11] The dentate nucleus in particular is thought to be implicated in higher level cognitive processing. It is enlarged in primates and humans and not observed in non-mammalian species.[12]

Cerebellar Nuclei

Cerebellar Nuclei
Fastigial Nucleus
Most medially located of the cerebellar nuclei. Receives input from the vermis and cerebellar afferents that carry vestibular, proximal somatosensory, auditory and visual information.
Interposed Nuclei
Consists of emboliform nucleus and globose nucleus. Interposed nuclei are situated laterally with respect to the fastigial nucleus. Receives input from intermediate zone and cerebellar afferents that carry spinal, proximal somatosensory, auditory and visual information.
Dentate Nucleus
Largest of the cerebellar nuclei. Lateral to interposed nuclei. Receives input from lateral hemisphere and cerebellar afferents that carry information from cerebral cortex.
Vestibular Nuclei
Located outside cerebellum in the medulla. Considered to be cerebellar nuclei as their connectivity patterns are identical to those of cerebellar nuclei. Receive input from flocculonodular lobe and from the vestibular labyrinth.
Links: cerebellum

Bergmann Glia

Glial cells of the cerebellum were described by Ramon y Cajal in 1911. He divided them into 3 main categories: the glia of the white matter, the astrocytes of the granule cell layer, and the Bergmann glia of the Purkinje cell layer. Also known as Goligi epithelial cells, Bergmann glia are unipolar astrocytes that have cell bodies located in the Purkinje cell layer and long processes projecting into the molecular layer. The Bergmann glia's processes interact with the dendrites of Purkinje cells at synapses with parallel and climbing fibers. Bergmann first characterized the long processes of cells he saw in the cerebellum of cats, dogs, and humans in 1857. Ramon y Cajal later described these cells as "epithelial cells with Bergmann fibers," giving the glia their name.[13]

Cerebellum Development


There are 3 germ layers present in the early embryo; ectoderm (most distal layer), mesoderm (middle layer) and endoderm (most proximal layer). The ectoderm differentiates into the nervous system, forming the spine, peripheral nerves, cerebrum and cerebellum. It also differentiates to form tooth enamel, epidermis, and the linings of the mouth, anus, sweat glands and nostrils.[14]

Figure 5: Diagram of a 2 Day Old Embryo Illustrating the Beginnings of Neural Development [15]

Neural Development

Neural development is one of the earliest systems to begin and the last to be completed after birth due to its highly complex structure. The first step in neural development occurs at the end of week 3 and involves the neural groove fusing to form the neural tube, which then folds to form the cranial and caudal region of the embryo, and ultimately form the cerebellum. There is a high chance of neural dysfunction and defects during the fetal neural development particularly due to the long development time frame and the need of certain nutrients such as folic acid to successfully close the tube. Neural tube defects (NTDs) such as spina bifida and anencephaly can arise if the tube does not close effectively.

Early Brain Vesicles

Primary Brain Vesicles

Primary Brain.png

Figure 6: (Week 4) 3 primary brain vesicles are formed; forebrain (prosencephalon) midbrain (mesencephalon), and hindbrain (rhombencephalon)[16]


Secondary brain vesicle.jpeg

Figure 7: (Week 5) 3 primary vesicles develop into 5 secondary vesicles [17];

  • Prosencephalon develops into telencephalon (which includes the endbrain and cerebral hemispheres) and diencephalon (located between the brain and forms an optic outgrowth)
  • Mesencephalon does not further develop into a secondary brain vesicle
  • Rhombencephalon develops into the metencephalon (behind the brain), and myelencephalon (contains medulla)


The metencephalon refers to the embryonic neural structure that eventually gives rise dorsally, to the cerebellum and ventrally, to the pons. The metencephalon is the anterior part of the rhombencephalon (hindbrain) and differentiates from the posterior part of the rhombencephalon (myencephalon) at week 5 of development.

The dorsal surface is characterised by its highly folded folia separated by grooves termed sulci. The median area is referred to as the vermis, which eventually becomes the most superior aspect of the cerebellum. [18] The first structure that belies the future cerebellum are the rhombic lips that appear on the metencephalon of a 5-6 week old embryo. The rhombic lips are aptly rhombus-shaped and denote the perimeter between the roof plate and the main body of the rhombencephalon. The anterior pair of lips mark the site at which the cerebellum will develop. [19]

Cerebellum Developmental Weeks

First Trimester

Week 3
Neurulation: Notochord and somites are formed under the ectoderm. The ectoderm then forms the neural plate which then forms the neural tube and then the brain and spinal chord.
Figure 8: Early stage of neurulation[20]
Figure 9: Late stages of neurulation[21]
Week 4
Prosencephalon, mesencephalon and rhombencephalon is developed.
Figure 10: Sagittal view of superior end of embryo [22]
Week 5
Prosencephalon develops into telencephalon and diencephalon. The rhombencephalon differentiates into metencephalon and myelencephalon. The metencephalon will later develop the pons and cerebellum.
Figure 11: Lateral view of embryo central nervous system at 5 weeks [23]
Week 6
A pair of thickenings on the lateral side of the alar plate is formed. This is called the rhombic lip.
Weeks 7-9
The rhombic lip is fused medially to the midbrain. The primitive choroid plexus is fused with the cerebellar hemisphere to form the centrally located eosinophilic matrix. During this process, the inferior olive develops into a thick medulla forming a 'bulbo-pontine extension' [24]. Development of cerebellum cell layer (future Purkinje cells) and choroid plexuses of the fourth and lateral ventricles [25].
Figure 12: Left lateral view of embryonic CNS[26]
Figure 13: Left medial view of lateral embryonic CNS [27]

Second Trimester

Figure 14: Inferior image of a fetal cerebellum at second trimester[28]

weeks 11-12
Cerebellar hemisphere grows in size and thickness. Laminar configuration becomes present and vermis fissures start to develop. Mechanical stress such as shear and rotation can be detected by the cerebellum, causing several deep fissures to be developed[24]
Weeks 15-16
Nodule and flocculus is developed. Several deep fissures are formed in the vermis which has increased in thickness similar to the hemispheres [24].
Figure 15: Cerebellar neuronal circuits (A): Representation of zebrafish cerebellar neurons (B): Sagittal section of the adult zebrafish cerebellum (C): Zebrafish cerebellar structure schematic representation.[29]
Figure 16: Cerebellum cell development: A 7 day old rat cerebellum that has been sectioned to show the 3 layers of cells - external granule layer, purkinje cells and internal granular layer (a). Showing granule cell precursors proliferating to differentiate into granule neurons (b). Cell organisation (c)[30]

Overview of Development

As the neural tube folds, the anterior portion develops the three brain vesicles:

  • Prosencephalon
  • Mesencephalon
  • Rhombencephalon

The rhombencephalon then further divides into the mesencephalic and myelincephalic vesicles on embryonic day 9. The neural tube failure to close then creates a gap along the dorsal sides and this produces a mouth-like structure as the tube bends to establish the pontine flexure. The pontine flexure further deepens bringing the mesencephalon (midbrain) closer to the primordium of the cerebellum (metencephalon); anterior aspects of the myelincephalon (brain stem) fold underneath developing the cerebellum plate[31]

The cerebellar territory is defined by the expression of Hoxa2 genes (from posterior) and Otx2 (from anterior) genes and these genes are controlled by proteins Wnt and fibroblast growth factor families which regulate the expression of these genes in order to establish the cerebellar territory[32]. Further development of the cerebellum begins between days 40 and 45 and it arises mostly from the metencephalon however the rhombic lips also contributes. The roof plate which is derived from the dorsal part of the alar plate thickens during development to become the cerebellum. The regulation of patterning involved when the primary fissure deepens by the end of the third month and thus divides the vermis, shows to be particularly important for development. The two lateral bulges are separated into the cranial anterior lob and caudal middle lobe. As the lobes divide further into lobules, fissures are formed and this continues throughout embryonic, fetal and postnatal life, thus increasing the surface area of the cerebellar cortex. The most primitive part of the cerebellum to form is the flocculonodular lobe, which is derived from separation of the first transverse fissure and this functions to keep connections with the vestibular system and it is also concerned with subconsciously controlling equilibrium. The flocculonodular lobe is separated from another crucial part of the cerebellum, corpus cerebelli, by the posterolateral fissure.

Overview of Cerebellar Cell Development

The cerebellum is connected to the brain stem via three pairs of peduncles and this allows the afferent and efferent pathways to enter and exit the cerebellum. Cerebellum afferent fibers can be grouped into two major types: mossy fibers and climbing fibres. Mossy fibres contribute to most of the afferent fibres in the cerebellum and they communicate with the cerebellar nuclei neurons and with Purkinje cells through granule cells embryonically, however postnatally they displace from Purkinje cells and synapse with their adult targets, the granule cell dendrites. Whilst mossy fibres originate from numerous sites in the nervous system, climbing fibers originate exclusively from the inferior olivary nucleus. Climbing fibers directly synapse with the cerebellar nuclei and Purkinje cells, relaying information to the cerebellum from several regions. The direction of these afferent fibres to their target neurons early in development are controlled by genes and molecules[33].

The cerebellum has a very basic structure consisting 2 principal classes of neurons and 3 layers; layers are shown in Figure 15.

  • Molecular Layer: consists of excitatory granular cell axons, purkinje cell dendritic fibres. stellate and basket cells.
  • Purkinje Cell Layer: consists of a single layer of inhibitory Purkinje cells.
  • Granular Cell Layer: Dense layer of excitatory granule cells, golgi cells and unipolar brush cells.

The granule cells receive inputs from outside the cerebellum and project these inputs to purkinje cells where the majority of these inputs are further projected to a variety of cerebellar nuclei in the white matter [34]. Within the layers there are some other main neuronal cell types, the stellate and basket cells are located in the molecular layer, whilst granule, golgi and unipolar brush cells are located in the granular layer [33]. Among these principal neurons, there is a diverse set of interneurons which are responsible for coordinating the output of the Purkinje cells to the cerebellar nuclei.

The nuclei from the cerebellum are formed by a complex process of neurogenesis and neuronal migration. The dorsomedial ventricular zone of the fourth ventricle gives rise to the principal neuronal output, the Purkinje cell and other neurons within the cerebellum The secondary germinal zone, coming from the adjacent rhombic lip generates the cerebellar granule cells as well as a subpopulation of neurons of cerebellar nuclei and several precerebellar nuclei [35]. Granule cells function in coordinating afferent input to and motor output from the cerebellum through excitatory connections with the Purkinje cell [32]. There are two types of grey matter in the cerebellum, the deep cerebellar nuclei and an external cerebellar cortex. There are 4 deep nuclei formed and the output of the cerebellar cortex are relayed through these nuclei, the ventricular layer produces 4 types of neurons that migrate to the cortex. Proper cerebellum function requires well-organised neuronal connections and the integration of afferent and efferent fibres throughout the cerebellar circuit [33]. The cerebellum functions in sensorimotor, balance control and vestibular ocular reflex, however recent studies have come out and shown that the cerebellum has a wide range of cognitive functions which include speech, memory and cognitive functions.[32]

Cellular Migration

Granule Cells

Granule cells migrate tangentially from the rhombic lip to form the transient structure, the external germinal layer (EGL). The EGL consists of an outer and inner layer that is sandwiched between the pia mater and the purkinje cell layer. During this tangential migration, granule cells extend two horizontal processes. Granule cells move from the outer layer of the EGL to differentiate in the inner layer of the EGL. Differentiated cells continue to move radially to the granule cell layer on the inner surface of the purkinje cell layer.[34] During radial migration, granule cells extend vertical processes and move through the purkinje cell layer on the radial processes of Bergmann glia.[36]

Purkinje Cells

Purkinje cells originate from the ventricular neuroepithelium and migrate radially towards the pial surface. Many studies have shown that purkinje cells use radial glia processes as a scaffold in this migration. The movement results in a 3 to 4 cell thick layer of purkinje cells beneath the EGL. This layer becomes 1 cell thick 1 week after birth.[37]

Granule Cell and Purkinje Cell Migration.png

Figure 17: Granule cell (yellow) and purkinje cell (green) migration timetable in mouse cerebellum. Top shows sagittal sections of entire cerebellum. Bottom shows movement of individual cells at interface of EGL and purkinje cell layer.[38]

Cell Signalling in Cerebellar Development

Figure 18: SHH (green) acts on EGL to stimulate proliferation, on Bergmann glia (B) to induce differentiation, and has an unknown function on purkinje cells (P). Laminin and heparan sulfate have a synergistic effect on SHH and fibronectin and vitronectin have an inhibitory effect on SHH.[39]

Proliferation in the EGL

Many different cell signalling pathways are involved with cell migration, proliferation, and differentiation in the cerebellum. Sonic hedgehog (SHH) is particularly important in the proliferation of granule cells in the external germinal layer. The external germinal layer (EGL) is the area of transit amplification of granule cell precursors. This layer is transient and lies on the external surface of the cerebellum until the cells differentiate and migrate radially to their final destination in the internal granule cell layer. SHH is secreted by the purkinje cells and acts locally, causing the granule cell precursors to undergo mitosis and Bergmann glia to differentiate. The autocrine function of SHH on the purkinje cells is unknown. [40] Proliferating cells in the EGL must also be positive for Atoh1, a transcription factor that represses differentiation and promotes division via SHH signalling. In a similar manner to SHH and Atoh1, the pia mater secretes Sdf1 which interacts with the receptor Cxcr4 to maintain proliferation in the EGL. Notch2 signalling and its stimulation of Atoh1 and repression of Bone Morphogenetic Protein (BMP).

Exit from the EGL

BMPs are involved in arresting granule cell proliferation in the EGL and stimulating differentiation.[41] Cells exit proliferation and move to the inner EGL where they differentiate upon expression of Neurod1 and interaction with the extracellular matrix components of the inner EGL, vitronectin, F3, and contactin.[34] Granule cell migration is stimulated by D-serine secreted by the Bergmann glia. This can be inhibited by DAAO or SR.[36]

Figure 19: Reelin is a large signalling molecule that initiates a signal transduction pathway to induce formation of a monolayer of purkinje cells and detach purkinje cells from radial glia.[42]

FGF and the Isthmus

Fibroblast Growth Factor (FGF) plays a role in allocating the isthmus area of the cerebellum. FGF8 is found in high concentrations in the rostral region of rhombomere 1 and decreased concentrations near the caudal region of rhombomere 1. It is necessary for the formation of the vermis of the cerebellum but the cerebellar hemispheres form independently of FGF8.[34]

Reelin and purkinje cells

Reelin is an important signalling molecule that plays a role in many different in the developing brain. Reelin is a glycoprotein secreted by cells in the EGL and rhombic lip and affects purkinje cells through a signal transduction pathway involving receptors VLDLR and ApoER2, adaptor protein Dab1, and many other further downstream intracellular signalling molecules. Reelin has shown to play a role in formation of the monolayer of purkinje cells and detachment of purkinje cells from radial glia. It may also affect other cell morphology and migration in the cerebellum.[43]

Transcription factors

The region of rhombomere 1, a segment of the metencephalon that forms the cerebellum, is bound by the expression of the transcription factors Hoxa2 and Otx2.  Otx2 is expressed in the midbrain and the lack of Otx2 marks the rostral border of the cerebellar primordium.  Hoxa2 is expressed in the hindbrain region and lack of Hoxa2 marks the caudal border of the cerebellar primordium.[41]

Key Historical Discoveries

Early 1500s
Galen, Vesalius and Varolio
Described the macroscopic anatomy of the cerebellum
Late 1700s
Luigi Rolando, Pierre Flourens, David Ferrier
Figure 20:Ferrier's findings on a monkey's cerebellum with stimulation points discovered[44]

Provided experimental evidence for the function of the cerebellum. Luigi Rolando identified a specifically motor impact after cerebellar lesions developed, as opposed to an intellectual or sensory effect. This led to the conclusion that the cerebellum incited and managed movement. Pierre Flourens, Luigi Luciani and David Ferrier were able to use this albeit crude experimentation to further define that the cerebellum coordinated movement instead of creating it, and also to differentiate between the short-term and long-term effects of cerebellar lesions, respectively.[45]

Early 1800s
Ernesto Lugaro
First defined "plasticity" as we know it in neuroscience, and also discovered the specific cells in the cerebellum that are named after him. He also furthered research into the functions of glia and defined "nervous conduction and transmission" in its current meaning.[46]
Early 1800s
Joseph Babinski and Gordon Holmes
Further defined the exact nature of the effect of cerebellar lesions on motor control, and found loss of coordination in antagonistic muscles and also basic loss of muscle control. It was also found that the side of the cerebellum the lesion developed on, affected the same side of the body.[45]
Mid 1800s
Ramon y Cajal
Figure 21: Drawing of Purkinje cells (A) and granule cells (B) from pigeon cerebellum. Drawn by Santiago Ramón y Cajal, 1899. [47]

Refuted Camillo Golgi's previous assertion that axons and dendrites would fuse, and also delineated the differing types of cells, most importantly of which were the mossy and climbing fibers of the cerebellum. However, this contribution could not be fully utilised until further technology was developed.

Olof Larsell
Developing a standard nomenclature for cerebellar anatomy that eventually spread world-wide, and for conducting a series of studies that illuminated our understanding of the rhombencephalon. [48]
John Eccles and Janos Szentágothai
Figure 22: Modular organisation of the cerebellum purkinje fibers by Janos Szentágothai[49]

Pieced together the first complete map of the functional anatomy of the cerebellum and define the excitatory and inhibitory nature of each cell type provided by Cajal. Further discoveries into the relationships between cell synapses, cell natures, and the minutiae of their structures by Jan Voogd, Olov Oscarsson and David Armstrong around the 1970's defined the organisation of Purkinje cells into "a series of longitudinal parasagittal bands", the specificity of which explains the solely Purkinje-axon-output of the cerebellar cortex.[50] The current focus in research now leans towards connecting cerebellar function with learning, emotion and perception of time.

Animal Studies

Animal Models

The mouse model is a primary model organism in the study of cerebellum development, but organisms such as Drosophila (fruit fly), C. elegans (roundworm), Saccharomyces cerevisiae (Baker's yeast), cats, dogs, and cattle are also used in some types of diseases.[51] Looking at a variety of different of organisms' cerebellar development can elucidate the evolution of the cerebellum and further understanding of cerebellar constituents.[34]

Figure 23: The Isthmic Organizer (IsO; shown in yellow) forms at the boundary of the posterior midbrain and anterior hindbrain: the IsO secretes Fgf8 and other growth factors, and is essential for defining the regions of the neural plate that will become the posterior midbrain (shown in blue) and the cerebellum (CB; green). [52]

Isthmic Organiser

Throughout history there have been many investigations on the cerebellum and how it has developed through research involving chicken embryos and mice. As previously mentioned the neural plate closes to form the neural tubes which have anterior-posterior (AP) and dorsal-ventral (DV) axes. Earlier experiments involving chick-quail chimera suggested that the cerebellum was derived from both midbrain and hindbrain. However, through successive gene expression and fate mapping studies, it was discovered that the anterior-most rhombomere of the hindbrain is where the cerebellum is formed from [53]. Once the axes are formed the isthmic organiser (IsO) is formed which plays a vital role in establishing the anterior limit of the cerebellar territory. The IsO in other words is the mid-hindbrain boundary [54]. However, the IsO does not position itself without the help of transcription factors. Studies of mouse and chicken embryos have shown that two homeo domain-containing transcription factors Otx2 and Gbx2 have an important role in positioning the isthmic organiser [54]. Surgical movement of the isthmic tissue to more anterior or posterior regions of the neural tube of 10-somite stage chick embryos led to ectopic midbrain and cerebellar structures[53], indicating that where the IsO is placed is an important factor in establishing where the cerebellum positions.

Figure 24: Schematic of the cerebellar circuitry in zebrafish. PN: Purkinje neuron; E: Eurydendroid cell; G: Granule cell; S: Stellate cell. [55]

Cell Structures

The cellular structures in the cerebellum (including Purkinje cells and granule cells) have been investigated in various animal models. One animal model is the zebra fish which is a bony fish (teleosts). Like mammals, the zebrafish cerebellum contains several types of neurons which function as either excitatory or inhibitory neurons [54]. Glutamate is utilised by excitatory neurons as their major neurotransmitter. Excitatory neurons include granule cells, unipolar brush cells and eurydendroid cells. The eurydendoid cells are predicted to be corresponding to the deep cerebellar neurons in mammals.[54] The inhibitory neurons use y-aminobutric acid (GABA) and/or glycine (also known as GABAergic neurons) for neurotransmission. Purkinje cells, Golgi and stellate cells are inhibitory neurons. However, a difference between mammal and teleosts is the lack of basket cells. Basket cells are GABAergic neurons that contribute project their axons to the Purkinje cells [54]. This is important, because as earlier highlighted Purkinje cells (inhibitory neurons) and granule cells (excitatory cells) contribute to the three cortical layers of the cerebellum. This model is important for understanding what structures contribute to the neurotransmission process in the cerebellum.


Abnormalities found within the posterior fossa of the cranium may affect the functioning and development of the cerebellum. The abnormalities affecting the cerebellum include Dandy-Walker-Malformation, Joubert Syndrome, Tecto-Cerebllar Dysraphism, Rhombencephalosynapsis and Medulloblastoma which will be explained in the table below.

Brain Imaging
Dandy-Walker Malformation
Dandy-Walker-Malformation (DWM) includes the incomplete development of the cerebellar vermis with cystic dilatation of the 4th ventricle and enlargement of the posterior fossa [56]. The cerebellar vermis (found at the medial, cortico-nuclear zone of the cerebellum[57]) may either be elevated or rotated upwards [56]. The communication of the 4th ventricle with the midline posterior fossa cyst can be seen on MRI scans of DWM [56]. Other structures that can be identified on MRI scans include upward displacement of the tentorium and anterolateral shift of cerebellar hemispheres [58]. The causes of DWM are still being researched and hence there has not been any clear causes. However, some causes include maternal diabetes, chromosomal defects that affect foetal brain development, infections in the mother that pass to the developing foetus and exposure of the unborn baby to certain toxins.[59] Symptoms of DWM include motor and speaking development delays, poor muscle coordination, vision and hearing impairment.[59]
Figure 25: Brain MRIs. Brain imaging of patients with Dandy-Walker malformation (CCM067, CCM095) and patients with normal cerebellum and posterior fossa (CCM001). A: sagittal midline T1-weighted images. B: axial T2-weighted images. [60]
Joubert Syndrome
Joubert syndrome (JS) is described as a rare inherited genetic disorder characterised by lack of muscle coordination, intellectual disability, respiratory disturbances and abnormal eye movement [61]. On neuroimaging, the cerebellar vermis is identified to have gone through hypoplasia (underdevelopment) or dysplasia (abnormal development) [56]. It is also described as the "molar tooth sign" on brain imaging, which the "molar tooth" shaped is caused by the defects in the midbrain-hindbrain development. JS is inherited as mutations in any of many genes, however, how mutations lead to JS is still being investigated. Mutations cause problems in the structure and function of cilia and hence signalling pathways may be disrupted during development [62].
Figure 26: Brain Imaging of Joubert Syndrome: Cranial MRI showing “molar tooth sign” (arrows)[63]
Chiari Syndrome I-III
Chiari Syndrome I-III is when the structures within the posterior cranial fossa protrude into the spinal canal [64] which can affect the development and functioning of the cerebellum in the long term. Chiari Syndrome can be classified into four types. The downward shift of the cerebellar tonsils to beneath the foramen magnum is type 1 and the downward movement of the vermis, medulla oblongata and pons with the fourth ventricle is type 2 [64]. When majority of the cerebellum lies in the foramen magnum it is type 3 and when it is completely in the foramen magnum (and therefore cannot develop normally) it is type 4[64]. As a result of genetic mutations or maternal diet lacking vitamins or nutrients, structural defects in the brain and spinal cord can occur during foetal development leading to Chiari Syndrome [65]
Figure 27: Cerebellar tonsils herniation on magnetic resonance imaging: Chiari malformation type I[66]
Rhombencephalosynapsis is a rare cerebellar defect whereby there is dorsal fusion of the cerebral hemispheres, fusion of dentate nuclei and superior cerebellar peduncles as well as the agenesis of the cerebella vermis [67]. Rhombencephalosynapsis is predicted to result from disturbed cerebellar development at approximately 33–34 days of gestation [68]. The cause of rhombencephalosynapsis is thought to be a genetic defect in the isthmic organizer, resulting in abnormal dorsal patterning, causing the mentioned defects [68]. Like other mentioned abnormalities there is development delay because of the underdeveloped cerebellum. Rhombencephalosynapsis can be identified from a range of symptoms, from involuntary muscle coordination, severe cerebral palsy or mental retardation[69].
Figure 28: Partial Rhombencephalosynapsis with fused upper parts of the cerebellum[70]
Medulloblastoma is a type of paediatric cancer of the cerebellum that occurs due to an over-proliferation of granule cell precursors in the External Germinal Layer. These frequently occur from an activation in SHH and Wnt pathways, disrupting the normal transient proliferation in the EGL. Therapies that promote differentiation of granule cells from the granule cell precursors in the EGL such as BMPs have shown to mitigate the disease [34]. Symptoms include headaches, nausea, vomit, tiredness, tilting the head to one side, difficulty in walking and balancing and problems with other motor skills. However these symptoms vary from patient to patient [71].
Figure 29: Brain magnetic resonance imaging of pediatric medulloblastomas: ( a) sagittal post-gadolinium WNT tumor; ( b) axial T2 of a SHH tumor. Red arrows delineate the tumor/leptomeningeal disease.[72]

Current Research

Emotional memory in depression

Figure 30: In this image you can see differences between the two groups of gray matter density in the cerebellar subregions. Cool color: decreased gray matter density in depression; Warm color: increased gray matter density in depression. [73]

Past investigations have concluded that damage to the posterior lobule of the cerebellum can cause individuals to show changes in manner or emotional instability, similar to a degree of depression or psychosis, without an outward cerebellar motor syndrome[74]. This is highly suggestive of the cerebellum's role in emotional memory despite its involvement with motor control. Patients with Major Depressive Disorder (MDD) display a tendency to only selectively recall aspects of scenarios that match their moods, conforming with the "mood-congruent memory (MCM)" theory [75]. This study was undertaken with that principle in mind, and investigated the depth of cerebellar involvement in emotional memory in depression. A link between the volume and density of cerebellar gray matter with measurements of emotional memory was hypothesised.

The experiment was conducted between patients with Major Depressive Disorder (MDD) and healthy controls (HCs)[76]. Patients with MDD displayed an atrophy in both gray matter and white matter, most severely in the posterior lobule. There was a significant impairment in emotional memory and decreased volume of the cerebellum in both anterior and posterior lobules. There was marked abnormalities in cortical density, but only a reduction in volume was found to be associated with decreased emotional memory. The severity of depressive symptoms correlated with both volume and density reduction in the grey matter. The posterior, anterior and flocculonodular lobes of patients with MDD displayed marked structural differences from the healthy controls, and a functional connectivity between lobules VI and VII of the cerebellum and the cerebrum could indicate that the decreased density in the lobules of MDD patients contributes to alterations in this connectivity. The flocculonodular lobe is especially implicated in MDD. The lobe is associated with vestibular regulation; Soza and Aviles (2007)[77] found that patients who experienced vestibular vertigo also experienced depressive symptoms. This study also determined that patients who experienced depression also experienced bouts of dizziness. Thus, an unprecedentedly widespread area of the cerebellum is displayed to be connected with emotional memory, in particular, with positive or negative memory retention and could lead towards a cure for depression.


Figure 31: Direct comparison of dystonia scores for animals with torsinA knockdown in the cerebellum alone (TorsinA CB, N = 20) compared with mice with knockdown in the cerebellum and basal ganglia (TorsinA CB+BG, N = 3) at three representative time points; 3 weeks, 11 weeks , and 13 weeks post-injection. There wasn't a significant difference in dystonia score between mice with torsinA knockdown in the cerebellum alone compared to those with knockdown in the cerebellum and basal ganglia [78]

This investigation into a potential link between dystonia -a disorder where muscles contract involuntarily- and the cerebellum attempts to delineate its pathophysiological role in the disease [79] . The main concern is that the etiology of dystonia appears to be extremely varied, and as such, unpredictable. There is no significant neural degeneration, but in secondary cases there may be structural lesions present in tissue which could be areas of pathophysiology in dystonia [80]. Dystonia may manifest itself in almost any body part, indicating that the neural area responsible most likely must not be very specific. This in combination with the involuntary nature of dystonia seems to indicate that the cerebellum is the more than likely involved in the disease.

Basal ganglia abnormalities are hinted to be a causative agent in dystonia.[81]. The gap in the knowledge of the true interactions between basal ganglia and the cerebellum with regards to dystonia have led to a hypothesis; that the difference in basal ganglia malfunctioning versus abnormal interaction between the ganglia and the cerebellum could reflect the heterogenous pathophysiology of dystonia; either primary or secondary. Some experimental evidence currently available implies that cerebellar dysfunction could affect the topographic distribution of the symptoms of dystonia, and therefore further research is warranted to investigate the full depth of basal ganglia involvement in the disease.

Adaptation to Delayed Action Effects

Figure 32: In real stimulation, a considerable increase in pre-stimulus low-frequency activity is only found in the right cerebellar hemisphere (near to the stimulation site). But in sham stimulation, pre-stimulus low-frequency activity increases in both the right cerebellar hemisphere and cerebellar vermis.[82].

Sensory attenuation refers to when individuals filters unnecessary information. When there is a perturbation between actions and the following-sound, the sensory attenuation is reduced [82]. An example of perturbation is when there is a delay when an individual presses a button with sound immediately expected, but instead the sound is delayed. Sensory attenuation can be further described by the forward model theory. The forward model theory suggests that predictions for sensory consequences (for example, sound that is heard) are made simultaneously with the motor movement[82]. Predictions and real sensory input (what really happens), after the sound delay is conducted, are compared in the model. If the prediction and real sensory input do not matchup, sensory attenuation is observed. The prediction errors are then relayed to other brain areas for further processing[82].

The process of sensory attenuation usually re-emerges after the disruption to the normal mechanism [82]. The re-emerging of this is a process of either correcting previous predictions or updating initial forward models to minimise prediction errors. The cerebellum is currently being researched on how it plays an important role in updating the forward model within the brain[82]. One investigation seeks to find evidence on the involvement of the cerebellum in learning to predict the unexpected delays. This investigation has found that low-frequency activity in the cerebellum, prior to the stimulation, plays a key role in adapting to the delayed stimulus [82].


Figure 33: Nissl staining showing the dopamine receptor expression within the cerebellum of a songbird [83]

The cerebellum has only recently been suspected to be involved in addictive behaviour, as some arguments provided for the initiation of research into the cerebellar role on addiction[84]. The cerebellum is shown to be intrinsically linked with dopamine release and reception[85]; with dopamine being the main hormone on which addiction is predicated, it is likely that the cerebellum could influence the response to the addictive stimuli. It has also been established that addictive drugs cause specific molecular mechanisms, changes in synapse plasticity[86], and influence intracellular transduction pathways as well as gene expression in the cerebellum[87]. The specificity of the drugs in targeting the cerebellum could highlight the link between the affected organ and addictive behaviour. Addictive drugs such as cocaine have been demonstrated to produce a behavioral sensitivity in mice, and an associated change in cerebellar plasticity. The change of the morphology of Purkinje cells and synaptic terminals in the mice most likely contributed to the difference in reception of the drug[88]. However, this link has not yet been fully investigated.

Future Questions

Although there are numerous articles and ongoing research on the cerebellum, there are still investigations yet to be performed. Some questions that could be answered in future research include:

  • Is the cerebellum size related to human intelligence?
  • Does the p53 gene function in cerebellum development? If so, does this function relate to the development of embryonic cancers? [89]
  • What changes in cerebellum development lead to the social impairments seen in those with Autism Spectrum Disorder?[90]
  • Do we need the cerebellum to actually function and survive?


  • ApoER2 – Works with VLDLR and is a very important receptor in the brain affecting neuronal function and development.
  • Basket cells– multipolar GABAergic interneurons. They are located on different regions of the brain and cerebellum. They function in making inhibitory synapses and control the overall potential of target cells.
  • Bergmann Glia – they are a type of radial astrocyte, cell bodies are in the Purkinje cell layer of the cerebellum.
  • Cerebellar nuclei – These cells receive inhibitory inputs from the purkinje cells, and excitatory inputs from mossy and climbing fibres.
  • Climbing fibres – provide excitatory input to the cerebellum, they have a crucial role in motor behaviors. Axons pass through the pons, then synapse with the deep cerebellar nuclei and purkinje cells.
  • Deep nuclei cells – Purkinje cells project to the deep nuclei cells and these are the only form of output cell in the cerebellar cortex. They also receive excitatory inputs from the mossy and climbing fibers.
  • Dendrites – an extension of a nerve cell, impulses travel along these extensions and they synapse at another cell body.
  • Dopamine – neurotransmitter and a precursor of substances including adrenaline.
  • Eurydendoid cells – cerebellar efferent neurons.
  • Flocculonodular lobe – lobe of the cerebellum that consists of a nodule and the flocculus. It is located on the anteroinferior surface of the cerebellum.
  • Glia cells – They are nonneuronal cells and they support cells and they surround neurons and insulate them, there are many types of glia cells: oligodendrocytes, ependymal cells, astrocytes, Schwann cells etc.
  • Granule cells – are small neurons, and they are the most numerous in the brain. They are packed in a thick layer of the cerebellar cortex and emit only 4 or 5 dendrites. They receive all input from mossy fibres.
  • Hoxa2 – a gene that encodes for a transcription factor which could be involved in the development of the positioning of the hindbrain.
  • Mossy fibres – major input of the cerebellum, relays sensory information from the pons to the granule cells and then sent to the purkinje cells for processing.
  • Neural tube – a hollow prenatal structure that forms the brain and spinal cord. Formed by the folding and fusion of the opposite ectodermal folds.
  • Otx2 – a protein that is involved with defining the layers and regions of the cerebral cortex and cerebellum.
  • Perturbation – (In the context of the Current Research) alternation to the normal mechanism that would happen in response to a stimulation
  • Plasticity – the brains ability to change at any age.
  • Pons – a part of the brain that links the medulla oblongata and the thalamus.
  • Purkinje cells – a class of GABAnergic neurons that are located in the cortex of the cerebellum, they are large, branched cells.
  • Stellate cells – in the cerebellum, they are located in the molecular layer and they synapse onto purkinje cells.
  • Tentorium – fold of the dura mater forming division between cerebrum and cerebellum.
  • VLDLR – Very-low-density-lipoprotein receptor, it’s a transmembrane lipoprotein receptor
  • Vermis – rounded and elongated section of the central part of cerebellum, lies between the two hemispheres.
  • Vetrobrobasilar System – consists of the two vertebral arteries and one basilar artery and these are located towards the back of the brain. Provide around 20% of the intracranial bloody supply.

Glossary Links

Glossary: A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z | Numbers | Symbols | Term Link


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