Uploads by Z3290379
From Embryology
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Date | Name | Thumbnail | Size | Description | Versions |
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15:02, 16 August 2011 | Stem cells neurospheres drived from Huntingtons Disease hippocampus.png (file) | 526 KB | Large stem cell-derived neurospheres were generated from 33-week old HD hippocampus, but not WT hippocampus. (A) Similar numbers of large (≥250 µm in diameter) hippocampal neurospheres were generated from HD (n = 4) and WT (n = 4) mice at 5 weeks of a | 1 | |
17:58, 10 September 2011 | Huntington Disease patient and control MRI.gif (file) | 139 KB | Figure samples of coronal and sagittal MR images showing outlines for caudate, putamen, cerebral and cerebellar volumes in a patient with Huntington’s disease (top) and a normal control (bottom). http://www.scielo.br/scielo.php?script=sci_arttext&pid=S | 1 | |
16:25, 11 September 2011 | HD patient with no treatment.mov (file) | 1.17 MB | Patient with Huntington's Disease Case 1 without valproic acid treatment http://www.biomedcentral.com/1471-2377/6/11 <ref><pubmed>16507108</pubmed></ref> ===References=== <references/> Attribution 2.0 Generic (CC BY 2.0) You are free to: - to Share | 1 | |
16:37, 16 September 2011 | SPECT scanner.jpg (file) | 161 KB | Some commercial preclinical SPECT systems. (a) A preclinical hybrid PET/SPECT device, the VECTor (Image courtesy of MI Labs), (b) Triumph Trimodality scanner (courtesy of Gamma Medica), (c) NanoSPECT (courtesy of BioScan, Inc), and (d) Inveon system (cour | 1 | |
16:33, 17 September 2011 | Huntington's disease MRI.jpg (file) | 163 KB | Modality: MRI Case Discussion: This patient with known Huntington's disease demonstrates marked atrophy of the caudate head bilaterally. Creative Commons Licence Under this license you may - copy contents and - alter / build upon it as long a | 1 | |
13:24, 18 September 2011 | Huntington disease atrophy 1.jpg (file) | 148 KB | ''Presentation:'' 50 year old male with movement disorder. ''Case Discussion:'' Note the marked focal atrophy of the caudate heads, consistent with the patient's known diagnosis of Huntington's disease. ''Modality:'' CT scan ''Creative Commons Licen | 1 | |
13:34, 18 September 2011 | Huntington disease atrophy 2.jpg (file) | 146 KB | 'Presentation:' 50 year old male with movement disorder. 'Case Discussion:' Note the marked focal atrophy of the caudate heads, consistent with the patient's known diagnosis of Huntington's disease. 'Creative Commons Licence' Under this license you m | 1 | |
13:39, 18 September 2011 | Huntington disease atrophy 3.jpg (file) | 144 KB | ''Presentation:'' 50 year old male with movement disorder. ''Case Discussion:'' Note the marked focal atrophy of the caudate heads, consistent with the patient's known diagnosis of Huntington's disease. ''Creative Commons Licence'' Under this license | 1 | |
14:23, 18 September 2011 | HD Interview questions.png (file) | 12 KB | '''Table 1''' Based on a review of the evidence, 7 interview questions assessing "Anger and Irritability" and 5 interview questions assessing "Obsessions and Compulsions" were developed for field testing (Table 1) '''Creative Commons Attribution 3.0 Un | 1 | |
14:25, 20 September 2011 | Neuroacanthocytosis.jpg (file) | 91 KB | '''Figure 2''' Coronal T2-weighted images showing features as described in Figure 1 (Figure 1 T2-weighted image is showing symmetrical hyperintense signal changes in anterior medial globus pallidus with surrounding hypointensity in the globus pallidus | 1 | |
15:06, 20 September 2011 | HD future research.jpg (file) | 78 KB | '''Culling out complex traits''' A consortium of international scientists is launching new mouse research initiatives to help elucidate genetic components of complex human diseases. Copyright This is an Open Access article: verbatim copying and redistri | 1 | |
16:54, 1 October 2011 | HD patients.jpg (file) | 52 KB | Fig 1. Phenotypically identical twins (A) and skull computed tomography showing head of caudate nucleus atrophy (B and C) Patients were female, 24 years-old when first examined, and phenotypically identical (Fig 1A). The onset of their disease, as report | 1 |