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Primary degenerative cerebellar ataxias in ethnic Bengalees in West Bengal: some observations, 12/2003
Seventy cases of primary degenerative cerebellar ataxias in ethnic Bengalees from southern West Bengal, India, were studied by the authors. Of these, 50 cases... 
Cerebellar ataxia, Autosomal recessive, Autosomal dominant, Ethnic variations
Journal
Case Report - Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL): A case report with review of literature, 01/2004
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) is an inherited arterial disease, commonly overlooked or... 
ni04025 Autosomal dominant arteriopathy, Subcortical dementia, Notch 3 gene | Neurology
Journal
2017, First edition., Human diseases and conditions collection, ISBN 9781944749743, xii, 71 pages
Book
Journal of Clinical Immunology, ISSN 0271-9142, 10/2018, Volume 38, Issue 7, pp. 739 - 741
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1007/s10875-018-0551-6 
SPORADIC MONOCYTOPENIA | AUTOSOMAL-DOMINANT | IMMUNOLOGY | Sarcoidosis
Journal Article
08/2008
Familial dyskeratotic comedones (FDC) is a rare autosomal dominant inherited condition, characterized by widespread, symmetrically scattered, comedone-like,... 
Autosomal dominant | Dyskeratosis | Familial dyskeratotic comedone | Comedone
Web Resource
Neurobiology of Aging, ISSN 0197-4580, 10/2019, Volume 82, pp. 40 - 47
The purpose was to compare longitudinal cognitive changes in and gene mutation carriers and noncarriers from four autosomal-dominant Alzheimer's disease (ADAD)... 
Autosomal dominant | APP | Cognition | Longitudinal | PSEN1 | Alzheimer's disease | Index Medicus
Journal Article
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, ISSN 0022-3565, 12/2015, Volume 355, Issue 3, pp. 397 - 409
Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are the most common genetic cause of familial and sporadic Parkinson's disease (PD). That the most... 
BRAIN PENETRANT | AUTOSOMAL-DOMINANT PARKINSONISM | GENE | DISEASE | PHARMACOLOGY & PHARMACY | HIGHLY POTENT | MUTATIONS | DISCOVERY
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 09/2019, Volume 404, pp. 16 - 18
Journal Article
REVISTA DE NEUROLOGIA, ISSN 0210-0010, 01/2017, Volume 64, Issue 1, pp. 45 - 47
Journal Article
Journal Article
Blood, ISSN 0006-4971, 06/2011, Volume 117, Issue 24, pp. 6406 - 6408
Journal Article
Academic Radiology, ISSN 1076-6332, 07/2018, Volume 25, Issue 7, pp. 850 - 855
Total kidney volume is an important biomarker for the evaluation of autosomal dominant polycystic kidney disease progression. In this study, we present a novel... 
computed tomography | Autosomal dominant polycystic kidney disease | kidney volume
Journal Article
Neuroscience Letters, ISSN 0304-3940, 12/2016, Volume 635, pp. 67 - 70
Amongst Parkinson's disease (PD) genetic factors, mutations in , , and genes are recognized causes of PD. Nonetheless, few genetic screenings have been... 
Autosomal dominant Parkinson’s disease | VPS35 | LRRK2 | Parkinson’s disease | GBA | SNCA
Journal Article
Ocular Immunology and Inflammation, ISSN 0927-3948, 07/2019, Volume 27, Issue 5, pp. 693 - 698
Purpose: We report two new CAPN5 mutations associated with a phenotype of Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy. Methods: We performed... 
UVEITIS | ADNIV | CALPAIN-5 | Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy | CAPN5
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 09/2010, Volume 30, Issue 39, pp. 13138 - 13149
Intraneuronal tau aggregations are distinctive pathological features of Parkinson's disease (PD) with autosomal-dominant mutations in leucine-rich repeat... 
ORGANIZATION | AUTOSOMAL-DOMINANT PARKINSONISM | MICROTUBULES | ALZHEIMERS-DISEASE | PROTEIN-KINASE | IN-VIVO | SITES | NEURODEGENERATION | DOPAMINERGIC-NEURONS | NEUROSCIENCES | DROSOPHILA
Journal Article
Korean Journal of Dermatology, ISSN 0494-4739, 02/2019, Volume 57, Issue 2, pp. 97 - 98
Journal Article
대한피부과학회지, ISSN 0494-4739, 2019, Volume 57, Issue 2, p. 97
Journal Article
Brain, ISSN 0006-8950, 10/2018, Volume 141, Issue 10, pp. 3065 - 3080
See Jacobs and Buckley (doi: 10.1093/brain/awy243 ) for a scientific commentary on this article. Despite the prevalence of white matter alterations in... 
white matter | diffusion tensor imaging | TREM2 | Alzheimer’s disease | autosomal dominant | Original
Journal Article
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