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Danse-thérapie et Parkinson - Exploration (Accueil)

Index « AbsEn.i » - entrée « genetic »
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genesis < genetic < genetically  Facettes :

List of bibliographic references indexed by genetic

Number of relevant bibliographic references: 16.
Ident.Authors (with country if any)Title
000025 (2015) Levente Szalárdy [Hongrie] ; Dénes Zádori [Hongrie] ; Péter Klivényi [Hongrie] ; J Zsef Toldi [Hongrie] ; Lászl Vécsei [Hongrie]Electron Transport Disturbances and Neurodegeneration: From Albert Szent-Györgyi's Concept (Szeged) till Novel Approaches to Boost Mitochondrial Bioenergetics
000049 (2014) Carlos Cepeda [États-Unis] ; Kerry P. S. Murphy [Royaume-Uni] ; Martin Parent [Canada] ; Michael S. Levine [États-Unis]The Role of Dopamine in Huntington’s Disease
000091 (2013) Jean-Marc BurgunderRecent advances in the management of choreas
000104 (2013) Jane Y. Chen ; Elizabeth A. Wang ; Carlos Cepeda ; Michael S. LevineDopamine imbalance in Huntington's disease: a mechanism for the lack of behavioral flexibility
000149 (2012) Richard Mayeux ; Yaakov SternEpidemiology of Alzheimer Disease
000156 (2012) David K. C. CooperA brief history of cross-species organ transplantation
000213 (2011) Adele DiamondBiological and social influences on cognitive control processes dependent on prefrontal cortex
000218 (2011) Yi Guo [République populaire de Chine] ; Wei-Dong Le [États-Unis] ; Joseph Jankovic [États-Unis] ; Hua-Rong Yang [République populaire de Chine] ; Hong-Bo Xu [République populaire de Chine] ; Wen-Jie Xie [États-Unis] ; Zhi Song [République populaire de Chine] ; Hao Deng [République populaire de Chine, États-Unis]Systematic genetic analysis of the PITX3 gene in patients with Parkinson disease
000241 (2010) Shreya Mitra ; Kwai W. Cheng ; Gordon B. MillsRab GTPases implicated in inherited and acquired disorders
000263 (2010) Program: Twenty Fourth Annual Symposium on Etiology, Pathogenesis, and Treatment of Parkinson's Disease and Other Movement Disorders
000272 (2009) Benjamin Bereznai [Hongrie] ; Mária Judit Molnar[Genetics and present therapy options in Parkinson's disease: a review].
000297 (2009) Sascha Hering [Autriche] ; Clemens Achmüller [Autriche] ; Andrea Köhler [Autriche] ; Werner Poewe [Autriche] ; Raine Schneider [Autriche] ; Sylvia M. Boesch [Autriche]Phenotype variability in spinocerebellar ataxia type 2: A longitudinal family survey and a case featuring an unusual benign course of disease
000367 (2005) A. WrightNeurogenetics II: complex disorders
000414 (2000) Mary M. Robertson [Royaume-Uni]Tourette syndrome, associated conditions and the complexities of treatment
000425 (1998) S. Frame ; R. Crombie ; J. Liddell ; D. Stuart ; S. Linardopoulos ; H. Nagase ; G. Portella ; K. Brown ; A. Street ; R. Akhurst ; A. BalmainEpithelial carcinogenesis in the mouse: correlating the genetics and the biology.
000474 (1991) G. Maraganore [Royaume-Uni, États-Unis] ; A. E. Harding [Royaume-Uni] ; C. D. Marsden [Royaume-Uni]A clinical and genetic study of familial Parkinson's disease

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