List of bibliographic references indexed by Nerve Degeneration (genetics)
Number of relevant bibliographic references: 15.
Ident. | Authors (with country if any) | Title |
---|
000005 (2015) |
Andrew Singleton [États-Unis] | X-linked Parkinson's disease. |
000494 (2014) |
Geetanjali S. Rathore [États-Unis] ; Christian P. Schaaf ; Amber J. Stocco | Novel mutation of the WDR45 gene causing beta-propeller protein-associated neurodegeneration. |
000B48 (2013) |
Maria Stamelou [Royaume-Uni] ; Niall P. Quinn ; Kailash P. Bhatia | "Atypical" atypical parkinsonism: new genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy-a diagnostic guide. |
000F10 (2012) |
Rita Horvath [Royaume-Uni] ; Elke Holinski-Feder ; Vivienne C M. Neeve ; Angela Pyle ; Helen Griffin ; Deephthi Ashok ; Charlotte Foley ; Gavin Hudson ; Bernd Rautenstrauss ; Gudrun Nürnberg ; Peter Nürnberg ; Jörg Kortler ; Birgit Neitzel ; Ingelore B Ssmann ; Thahira Rahman ; Bernard Keavney ; John Loughlin ; Sophie Hambleton ; Benedikt Schoser ; Hanns Lochmüller ; Mauro Santibanez-Koref ; Patrick F. Chinnery | A new phenotype of brain iron accumulation with dystonia, optic atrophy, and peripheral neuropathy. |
001650 (2011) |
Zhenyu Yue [États-Unis] ; M. Lenard Lachenmayer [États-Unis, Allemagne] | Genetic LRRK2 models of Parkinson's disease: Dissecting the pathogenic pathway and exploring clinical applications |
001A40 (2010) |
Alisdair Mcneill [Royaume-Uni] | Response to: ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation |
001E75 (2010) |
Susanne A. Schneider [Royaume-Uni, Allemagne] ; Coro Paisan-Ruiz [Royaume-Uni] ; Niall P. Quinn [Royaume-Uni] ; Andrew Lees (neurologue) [Royaume-Uni] ; Henry Houlden [Royaume-Uni] ; John Hardy [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] | ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation |
003423 (2006) |
Angelo Antonini [Italie] ; Stefano Goldwurm [Italie] ; Riccardo Benti [Italie] ; Holger Prokisch [Allemagne] ; Monika Ebhardt [Allemagne] ; Roberto Cilia [Italie] ; Michela Zini [Italie] ; Andrea Righini [Italie] ; Giovanni Cossu [Italie] ; Gianni Pezzoli [Italie] | Genetic, clinical, and imaging characterization of one patient with late‐onset, slowly progressive, pantothenate kinase‐associated neurodegeneration |
003776 (2005) |
Tomaso Scaravilli [Italie] ; Eduardo Tolosa [Espagne] ; Isidre Ferrer [Espagne] | Progressive supranuclear palsy and corticobasal degeneration: Lumping versus splitting |
003888 (2005) |
Nadia Stefanova [Autriche] ; Markus Reindl [Autriche] ; Werner Poewe [Autriche] ; Gregor K. Wenning [Autriche] | In vitro models of multiple system atrophy |
005298 (1997) |
Tanya Stojkovic [France] ; Luc Defebvre [France] ; Xavier Quilliet ; Eric Eveno ; Alain Sarasin ; Mauro Mezzina ; Destée | Neurological manifestations in two related xeroderma pigmentosum group d patients: Complications of the late‐onset type of the juvenile form |
005366 (1997) |
M. W. Becher [Royaume-Uni] ; D. C. Rubinsztein [Royaume-Uni] ; J. Leggo [Royaume-Uni] ; M. V. Wagster [Royaume-Uni] ; O. C. Stine [Royaume-Uni] ; N. G. Ranen [Royaume-Uni] ; M. L. Franz [Royaume-Uni] ; M. H. Abbott [Royaume-Uni, États-Unis] ; M. Sherr [Royaume-Uni] ; J. C. Macmillan ; L. Barron [Royaume-Uni] ; M. Porteous [Royaume-Uni] ; P. S. Harper ; Ross [Royaume-Uni, États-Unis] | Dentatorubral and pallidoluysian atrophy (DRPLA) Clinical and neuropathological findings in genetically confirmed north american and european pedigrees |
005591 (1996) |
Taylor‐Robinson [Royaume-Uni] ; R. A. Weeks [Royaume-Uni] ; D. J. Bryant [Royaume-Uni] ; J. Sargentoni [Royaume-Uni] ; C. D. Marcus [Royaume-Uni] ; A. E. Harding [Royaume-Uni] ; D. J. Brooks [Royaume-Uni] | Proton magnetic resonance spectroscopy in Huntington's disease: Evidence in favour of the glutamate excitotoxic theory? |
005C15 (1994) |
T. T. Warner ; G. G. Lennox ; I. Janota [Royaume-Uni] ; Harding | Autosomal‐dominant dentatorubropallidoluysian atrophy in the United Kingdom |
006294 (1990) |
Wahnschaffe [Allemagne] ; Gabriele Fredow [Allemagne] ; Peter Heintz [Allemagne] ; Wolfgang Löscher [Allemagne] | Neuropathological studies in a mutant hamster model of paroxysmal dystonia |
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