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Movement Disorders (revue) - Merge (PascalFrancis)

Index « FA11s1.i » - entrée « HOULDEN (Henry) »
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HOUGHTON (William H.) < HOULDEN (Henry) < HOULE (Sylvain)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 9.
Ident.Authors (with country if any)Title
002164 (2010) Joyce Van De Leemput ; Fabienne Wavrant-De Vrieze ; Ian Rafferty ; Jose M. Bras ; Paola Giunti ; Elizabeth Mc Fisher ; John A. Hardy ; Andrew B. Singleton ; Henry HouldenSequencing Analysis of the ITPR1 Gene in a Pure Autosomal Dominant Spinocerebellar Ataxia Series
002254 (2010) Susanne A. Schneider ; Coro Paisan-Ruiz ; Niall P. Quinn ; Andrew J. Lees ; Henry Houlden ; John Hardy ; Kailash P. BhatiaATP13A2 Mutations (PARK9) Cause Neurodegeneration with Brain Iron Accumulation
002324 (2010) Annu Aggarwal ; Susanne A. Schneider ; Henry Houlden ; Monty Silverdale ; Reema Paudel ; Coro Paisan-Ruiz ; Shrinivas Desai ; Mihir Munshi ; Darshana Sanghvi ; John Hardy ; Kailash P. Bhatia ; Mohit BhattIndian-Subcontinent NBIA: Unusual Phenotypes, Novel PANK2 Mutations, and Undetermined Genetic Forms
002390 (2010) Coro Paisan-Ruiz ; Rocio Guevara ; Monica Federoff ; Hasmet Hanagasi ; Fardaz Sina ; Elahe Elahi ; Susanne A. Schneider ; Petra Schwingenschuh ; Nin Bajaj ; Murat Emre ; Andrew B. Singleton ; John Hardy ; Kailash P. Bhatia ; Sebastian Brandner ; Andrew J. Lees ; Henry HouldenEarly-Onset L-dopa-Responsive Parkinsonism with Pyramidal Signs Due to ATP13A2, PLA2G6, FBX07 and Spatacsin Mutations
002452 (2010) Marianne J. U. Novak ; Mary G. Sweeney ; Abi Li ; Colm Treacy ; Hoskote S. Chandrashekar ; Paola Giunti ; Robert G. Goold ; Mary B. Davis ; Henry Houlden ; Sarah J. TabriziAn ITPR1 Gene Deletion Causes Spinocerebellar Ataxia 15/16: A Genetic, Clinical and Radiological Description
002918 (2011) Katrina Gwinn ; Michael J. Devine ; Lee-Way Jin ; Janel Johnson ; Thomas Bird ; Manfred Muenter ; Cheryl Waters ; Charles H. Adler ; Richard Caselli ; Henry Houlden ; Grisel Lopez ; Amanda Singleton ; John Hardy ; Andrew SingletonClinical Features, with Video Documentation, of the Original Familial Lewy Body Parkinsonism Caused By α-Synuclein Triplication (Iowa Kindred)
002A97 (2012) Núria Seto-Salvia ; Javier Pagonabarraga ; Henry Houlden ; Berta Pascual-Sedano ; Oriol Dols-Icardo ; Arianna Tucci ; Coro Paisan-Ruiz ; Antonia Campolongo ; Sofia Anton-Aguirre ; Inés Martin ; Laia Munoz ; Enric Bufill ; Lluïsa Vilageliu ; Daniel Grinberg ; M Nica Cozar ; Rafael Blesa ; Alberto Lleo ; John Hardy ; Jaime Kulisevsky ; Jordi ClarimonGlucocerebrosidase Mutations Confer a Greater Risk of Dementia during Parkinson's Disease Course
002C21 (2012) Georgia Xiromerisiou ; Henry Houlden ; Nikolaos Scarmeas ; Maria Stamelou ; Eleanna Kara ; John Hardy ; Andrew J. Lees ; Prasad Korlipara ; Patricia Limousin ; Reema Paudel ; Georgios M. Hadjigeorgiou ; Kailash P. BhatiaTHAP1 Mutations And Dystonia Phenotypes: Genotype Phenotype Correlations
002D05 (2012) Maja Kojovic ; Una-Marie Sheerin ; Ignacio Rubio-Agusti ; Anirban Saha ; Jose Bras ; Vaneesha Gibbons ; Rodger Palmer ; Henry Houlden ; John Hardy ; Nicholas W. Wood ; Kailash P. BhatiaYoung-Onset Parkinsonism due to Homozygous Duplication of α-Synuclein in a Consanguineous Family

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