List of bibliographic references
Number of relevant bibliographic references: 34.
[0-20] [
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20-40]
| Ident. | Authors (with country if any) | Title |
|---|
| 000009 (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. Bhatia | Young-Onset Parkinsonism due to Homozygous Duplication of α-Synuclein in a Consanguineous Family |
| 000093 (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. Bhatia | THAP1 Mutations And Dystonia Phenotypes: Genotype Phenotype Correlations |
| 000217 (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 Clarimon | Glucocerebrosidase Mutations Confer a Greater Risk of Dementia during Parkinson's Disease Course |
| 000235 (2012) |
Alisdair Mcneill ; Raquel Duran ; Christos Proukakis ; Jose Bras ; Derralyn Hughes ; Atuhl Mehta ; John Hardy ; Nicholas W. Wood ; Anthony H. V. Schapira | Hyposmia and Cognitive Impairment in Gaucher Disease Patients and Carriers |
| 000309 (2012) |
Susanne A. Schneider ; John Hardy ; Kailash P. Bhatia | Syndromes of Neurodegeneration with Brain Iron Accumulation (NBIA): an Update on Clinical Presentations, Histological and Genetic Underpinnings, and Treatment Considerations |
| 000386 (2011) |
Michael J. Devine ; Katrina Gwinn ; Andrew Singleton ; John Hardy | Parkinson's Disease and α-Synuclein Expression |
| 000400 (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 Singleton | Clinical Features, with Video Documentation, of the Original Familial Lewy Body Parkinsonism Caused By α-Synuclein Triplication (Iowa Kindred) |
| 000569 (2011) |
Thomas Gasser ; John Hardy ; Yoshikuni Mizuno | Milestones in PD Genetics |
| 000929 (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 Houlden | Early-Onset L-dopa-Responsive Parkinsonism with Pyramidal Signs Due to ATP13A2, PLA2G6, FBX07 and Spatacsin Mutations |
| 000995 (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 Bhatt | Indian-Subcontinent NBIA: Unusual Phenotypes, Novel PANK2 Mutations, and Undetermined Genetic Forms |
| 000A65 (2010) |
Susanne A. Schneider ; Coro Paisan-Ruiz ; Niall P. Quinn ; Andrew J. Lees ; Henry Houlden ; John Hardy ; Kailash P. Bhatia | ATP13A2 Mutations (PARK9) Cause Neurodegeneration with Brain Iron Accumulation |
| 000D78 (2009) |
Susanne A. Schneider ; Coro Paisan-Ruiz ; Ines Garcia-Gorostiaga ; Niall P. Quinn ; Yvonne G. Weber ; Holger Lerche ; John Hardy ; Kailash P. Bhatia | GLUT1 Gene Mutations Cause Sporadic Paroxysmal Exercise-Induced Dyskinesias |
| 000F20 (2009) |
Sarah Teixeira Camargos ; Leonardo Oliveira Dornas ; Parastoo Momeni ; Andrew Lees ; John Hardy ; Andrew Singleton ; Francisco Cardoso | Familial Parkinsonism and Early Onset Parkinson's Disease in a Brazilian Movement Disorders Clinic : Phenotypic Characterization and Frequency of SNCA, PRKN, PINK1, and LRRK2 Mutations |
| 000F43 (2009) |
Susanne A. Schneider ; Kailash P. Bhatia ; John Hardy | Complicated Recessive Dystonia Parkinsonism Syndromes |
| 001206 (2008) |
Rita Joao Guerreiro ; Isabel Santana ; Jose Miguel Bras ; Tamas Revesz ; Olinda Rebelo ; Maria Helena Ribeiro ; Beatriz Santiago ; Catarina Resende Oliveira ; Andrew Singleton ; John Hardy | Novel Progranulin Mutation : Screening for PGRN Mutations in a Portuguese Series of FTD/CBS Cases |
| 001371 (2008) |
Sarah Teixeira Camargos ; Francisco Cardoso ; Parastoo Momeni ; Juliana Gurgel Gianetti ; Andrew Lees ; John Hardy ; Andrew Singleton | Novel GCH1 Mutation in a Brazilian Family with Dopa-Responsive Dystonia |
| 001A73 (2006) |
Liana Fidani ; Kallirhoe Kalinderi ; Sevasti Bostantjopoulou ; Jordi Clarimon ; Antonis Goulas ; Zoe Katsarou ; John Hardy ; Alexandros Kotsis | Association of the Tau haplotype with Parkinson's disease in the greek population |
| 001B10 (2006) |
Hon-Chung Fung ; Chiung-Mei Chen ; John Hardy ; Dena Hernandez ; Andrew Singleton ; Yih-Ru Wu | Lack of G2019S LRRK2 mutation in a cohort of taiwanese with sporadic parkinson's disease |
| 001C18 (2005) |
Jose Miguel Bras ; Rita Joao Guerreiro ; Maria Helena Ribeiro ; Cristina Januario ; Ana Morgadinho ; Catarina Resende Oliveira ; Luis Cunha ; John Hardy ; Andrew Singleton | G2019S dardarin substitution is a common cause of parkinson's disease in a portuguese cohort |
| 001C24 (2005) |
Parastoo Momeni ; Chin-Song Lu ; Yah-Huei Wu Chou ; Hsiu-Chen Chang ; Rou-Shayn Chen ; Chiung-Chu Chen ; Jin-Tian Hsu ; Andrew Singleton ; John Hardy | Taiwanese cases of SCA2 are derived from a single founder |
| 001D81 (2005) |
John Hardy ; Andrew J. Lees | Parkinson's disease : A broken nosology |
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