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Index « FA11s1.i » - entrée « SINGLETON (Andrew) »
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SINGLETON (Andrew B.) < SINGLETON (Andrew) < SINGMANEESAKULCHAI (Surat)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 20.
Ident.Authors (with country if any)Title
000494 (2002) Virgilio Gerald H. Evidente ; Katrina Gwinn-Hardy ; John Hardy ; Dena Hernandez ; Andrew SingletonX-linked dystonia ("Lubag") presenting predominantly with parkinsonism: A more benign phenotype?
000687 (2002) S. H. Subramony ; Dena Hernandez ; Amanda Adam ; Stephanie Smith-Jefferson ; Jennifer Hussey ; Katrina Gwinn-Hardy ; Timothy Lynch ; Olga Mcdaniel ; John Hardy ; Matt Farrer ; Andrew SingletonEthnic differences in the expression of neurodegenerative disease: Machado-Joseph disease in Africans and Caucasians
000727 (2002) Virgilio Gerald H. Evidente ; Joel Advincula ; Raymund Esteban ; Paul Pasco ; Jhoe Anthony Alfon ; Filipinas F. Natividad ; Joven Cuanang ; Amado San Luis ; Katrina Gwinn-Hardy ; John Hardy ; Dena Hernandez ; Andrew SingletonPhenomenology of "Lubag" or X-linked dystonia-parkinsonism
000B58 (2004) Michiko K. Bruno ; Bernard Ravina ; Gaetan Garraux ; Mark Hallett ; Louis Ptacek ; Amanda Singleton ; Janel Johnson ; Andrew Singleton ; Melissa Hanson ; Elaine Considine ; Katrina Gwinn-HardyExercise-induced dystonia as a preceding symptom of familial Parkinson's disease
000C03 (2004) Okan Dogu ; Janel Johnson ; Dena Hernandez ; Melissa Hanson ; John Hardy ; Hulya Apaydin ; Sibel Özekmekci ; Serhan Sevim ; Katrina Gwinn-Hardy ; Andrew SingletonA consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletion
000C15 (2004) Lorraine N. Clark ; Shehla Afridi ; Helen Mejia-Santana ; Juliette Harris ; Elan D. Louis ; Lucien J. Cote ; Howard Andrews ; Andrew Singleton ; Fabienne Wavrant De-Vrieze ; John Hardy ; Richard Mayeux ; Stanley Fahn ; Cheryl Waters ; Blair Ford ; Steven Frucht ; Ruth Ottman ; Karen MarderAnalysis of an early-onset Parkinson's disease cohort for DJ-1 mutations
000E17 (2005) Naheed L. Khan ; Wagner Horta ; Louise Eunson ; Elizabeth Graham ; Janel O. Johnson ; SHANNON CHANG ; Mary Davis ; Andrew Singleton ; Nicholas W. Wood ; Andrew J. LeesParkin disease in a brazilian kindred : Manifesting heterozygotes and clinical follow-up over 10 years
000E85 (2005) Jordi Clarimon ; Janel Johnson ; Ruth Djaldetti ; Dena Hernandez ; Nobutaka Hattori ; Hava Sroka ; Yael Barhom ; Andrew SingletonMutation of the parkin gene in a persian family : Clinical progression over a 40-year period
001097 (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 HardyTaiwanese cases of SCA2 are derived from a single founder
001103 (2005) Jose Miguel Bras ; Rita Joao Guerreiro ; Maria Helena Ribeiro ; Cristina Januario ; Ana Morgadinho ; Catarina Resende Oliveira ; Luis Cunha ; John Hardy ; Andrew SingletonG2019S dardarin substitution is a common cause of parkinson's disease in a portuguese cohort
001150 (2006) Georgios M. Hadjigeorgiou ; Georgia Xiromerisiou ; Vanessa Gourbali ; Kostantinos Aggelakis ; Nikolaos Scarmeas ; Alexandros Papadimitriou ; Andrew SingletonAssociation of α-synuclein Rep1 polymorphism and parkinson's disease : Influence of Rep1 on age at onset
001211 (2006) Hon-Chung Fung ; Chiung-Mei Chen ; John Hardy ; Dena Hernandez ; Andrew Singleton ; Yih-Ru WuLack of G2019S LRRK2 mutation in a cohort of taiwanese with sporadic parkinson's disease
001496 (2007) Hasmet Ayhan Hanagasi ; Andrew Lees ; Janel O. Johnson ; Andrew Singleton ; Murat EmreSmoking-responsive juvenile-onset Parkinsonism
001948 (2008) Sarah Teixeira Camargos ; Francisco Cardoso ; Parastoo Momeni ; Juliana Gurgel Gianetti ; Andrew Lees ; John Hardy ; Andrew SingletonNovel GCH1 Mutation in a Brazilian Family with Dopa-Responsive Dystonia
001A84 (2008) Sonja Scholz ; Andrew SingletonSusceptibility Gènes in Movement Disorders
001B13 (2008) Rita Joao Guerreiro ; Isabel Santana ; Jose Miguel Bras ; Tamas Revesz ; Olinda Rebelo ; Maria Helena Ribeiro ; Beatriz Santiago ; Catarina Resende Oliveira ; Andrew Singleton ; John HardyNovel Progranulin Mutation : Screening for PGRN Mutations in a Portuguese Series of FTD/CBS Cases
001D87 (2009) Giovanni Defazio ; Mar Matarin ; Elizabeth L. Peckham ; Davide Martino ; Enza M. Valente ; Andrew Singleton ; Anthony Crawley ; Maria Stella Aniello ; Francesco Brancati ; Giovanni Abbruzzese ; Paolo Girlanda ; Paolo Livrea ; Mark Hallett ; Alfredo BerardelliThe TOR1A Polymorphism rsll82 and the Risk of Spread in Primary Blepharospasm
001D99 (2009) Sarah Teixeira Camargos ; Leonardo Oliveira Dornas ; Parastoo Momeni ; Andrew Lees ; John Hardy ; Andrew Singleton ; Francisco CardosoFamilial Parkinsonism and Early Onset Parkinson's Disease in a Brazilian Movement Disorders Clinic : Phenotypic Characterization and Frequency of SNCA, PRKN, PINK1, and LRRK2 Mutations
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)
002932 (2011) Michael J. Devine ; Katrina Gwinn ; Andrew Singleton ; John HardyParkinson's Disease and α-Synuclein Expression

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