Movement Disorders (revue) - Corpus (Istex)

Index « Auteurs » - entrée « Andrew Singleton »
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Andrew Siegel < Andrew Singleton < Andrew Taylor  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 21.
[0-20] [0 - 20][0 - 21][20-20][20-40]
Ident.Authors (with country if any)Title
000B89 (2011) Michael J. Devine ; Katrina Gwinn ; Andrew Singleton ; John HardyParkinson's disease and α‐synuclein expression
001198 (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 rs1182 and the risk of spread in primary blepharospasm
001215 (2008) Sonja Scholz ; Andrew SingletonSusceptibility genes in movement disorders
001401 (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
001908 (2004) Okan Dogu ; Janel Johnson ; Dena Hernandez ; Melissa Hanson ; John Hardy ; Hulya Apaydin ; Sibel Özekmekçi ; Serhan Sevim ; Katrina Gwinn-Hardy ; Andrew SingletonA consanguineous Turkish family with early‐onset Parkinson's disease and an exon 4 parkin deletion
001A87 (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
001C76 (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
001E09 (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?
001E52 (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
001F34 (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
002311 (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)
002A78 (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
002C79 (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
002E17 (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
003566 (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
003577 (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
003578 (2007) Hasmet Ayhan Hanagasi ; Andrew Lees ; Janel O. Johnson ; Andrew Singleton ; Murat EmreSmoking‐responsive juvenile‐onset Parkinsonism
003713 (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
003745 (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
003C34 (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
004043 (2006) Michael J. Eblan ; Joann Nguyen ; Shira G. Ziegler ; Alicia Lwin ; Melissa Hanson ; Marisol Gallardo ; Roberto Weiser ; Marisel De Lucca ; Andrew Singleton ; Ellen SidranskyGlucocerebrosidase mutations are also found in subjects with early‐onset parkinsonism from Venezuela

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