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Movement Disorders (revue) - Curation (Ncbi)

Index « Keywords » - entrée « Genetic Markers »
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Genetic Loci (genetics) < Genetic Markers < Genetic Markers (genetics)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 19.
Ident.Authors (with country if any)Title
000091 (1999) C. Kamm [Allemagne] ; E. Castelon-Konkiewitz ; M. Naumann ; F. Heinen ; M. Brack ; A. Nebe ; A. Ceballos-Baumann ; T. GasserGAG deletion in the DYT1 gene in early limb-onset idiopathic torsion dystonia in Germany.
000350 (2000) A. Münchau [Royaume-Uni] ; E M Valente ; M B Davis ; V. Stinton ; N W Wood ; N P Quinn ; K P BhatiaA Yorkshire family with adult-onset cranio-cervical primary torsion dystonia.
000366 (2000) S N Illarioshkin [Russie] ; I A Ivanova-Smolenskaya ; R A Rahmonov ; E D Markova ; G. Stevanin ; A. BriceClinical and genetic study of familial essential tremor in an isolate of Northern Tajikistan.
000501 (2001) L I Golbe [États-Unis] ; A M Lazzarini ; J R Spychala ; W G Johnson ; E S Stenroos ; M H Mark ; J I SageThe tau A0 allele in Parkinson's disease.
000517 (2001) S. Bohlega [Arabie saoudite] ; A. Al-Tahan ; M. Kambouris ; M. DivakaranNeurodegenerative Huntington-like disorder.
000799 (2002) Pau Pastor [Espagne] ; Mario Ezquerra ; Eduardo Tolosa ; Esteban Mu Oz ; María José Martí ; Francesc Valldeoriola ; José Luís Molinuevo ; Matilde Calopa ; Rafael OlivaFurther extension of the H1 haplotype associated with progressive supranuclear palsy.
000911 (2002) S H Subramony [États-Unis] ; 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.
000A04 (2003) Giovanni Defazio [Italie] ; Francesco Brancati ; Enza Maria Valente ; Viviana Caputo ; Antonio Pizzuti ; Davide Martino ; Giovanni Abbruzzese ; Paolo Livrea ; Alfredo Berardelli ; Bruno DallapiccolaFamilial blepharospasm is inherited as an autosomal dominant trait and relates to a novel unassigned gene.
000A67 (2003) Eng-King Tan [Singapour] ; Yanni Tan ; Anthea Chai ; Christopher Tan ; Hui Shen ; Sau-Ying Lum ; Stephanie M C. Fook-Cheong ; Mei-Ling Teoh ; Yuan Yih ; Meng-Cheong Wong ; Yi ZhaoDopamine D2 receptor TaqIA and TaqIB polymorphisms in Parkinson's disease.
000E83 (2004) Christoph Kamm [États-Unis] ; Joanne Leung ; Soni Joseph ; William B. Dobyns ; Alison Brashear ; Xandra O. Breakefield ; Laurie J. OzeliusRefined linkage to the RDP/DYT12 locus on 19q13.2 and evaluation of GRIK5 as a candidate gene.
001024 (2004) Jacek Zaremba [Pologne] ; Hanna Mierzewska ; Zofia Lysiak ; Patricia Kramer ; Laurie J. Ozelius ; Allison BrashearRapid-onset dystonia-parkinsonism: a fourth family consistent with linkage to chromosome 19q13.
001282 (2005) Roongroj Bhidayasiri [États-Unis] ; Joanna C. Jen ; Robert W. BalohThree brothers with a very-late-onset writer's cramp.
001683 (2006) Florian D. Vogl [Italie] ; Irene Pichler ; Susanna Adel ; Gerd K. Pinggera ; Stefano Bracco ; Alessandro De Grandi ; Claudia Beu Volpato ; Paolo Aridon ; Thomas Mayer ; Thomas Meitinger ; Christine Klein ; Giorgio Casari ; Peter P. PramstallerRestless legs syndrome: epidemiological and clinicogenetic study in a South Tyrolean population isolate.
001970 (2007) David Kemlink [Allemagne] ; Olli Polo ; Pasquale Montagna ; Federica Provini ; Karin Stiasny-Kolster ; Wolfgang Oertel ; Al De Weerd ; Sona Nevsimalova ; Karel Sonka ; Birgit Högl ; Birgit Frauscher ; Werner Poewe [Autriche] ; Claudia Trenkwalder ; Peter P. Pramstaller ; Luigi Ferini-Strambi ; Marco Zucconi ; Eric Konofal ; Isabelle Arnulf ; Georgios M. Hadjigeorgiou ; Svenja Happe ; Christine Klein ; Anja Hiller ; Peter Lichtner ; Thomas Meitinger ; Betram Müller-Myshok ; Juliane WinkelmannFamily-based association study of the restless legs syndrome loci 2 and 3 in a European population.
001A28 (2007) Kristoffer Haugarvoll [États-Unis] ; Mathias Toft ; Owen A. Ross ; Jeremy T. Stone ; Michael G. Heckman ; Linda R. White ; Timothy Lynch ; John Mark Gibson ; Zbigniew K. Wszolek ; Ryan J. Uitti ; Jan O. Aasly ; Matthew J. FarrerELAVL4, PARK10, and the Celts.
003412 (2011) Robert A. Wilcox [Australie] ; Susen Winkler ; Katja Lohmann ; Christine KleinWhispering dysphonia in an Australian family (DYT4): a clinical and genetic reappraisal.
004580 (1988) V P Misra [Royaume-Uni] ; M. Baraitser ; A E HardingGenetic prediction in Huntington's disease: what are the limitations imposed by pedigree structure?
004E75 (1998) G. De Boo [Pays-Bas] ; A. Tibben ; J. Hermans ; A. Maat ; R A RoosSubtle involuntary movements are not reliable indicators of incipient Huntington's disease.
005084 (1998) J J Higgins [États-Unis] ; J M Loveless ; Joseph Jankovic [États-Unis] ; P I PatelEvidence that a gene for essential tremor maps to chromosome 2p in four families.

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