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Movement Disorders (revue) - Curation (Ncbi)

Index « Keywords » - entrée « Genetic Markers (genetics) »
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Genetic Markers < Genetic Markers (genetics) < Genetic Predisposition to Disease  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 16.
Ident.Authors (with country if any)Title
000173 (1999) M G Sieberer [Allemagne] ; P. Vieregge ; C. Klein ; L J Ozelius ; K P WandingerConcordant late onset of craniocervical dystonia in a pair of monozygotic twins.
000736 (2002) Francesco Brancati [Italie] ; Giovanni Defazio ; Viviana Caputo ; Enza Maria Valente ; Antonio Pizzuti ; Paolo Livrea ; Alfredo Berardelli ; Bruno DallapiccolaNovel Italian family supports clinical and genetic heterogeneity of primary adult-onset torsion dystonia.
000831 (2002) Sian D. Spacey [Royaume-Uni] ; Enza-Maria Valente ; Gurusidheshwar M. Wali ; Thomas T. Warner ; Paul R. Jarman ; Anthony H V. Schapira ; Peter H. Dixon ; Mary B. Davis ; Kailash P. Bhatia ; Nicholas W. WoodGenetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD gene.
000850 (2002) Marina A J. Tijssen [Pays-Bas] ; Monique N. Vergouwe ; J Gert Van Dijk ; Michelle Rees ; Rune R. Frants ; Peter BrownMajor and minor form of hereditary hyperekplexia.
000930 (2002) David A. Grimes [Canada] ; J David Grimes ; Lem Racacho ; Kylie A. Scoggan ; Fabin Han ; Betty Anne Schwarz ; John Woulfe ; Dennise BulmanLarge French-Canadian family with Lewy body parkinsonism: exclusion of known loci.
000939 (2002) Virgilio Gerald H. Evidente [États-Unis] ; 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.
000A37 (2003) Saeed Bohlega [Arabie saoudite] ; Adel Al-Jishi ; Carol Dobson-Stone ; Luca Rampoldi ; Parthasarathi Saha ; Hatem Murad ; Abid Kareem ; George Roberts ; Anthony P. MonacoChorea-acanthocytosis: clinical and genetic findings in three families from the Arabian peninsula.
000C99 (2004) Jacob Appel ; Joseph H. FriedmanGenetic markers and the majority's right not to know.
001427 (2006) Paola Valentino [Italie] ; Grazia Annesi ; Innocenza C. Cir Candiano ; Ferdinanda Annesi ; Donatella Civitelli ; Patrizia Tarantino ; Francesco Naso ; Patrizia Spadafora ; Sara Carrideo ; Elvira V. De Marco ; Domenico Consoli ; Mario Zappia ; Antonio Gambardella ; Aldo QuattroneGenetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern.
001726 (2006) Katja Hedrich [Allemagne] ; Susen Winkler ; Johann Hagenah ; Kemal Kabakci ; Meike Kasten ; Eberhard Schwinger ; Jens Volkmann ; Peter P. Pramstaller ; Vladimir Kostic ; Peter Vieregge ; Christine KleinRecurrent LRRK2 (Park8) mutations in early-onset Parkinson's disease.
001D95 (2007) Penelope Hogarth [États-Unis] ; Luca Lovrecic ; Dimitri KraincSodium phenylbutyrate in Huntington's disease: a dose-finding study.
004772 (1994) S B Bressman [États-Unis] ; A L Hunt ; G A Heiman ; M F Brin ; R E Burke ; S. Fahn ; J M Trugman ; D. De Leon ; P L Kramer ; K C WilhelmsenExclusion of the DYT1 locus in a non-Jewish family with early-onset dystonia.
004A76 (1996) T. Gasser [États-Unis] ; C M Bove ; L J Ozelius ; M. Hallett ; M E Charness ; F H Hochberg ; X O BreakefieldHaplotype analysis at the DYT1 locus in Ashkenazi Jewish patients with occupational hand dystonia.
004B65 (1996) T. Gasser [Allemagne] ; B. Bereznai ; B. Müller ; R. Pruszak-Seel ; R. Damrich ; G. Deuschl ; W H OertelLinkage studies in alcohol-responsive myoclonic dystonia.
004B70 (1996) C M Haw [Royaume-Uni] ; T R Barnes ; K. Clark ; P. Crichton ; D. KohenMovement disorder in Down's syndrome: a possible marker of the severity of mental handicap.
004F02 (1998) O. Bandmann [Royaume-Uni] ; C D Marsden ; N W WoodGenetic aspects of Parkinson's disease.

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