Chromosome Deletion < Chromosome Disorders < Chromosome Disorders (complications)

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 34.
[0-20] [0 - 20][0 - 34][20-33][20-40]

Ident.	Authors (with country if any)	Title
000115 (1999)	H R Morris [Royaume-Uni] ; A J Lees ; N W Wood	Neurofibrillary tangle parkinsonian disorders--tau pathology and tau genetics.
000126 (1999)	E. Cassetta [Italie] ; N. Del Grosso ; A R Bentivoglio ; E M Valente ; M. Frontali ; A. Albanese	Italian family with cranial cervical dystonia: clinical and genetic study.
000226 (2000)	A. Schrag [Royaume-Uni] ; N P Quinn ; K P Bhatia ; C D Marsden	Benign hereditary chorea--entity or syndrome?
000285 (2000)	J J Higgins [États-Unis] ; K. Kluetzman ; J. Berciano ; O. Combarros ; J M Loveless	Posterior column ataxia and retinitis pigmentosa: a distinct clinical and genetic disorder.
000296 (2000)	T. Klockgether [Allemagne] ; U. Wüllner ; A. Spauschus ; B. Evert	The molecular biology of the autosomal-dominant cerebellar ataxias.
000551 (2001)	T. Perniola [Italie] ; L. Margari ; M G De Iaco ; A. Presicci ; P. Ventura ; E. Ferrannini ; G. Illiceto	Familial paroxysmal exercise-induced dyskinesia, epilepsy, and mental retardation in a family with autosomal dominant inheritance.
001452 (1992)	R N Rosenberg	Machado-Joseph disease: an autosomal dominant motor system degeneration.
001453 (1992)	L. Sudarsky [États-Unis] ; L. Corwin ; D M Dawson	Machado-Joseph disease in New England: clinical description and distinction from the olivopontocerebellar atrophies.
004702 (1995)	A. Ishikawa [Japon] ; T. Miyatake	A family with hereditary juvenile dystonia-parkinsonism.
004709 (1995)	S. Bohlega [Arabie saoudite] ; B. Stigsby ; M Z Al-Kawi ; D R Mclean ; P. Ozand ; S. Omer ; P. Coates	Familial tremulous and myoclonic dystonia with white matter changes in brain magnetic resonance imaging.
004846 (1994)	T T Warner [Royaume-Uni] ; G G Lennox ; I. Janota ; A E Harding	Autosomal-dominant dentatorubropallidoluysian atrophy in the United Kingdom.
004896 (1994)	S. Micheli [Argentine] ; M. Fernández-Pardal ; P. Quesada ; T. Brannan ; J A Obeso	Variable onset of adult inherited focal dystonia: a problem for genetic studies.
004937 (1993)	R J Uitti [États-Unis] ; D M Maraganore	Adult onset familial cervical dystonia: report of a family including monozygotic twins.
004970 (1993)	D. Conway [Royaume-Uni] ; P G Bain ; T T Warner ; M B Davis ; L J Findley ; P D Thompson ; C D Marsden ; A E Harding	Linkage analysis with chromosome 9 markers in hereditary essential tremor.
004A70 (1996)	N P Quinn [Royaume-Uni]	Essential myoclonus and myoclonic dystonia.
004A76 (1996)	T. Gasser [États-Unis] ; C M Bove ; L J Ozelius ; M. Hallett ; M E Charness ; F H Hochberg ; X O Breakefield	Haplotype analysis at the DYT1 locus in Ashkenazi Jewish patients with occupational hand dystonia.
004B21 (1995)	M A Tijssen [Pays-Bas] ; E. Bollen ; E. Van Exel ; J G Van Dijk	Saccadic eye movements in hyperekplexia.
004B59 (1996)	C. Nicolosi ; P. Girlanda ; G. Vita ; C. Messina	Cat eye syndrome and dystonia.
004B65 (1996)	T. Gasser [Allemagne] ; B. Bereznai ; B. Müller ; R. Pruszak-Seel ; R. Damrich ; G. Deuschl ; W H Oertel	Linkage studies in alcohol-responsive myoclonic dystonia.
004B69 (1996)	C. Trenkwalder [Allemagne] ; V C Seidel ; T. Gasser ; W H Oertel	Clinical symptoms and possible anticipation in a large kindred of familial restless legs syndrome.
004B97 (1996)	J E Nielsen [Danemark] ; S A S Rensen ; L. Hasholt ; A. N Rrem Lle	Dentatorubral-pallidoluysian atrophy. Clinical features of a five-generation Danish family.

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