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Literature DB >> 3400498

Hereditary myoclonic dystonia, hereditary torsion dystonia and hereditary essential myoclonus: an area of confusion.

N P Quinn¹, J C Rothwell, P D Thompson, C D Marsden.

Abstract

Entities: Disease

Mesh：

Substances：
Ethanol

Year: 1988 PMID： 3400498

Source DB: PubMed Journal: Adv Neurol ISSN： 0091-3952

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Cited

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10 in total

1. Association of a missense change in the D2 dopamine receptor with myoclonus dystonia.

Authors: C Klein; M F Brin; P Kramer; M Sena-Esteves; D de Leon; D Doheny; S Bressman; S Fahn; X O Breakefield; L J Ozelius
Journal: Proc Natl Acad Sci U S A Date: 1999-04-27 Impact factor: 11.205

Review 2. The dystonias.

Authors: C D Marsden; N P Quinn
Journal: BMJ Date: 1990-01-20

3. Myoclonic dystonia.

Authors: S M Pueschel; J H Friedman; T Shetty
Journal: Childs Nerv Syst Date: 1992-03 Impact factor: 1.475

Review 4. The genetics of primary torsion dystonia.

Authors: U Müller; K G Kupke
Journal: Hum Genet Date: 1990-01 Impact factor: 4.132

5. Dopamine beta-hydroxylase gene excluded in four subtypes of hereditary dystonia.

Authors: D Schuback; P Kramer; L Ozelius; G Holmgren; L Forsgren; M Kyllerman; J Wahlström; C M Craft; T Nygaard; M Brin
Journal: Hum Genet Date: 1991-07 Impact factor: 4.132

6. Distinguishing SWEDDs patients with asymmetric resting tremor from Parkinson's disease: a clinical and electrophysiological study.

Authors: Petra Schwingenschuh; Diane Ruge; Mark J Edwards; Carmen Terranova; Petra Katschnig; Fatima Carrillo; Laura Silveira-Moriyama; Susanne A Schneider; Georg Kägi; Francisco J Palomar; Penelope Talelli; John Dickson; Andrew J Lees; Niall Quinn; Pablo Mir; John C Rothwell; Kailash P Bhatia
Journal: Mov Disord Date: 2010-04-15 Impact factor: 10.338

Hereditary myoclonic dystonia, hereditary torsion dystonia and hereditary essential myoclonus: an area of confusion.

1. Association of a missense change in the D2 dopamine receptor with myoclonus dystonia.

Review 2. The dystonias.

3. Myoclonic dystonia.

Review 4. The genetics of primary torsion dystonia.

5. Dopamine beta-hydroxylase gene excluded in four subtypes of hereditary dystonia.

6. Distinguishing SWEDDs patients with asymmetric resting tremor from Parkinson's disease: a clinical and electrophysiological study.

Review 7. Clinical variants of idiopathic torsion dystonia.

8. Abnormal motor patterns in the framework of the equilibrium-point hypothesis: a cause for dystonic movements?

Review 9. Electrophysiologic evaluation of psychogenic movement disorders.

10. Sporadic and familial myoclonic dystonia: Report of three cases and review of literature.