Levodopa-responsive dystonia-Reference-Cited by-同舟云学术

Levodopa-responsive dystonia

Published:2000-06 Issue:6 Volume:123 Page:1112-1121
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

Tassin Johann,Dürr Alexandra,Bonnet Anne-Marie,Gil Roger,Vidailhet Marie,Lücking Christoph B.,Goas Jean-Yves,Durif Franck,Abada Myriem,Echenne Bernard,Motte Jacques,Lagueny Alain,Lacomblez Lucette,Jedynak Pierre,Bartholomé Barbara,Agid Yves,Brice Alexis

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/123/6/1112/17873677/1231112.pdf

Reference30 articles.

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2. Bandmann O, Nygaard TG, Surtees R, Marsden CD, Wood NW, Harding AE. Dopa-responsive dystonia in British patients: new mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneity. Hum Mol Genet1996; 5: 403–6.

3. Bandmann O, Valente EM, Holmans P, Surtees RA, Walters JH, Wevers RA, et al. Dopa-responsive dystonia: a clinical and molecular genetic study. Ann Neurol1998; 44: 649–56.

4. Beyer K, Lao-Villadoniga JI, Vecino-Bilbao B, Cacabelos R, De la Fuente-Fernandez R. A novel point mutation in the GTP cyclohydrolase I gene in a Spanish family with hereditary progressive and dopa responsive dystonia [letter]. J Neurol Neurosurg Psychiatry1997; 62: 420–1.

5. Blau N, Ichinose H, Nagatsu T, Heizmann CW, Zacchello F, Burlina AB. A missense mutation in a patient with guanosine triphosphate cyclohydrolase I deficiency missed in the newborn screening program. J Pediatr1995; 126: 401–5.

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