Scoliosis in a dopa-responsive dystonia family with a mutation of the GTP cyclohydrolase I gene-Reference-Cited by-同舟云学术

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Scoliosis in a dopa-responsive dystonia family with a mutation of the GTP cyclohydrolase I gene

Published:2000-06-13 Issue:11 Volume:54 Page:2187-2187
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Furukawa Yoshiaki,Kish Stephen J.,Lang Anthony E.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Reference7 articles.

1. Dopa-responsive dystonia: Recent advances and remaining issues to be addressed

2. Dopa-responsive dystonia: The spectrum of clinical manifestations in a large North American family

3. Dopa-Responsive Dystonia Masquerading as Idiopathic Kyphoscoliosis

4. Clinical and molecular genetics of primary dystonias

5. Nygaard TG, Duvoisin RC. Hereditary progressive dystonia/dopa-responsive dystonia. In: Joseph AB, Young RR, eds. Movement disorders in neurology and neuropsychiatry. 2nd ed. Malden, MA:Blackwell Science, 1999: 531–537.

Cited by 19 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Dopa-Responsive Dystonia and Related Disorders;Movement Disorder Emergencies;2021-10-03

2. Early-onset autosomal dominant GTP-cyclohydrolase I deficiency: Diagnostic delay and residual motor signs;Brain and Development;2021-08

3. Scoliosis Secondary to Dystonia;JBJS Case Connector;2017-07-12

4. Dopa-responsive dystonia—clinical and genetic heterogeneity;Nature Reviews Neurology;2015-06-23

5. Exploring the Link Between Dystonia Genes and Idiopathic Scoliosis;Journal of Pediatric Orthopaedics;2013-09

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