Investigation of the role of SMN1 and SMN2 haploinsufficiency as a risk factor for Hirayama's disease: Clinical, neurophysiological and genetic characteristics in a Spanish series of 13 patients-Reference-Cited by-同舟云学术

Investigation of the role of SMN1 and SMN2 haploinsufficiency as a risk factor for Hirayama's disease: Clinical, neurophysiological and genetic characteristics in a Spanish series of 13 patients

Published:2007-12 Issue:10 Volume:109 Page:844-848
ISSN:0303-8467
Container-title:Clinical Neurology and Neurosurgery
language:en
Short-container-title:Clinical Neurology and Neurosurgery

Author:

Gamez Josep,Also Eva,Alias Laura,Corbera-Bellalta Marc,Barceló Maria J.,Centeno Maria,Raguer Nuria,Gratacós Margarita,Baiget Montserrat,Tizzano Eduardo F.

Publisher

Elsevier BV

Subject

Clinical Neurology,General Medicine,Surgery

Reference42 articles.

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2. Juvenile muscular atrophy unilateral upper extremity;Hirayama;Neurology,1963

3. Juvenile non-progressive muscular atrophy localized in the hand and forearm–observations in 38 cases (in Japanese, abstract in English);Hirayama;Rinsho Shinkeigaku (Clin Neurol),1972

4. Focal cervical poliopathy causing juvenile muscular atrophy of distal upper extremity: a pathological study;Hirayama;J Neurol Neurosurg Psychiatry,1987

5. Non-progressive juvenile spinal muscular atrophy of the distal upper limb (Hirayama's disease);Hirayama,1991

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