An evaluation of some carrier detection techniques in Duchenne muscular dystrophy-Reference-Cited by-同舟云学术

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An evaluation of some carrier detection techniques in Duchenne muscular dystrophy

Published:1979-11 Issue:3 Volume:43 Page:377-394
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Lane R.J.M.,Maskrey P.,Nicholson G.A.,Siddiqui P.Q.R.,Nicholson Megan,Gascoigne Patsy,Pennington R.J.T.,Gardner-Medwin D.,Walton J.N.

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference80 articles.

1. Myoglobinaemia in Duchenne muscular dystrophy patients and carriers — A new adjunct to carrier detection;Adornato;Lancet,1978

2. A possible role for electron microscopy in the detection of carriers of Duchenne type muscular dystrophy;Afifi;J. Neurol., Neurosurg., Psychiat.,1973

3. Serum pyruvate kinase in muscle disease and carrier states;Alberts;Neurology (Minneap.),1974

4. Ouabain and erythrocyte ghost adenosine triphosphatase;Araki;Arch. Neurol. (Chic.),1971

5. Identification of the agent responsible for the abnormal immunoelectrophoretic pattern of serum in Duchenne's progressive muscular dystrophy;Askanas;Life Sci.,1966

Cited by 9 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. Clinical, Biochemical and Histological Responses to Treatment in Polymyositis: A Prospective Study;Journal of the Royal Society of Medicine;1989-06

2. Neuromuskuläre Erkrankungen mit Myokardbeteiligung;Myokarderkrankungen Perikarderkrankungen Herztumoren;1989

3. Evaluation of carrier detection of Duchenne muscular dystrophy using carbonic anhydrase III and creatine kinase;American Journal of Medical Genetics;1985-06

4. Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention;Human Genetics;1984-03

5. Improved detection of Duchenne muscular dystrophy heterozygotes using discriminant analysis of creatine kinase levels;American Journal of Medical Genetics;1983-01

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