Significance of serum myoglobin in neuromuscular diseases and in carrier detection of Duchenne muscular dystrophy
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0404.1982.tb04523.x/fullpdf
Reference23 articles.
1. Myoglobinemia in Duchenne muscular dystrophy patients and carriers: a new adjunct to carrier detection;Adernato;Lancet,1978
2. Muscle disorders in childhood;Dubowitz;Major problems in clinical pediatrics,1978
3. Creatine kinase B-subunit activity in serum after immunoinhibition of M-subunit activity;Gerhardt;Clin. Chem.,1979
4. Creatine kinase isoenzyme patterns in Duchenne muscular dystrophy;Goedde;Clin. Gen.,1978
5. Creatine phosphokinase in pathological human serum;Goto;Clin. Chim. Acta,1970
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3. Myoglobin, creatine kinase and creatine kinase subunit-B in serum from patients and relatives with hypokaliaemic familial periodic paralysis;Acta Neurologica Scandinavica;2009-01-29
4. Carrier detection in Duchenne muscular dystrophy: A review of current issues and approaches;Clinica Chimica Acta;1987-01
5. Serum carbonic anhydrase III in neuromuscular disorders and in healthy persons after a long-distance run;Journal of the Neurological Sciences;1985-10
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