Chondrodystrophic myotonia: electromyographic and cardiac features of a case
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0404.1979.tb02975.x/fullpdf
Reference17 articles.
1. Myotonia, dwarfism, diffuse bone disease and unusual ocular and facial abnormalities (a new syndrome);Aberfeld;Brain,1965
2. Chondrodystrophic myotonia: report of two cases. Myotonia, dwarfism, diffuse bone disease and unusual ocular and facial abnormalities;Aberfeld;Arch. Neurol. (Chic.),1970
3. Persistent motor neuron discharges of central origin present in the resting state;Blank;Neurol. (Minneap.),1974
4. E.M.G. studies of two family cases of the Schwartz and Jampel syndrome;Cadilhac;Electromyogr. Clin. Neurophysiol.,1975
5. Syndrome de Schwartz;Cordeiro Ferreira;Bordeaux Méd.,1973
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2. Schwartz-Jampel Syndrome in Saudi Children;Annals of Saudi Medicine;1994-03
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4. Neuromuskuläre Erkrankungen mit Myokardbeteiligung;Myokarderkrankungen Perikarderkrankungen Herztumoren;1989
5. Bilateral carpal tunnel in childhood associated with Schwartz-Jampel syndrome;Muscle & Nerve;1984-01
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