Progressive peroneal muscular atrophy (Charcot-Marie-Tooth disease) associated with β-thalassemia trait and glucose-6-phosphate dehydrogenase (G-6-PD) deficiency. A clinical and nerve biopsy case
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,General Neuroscience,Psychiatry and Mental health,Clinical Neurology,Dermatology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/BF02335407.pdf
Reference23 articles.
1. Behse F., Buchtal F.:Peroneal muscular atrophy (PMA) and related disorders II, Brain 100: 67–85.
2. Bradley W.G., Madrid R., Davis C.J.F. (1977):The peroneal muscular atrophy syndrome-clinical, genetic, electrophysiological and nerve biopsy studies, Part 3 (Clinical electrophysiological and pathological correlations), J. Neurol. Scie. 32 (1): 123–136.
3. Buchtal F., Behse F. (1977):Peroneal muscular atrophy (PMA) and related disorders-I, Brain 100: 41–66.
4. Burt A.M., Wenger B.S. 1961G-6-P dehydrogenase activity in the brain of developing chick, Develop. Biol. 3: 84–95.
5. Burt A.M.: (1965)Glucose metabolism and chick neurogenesis. G-6-P dehydrogenase activity in the embryonic brachial spinal cord. Develop. Biol. 12: 213–232.
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