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3. Sorbitol dehydrogenase in muscle disease. Kar NC; Pearson CM Lancet; 1973 Mar; 1(7804):673. PubMed ID: 4121883 [No Abstract] [Full Text] [Related]
4. [Malate dehydrogenase activity in patients with different forms of progressive muscular dystrophy]. Gil'manov VKh Zh Nevropatol Psikhiatr Im S S Korsakova; 1970; 70(9):1309-12. PubMed ID: 5511109 [No Abstract] [Full Text] [Related]
5. The role of histochemistry in muscle disease. Dubowitz V Mod Trends Neurol; 1970; 5(0):189-208. PubMed ID: 4277721 [No Abstract] [Full Text] [Related]
7. [Importance of enzyme histochemistry in the diagnosis of neurogenic muscular disease. Discussion of some special aspects]. De Giacomo P; Buscaino GA; Perniola T Riv Patol Nerv Ment; 1969 Apr; 90(2):121-6. PubMed ID: 4255923 [No Abstract] [Full Text] [Related]
8. [Contribution to enzymatic study in liquor and serum of different amyotrophic entities (author's transl)]. Nieto Vales JM; RodrÃguez Navarro I Folia Clin Int (Barc); 1973 Feb; 23(2):86-109. PubMed ID: 4804725 [No Abstract] [Full Text] [Related]
9. [Clinical study of muscular atrophy]. Shinoda M Hokkaido Igaku Zasshi; 1974 Jan; 49(1):23-31. PubMed ID: 4376121 [No Abstract] [Full Text] [Related]
10. [Muscle LDH isoenzymes in neuromuscular diseases and in carriers of recessive X-linked muscular dystrophy (duchenne)]. Kowalewski S; Rotthauwe HW Z Kinderheilkd; 1972; 113(1):55-70. PubMed ID: 5056500 [No Abstract] [Full Text] [Related]
14. [Mental development of children with the Duchenne type of progressive muscular dystrophy]. Kozicka A Neurol Neurochir Pol; 1971; 5(4):523-8. PubMed ID: 5122056 [No Abstract] [Full Text] [Related]
15. [Carbohydrate metabolism disorders in hereditary forms of neuromuscular diseases]. Golubeva VV Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(8):1153-9. PubMed ID: 5136819 [No Abstract] [Full Text] [Related]
16. Serum lactate dehydrogenase isoenzymes in neuromuscular diseases. Hooshmand H Dis Nerv Syst; 1975 Nov; 36(11):607-11. PubMed ID: 1183304 [TBL] [Abstract][Full Text] [Related]
17. [A genetic questionnaire. The genetic aspects of a case of benign spinal muscular dystrophy]. Klein D J Genet Hum; 1970 Dec; 18(4):421-2. PubMed ID: 5524821 [No Abstract] [Full Text] [Related]
18. [Serum aldolase activity in patients with myopathies and in their close reltives]. Dzhuraev A Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(8):1159-63. PubMed ID: 5136820 [No Abstract] [Full Text] [Related]