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25. [Chronic progressive external ophthalmoplegia in the current views of isolated and evolutive ocular myopathy. Diagnostic and prognostic judgment by means of electromyography and determination of muscle enzymes in the blood]. Morra M Minerva Oftalmol; 1970; 12(2):47-58. PubMed ID: 5507455 [No Abstract] [Full Text] [Related]
26. The effect of exercise on serum enzymes. Fowler WM; Gardner GW; Kazerunian HH; Lauvstad WA Arch Phys Med Rehabil; 1968 Oct; 49(10):554-65. PubMed ID: 5685050 [No Abstract] [Full Text] [Related]
27. Carrier detection in X-linked Duchenne type muscular dystrophy. A pluridimensional investigation. Radu H; Migea S; Török Z; Bordeianu L; Radu A J Neurol Sci; 1968; 6(2):289-300. PubMed ID: 4179111 [No Abstract] [Full Text] [Related]
28. [Contribution on the study of pseudohypertrophic muscular dystrophies. II. Pseudohypertrophic muscular dystrophies in females]. Radu H; Stenzel K Dtsch Z Nervenheilkd; 1969; 196(2):116-35. PubMed ID: 5800953 [No Abstract] [Full Text] [Related]
29. Muscular dystrophy in young girls. Penn AS; Lisak RP; Rowland LP Neurology; 1970 Feb; 20(2):147-59. PubMed ID: 5460703 [No Abstract] [Full Text] [Related]
31. Evidence against the existence of a subclinical form of X-linked Duchenne muscular dystrophy. Emery AE; Spikesman A J Neurol Sci; 1970 Jun; 10(6):523-33. PubMed ID: 5422556 [No Abstract] [Full Text] [Related]
33. The biochemical identification of the carrier state in X-linked recessive (Duchenne) muscular dystrophy. Thomson WH Clin Chim Acta; 1969 Nov; 26(2):207-21. PubMed ID: 5352692 [No Abstract] [Full Text] [Related]
34. Marked cardiac involvement in limb-girdle muscular dystrophy. Kawashima S; Ueno M; Kondo T; Yamamoto J; Iwasaki T Am J Med Sci; 1990 Jun; 299(6):411-4. PubMed ID: 2356853 [TBL] [Abstract][Full Text] [Related]
35. [Histological, serum enzyme and electromyographic studies in thyreomyopathies in children (research on hypothroid patients)]. Iafusco F; Canani MB; Granata E Pediatria (Napoli); 1967 Dec; 75(6):893-913. PubMed ID: 5617794 [No Abstract] [Full Text] [Related]
36. [Enzyme diagnosis in progressive muscular dystrophies, especially in the Duchenne type]. Pernice W; Beckmann R; Renner S; Wais U Klin Padiatr; 1989; 201(3):167-76. PubMed ID: 2739342 [TBL] [Abstract][Full Text] [Related]
37. Interstitial myofibrositis: hypothesis of the mechanism. Awad EA Arch Phys Med Rehabil; 1973 Oct; 54(10):449-53. PubMed ID: 4126445 [No Abstract] [Full Text] [Related]
38. Distal muscular dystrophy with autosomal recessive inheritance. Scoppetta C; Vaccario ML; Casali C; Di Trapani G; Mennuni G Muscle Nerve; 1984; 7(6):478-81. PubMed ID: 6543900 [TBL] [Abstract][Full Text] [Related]
39. A possible role for electron microscopy in detection of carriers of Duchenne type muscular dystrophy. Afifi AK; Bergman RA; Zellweger H J Neurol Neurosurg Psychiatry; 1973 Aug; 36(4):643-50. PubMed ID: 4731334 [TBL] [Abstract][Full Text] [Related]