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22. [Progressive muscular dystrophy: CPK, LDH, ALD (aldolase)--EMG, ECG in patients and their families]. Diotallevi P; Bargilli E; Danni M; Dellantonio R; Tocchini M; Milani-Comparetti M Boll Soc Ital Biol Sper; 1988 Jun; 64(6):523-30. PubMed ID: 3190905 [No Abstract] [Full Text] [Related]
23. [Changes in the activity of blood serum enzymes in relatives of children with myopathy]. Grinio LP Vopr Med Khim; 1966; 12(6):600-3. PubMed ID: 6000902 [No Abstract] [Full Text] [Related]
25. Investigation on healthy individuals from families of patients with Duchenne type muscular dystrophy. Hausmanowa-Petrusewicz I; Prot J; Niebrój-Dobosz I; Emeryk B; Wasowicz B; Slucka C; Hetnarska L; Bendarzewska B; Pucek Z Pol Med J; 1968; 7(1):228-37. PubMed ID: 5652928 [No Abstract] [Full Text] [Related]
26. [Enzymatic activity of the serum in the family of a progressive muscular dystrophy patient]. Esaki K; Tokoro T; Yamamoto K; Kato T; Asano B Iryo; 1969 Oct; 23(10):1306-11. PubMed ID: 5364982 [No Abstract] [Full Text] [Related]
28. [On Becker's benign muscular dystrophy: study of a family with 10 affected members in 6 generations]. Caruso G; Campanella G Acta Neurol (Napoli); 1968; 23(4):709-31. PubMed ID: 5747395 [No Abstract] [Full Text] [Related]
29. [Serum aldolase and creatine phosphokinase in progressive muscular dystrophy]. Ceccarelli A; Leone P Clin Pediatr (Bologna); 1967 May; 49(5):237-45. PubMed ID: 6080497 [No Abstract] [Full Text] [Related]
30. [Clinico-statistical considerations on a group of 22 patients with progressive muscular dystrophy]. Garofalo E; Marcer V Fracastoro; 1966; 59(6):621-38. PubMed ID: 5998705 [No Abstract] [Full Text] [Related]
31. [Differentiation and dedifferentiation of muscular dystrophy]. Ueda K; Ito T; Nakata T; Ohara T; Matsumoto K Nihon Rinsho; 1968 Oct; 26(10):2423-42. PubMed ID: 5752013 [No Abstract] [Full Text] [Related]
33. Serum enzyme changes in muscle disease and their relation to tissue change. HUGHES BP Proc R Soc Med; 1963 Mar; 56(3):179-82. PubMed ID: 13955533 [No Abstract] [Full Text] [Related]
34. [Contribution to the study of the enzymology of primary myopathies of childhood]. Vitetta M Biol Lat; 1965; 18(4):359-66. PubMed ID: 5871253 [No Abstract] [Full Text] [Related]
35. [Plasma level of hemopexin (Hpx) in families with progressive muscular dystrophy (PMD)]. Diotallevi P; Balducci E; Canapa A; Danni M; Giamagli CA; Lucesoli S; Ravaglia P; Milani-Comparetti M Boll Soc Ital Biol Sper; 1988 Jun; 64(6):531-8. PubMed ID: 3190906 [No Abstract] [Full Text] [Related]
36. Slowly progressive X-linked recessive muscular dystrophy (type 3b). Report of cases and review of the literature. Zellweger H; Hanson JW Arch Intern Med; 1967 Nov; 120(5):525-35. PubMed ID: 6054585 [No Abstract] [Full Text] [Related]
37. [Biological anomalies in the apparently healthy transmitters of muscular dystrophy]. DEMOS J; DREYFUS JC; SCHAPIRA F; SCHAPIRA G Rev Can Biol; 1962; 21():587-97. PubMed ID: 14026924 [No Abstract] [Full Text] [Related]
38. Myoglobin is a sensitive marker of increased muscle membrane vulnerability. Driessen-Kletter MF; Amelink GJ; Bär PR; van Gijn J J Neurol; 1990 Jul; 237(4):234-8. PubMed ID: 2391544 [TBL] [Abstract][Full Text] [Related]