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Journal Abstract Search
365 related items for PubMed ID: 5800957
1. [Contribution on the study of pseudohypertrophic muscular dystrophies. I. Benign pseudohypertrophic muscular dystrophy]. Radu H, Stenzel K. Dtsch Z Nervenheilkd; 1969; 196(2):92-115. PubMed ID: 5800957 [No Abstract] [Full Text] [Related]
2. [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]
6. Pseudohypertrophic muscular dystrophy of Cuchenne with manifestations in the heterozygote. Walker BA. Birth Defects Orig Artic Ser; 1971 Feb; 7(2):108-9. PubMed ID: 5173116 [No Abstract] [Full Text] [Related]
7. Benign congenital muscular dystrophy: a special form of congenital hypotonia. Zellweger H, Afifi A, McCormick WF, Mergner W. Clin Pediatr (Phila); 1967 Nov; 6(11):655-63. PubMed ID: 6058423 [No Abstract] [Full Text] [Related]
8. [Progressive muscle dystrophy. II. Enzyme activity chages in serum in progressive muscle dystrophy]. Lujf A, Sluga E, Moser K. Wien Klin Wochenschr; 1971 Feb 19; 83(7):109-13. PubMed ID: 5547427 [No Abstract] [Full Text] [Related]
9. Blood enzymes in Duchene's progressive muscular dystrophy and their correlation with the clinical and histological pictures. Niebrój-Dobosz I, Jedrzejowska H, Hetnarska L. Acta Med Pol; 1970 Feb 19; 11(4):387-93. PubMed ID: 5493781 [No Abstract] [Full Text] [Related]
10. Biochemical aspects of genetically determined progressive muscular dystrophies. Luca N, Haţegan D. Rev Roum Neurol; 1973 Feb 19; 10(6):531-7. PubMed ID: 4771091 [No Abstract] [Full Text] [Related]
11. Serum enzyme alterations in neuromuscular disorders. Munsat TL, Baloh R, Pearson CM, Fowler W. JAMA; 1973 Dec 24; 226(13):1536-43. PubMed ID: 4800933 [No Abstract] [Full Text] [Related]
12. The biochemical identification of the carrier state in X-linked recessive (Duchenne) muscular dystrophy. Thomson WH. Clin Chim Acta; 1969 Nov 24; 26(2):207-21. PubMed ID: 5352692 [No Abstract] [Full Text] [Related]
13. The effect of exercise on serum enzymes. Fowler WM, Gardner GW, Kazerunian HH, Lauvstad WA. Arch Phys Med Rehabil; 1968 Oct 24; 49(10):554-65. PubMed ID: 5685050 [No Abstract] [Full Text] [Related]
14. Benign sex-linked muscular dystrophy. Clinical and pathological features. Markand ON, North RR, D'Agostino AN, Daly DD. Neurology; 1969 Jul 24; 19(7):617-33. PubMed ID: 5815127 [No Abstract] [Full Text] [Related]
15. A serum isozyme study in muscular dystrophy. Particular reference to creatine kinase, aspartate aminotransferase, and lactic acid dehydrogenase isozymes. Somer H, Donner M, Murros J, Konttinen A. Arch Neurol; 1973 Nov 24; 29(5):343-5. PubMed ID: 4743886 [No Abstract] [Full Text] [Related]
16. Poikiloderma atrophicans vasculare associated with muscular dystrophy. Woolfson H, McQueen A. Arch Dermatol; 1973 Jan 24; 107(1):115-7. PubMed ID: 4682534 [No Abstract] [Full Text] [Related]
17. THE USE OF SERUM CREATINE PHOSPHOKINASE AND OTHER SERUM ENZYMES IN THE DIAGNOSIS OF PROGRESSIVE MUSCULAR DYSTROPHY. SWAIMAN KF, SANDLER B. J Pediatr; 1963 Dec 24; 63():1116-9. PubMed ID: 14089817 [No Abstract] [Full Text] [Related]
18. The diagnostic significance of serum enzymes and electrocardiogram in various muscular dystrophies. Zellweger H, Durnin R, Simpson J. Acta Neurol Scand; 1972 Dec 24; 48(1):87-101. PubMed ID: 5019834 [No Abstract] [Full Text] [Related]
19. [Enzyme diagnosis in progressive muscular dystrophies, especially in the Duchenne type]. Pernice W, Beckmann R, Renner S, Wais U. Klin Padiatr; 1989 Dec 24; 201(3):167-76. PubMed ID: 2739342 [Abstract] [Full Text] [Related]
20. Evidence against the existence of a subclinical form of X-linked Duchenne muscular dystrophy. Emery AE, Spikesman A. J Neurol Sci; 1970 Jun 24; 10(6):523-33. PubMed ID: 5422556 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]