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2. Biochemical abnormalities of the sarcoplasmic reticulum in muscular dystrophy. Samaha FJ; Gergely J N Engl J Med; 1969 Jan; 280(4):184-8. PubMed ID: 4235816 [No Abstract] [Full Text] [Related]
3. Echinogenic action of L-alpha-lysophosphatidylcholine in Duchenne muscular dystrophy: a study on carrier detection. Tangorra A; Curatola G; Milani-Comparetti M; Ferretti G Am J Med Genet; 1989 Apr; 32(4):540-4. PubMed ID: 2774000 [TBL] [Abstract][Full Text] [Related]
5. [Clinico-biochemical and genetic studies of myopathy]. Davidenkova EF; Droznina TA; Markelov IM Zh Nevropatol Psikhiatr Im S S Korsakova; 1966; 66(11):1623-8. PubMed ID: 6001049 [No Abstract] [Full Text] [Related]
6. Muscle and serum enzymes and isoenzymes in muscular dystrophies. Ibrahim GA; Zweber BA; Awad EA Arch Phys Med Rehabil; 1981 Jun; 62(6):265-9. PubMed ID: 7235920 [TBL] [Abstract][Full Text] [Related]
14. [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]
15. [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]
16. [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]
17. Membrane abnormalities in Duchenne muscular dystrophy. Jones GE; Witkowski JA J Neurol Sci; 1983 Feb; 58(2):159-74. PubMed ID: 6300338 [No Abstract] [Full Text] [Related]
18. 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]
19. [Autosomal recessive severe, proximal myopathy in children, common in Tunisia]. Ben Hamida M; Attia N; Chabouni H; Fardeau M Rev Neurol (Paris); 1983; 139(4):289-97. PubMed ID: 6612142 [TBL] [Abstract][Full Text] [Related]
20. [Effects of administration of phosphocreatine on the clinical, biochemical and electromyographic evolution of Duchenne's progressive muscular dystrophy]. Radu H; Keresztes L; Stenzel K Minerva Med; 1968 Dec; 59(99):5524-9. PubMed ID: 5718841 [No Abstract] [Full Text] [Related] [Next] [New Search]