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23. Practical aspects of myoblast implantation: investigations on two inherited myopathies in animals. Morgan JE Adv Exp Med Biol; 1990; 280():89-94; discussion 95-6. PubMed ID: 2248159 [No Abstract] [Full Text] [Related]
24. Genetic counseling of isolated carriers of Duchenne muscular dystrophy. Hoffman EP; Pegoraro E; Scacheri P; Burns RG; Taber JW; Weiss L; Spiro A; Blattner P Am J Med Genet; 1996 Jun; 63(4):573-80. PubMed ID: 8826437 [TBL] [Abstract][Full Text] [Related]
25. Invited review: myoblast transfer: a possible therapy for inherited myopathies? Partridge TA Muscle Nerve; 1991 Mar; 14(3):197-212. PubMed ID: 2041542 [TBL] [Abstract][Full Text] [Related]
26. The clinical consequences of X-chromosome inactivation: Duchenne muscular dystrophy in one of monozygotic twins. Pena SD; Karpati G; Carpenter S; Fraser FC J Neurol Sci; 1987 Jul; 79(3):337-44. PubMed ID: 3612177 [TBL] [Abstract][Full Text] [Related]
27. Use of quantitative myometry in the evaluation of myoblast transfer therapy. Munsat TL Adv Exp Med Biol; 1990; 280():227-9. PubMed ID: 2248142 [No Abstract] [Full Text] [Related]
28. Purification and proliferation of human myoblasts isolated with fluorescence activated cell sorting. Blau HM; Webster C; Pavlath GK Adv Exp Med Biol; 1990; 280():97-100. PubMed ID: 2248160 [No Abstract] [Full Text] [Related]
29. Myoblast transfer in DMD: problems in the interpretation of efficiency. Karpati G; Holland P; Worton RG Muscle Nerve; 1992 Oct; 15(10):1209-10. PubMed ID: 1406777 [No Abstract] [Full Text] [Related]
30. Dystrophin negative skeletal and myocardial muscle cells in a carrier of Duchenne's muscular dystrophy. Watanabe K; Izumi T; Natsui M; Matsubara N; Miyakita Y; Koyama S; Inomata T; Suzuki M; Shibata A Eur Heart J; 1993 Jul; 14(7):989-92. PubMed ID: 8375425 [TBL] [Abstract][Full Text] [Related]
32. Quantitation of muscle mass and muscle protein synthesis rate: documenting a response to myoblast transfer. Griggs RC Adv Exp Med Biol; 1990; 280():235-40. PubMed ID: 2248144 [TBL] [Abstract][Full Text] [Related]
33. [Monozygotic twins with progressive muscular dystrophy]. Radu H; Killyen I; Rosu AM; Ionescu V Z Neurol; 1972; 202(3):241-6. PubMed ID: 4120053 [No Abstract] [Full Text] [Related]
34. Integrated dystrophin analysis using immunocytochemical, biochemical and genetic techniques. Nicholson LV; Johnson MA; Davies KE Basic Appl Histochem; 1990; 34(3):169-75. PubMed ID: 1702616 [TBL] [Abstract][Full Text] [Related]
35. Immunosuppressive therapy in Duchenne muscular dystrophy: considerations for myoblast transfer studies. Mendell JR Adv Exp Med Biol; 1990; 280():287-95. PubMed ID: 2248150 [No Abstract] [Full Text] [Related]
36. [DNA and dystrophin analysis in Duchenne's and Becker's disease; benefit to the patient]. Jennekens FG; Ippel PF Ned Tijdschr Geneeskd; 1993 Jan; 137(2):61-3. PubMed ID: 8421528 [No Abstract] [Full Text] [Related]
37. Cell and gene therapy in Duchenne muscular dystrophy. Morgan JE Hum Gene Ther; 1994 Feb; 5(2):165-73. PubMed ID: 7514447 [TBL] [Abstract][Full Text] [Related]
38. Immunostaining of dystrophin and utrophin in skeletal muscle of dystrophinopathies. Sahashi K; Ibi T; Suoh H; Nakao N; Tashiro M; Marui K; Arahata K; Sugita H Intern Med; 1994 May; 33(5):277-83. PubMed ID: 7949630 [TBL] [Abstract][Full Text] [Related]
39. On dystrophin abundance and C-terminal missense mutations in dystrophinopathies. Oexle K; Heyer R Ann Neurol; 1999 Jul; 46(1):137-8. PubMed ID: 10401797 [No Abstract] [Full Text] [Related]
40. Normal and dystrophin-deficient muscle fibers in carriers of the gene for Duchenne muscular dystrophy. Bonilla E; Schmidt B; Samitt CE; Miranda AF; Hays AP; de Oliveira AB; Chang HW; Servidei S; Ricci E; Younger DS Am J Pathol; 1988 Dec; 133(3):440-5. PubMed ID: 3059802 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]