254 related articles for article (PubMed ID: 930487)
21. Progressive muscle disease in a young woman with family history of Duchenne's muscular dystrophy.
Olson BJ; Fenichel GM
Arch Neurol; 1982 Jun; 39(6):378-80. PubMed ID: 7092617
[TBL] [Abstract][Full Text] [Related]
22. [Molecular biology of Duchenne's muscular dystrophy].
Coral-Vázquez R; Salamanca-Gómez F
Gac Med Mex; 1996; 132(2):221-2. PubMed ID: 8964357
[No Abstract] [Full Text] [Related]
23. Duchenne's muscular dystrophy: review and recent scientific findings.
Evans BK; Goyne C
Am J Med Sci; 1991 Aug; 302(2):118-23. PubMed ID: 1897557
[TBL] [Abstract][Full Text] [Related]
24. [Detection of the cause of genetic fault in Duchenne's dystrophy].
Palotie L; Somer H
Duodecim; 1988; 104(20):1588-96. PubMed ID: 3056698
[No Abstract] [Full Text] [Related]
25. Gastric hypomotility in Duchenne's muscular dystrophy.
Barohn RJ; Levine EJ; Olson JO; Mendell JR
N Engl J Med; 1988 Jul; 319(1):15-8. PubMed ID: 3380114
[TBL] [Abstract][Full Text] [Related]
26. Duchenne muscular dystrophy in a girl with an (X;15) translocation.
Ribeiro MC; Melaragno MI; Schmidt B; Brunoni D; Gabbai AA; Hackel C
Am J Med Genet; 1986 Oct; 25(2):231-6. PubMed ID: 3777020
[TBL] [Abstract][Full Text] [Related]
27. Update: Duchenne muscular dystrophy.
Fenichel GM; Robison JD
Compr Ther; 1988 Jul; 14(7):29-32. PubMed ID: 3060302
[No Abstract] [Full Text] [Related]
28. [Clinico-genealogic analysis of the malignancy of Duchenne's progressive muscular dystrophy].
Kavtaradze NP; Mindadze BA; Natriashvili GD
Zh Nevropatol Psikhiatr Im S S Korsakova; 1982; 82(11):26-8. PubMed ID: 7180299
[No Abstract] [Full Text] [Related]
29. Leber's congenital amaurosis with Duchenne's muscular dystrophy.
Hazariwala K; Brownstein S; Polomeno R; Little JM; Labuda D
Can J Ophthalmol; 1990 Jun; 25(4):202-7. PubMed ID: 1972344
[TBL] [Abstract][Full Text] [Related]
30. X;autosome translocations in females with Duchenne or Becker muscular dystrophy.
Dubowitz V
Nature; 1986 Jul 17-23; 322(6076):291-2. PubMed ID: 3461282
[No Abstract] [Full Text] [Related]
31. [Importance of recombinant DNA studies for the identification of carriers of Duchenne's muscular dystrophy].
Veenema H; Leschot NJ; van Ommen GJ; Pearson PL
Ned Tijdschr Geneeskd; 1985 Jun; 129(24):1137-41. PubMed ID: 4022155
[No Abstract] [Full Text] [Related]
32. Duchenne's muscular dystrophy: socioreligious belief delays diagnosis and genetic counselling.
Lyn PC
Singapore Med J; 1986 Feb; 27(1):68-71. PubMed ID: 3715493
[No Abstract] [Full Text] [Related]
33. Mosaicism 45,X/46,X, t dic(Xp:Xp) in a girl with short stature.
Abulhasan SJ; Teebi AS; Zaki M; Hammad I; Al-Awadi SA; Krishna Murthy DS
Ann Genet; 1990; 33(4):234-8. PubMed ID: 2095706
[TBL] [Abstract][Full Text] [Related]
34. [Phenotype manifestation of disease in a heterozygote for Duchenne's form of muscular dystrophy].
Gencík A; Traubner P
Cesk Neurol Neurochir; 1979 May; 42(3):205-11. PubMed ID: 455525
[No Abstract] [Full Text] [Related]
35. Analysis of dystrophin expression after activation of myogenesis in amniocytes, chorionic-villus cells, and fibroblasts. A new method for diagnosing Duchenne's muscular dystrophy.
Sancho S; Mongini T; Tanji K; Tapscott SJ; Walker WF; Weintraub H; Miller AD; Miranda AF
N Engl J Med; 1993 Sep; 329(13):915-20. PubMed ID: 8361505
[TBL] [Abstract][Full Text] [Related]
36. Observations on the electrocardiogram in Duchenne's progressive muscular dystrophy.
Durnin RE; Ziska JH; Zellweger H
Helv Paediatr Acta; 1971 Aug; 26(3):331-9. PubMed ID: 5116168
[No Abstract] [Full Text] [Related]
37. [Carrier detection and prenatal diagnosis of Duchenne's muscular dystrophy based on DNA analysis].
Evgrafov OV; Badalian LO; Poliakov AV; Zaĭtseva SP; Malygina NA; Vinogradov SV; Bakharev VA; Mil'man FA; Lisova LP; Zaretskaia NV
Zh Nevropatol Psikhiatr Im S S Korsakova; 1990; 90(8):29-33. PubMed ID: 2175114
[TBL] [Abstract][Full Text] [Related]
38. [DNA markers, genetic counseling and prenatal diagnosis of hereditary diseases. A study of 3 families with Duchenne's muscular dystrophy].
Schwartz M; Nørby S; Brandt NJ
Ugeskr Laeger; 1985 Jul; 147(30):2382-6. PubMed ID: 3864307
[No Abstract] [Full Text] [Related]
39. The X chromosome in Duchenne's muscular dystrophy.
Katsantoni A
Clin Genet; 1976 Mar; 9(3):371-3. PubMed ID: 1261076
[TBL] [Abstract][Full Text] [Related]
40. [Presentation of a complex monitoring and therapy program in neuromuscular diseases, exemplified by X chromosomal muscular dystrophies. 1: Etiology, development, clinical and paraclinical findings].
Hoffmann W; Ullrich KP
Padiatr Grenzgeb; 1987; 26(4):271-8. PubMed ID: 3658476
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]