These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 8964357)

  • 1. [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]  

  • 2. [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]  

  • 3. [A combination of Duchenne's progressive muscular dystrophy with congenital ichthyosis--a deletion or 2 independent gene mutations at Xp21--Xp22?].
    Badalian LO; Temin PA; Kamennykh LN; Zavadenko NN; Arkhipov BA
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1988; 88(8):48-51. PubMed ID: 3195282
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Deletion analysis of the dystrophin gene in patients with Duchenne's muscular dystrophy in Tajikistan].
    Odinokova ON; Puzyrev VP; Radzhabaliev ShF; Rakhmonov RA
    Genetika; 1996 Oct; 32(10):1392-5. PubMed ID: 9091412
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Clinical polymorphism and genetic heterogeneity in Duchenne's progressive muscular dystrophy in girls (a review)].
    Zavadenko NN; Temin PA; Malygina NA
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1988; 88(11):123-6. PubMed ID: 3066079
    [No Abstract]   [Full Text] [Related]  

  • 6. [Duchenne's muscular dystrophy in a girl with 45,X/46,XX chromosomal mosaicism].
    Aver'ianov IuN; Bogomazov EA; Logunova LV
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1977; 77(10):1449-52. PubMed ID: 930487
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular biology of Duchenne and Becker's muscular dystrophy: clinical applications.
    Gutmann DH; Fischbeck KH
    Ann Neurol; 1989 Aug; 26(2):189-94. PubMed ID: 2673003
    [TBL] [Abstract][Full Text] [Related]  

  • 8. X-linked muscular dystrophy--phenotypic/genotypic correlation.
    Guard E; Roadley G; Watt A; Mueller RF
    N Z Med J; 1992 Aug; 105(939):319. PubMed ID: 1501822
    [No Abstract]   [Full Text] [Related]  

  • 9. Six novel mutations in the emerin gene causing X-linked Emery-Dreifuss muscular dystrophy.
    Wulff K; Parrish JE; Herrmann FH; Wehnert M
    Hum Mutat; 1997; 9(6):526-30. PubMed ID: 9195226
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The Emery-Dreifuss Muscular Dystrophy Mutation Database.
    Yates JR; Wehnert M
    Neuromuscul Disord; 1999 May; 9(3):199. PubMed ID: 10382916
    [No Abstract]   [Full Text] [Related]  

  • 11. [Duchenne muscular dystrophy. Fragile X syndrome. Epidemiology, genetics, diagnosis].
    Pinson S; Plauchu H
    Rev Prat; 1998 Mar; 48(5):565-9. PubMed ID: 9781124
    [No Abstract]   [Full Text] [Related]  

  • 12. [X-linked muscular dystrophy: is prevention possible?].
    Plauchu H
    Pediatrie; 1990; 45(5):297-9. PubMed ID: 2165239
    [No Abstract]   [Full Text] [Related]  

  • 13. Serum cytoplasmic and mitochondrial aspartate aminotransferase in Duchenne's progressive muscular dystrophy.
    Janik P; Nowak I; Niebrój-Dobosz I
    Mater Med Pol; 1994; 26(3):101-4. PubMed ID: 7603078
    [TBL] [Abstract][Full Text] [Related]  

  • 14. DNA diagnostic tests in Xp21 dystrophy families for prenatal diagnosis.
    Dinçer P; Topaloğlu H; Ayter S
    Turk J Pediatr; 1998; 40(3):347-55. PubMed ID: 9763898
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Emery Dreifuss muscular dystrophy--a case report.
    Chakraborty SK; Das SK; Banerjee A; Pahari DK; Ganguly G; Saha S
    J Assoc Physicians India; 1995 Nov; 43(11):807-8. PubMed ID: 8773049
    [No Abstract]   [Full Text] [Related]  

  • 16. 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]  

  • 17. Muscle fiber immaturity and inactivity reduce myonecrosis in Duchenne muscular dystrophy.
    Kimura S; Sugino S; Ohtani Y; Matsukura M; Nishino I; Ikezawa M; Sakata A; Kondo Y; Yoshioka K; Huard J; Nonaka I; Miike T
    Ann Neurol; 1998 Dec; 44(6):967-71. PubMed ID: 9851444
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [A manifested carrier of late onset Duchenne type muscular dystrophy].
    Wakata N; Uchida A; Kinoshita M
    Rinsho Shinkeigaku; 1987 May; 27(5):630-3. PubMed ID: 3621760
    [No Abstract]   [Full Text] [Related]  

  • 19. Inside out, boy you turn me?
    Phimister B
    Nat Genet; 1997 May; 16(1):11. PubMed ID: 9140386
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.