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 *

77 related articles for article (PubMed ID: 3166446)

  • 1. Duchenne muscular dystrophy and acute lymphoblastic leukaemia.
    Svarch E; Menéndez A; González A
    Haematologia (Budap); 1988; 21(2):123-4. PubMed ID: 3166446
    [No Abstract]   [Full Text] [Related]  

  • 2. The muscular dystrophies.
    Seiler J; Bope ET
    Am Fam Physician; 1986 Jul; 34(1):123-8. PubMed ID: 3728255
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Xp21/autosome translocations. Case report and risk for Duchenne muscular dystrophy.
    Holden JJ; Smith A; MacLeod PM; Masotti R; Duncan AM
    Clin Genet; 1986 Jun; 29(6):516-22. PubMed ID: 3742857
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Trisomy 21 in a boy with progressive muscular dystrophy (Duchenne)].
    Moser H
    Z Kinderheilkd; 1971; 109(4):318-25. PubMed ID: 4252123
    [No Abstract]   [Full Text] [Related]  

  • 5. Malignant hyperthermia in a child with Duchenne muscular dystrophy.
    Kelfer HM; Singer WD; Reynolds RN
    Pediatrics; 1983 Jan; 71(1):118-9. PubMed ID: 6848959
    [No Abstract]   [Full Text] [Related]  

  • 6. The linkage between Duchenne-type progressive muscular dystrophy and color blindness.
    Prot J; Laska M
    Pol Med J; 1970; 9(5):1207-11. PubMed ID: 5313771
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. [Estimation of the probability of heterozygosity in Duchenne-type progressive muscular dystrophy].
    Guízar Vázquez J; Navarrete Cadena C; Rico R; Mora G; Zavala C
    Bol Med Hosp Infant Mex; 1981; 38(1):23-33. PubMed ID: 7284070
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hypokalemia complicating Duchenne muscular dystrophy.
    McDonald B; Rosenthal SA
    Yale J Biol Med; 1987; 60(5):405-8. PubMed ID: 3424874
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Lifelong care of the child with Duchenne muscular dystrophy.
    Brady MH
    MCN Am J Matern Child Nurs; 1979; 4(4):227-30. PubMed ID: 109725
    [No Abstract]   [Full Text] [Related]  

  • 11. [Sex-related neurologic diseases. Duchenne muscular dystrophy. Lowe's disease].
    Castro-Gago M
    An Esp Pediatr; 1984 Oct; 21 Suppl 20():51-4. PubMed ID: 6517412
    [No Abstract]   [Full Text] [Related]  

  • 12. [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]  

  • 13. Variability of X-linked muscular dystrophy.
    Fischbeck KH; Schotland DL
    Ann Neurol; 1983 Feb; 13(2):217. PubMed ID: 6830187
    [No Abstract]   [Full Text] [Related]  

  • 14. Neuroblastoma in Duchenne muscular dystrophy.
    Johnston KM; Zoger S; Golabi M; Mulvihill JJ
    Pediatrics; 1986 Dec; 78(6):1170-1. PubMed ID: 3786049
    [No Abstract]   [Full Text] [Related]  

  • 15. Myocardial infarction in a child aged ten with Duchenne muscular dystrophy.
    Fiorista F; Brambilla G; Saviotti M; Diaco T; Morpurgo M
    Z Kardiol; 1981 Oct; 70(10):784-8. PubMed ID: 7303802
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Acute hypokalemia as a possible cause of death in a patient with advanced muscular dystrophy.
    Soloway SS; Mudge GH
    Johns Hopkins Med J; 1979 May; 144(5):166-7. PubMed ID: 449173
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Experience with DNA analysis in Duchenne and Becker muscular dystrophy families in NSW.
    Morgan G; Donald JA; Chen J; Serravalle S; Colley P; Denton MJ
    Aust Paediatr J; 1988; 24 Suppl 1():98-9. PubMed ID: 3202741
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [New aspects of carrier diagnosis and human genetic counseling in Duchenne and Becker muscular dystrophy].
    Spiegler AW; Huppert P; Werner W; Metzke H; Strobel U; Köhler K; Gerhardt R; Kaufmann J; Herrmann FH
    Z Arztl Fortbild (Jena); 1988; 82(22):1139-42. PubMed ID: 3247797
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 4.