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 *

124 related articles for article (PubMed ID: 3835047)

  • 21. Muscle damage progression in Duchenne muscular dystrophy evaluated by a new quantitative computed tomography method.
    Liu M; Chino N; Ishihara T
    Arch Phys Med Rehabil; 1993 May; 74(5):507-14. PubMed ID: 8489361
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Plasma acetylcholinesterase in Duchenne muscular dystrophy.
    Sketelj J; Sasel B; Zupancic N; Brzin M
    Exp Neurol; 1983 May; 80(2):329-36. PubMed ID: 6840242
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [CT findings of muscular dystrophy: limb girdle type (LG), myotonic type (MYD) and Duchenne type (DMD)].
    Saitoh H
    Nihon Igaku Hoshasen Gakkai Zasshi; 1991 Jul; 51(7):790-8. PubMed ID: 1891345
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Investigation of human skeletal muscle structure and composition by X-ray computerised tomography.
    Grindrod S; Tofts P; Edwards R
    Eur J Clin Invest; 1983 Dec; 13(6):465-8. PubMed ID: 6416864
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [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]  

  • 26. Carrier detection in Duchenne muscular dystrophy using computed tomography.
    Stern LM; Caudrey DJ; Clark MS; Perrett LV; Boldt DW
    Clin Genet; 1985 Apr; 27(4):392-7. PubMed ID: 3995788
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Creatine phosphokinase activities in various skeletal muscles in a case of progressive muscular dystrophy (Duchenne type). Enzymatic measurements at autopsy].
    Araki S; Inokuchi T; Narazaki T
    Igaku To Seibutsugaku; 1967 Oct; 75(4):145-8. PubMed ID: 5627037
    [No Abstract]   [Full Text] [Related]  

  • 28. [Serum creatine kinase activity in patients with Duchenne-type dystrophy and in their mothers following physical effort].
    Hetnarska L
    Neurol Neurochir Pol; 1971; 5(5):653-7. PubMed ID: 5161075
    [No Abstract]   [Full Text] [Related]  

  • 29. Computed tomography of muscle.
    Bulcke JA; Crolla D; Termote JL; Baert A; Palmers Y; Van den Bergh R
    Muscle Nerve; 1981; 4(1):67-72. PubMed ID: 7231448
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Lower extremity involvement in Duchenne's muscular dystrophy.
    Reinherz R; Mann I
    J Am Podiatry Assoc; 1977 Nov; 67(11):796-801. PubMed ID: 915190
    [No Abstract]   [Full Text] [Related]  

  • 31. Spinal muscular atrophy and probable Duchenne muscular dystrophy occurring separately in closely related Melanesian families in Papua, New Guinea.
    Scrimgeour EM; Mastaglia FL; Kevau I
    Am J Med Genet; 1992 Aug; 43(6):1044-5. PubMed ID: 1415334
    [No Abstract]   [Full Text] [Related]  

  • 32. Serum creatine kinase isoenzymes in Duchenne muscular dystrophy determined by sensitive enzyme immunoassay methods.
    Mokuno K; Riku S; Sugimura K; Takahashi A; Kato K; Osugi S
    Muscle Nerve; 1987 Jun; 10(5):459-63. PubMed ID: 3302699
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Identification of the carrier state in the severe recessive X-linked muscular dystrophy (Duchenne type). I. Assay of activated serum creatine kinase activity in serum (author's transl)].
    Rotthauwe HW; Kowalewski S
    Z Kinderheilkd; 1973 Nov; 115(4):333-42. PubMed ID: 4591596
    [No Abstract]   [Full Text] [Related]  

  • 34. [Distribution of skeletal muscle involvement in autosomal recessive distal muscular dystrophy: a clinical and computed tomographic study].
    Mizusawa H; Kobayashi F; Nakanishi T
    Rinsho Shinkeigaku; 1987 Feb; 27(2):177-84. PubMed ID: 3581592
    [No Abstract]   [Full Text] [Related]  

  • 35. [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]  

  • 36. [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]  

  • 37. [Human embryonal muscles in Duchenne muscular dystrophy].
    Grinio LP
    Vopr Med Khim; 1990; 36(1):37-9. PubMed ID: 2343572
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Serum alpha-galactosidase activity in children with Duchenne-type muscular dystrophy and in gene carriers.
    László A; Havass Z
    Acta Paediatr Hung; 1983; 24(4):327-9. PubMed ID: 6324830
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Duchenne muscular dystrophy, preclinical diagnosis.
    Murdoch JL
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):110. PubMed ID: 5173117
    [No Abstract]   [Full Text] [Related]  

  • 40. Investigation of scoliosis in Duchenne dystrophy using computerized tomography.
    Stern LM; Clark BE
    Muscle Nerve; 1988 Jul; 11(7):775-83. PubMed ID: 3405244
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.