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 *

70 related articles for article (PubMed ID: 7134759)

  • 21. [Analysis of the interference pattern in patients with muscular dystrophy].
    Escobar-Cedillo RE; Miranda A; Lona S; Castillo M
    Rev Neurol; 2004 Sep 16-30; 39(6):517-20. PubMed ID: 15467987
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Congenital muscular dystrophy: report on 10 cases].
    Olivé M; Roig M; Bonaventura I; Navarro C
    Neurologia; 1994 Nov; 9(9):387-92. PubMed ID: 7811489
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The congenital and limb-girdle muscular dystrophies: sharpening the focus, blurring the boundaries.
    Kirschner J; Bönnemann CG
    Arch Neurol; 2004 Feb; 61(2):189-99. PubMed ID: 14967765
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Carnitine levels in normal children and adults and in patients with diseases muscle.
    Carrier HN; Berthillier G
    Muscle Nerve; 1980; 3(4):326-34. PubMed ID: 7412776
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [The place of electromyography in the diagnosis of myopathy in children].
    Raimbault J; Renault F; Laget P
    Ann Pediatr (Paris); 1977; 24(6-7):451-8. PubMed ID: 16211924
    [No Abstract]   [Full Text] [Related]  

  • 26. Intramuscular renin-angiotensin system is activated in human muscular dystrophy.
    Sun G; Haginoya K; Dai H; Chiba Y; Uematsu M; Hino-Fukuyo N; Onuma A; Iinuma K; Tsuchiya S
    J Neurol Sci; 2009 May; 280(1-2):40-8. PubMed ID: 19232644
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The functional staging of Duchenne muscular dystrophy using in vivo 31P MR spectroscopy.
    Ikehira H; Nishikawa S; Matsumura K; Hasegawa T; Arimizu N; Tateno Y
    Radiat Med; 1995; 13(2):63-5. PubMed ID: 7667509
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Glycocyaminuria in normal and myodystrophic children; its significance in the metabolic disorder of progressive muscular dystrophy].
    SVILOKOS N; SERAFINI L; VERDURA G
    Minerva Pediatr; 1958 May; 10(19-20):549-52. PubMed ID: 13565816
    [No Abstract]   [Full Text] [Related]  

  • 29. Full circle to cobbled brain.
    Ross ME
    Nature; 2002 Jul; 418(6896):376-7. PubMed ID: 12140540
    [No Abstract]   [Full Text] [Related]  

  • 30. Distal muscular dystrophy of the Miyoshi type.
    Yildiz H; Emre U; Coskun O; Ergün U; Atasoy HT; Inan LE
    Clin Neuropathol; 2003; 22(4):204-8. PubMed ID: 12908758
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Inherited myopathies and muscular dystrophies.
    Cardamone M; Darras BT; Ryan MM
    Semin Neurol; 2008 Apr; 28(2):250-9. PubMed ID: 18351526
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Muscular dystrophies in childhood. I. Current aspects of classification, pathogenesis, diagnosis, clinical course and therapy].
    John R; Daute KH
    Kinderarztl Prax; 1980 Dec; 48(12):633-9. PubMed ID: 7206463
    [No Abstract]   [Full Text] [Related]  

  • 33. Using electromyography to assess function in humans and animal models of muscular dystrophy.
    Han JJ; Carter GT; Weiss MD; Shekar C; Kornegay JN
    Phys Med Rehabil Clin N Am; 2005 Nov; 16(4):981-97, x. PubMed ID: 16214055
    [No Abstract]   [Full Text] [Related]  

  • 34. Basic and clinical studies on mouth occlusion pressure in healthy subjects and patients with pulmonary and muscular diseases.
    Yunus F
    Hiroshima J Med Sci; 1982 Dec; 31(4):233-58. PubMed ID: 7182382
    [No Abstract]   [Full Text] [Related]  

  • 35. Diagnostic value of satellite potentials in clinical EMG.
    Rowińska-Marcińska K; Ryniewicz B; Hausmanowa-Petrusewicz I; Karwańska A
    Electromyogr Clin Neurophysiol; 1997; 37(8):483-9. PubMed ID: 9444488
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Hepatic, renal, muscular and myocardial pentoses in hereditary myodystrophic mice].
    MAGGI V; MAGARO M; SENSI S; GRECO AV; GAMBASSI G
    Boll Soc Ital Biol Sper; 1959 Jul; 35():877-8. PubMed ID: 14419817
    [No Abstract]   [Full Text] [Related]  

  • 37. [Better knowledge of oculo-pharyngeal muscular dystrophy for better diagnosis].
    Tymchyk-Tremblay S
    Infirm Que; 1996; 4(2):25-8. PubMed ID: 9136361
    [No Abstract]   [Full Text] [Related]  

  • 38. [New advances in muscular dystrophy: an up-to-date diagnostic plan].
    Lin S; Liechti-Gallati S; Burgunder JM
    Schweiz Med Wochenschr; 1999 Aug; 129(33):1141-51. PubMed ID: 10483667
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Analytic determination of metmyoglobin and its clinical use].
    Peham H
    Verh Dtsch Ges Inn Med; 1971; 77():1121-3. PubMed ID: 5155977
    [No Abstract]   [Full Text] [Related]  

  • 40. [Vascular disorders in progressive muscular dystrophy].
    Badalian LO; Temin PA; Il'in IL; Dzhabarov BD
    Klin Med (Mosk); 1981 Feb; 59(2):15-8. PubMed ID: 7289479
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.