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 *

80 related articles for article (PubMed ID: 3229402)

  • 21. [Inborn errors of metabolism in muscle cells].
    Sengers RC; Stadhouders AM; Trijbels JM; Bookelman H
    Ned Tijdschr Geneeskd; 1977 Mar; 121(12):493-9. PubMed ID: 321979
    [No Abstract]   [Full Text] [Related]  

  • 22. A new variant of late-onset myophosphorylase deficiency.
    Kost GJ; Verity MA
    Muscle Nerve; 1980; 3(3):195-201. PubMed ID: 6929403
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Gentamicin treatment in McArdle disease: failure to correct myophosphorylase deficiency.
    Schroers A; Kley RA; Stachon A; Horvath R; Lochmüller H; Zange J; Vorgerd M
    Neurology; 2006 Jan; 66(2):285-6. PubMed ID: 16434679
    [No Abstract]   [Full Text] [Related]  

  • 24. [Muscular intolerance of exercise. Current data].
    Serratrice G
    Presse Med; 1998 Oct; 27(33):1683-6. PubMed ID: 9834785
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Complex phenotypes in metabolic muscle diseases.
    Vladutiu GD
    Muscle Nerve; 2000 Aug; 23(8):1157-9. PubMed ID: 10918250
    [No Abstract]   [Full Text] [Related]  

  • 26. Biochemistry of striated muscle during human muscular diseases.
    Schapira G; Dreyfus JC; Schapira F
    Enzymol Biol Clin (Basel); 1970; 11(1):8-31. PubMed ID: 4905517
    [No Abstract]   [Full Text] [Related]  

  • 27. Metabolic response to exercise and muscle disease.
    Sahgal V; Solomon R
    Compr Ther; 1986 Jan; 12(1):31-8. PubMed ID: 2936540
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Metabolic diseases of skeletal muscle: clues to understanding exercise physiology.
    Scheen AJ
    Eur J Med; 1992 Dec; 1(8):453-6. PubMed ID: 1341203
    [No Abstract]   [Full Text] [Related]  

  • 29. Myophosphorylase deficiency impairs muscle oxidative metabolism.
    Haller RG; Lewis SF; Cook JD; Blomqvist CG
    Ann Neurol; 1985 Feb; 17(2):196-9. PubMed ID: 3856415
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Late-onset McArdle's disease mimicking treatment-resistant polymyositis. Report of a case and review of the literature.
    Pego R; González-Gay MA; García-Porrúa C; Brañas F; Navarro C
    Rev Rhum Engl Ed; 1999 Apr; 66(4):236-7. PubMed ID: 10339783
    [No Abstract]   [Full Text] [Related]  

  • 31. Metabolic myopathies: evaluation by graded exercise testing.
    Elliot DL; Buist NR; Goldberg L; Kennaway NG; Powell BR; Kuehl KS
    Medicine (Baltimore); 1989 May; 68(3):163-72. PubMed ID: 2716515
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Metabolic myopathies].
    Zellweger H
    Padiatr Grenzgeb; 1984; 23(5):327-38. PubMed ID: 6504540
    [No Abstract]   [Full Text] [Related]  

  • 33. [Exercise-induced muscular weakness, myalgia and contractures. I. A clinical review].
    Mattle H; Jerusalem F
    Schweiz Med Wochenschr; 1977 Apr; 107(13):428-36. PubMed ID: 139680
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Exercise tolerance and daily life in McArdle's disease.
    Ollivier K; Hogrel JY; Gomez-Merino D; Romero NB; Laforêt P; Eymard B; Portero P
    Muscle Nerve; 2005 May; 31(5):637-41. PubMed ID: 15614801
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The role of histochemistry in muscle disease.
    Dubowitz V
    Mod Trends Neurol; 1970; 5(0):189-208. PubMed ID: 4277721
    [No Abstract]   [Full Text] [Related]  

  • 36. An A-to-C substitution involving the translation initiation codon in a patient with myophosphorylase deficiency (McArdle's disease).
    Tsujino S; Rubin LA; Shanske S; DiMauro S
    Hum Mutat; 1994; 4(1):73-5. PubMed ID: 7951262
    [No Abstract]   [Full Text] [Related]  

  • 37. [Late diagnosis of a McArdle disease's case (type V glycogenosis)].
    Flavier S; Rolland MO; Eude M; Fédou C; Brun JF; Maire I; Mercier J; Raynaud E
    Ann Biol Clin (Paris); 2007; 65(5):550-4. PubMed ID: 17913675
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Myopathy in McArdle's syndrome. Improvement with a high-protein diet.
    Slonim AE; Goans PJ
    N Engl J Med; 1985 Feb; 312(6):355-9. PubMed ID: 3855499
    [No Abstract]   [Full Text] [Related]  

  • 39. Adult muscle phosphorylase "b" kinase deficiency.
    Abarbanel JM; Bashan N; Potashnik R; Osimani A; Moses SW; Herishanu Y
    Neurology; 1986 Apr; 36(4):560-2. PubMed ID: 3083284
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [2 causes of muscle ache and reddish-brown urine following exertion].
    Jennekens FG; Scholte HR; Koster JF; Bouvy JJ
    Ned Tijdschr Geneeskd; 1979 Sep; 123(36):1562-8. PubMed ID: 289908
    [No Abstract]   [Full Text] [Related]  

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