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 *

188 related articles for article (PubMed ID: 9127121)

  • 21. [Study of human muscle biopsies with muscle glycogen storage diseases using 1H nuclear magnetic resonance spectroscopy (NMRS)--analysis of perchloric acid extracts of muscles].
    Sugie H; Sugie Y; Ito M; Tsurui S
    Rinsho Shinkeigaku; 1991 Jun; 31(6):616-8. PubMed ID: 1657479
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Glycogen storage myopathy with abnormal lactate dehydrogenase.
    Nagata N; Miike T; Matsuda I; Shikama H; Tokumitsu Y; Ui M
    Neuropediatrics; 1982 May; 13(2):103-7. PubMed ID: 6957732
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Specific enzyme diagnosis in mitochondrial myopathies and encephalomyopathies].
    László A; Sümegi B; Alkonyi I; Horváth E; Sztriha L; Várkonyi A; Zombori J
    Orv Hetil; 1994 Apr; 135(14):747-50. PubMed ID: 8170674
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Skeletal muscle glycolytic capacity and phosphofructokinase regulation in horses with polysaccharide storage myopathy.
    Valberg SJ; Townsend D; Mickelson JR
    Am J Vet Res; 1998 Jun; 59(6):782-5. PubMed ID: 9622752
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Enzyme histochemistry in the biopsy diagnosis of skeletal muscle diseases].
    Gullotta F
    Acta Histochem Suppl; 1983; 28():75-84. PubMed ID: 6412312
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Nation-wide survey on muscle glycogen storage disease (MGSDs) and comparison with our experiences in diagnosis of MGSDs].
    Fukuda T; Sugie H; Ito M; Sugie Y; Saito K; Nishino I; Shimizu T
    Rinsho Shinkeigaku; 2003 May; 43(5):243-8. PubMed ID: 12931628
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
    Auré K; Fayet G; Leroy JP; Lacène E; Romero NB; Lombès A
    Brain; 2006 May; 129(Pt 5):1249-59. PubMed ID: 16537564
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Glycogenosis with amylopectinoid deposits in a 13-year-old girl.
    Tuñón T; Bengoechea O; Narbona J
    Clin Neuropathol; 1988; 7(3):100-4. PubMed ID: 3203479
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Investigation of children for mitochondriopathy confirms need for strict patient selection, improved morphological criteria, and better laboratory methods.
    Miles L; Wong BL; Dinopoulos A; Morehart PJ; Hofmann IA; Bove KE
    Hum Pathol; 2006 Feb; 37(2):173-84. PubMed ID: 16426917
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Glycogen storage myopathies.
    Tsujino S; Nonaka I; DiMauro S
    Neurol Clin; 2000 Feb; 18(1):125-50. PubMed ID: 10658171
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Clinical and biochemical analysis of 27 patients with myoglobinuria of unknown causes].
    Tsurui S; Sugie H; Ito M; Igarashi Y
    Rinsho Shinkeigaku; 1995 Jan; 35(1):24-8. PubMed ID: 7781210
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Spectrum of myopathic findings in 50 patients with the 3243A>G mutation in mitochondrial DNA.
    Kärppä M; Herva R; Moslemi AR; Oldfors A; Kakko S; Majamaa K
    Brain; 2005 Aug; 128(Pt 8):1861-9. PubMed ID: 15857931
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Clinical features, diagnosis and treatment of McArdle's glycogenosis].
    Lobzin VS; Saĭkova LA
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(3):342-5. PubMed ID: 6586038
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Exercise intolerance caused by muscular phosphorylase kinase deficiency. Contribution of in vivo metabolic studies].
    Laforêt P; Eymard B; Lombès A; Duboc D; Jehenson P; Rocchiccioli F; Chaussain M; Chateau D; Brunet P; Fardeau M
    Rev Neurol (Paris); 1996; 152(6-7):458-64. PubMed ID: 8944243
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Ultrastructural examination of the axillary skin biopsy in the diagnosis of metabolic diseases.
    Abramovich CM; Prayson RA; McMahon JT; Cohen BH
    Hum Pathol; 2001 Jun; 32(6):649-55. PubMed ID: 11431721
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Adult-onset glycogen storage disease type 2: clinico-pathological phenotype revisited.
    Schoser BG; Müller-Höcker J; Horvath R; Gempel K; Pongratz D; Lochmüller H; Müller-Felber W
    Neuropathol Appl Neurobiol; 2007 Oct; 33(5):544-59. PubMed ID: 17573812
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Fatal familial infantile glycogen storage disease: multisystem phosphofructokinase deficiency.
    Amit R; Bashan N; Abarbanel JM; Shapira Y; Sofer S; Moses S
    Muscle Nerve; 1992 Apr; 15(4):455-8. PubMed ID: 1533013
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Myasthenic form of a metabolic myopathy with dystrophic changes due to storage and symptoms resembling McArdle's syndrome (a case report)].
    Wagner A; Zett W
    Psychiatr Neurol Med Psychol (Leipz); 1971 Nov; 23(11):650-7. PubMed ID: 5291479
    [No Abstract]   [Full Text] [Related]  

  • 39. [The importance of muscle biopsy in the diagnosis of neuromuscular diseases].
    Bleggi-Torres LF; de Noronha L
    Arq Neuropsiquiatr; 1994 Sep; 52(3):370-5. PubMed ID: 7893212
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [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]  

    [Previous]   [Next]    [New Search]
    of 10.