BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

182 related articles for article (PubMed ID: 11100052)

  • 1. Succinate dehydrogenase deficiency.
    Vladutiu GD; Heffner RR
    Arch Pathol Lab Med; 2000 Dec; 124(12):1755-8. PubMed ID: 11100052
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Isolated mitochondrial myopathy associated with muscle coenzyme Q10 deficiency.
    Lalani SR; Vladutiu GD; Plunkett K; Lotze TE; Adesina AM; Scaglia F
    Arch Neurol; 2005 Feb; 62(2):317-20. PubMed ID: 15710863
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A patient with mitochondrial myopathy associated with isolated succinate dehydrogenase deficiency.
    Sugimoto J; Shimohira M; Osawa Y; Matsubara M; Yamamoto H; Goto Y; Nonaka I
    Brain Dev; 2000 May; 22(3):158-62. PubMed ID: 10814897
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sarcoid myopathy and mitochondrial respiratory chain defects: clinicopathological, biochemical and molecular biological analyses.
    Reichmann H; Schalke B; Seibel P; Naumann M; Toyka K
    Neuromuscul Disord; 1995 Jul; 5(4):277-83. PubMed ID: 7580239
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Biochemical investigations and immunoblot analyses of two unrelated patients with an isolated deficiency in complex II of the mitochondrial respiratory chain.
    Birch-Machin MA; Marsac C; Ponsot G; Parfait B; Taylor RW; Rustin P; Munnich A
    Biochem Biophys Res Commun; 1996 Mar; 220(1):57-62. PubMed ID: 8602857
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Characterization of mitochondrial myopathies through the evaluation of the enzymatic activities involved in energy metabolism].
    Pedroso FC; Campello AP; Werneck LC; Klüppel ML
    Arq Neuropsiquiatr; 1997 Jun; 55(2):249-57. PubMed ID: 9629385
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Succinate Dehydrogenase B (SDHB) Immunohistochemistry for the Evaluation of Muscle Biopsies.
    Punsoni M; Mangray S; Lombardo KA; Heath N; Stopa EG; Yakirevich E
    Appl Immunohistochem Mol Morphol; 2017 Oct; 25(9):645-650. PubMed ID: 27556822
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Single muscle fibre analyses in 2 brothers with succinate dehydrogenase deficiency.
    Reichmann H; Angelini C
    Eur Neurol; 1994; 34(2):95-8. PubMed ID: 8174601
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Progressive myopathy with a combined respiratory chain defect including Complex II.
    Rodrigues Ade S; Kiyomoto BH; Oliveira AS; Gabbai AA; Schmidt B; Tengan CH
    J Neurol Sci; 2008 Jan; 264(1-2):182-6. PubMed ID: 17850823
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Respiratory chain enzyme defects in patients with idiopathic inflammatory myopathy.
    Campos Y; Arenas J; Cabello A; Gomez-Reino JJ
    Ann Rheum Dis; 1995 Jun; 54(6):491-3. PubMed ID: 7632092
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cytochrome c oxidase-intermediate fibres: importance in understanding the pathogenesis and treatment of mitochondrial myopathy.
    Murphy JL; Ratnaike TE; Shang E; Falkous G; Blakely EL; Alston CL; Taivassalo T; Haller RG; Taylor RW; Turnbull DM
    Neuromuscul Disord; 2012 Aug; 22(8):690-8. PubMed ID: 22647770
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial myopathy with succinate dehydrogenase and aconitase deficiency. Abnormalities of several iron-sulfur proteins.
    Hall RE; Henriksson KG; Lewis SF; Haller RG; Kennaway NG
    J Clin Invest; 1993 Dec; 92(6):2660-6. PubMed ID: 8254022
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel immunofluorescent assay to investigate oxidative phosphorylation deficiency in mitochondrial myopathy: understanding mechanisms and improving diagnosis.
    Rocha MC; Grady JP; Grünewald A; Vincent A; Dobson PF; Taylor RW; Turnbull DM; Rygiel KA
    Sci Rep; 2015 Oct; 5():15037. PubMed ID: 26469001
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Evaluation of patients with lactic acidosis using microphotometric mitochondrial enzyme assay in single muscle fibers.
    Sugie H; Sugie Y; Ito M; Tsurui S; Shimizu K; Nakajima H; Fukuda T; Ishikawa A; Sato H; Hirano K
    Brain Dev; 1994; 16(4):315-9. PubMed ID: 7818028
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical manifestation and a new ISCU mutation in iron-sulphur cluster deficiency myopathy.
    Kollberg G; Tulinius M; Melberg A; Darin N; Andersen O; Holmgren D; Oldfors A; Holme E
    Brain; 2009 Aug; 132(Pt 8):2170-9. PubMed ID: 19567699
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Deficiency of skeletal muscle succinate dehydrogenase and aconitase. Pathophysiology of exercise in a novel human muscle oxidative defect.
    Haller RG; Henriksson KG; Jorfeldt L; Hultman E; Wibom R; Sahlin K; Areskog NH; Gunder M; Ayyad K; Blomqvist CG
    J Clin Invest; 1991 Oct; 88(4):1197-206. PubMed ID: 1918374
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mitochondrial myopathy in a german shepherd dog.
    Paciello O; Maiolino P; Fatone G; Papparella S
    Vet Pathol; 2003 Sep; 40(5):507-11. PubMed ID: 12949407
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL family.
    de la Peña P; Bornstein B; del Hoyo P; Fernández-Moreno MA; Martín MA; Campos Y; Gómez-Escalonilla C; Molina JA; Cabello A; Arenas J; Garesse R
    Neurology; 2001 Oct; 57(7):1235-8. PubMed ID: 11591842
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Diagnostic yield muscle biopsy in patients with clinical evidence of mitochondrial cytopathy.
    Rollins S; Prayson RA; McMahon JT; Cohen BH
    Am J Clin Pathol; 2001 Sep; 116(3):326-30. PubMed ID: 11554158
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.