BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

102 related articles for article (PubMed ID: 11933462)

  • 21. Mitochondrial myopathy with anemia, cardiomyopathy, and lactic acidosis: a distinct late onset mitochondrial disorder.
    Van Hove JL; Shanske S; Ciacci F; Ballinger S; Shoffner JS; Wallace DC; Hanioka T; Folkers K; Bossen EH; Kussin PS
    Am J Med Genet; 1994 Jun; 51(2):114-20. PubMed ID: 8092186
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Mitochondrial fatty acid oxidation disorders in Thai infants: a report of 3 cases.
    Wasant P; Matsumoto I; Naylor E; Liammongkolkul S
    J Med Assoc Thai; 2002 Aug; 85 Suppl 2():S710-9. PubMed ID: 12403251
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Hypertrophic cardiomyopathy with mitochondrial DNA depletion and respiratory enzyme defects.
    Marin-Garcia J; Ananthakrishnan R; Goldenthal MJ
    Pediatr Cardiol; 1998; 19(3):266-8. PubMed ID: 9568229
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Regional absence of mitochondria causing energy depletion in the myocardium of muscle LIM protein knockout mice.
    van den Bosch BJ; van den Burg CM; Schoonderwoerd K; Lindsey PJ; Scholte HR; de Coo RF; van Rooij E; Rockman HA; Doevendans PA; Smeets HJ
    Cardiovasc Res; 2005 Feb; 65(2):411-8. PubMed ID: 15639480
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Mitochondrial cardiomyopathy with a high degree of heart muscle hypertrophy].
    Grantzow R; Hübner G
    Monatsschr Kinderheilkd; 1982 Dec; 130(12):909-10. PubMed ID: 6891436
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mitochondrial tRNA gene mutations in patients having mitochondrial disease with lactic acidosis.
    Ueki I; Koga Y; Povalko N; Akita Y; Nishioka J; Yatsuga S; Fukiyama R; Matsuishi T
    Mitochondrion; 2006 Feb; 6(1):29-36. PubMed ID: 16337222
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Mitochondrial diseases in adults].
    Serratrice J; Desnuelle C; Granel B; de Roux-Serratrice C; Disdier P; Weiller PJ
    Rev Med Interne; 2001 Dec; 22 Suppl 3():356s-366s. PubMed ID: 11794880
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Diagnosis and therapy of mitochondriopathies].
    Sperl W
    Wien Klin Wochenschr; 1997 Feb; 109(3):93-9. PubMed ID: 9139466
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Fatal neonatal cardiomyopathy associated with cataract and mitochondrial myopathy.
    Smeitink JA; Sengers RC; Trijbels JM; Ruitenbeek W; Daniëls O; Stadhouders AM; Kock-Jansen MJ
    Eur J Pediatr; 1989 Jun; 148(7):656-9. PubMed ID: 2744041
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mitochondrial citrate synthase crystals: novel finding in Sengers syndrome caused by acylglycerol kinase (AGK) mutations.
    Siriwardena K; Mackay N; Levandovskiy V; Blaser S; Raiman J; Kantor PF; Ackerley C; Robinson BH; Schulze A; Cameron JM
    Mol Genet Metab; 2013 Jan; 108(1):40-50. PubMed ID: 23266196
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Severe obstructive hypertrophic cardiomyopathy occurring secondary to mitochondrial disease.
    Izgi C; Cevik C; Bakal RB; Ozkan M
    Turk Kardiyol Dern Ars; 2009 Jul; 37(5):332-6. PubMed ID: 19875907
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mitochondrial defects in cardiomyopathy and neuromuscular disease.
    Wallace DC
    Am Heart J; 2000 Feb; 139(2 Pt 3):S70-85. PubMed ID: 10650320
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Exercise intolerance in patients with McArdle's disease or mitochondrial myopathies.
    Chaussain M; Camus F; Defoligny C; Eymard B; Fardeau M
    Eur J Med; 1992 Dec; 1(8):457-63. PubMed ID: 1341204
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Activities of respiratory chain complexes and pyruvate dehydrogenase in isolated muscle mitochondria in premature neonates.
    Honzik T; Wenchich L; Böhm M; Hansikova H; Pejznochova M; Zapadlo M; Plavka R; Zeman J
    Early Hum Dev; 2008 Apr; 84(4):269-76. PubMed ID: 17698302
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The hepatic mitochondrial DNA depletion syndrome: ultrastructural changes in liver biopsies.
    Mandel H; Hartman C; Berkowitz D; Elpeleg ON; Manov I; Iancu TC
    Hepatology; 2001 Oct; 34(4 Pt 1):776-84. PubMed ID: 11584375
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Microdialysis and electromyography of experimental muscle fatigue in healthy volunteers and patients with mitochondrial myopathy.
    Axelson HW; Melberg A; Ronquist G; Askmark H
    Muscle Nerve; 2002 Oct; 26(4):520-6. PubMed ID: 12362418
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mitochondrial cardiomyopathy: molecular and biochemical analysis.
    Marin-Garcia J; Goldenthal MJ
    Pediatr Cardiol; 1997; 18(4):251-60. PubMed ID: 9175519
    [TBL] [Abstract][Full Text] [Related]  

  • 38. CMR gives clue to "ragged red fibers" in the heart in a patient with mitochondrial myopathy.
    Jose T; Gdynia HJ; Mahrholdt H; Vöhringer M; Klingel K; Kandolf R; Bornemann A; Yilmaz A
    Int J Cardiol; 2011 May; 149(1):e24-7. PubMed ID: 19344965
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Heart mitochondrial respiratory chain complexes are functionally unaffected in heavy ethanol drinkers without cardiomyopathy.
    Miró O; Robert J; Casademont J; Alonso JR; Nicolás JM; Fernández-Solá J; Urbano-Márquez A; Hoek JB; Cardellach F
    Alcohol Clin Exp Res; 2000 Jun; 24(6):859-64. PubMed ID: 10888075
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mitochondrial cardiomyopathy and scapuloperoneal spinal muscular atrophy in a child.
    Malcić I; Barisić N; Pazanin L; Richter D; Jadro-Santel D; Senecić I; Jelić I; Hlavka V
    Acta Med Croatica; 1993; 47(1):47-50. PubMed ID: 7693085
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.