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 *

135 related articles for article (PubMed ID: 11757584)

  • 21. Mitochondrial cytopathies: clinical, morphological and genetic characteristics.
    Kierdaszuk B; Jamrozik Z; Tońska K; Bartnik E; Kaliszewska M; Kamińska A; Kwieciński H
    Neurol Neurochir Pol; 2009; 43(3):216-27. PubMed ID: 19618304
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Comprehensive molecular diagnosis of mitochondrial disorders: qualitative and quantitative approach.
    Wong LJ
    Ann N Y Acad Sci; 2004 Apr; 1011():246-58. PubMed ID: 15126301
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Random mtDNA deletions and functional consequence in aged human skeletal muscle.
    Chabi B; Mousson de Camaret B; Chevrollier A; Boisgard S; Stepien G
    Biochem Biophys Res Commun; 2005 Jul; 332(2):542-9. PubMed ID: 15896715
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Childhood encephalopathies and myopathies: a prospective study in a defined population to assess the frequency of mitochondrial disorders.
    Uusimaa J; Remes AM; Rantala H; Vainionpää L; Herva R; Vuopala K; Nuutinen M; Majamaa K; Hassinen IE
    Pediatrics; 2000 Mar; 105(3 Pt 1):598-603. PubMed ID: 10699115
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Impaired energy metabolism and abnormal muscle histology in mut- methylmalonic aciduria.
    Østergaard E; Wibrand F; Ørngreen MC; Vissing J; Horn N
    Neurology; 2005 Sep; 65(6):931-3. PubMed ID: 16186538
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Neuromuscular implications in CADASIL.
    Finsterer J
    Cerebrovasc Dis; 2007; 24(5):401-4. PubMed ID: 17878719
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Epileptic phenotypes in children with respiratory chain disorders.
    El Sabbagh S; Lebre AS; Bahi-Buisson N; Delonlay P; Soufflet C; Boddaert N; Rio M; Rötig A; Dulac O; Munnich A; Desguerre I
    Epilepsia; 2010 Jul; 51(7):1225-35. PubMed ID: 20196775
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Clinical, biochemical, molecular, and histological features of 65 Portuguese patients with mitochondrial disorders.
    Cruz S; Taipa R; Nogueira C; Pereira C; Almeida LS; Neiva R; Geraldes T; Guimarães A; Melo-Pires M; Vilarinho L
    Muscle Nerve; 2017 Nov; 56(5):868-872. PubMed ID: 28128857
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Reversion of mtDNA depletion in a patient with TK2 deficiency.
    Vilà MR; Segovia-Silvestre T; Gámez J; Marina A; Naini AB; Meseguer A; Lombès A; Bonilla E; DiMauro S; Hirano M; Andreu AL
    Neurology; 2003 Apr; 60(7):1203-5. PubMed ID: 12682338
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic study.
    Hammans SR; Sweeney MG; Hanna MG; Brockington M; Morgan-Hughes JA; Harding AE
    Brain; 1995 Jun; 118 ( Pt 3)():721-34. PubMed ID: 7600089
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Re-evaluation of the dysfunction of mitochondrial respiratory chain in skeletal muscle of patients with Parkinson's disease.
    Winkler-Stuck K; Kirches E; Mawrin C; Dietzmann K; Lins H; Wallesch CW; Kunz WS; Wiedemann FR
    J Neural Transm (Vienna); 2005 Apr; 112(4):499-518. PubMed ID: 15340872
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis.
    Vielhaber S; Kunz D; Winkler K; Wiedemann FR; Kirches E; Feistner H; Heinze HJ; Elger CE; Schubert W; Kunz WS
    Brain; 2000 Jul; 123 ( Pt 7)():1339-48. PubMed ID: 10869047
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mitofusin 2 mutations affect mitochondrial function by mitochondrial DNA depletion.
    Vielhaber S; Debska-Vielhaber G; Peeva V; Schoeler S; Kudin AP; Minin I; Schreiber S; Dengler R; Kollewe K; Zuschratter W; Kornblum C; Zsurka G; Kunz WS
    Acta Neuropathol; 2013 Feb; 125(2):245-56. PubMed ID: 22926664
    [TBL] [Abstract][Full Text] [Related]  

  • 34. In vivo functional investigations of lactic acid in patients with respiratory chain disorders.
    Touati G; Rigal O; Lombès A; Frachon P; Giraud M; Ogier de Baulny H
    Arch Dis Child; 1997 Jan; 76(1):16-21. PubMed ID: 9059154
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mitochondrial biogenesis: pharmacological approaches.
    Valero T
    Curr Pharm Des; 2014; 20(35):5507-9. PubMed ID: 24606795
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. A novel mutation in the mitochondrial tRNA(Ser(AGY)) gene associated with mitochondrial myopathy, encephalopathy, and complex I deficiency.
    Wong LJ; Yim D; Bai RK; Kwon H; Vacek MM; Zane J; Hoppel CL; Kerr DS
    J Med Genet; 2006 Sep; 43(9):e46. PubMed ID: 16950817
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The kidney in mitochondrial cytopathies.
    Niaudet P; Rotig A
    Kidney Int; 1997 Apr; 51(4):1000-7. PubMed ID: 9083263
    [No Abstract]   [Full Text] [Related]  

  • 39. [Ultrastructural and clinical findings of mitochondrial encephalomyopathy:report of 27 cases].
    Zhang Q; Sun YL; Zhang CP; Qu BQ; Zhang ZQ
    Zhonghua Bing Li Xue Za Zhi; 2019 Apr; 48(4):298-302. PubMed ID: 30955266
    [No Abstract]   [Full Text] [Related]  

  • 40. Somatic mitochondrial DNA mutations in mammalian aging.
    Larsson NG
    Annu Rev Biochem; 2010; 79():683-706. PubMed ID: 20350166
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.