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 *

180 related articles for article (PubMed ID: 9810590)

  • 21. Mitochondrial myopathies-clinicopathological features and diagnostic modalities.
    Tatke M
    Indian J Pathol Microbiol; 2007 Jul; 50(3):467-77. PubMed ID: 17883111
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Mitochondrial myopathies.
    Larsson NG; Oldfors A
    Acta Physiol Scand; 2001 Mar; 171(3):385-93. PubMed ID: 11412152
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. 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]  

  • 25. Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene.
    Mancuso M; Filosto M; Bonilla E; Hirano M; Shanske S; Vu TH; DiMauro S
    Arch Neurol; 2003 Jul; 60(7):1007-9. PubMed ID: 12873860
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Aerobic training is safe and improves exercise capacity in patients with mitochondrial myopathy.
    Jeppesen TD; Schwartz M; Olsen DB; Wibrand F; Krag T; Dunø M; Hauerslev S; Vissing J
    Brain; 2006 Dec; 129(Pt 12):3402-12. PubMed ID: 16815877
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Congenital nemaline myopathy with mitochondrial abnormalities. An adult case report].
    Oya Y; Segawa M; Ogawa M; Goto Y; Nonaka I; Kawai M
    Rinsho Shinkeigaku; 2000 May; 40(5):452-8. PubMed ID: 11002727
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Detection of mitochondrial defects by laser fluorimetry.
    Kunz WS; Winkler K; Kuznetsov AV; Lins H; Kirches E; Wallesch CW
    Mol Cell Biochem; 1997 Sep; 174(1-2):97-100. PubMed ID: 9309672
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Mitochondrial nature of cardiomyopathies in children (analysis of skeletal muscle biopsies)].
    Sukhorukov VS; Klembovskiĭ AI; Nevstrueva VV; Leont'eva IV; Belozerov IuM; Sebeleva AI
    Arkh Patol; 1997; 59(5):12-8. PubMed ID: 9446528
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Neurotrophin-4 is up-regulated in ragged-red fibers associated with pathogenic mitochondrial DNA mutations.
    Walker UA; Schon EA
    Ann Neurol; 1998 Apr; 43(4):536-40. PubMed ID: 9546339
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Neuropathology of mitochondrial diseases.
    Filosto M; Tomelleri G; Tonin P; Scarpelli M; Vattemi G; Rizzuto N; Padovani A; Simonati A
    Biosci Rep; 2007 Jun; 27(1-3):23-30. PubMed ID: 17541738
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies.
    Filosto M; Mancuso M; Vives-Bauza C; Vilà MR; Shanske S; Hirano M; Andreu AL; DiMauro S
    Ann Neurol; 2003 Oct; 54(4):524-6. PubMed ID: 14520667
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Mitochondrial diseases].
    Serratrice G
    Rev Prat; 1993 Apr; 43(7):868-74. PubMed ID: 8346403
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Relationship of primary mitochondrial respiratory chain dysfunction to fiber type abnormalities in skeletal muscle.
    Enns GM; Hoppel CL; DeArmond SJ; Schelley S; Bass N; Weisiger K; Horoupian D; Packman S
    Clin Genet; 2005 Oct; 68(4):337-48. PubMed ID: 16143021
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Comparative diagnostic value of the analysis of the skeletal muscle and lymphocytes in mitochondrial diseases].
    Sukhorukov VS; Nartsissov RP; Petrichuk SV; Vasil'ev S; Nikolaeva EA; Kleĭmenova NV; Klembovskiĭ AI; Kazantseva LZ
    Arkh Patol; 2000; 62(2):19-21. PubMed ID: 10789008
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects.
    De Paepe B; Smet J; Lammens M; Seneca S; Martin JJ; De Bleecker J; De Meirleir L; Lissens W; Van Coster R
    J Clin Pathol; 2009 Feb; 62(2):172-6. PubMed ID: 19181635
    [TBL] [Abstract][Full Text] [Related]  

  • 37. SCID mice containing muscle with human mitochondrial DNA mutations. An animal model for mitochondrial DNA defects.
    Clark KM; Watt DJ; Lightowlers RN; Johnson MA; Relvas JB; Taanman JW; Turnbull DM
    J Clin Invest; 1998 Dec; 102(12):2090-5. PubMed ID: 9854044
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Diagnosis of mitochondrial diseases: clinical and histological study of sixty patients with ragged red fibers.
    Challa S; Kanikannan MA; Murthy JM; Bhoompally VR; Surath M
    Neurol India; 2004 Sep; 52(3):353-8. PubMed ID: 15472426
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Thymidine kinase 2 defects can cause multi-tissue mtDNA depletion syndrome.
    Götz A; Isohanni P; Pihko H; Paetau A; Herva R; Saarenpää-Heikkilä O; Valanne L; Marjavaara S; Suomalainen A
    Brain; 2008 Nov; 131(Pt 11):2841-50. PubMed ID: 18819985
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Distribution of COX-negative mitochondria in myofibers of rats intoxicated with Senna occidentalis seeds.
    Calore NM; Calore EE; Sesso A; Correia H; Marcondes MC; Vilela de Almeida L
    J Submicrosc Cytol Pathol; 2002 Apr; 34(2):227-31. PubMed ID: 12117285
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.