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 *

207 related articles for article (PubMed ID: 10593563)

  • 21. Disorders of mitochondria and related metabolism.
    Zeviani M; Fernandez-Silva P; Tiranti V
    Curr Opin Neurol; 1997 Apr; 10(2):160-7. PubMed ID: 9146998
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Mitochondrial diseases. Clinical features, investigation and genetics].
    Østergaard E; Wibrand F; Horn N; Brøndum-Nielsen K
    Ugeskr Laeger; 2003 Feb; 165(7):663-8. PubMed ID: 12617042
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mitochondrial encephalopathies.
    Maertens P
    Semin Pediatr Neurol; 1996 Dec; 3(4):279-97. PubMed ID: 8969010
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mitochondrial encephalomyopathy.
    Goto Y
    Neuropathology; 2000 Sep; 20 Suppl():S82-4. PubMed ID: 11037195
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mitochondrial respiratory-chain defects presenting as nonspecific features in children.
    Tsao CY; Mendell JR; Lo WD; Luquette M; Rusin J
    J Child Neurol; 2000 Jul; 15(7):445-8. PubMed ID: 10921514
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mitochondrial disease criteria: diagnostic applications in children.
    Morava E; van den Heuvel L; Hol F; de Vries MC; Hogeveen M; Rodenburg RJ; Smeitink JA
    Neurology; 2006 Nov; 67(10):1823-6. PubMed ID: 17130416
    [TBL] [Abstract][Full Text] [Related]  

  • 27. SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness.
    Carrozzo R; Dionisi-Vici C; Steuerwald U; Lucioli S; Deodato F; Di Giandomenico S; Bertini E; Franke B; Kluijtmans LA; Meschini MC; Rizzo C; Piemonte F; Rodenburg R; Santer R; Santorelli FM; van Rooij A; Vermunt-de Koning D; Morava E; Wevers RA
    Brain; 2007 Mar; 130(Pt 3):862-74. PubMed ID: 17301081
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Novel mutation in SUCLA2 identified on sequencing analysis.
    Güngör O; Özkaya AK; Güngör G; Karaer K; Dilber C; Aydin K
    Pediatr Int; 2016 Jul; 58(7):659-61. PubMed ID: 26952923
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Respiratory chain encephalomyopathies: a diagnostic classification.
    Walker UA; Collins S; Byrne E
    Eur Neurol; 1996; 36(5):260-7. PubMed ID: 8864705
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Pathogenic Mitochondria DNA Mutations: Current Detection Tools and Interventions.
    Mustafa MF; Fakurazi S; Abdullah MA; Maniam S
    Genes (Basel); 2020 Feb; 11(2):. PubMed ID: 32059522
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Variable phenotypes in a family with mitochondrial encephalomyopathy harboring a 3291T > C mutation in mitochondrial DNA.
    Sunami Y; Sugaya K; Chihara N; Goto Y; Matsubara S
    Neurol Sci; 2011 Oct; 32(5):861-4. PubMed ID: 21863273
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mitochondrial encephalomyopathy lactic acidosis and strokelike episodes mimicking occipital idiopathic epilepsy.
    Cesaroni E; Scarpelli M; Zamponi N; Polonara G; Zeviani M
    Pediatr Neurol; 2009 Aug; 41(2):131-4. PubMed ID: 19589463
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Rolandic mitochondrial encephalomyelopathy and MT-ND3 mutations.
    Werner KG; Morel CF; Kirton A; Benseler SM; Shoffner JM; Addis JB; Robinson BH; Burrowes DM; Blaser SI; Epstein LG; Feigenbaum AS
    Pediatr Neurol; 2009 Jul; 41(1):27-33. PubMed ID: 19520270
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Different tissue distribution of a mitochondrial DNA duplication and the corresponding deletion in a patient with a mild mitochondrial encephalomyopathy: deletion in muscle, duplication in blood.
    Houshmand M; Gardner A; Hällström T; Müntzing K; Oldfors A; Holme E
    Neuromuscul Disord; 2004 Mar; 14(3):195-201. PubMed ID: 15036329
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Cellular models for pathogenesis in mitochondrial diseases.
    Di Donato S
    Curr Opin Neurol; 1996 Dec; 9(6):469-72. PubMed ID: 9007407
    [No Abstract]   [Full Text] [Related]  

  • 36. New mutations in TK2 gene associated with mitochondrial DNA depletion.
    Galbiati S; Bordoni A; Papadimitriou D; Toscano A; Rodolico C; Katsarou E; Sciacco M; Garufi A; Prelle A; Aguennouz M'; Bonsignore M; Crimi M; Martinuzzi A; Bresolin N; Papadimitriou A; Comi GP
    Pediatr Neurol; 2006 Mar; 34(3):177-85. PubMed ID: 16504786
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Mitochondrial encephalomyopathies starting in childhood and adolescence].
    Castro-Gago M; Novo-Rodríguez MI; Eirís-Puñal J
    Rev Neurol; 1998 Apr; 26 Suppl 1():S61-71. PubMed ID: 9810592
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Additive effect of nuclear and mitochondrial mutations in a patient with mitochondrial encephalomyopathy.
    Nesti C; Meschini MC; Meunier B; Sacchini M; Doccini S; Romano A; Petrillo S; Pezzini I; Seddiki N; Rubegni A; Piemonte F; Donati MA; Brasseur G; Santorelli FM
    Hum Mol Genet; 2015 Jun; 24(11):3248-56. PubMed ID: 25736212
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Diseases of oxidative phosphorylation due to mtDNA mutations.
    DiMauro S; Andreu AL; Musumeci O; Bonilla E
    Semin Neurol; 2001 Sep; 21(3):251-60. PubMed ID: 11641815
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mitochondrial encephalomyopathies.
    Shoubridge EA
    Curr Opin Neurol; 1998 Oct; 11(5):491-6. PubMed ID: 9847999
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.