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 *

178 related articles for article (PubMed ID: 11596342)

  • 1. [Complex I (NADH-ubiquinone oxidoreductase) deficiency].
    Nonaka I
    Ryoikibetsu Shokogun Shirizu; 2001; (36):129-31. PubMed ID: 11596342
    [No Abstract]   [Full Text] [Related]  

  • 2. Respiratory chain complex I deficiency.
    Triepels RH; Van Den Heuvel LP; Trijbels JM; Smeitink JA
    Am J Med Genet; 2001; 106(1):37-45. PubMed ID: 11579423
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Leigh disease caused by the mitochondrial DNA G14459A mutation in unrelated families.
    Kirby DM; Kahler SG; Freckmann ML; Reddihough D; Thorburn DR
    Ann Neurol; 2000 Jul; 48(1):102-4. PubMed ID: 10894222
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Low mutant load of mitochondrial DNA G13513A mutation can cause Leigh's disease.
    Kirby DM; Boneh A; Chow CW; Ohtake A; Ryan MT; Thyagarajan D; Thorburn DR
    Ann Neurol; 2003 Oct; 54(4):473-8. PubMed ID: 14520659
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Electron transfer complex I deficiency].
    Goto Y
    Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):488-90. PubMed ID: 9645116
    [No Abstract]   [Full Text] [Related]  

  • 6. [Fatal infantile mitochondrial disease].
    Murakami N
    Ryoikibetsu Shokogun Shirizu; 2001; (36):173-5. PubMed ID: 11596361
    [No Abstract]   [Full Text] [Related]  

  • 7. [Complex II (succinate-ubiquinone reductase) deficiency].
    Nonaka I
    Ryoikibetsu Shokogun Shirizu; 2001; (36):132-4. PubMed ID: 11596343
    [No Abstract]   [Full Text] [Related]  

  • 8. Human mitochondrial complex I deficiency: investigating transcriptional responses by microarray.
    van der Westhuizen FH; van den Heuvel LP; Smeets R; Veltman JA; Pfundt R; van Kessel AG; Ursing BM; Smeitink JA
    Neuropediatrics; 2003 Feb; 34(1):14-22. PubMed ID: 12690563
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Complex IV (cytochrome c oxidase) deficiency].
    Nonaka I
    Ryoikibetsu Shokogun Shirizu; 2001; (36):137-41. PubMed ID: 11596345
    [No Abstract]   [Full Text] [Related]  

  • 10. Isolated complex I deficiency in children: clinical, biochemical and genetic aspects.
    Loeffen JL; Smeitink JA; Trijbels JM; Janssen AJ; Triepels RH; Sengers RC; van den Heuvel LP
    Hum Mutat; 2000; 15(2):123-34. PubMed ID: 10649489
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Complex I deficiency due to NDUFS8 gene mutation].
    Ito M
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():441-3. PubMed ID: 12013907
    [No Abstract]   [Full Text] [Related]  

  • 12. Mitochondrial complex I deficiency caused by a deleterious NDUFA11 mutation.
    Berger I; Hershkovitz E; Shaag A; Edvardson S; Saada A; Elpeleg O
    Ann Neurol; 2008 Mar; 63(3):405-8. PubMed ID: 18306244
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Respiratory chain enzyme complex I].
    Koga Y; Ueki I
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():478-81. PubMed ID: 12013918
    [No Abstract]   [Full Text] [Related]  

  • 14. Infantile mitochondrial disorders.
    Carrozzo R; Piemonte F; Tessa A; Lucioli S; Rizza T; Meschini MC; Fattori F; Santorelli FM
    Biosci Rep; 2007 Jun; 27(1-3):105-12. PubMed ID: 17486440
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sporadic heteroplasmic single 5.5 kb mitochondrial DNA deletion associated with cerebellar ataxia, hypogonadotropic hypogonadism, choroidal dystrophy, and mitochondrial respiratory chain complex I deficiency.
    Barrientos A; Casademont J; Genís D; Cardellach F; Fernández-Real JM; Grau JM; Urbano-Márquez A; Estivill X; Nunes V
    Hum Mutat; 1997; 10(3):212-6. PubMed ID: 9298821
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CIA30 complex I assembly factor: a candidate for human complex I deficiency?
    Janssen R; Smeitink J; Smeets R; van Den Heuvel L
    Hum Genet; 2002 Mar; 110(3):264-70. PubMed ID: 11935339
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Optic atrophy/dystonia].
    Ishii A; Ohkoshi N
    Ryoikibetsu Shokogun Shirizu; 2001; (36):203-8. PubMed ID: 11596371
    [No Abstract]   [Full Text] [Related]  

  • 18. The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency.
    Chol M; Lebon S; Bénit P; Chretien D; de Lonlay P; Goldenberg A; Odent S; Hertz-Pannier L; Vincent-Delorme C; Cormier-Daire V; Rustin P; Rötig A; Munnich A
    J Med Genet; 2003 Mar; 40(3):188-91. PubMed ID: 12624137
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Leigh syndrome due to mitochondrial respiratory chain complex II deficiency].
    Ma YY; Wu TF; Liu YP; Wang Q; Song JQ; Xiao JX; Jiang YW; Yang YL
    Zhongguo Dang Dai Er Ke Za Zhi; 2011 Jul; 13(7):569-72. PubMed ID: 21752325
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Mitochondrial diseases with recurrent myoglobinuria].
    Murakami N
    Ryoikibetsu Shokogun Shirizu; 2001; (36):183-5. PubMed ID: 11596365
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.