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 *

151 related articles for article (PubMed ID: 7625545)

  • 21. Remarkable improvement in adult Leigh syndrome with partial cytochrome c oxidase deficiency.
    Goldenberg PC; Steiner RD; Merkens LS; Dunaway T; Egan RA; Zimmerman EA; Nesbit G; Robinson B; Kennaway NG
    Neurology; 2003 Mar; 60(5):865-8. PubMed ID: 12629249
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Leigh syndrome: clinical features and biochemical and DNA abnormalities.
    Rahman S; Blok RB; Dahl HH; Danks DM; Kirby DM; Chow CW; Christodoulou J; Thorburn DR
    Ann Neurol; 1996 Mar; 39(3):343-51. PubMed ID: 8602753
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Cytochrome c oxidase deficiency--SURF1 mutations].
    Naito E; Ogawa Y
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():446-9. PubMed ID: 12013909
    [No Abstract]   [Full Text] [Related]  

  • 24. The first patient diagnosed with cytochrome c oxidase deficient Leigh syndrome: progress report.
    Coenen MJ; Smeitink JA; Farhoud MH; Nijtmans LG; Rodenburg R; Janssen A; van Kaauwen EP; Trijbels FJ; van den Heuvel LP
    J Inherit Metab Dis; 2006 Feb; 29(1):212-3. PubMed ID: 16601896
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A previously undescribed leukodystrophy in Leigh syndrome associated with T9176C mutation of the mitochondrial ATPase 6 gene.
    Hung PC; Wang HS
    Dev Med Child Neurol; 2007 Jan; 49(1):65-7. PubMed ID: 17209980
    [TBL] [Abstract][Full Text] [Related]  

  • 26. SURF1 gene mutations in three cases with Leigh syndrome and cytochrome c oxidase deficiency.
    Moslemi AR; Tulinius M; Darin N; Aman P; Holme E; Oldfors A
    Neurology; 2003 Oct; 61(7):991-3. PubMed ID: 14557577
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Early mitochondrial encephalomyopathy due to complex IV deficiency consistent with Alpers-Huttenlocher syndrome: report of two cases].
    Castro-Gago M; González-Conde V; Fernández-Seara MJ; Rodrigo-Sáez E; Fernández-Cebrián S; Alonso-Martín A; Campos Y; Arenas J; Eirís-Puñal J
    Rev Neurol; 1999 Nov 16-30; 29(10):912-7. PubMed ID: 10637838
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Loss-of-function mutations of SURF-1 are specifically associated with Leigh syndrome with cytochrome c oxidase deficiency.
    Tiranti V; Jaksch M; Hofmann S; Galimberti C; Hoertnagel K; Lulli L; Freisinger P; Bindoff L; Gerbitz KD; Comi GP; Uziel G; Zeviani M; Meitinger T
    Ann Neurol; 1999 Aug; 46(2):161-6. PubMed ID: 10443880
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Complementation analysis of systemic cytochrome oxidase deficiency presenting as Leigh syndrome.
    Brown RM; Brown GK
    J Inherit Metab Dis; 1996; 19(6):752-60. PubMed ID: 8982948
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Human cytochrome oxidase deficiency.
    Robinson BH
    Pediatr Res; 2000 Nov; 48(5):581-5. PubMed ID: 11044474
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Leigh Syndrome with COX deficiency and SURF1 gene mutations: MR imaging findings.
    Rossi A; Biancheri R; Bruno C; Di Rocco M; Calvi A; Pessagno A; Tortori-Donati P
    AJNR Am J Neuroradiol; 2003; 24(6):1188-91. PubMed ID: 12812953
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Progressive cytochrome c oxidase deficiency in a case of Leigh's encephalomyelopathy.
    Koga Y; Nonaka I; Nakao M; Yoshino M; Tanaka M; Ozawa T; Nakase H; DiMauro S
    J Neurol Sci; 1990 Jan; 95(1):63-76. PubMed ID: 2159985
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Leigh syndrome with cytochrome-c oxidase deficiency and a single T insertion nt 5537 in the mitochondrial tRNATrp gene.
    Tulinius M; Moslemi AR; Darin N; Westerberg B; Wiklund LM; Holme E; Oldfors A
    Neuropediatrics; 2003 Apr; 34(2):87-91. PubMed ID: 12776230
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Symmetric lesions of the subthalamic nuclei in mitochondrial encephalopathies: an almost distinctive Mark of Leigh disease with COX deficiency.
    Savoiardo M; Ciceri E; D'Incerti L; Uziel G; Scotti G
    AJNR Am J Neuroradiol; 1995 Sep; 16(8):1746-7. PubMed ID: 7502989
    [No Abstract]   [Full Text] [Related]  

  • 35. [Cytochrome c oxydase-deficient Leigh syndrome with homozygous mutation in SURF1 gene].
    Monnot S; Chabrol B; Cano A; Pellissier JF; Collignon P; Montfort MF; Paquis-Flucklinger V
    Arch Pediatr; 2005 May; 12(5):568-71. PubMed ID: 15885549
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Sulfite oxidase deficiency presenting as Leigh syndrome].
    Amiel J; Gagey V; Rabier D; Dorche C; Bonnefont JP; Dufier JL; Saudubray JM; Rey J; Munnich A
    Arch Pediatr; 1994 Nov; 1(11):1023-7. PubMed ID: 7834040
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Leigh syndrome: serial CT and MR imaging findings].
    Ariga H; Takahashi S; Miyabayashi S; Ohnuma A; Higano S; Kurihara N; Sakamoto K
    Nihon Igaku Hoshasen Gakkai Zasshi; 1996 Oct; 56(12):839-45. PubMed ID: 8940814
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A novel mutation in SURF1 causes skipping of exon 8 in a patient with cytochrome c oxidase-deficient leigh syndrome and hypertrichosis.
    Williams SL; Taanman JW; Hansíková H; Houst'ková H; Chowdhury S; Zeman J; Houstek J
    Mol Genet Metab; 2001 Aug; 73(4):340-3. PubMed ID: 11509016
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Clinical, pathological, and neuroimaging analyses of two cases of Leigh syndrome in a Chinese family.
    Jin T; Shen H; Zhao Z; Hu J
    J Child Neurol; 2014 Nov; 29(11):NP143-8. PubMed ID: 24413359
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Unusual clinical presentations in four cases of Leigh disease, cytochrome C oxidase deficiency, and SURF1 gene mutations.
    Tay SK; Sacconi S; Akman HO; Morales JF; Morales A; De Vivo DC; Shanske S; Bonilla E; DiMauro S
    J Child Neurol; 2005 Aug; 20(8):670-4. PubMed ID: 16225813
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.