152 related articles for article (PubMed ID: 7625545)
1. Deficiency in complex IV (cytochrome c oxidase) of the respiratory chain, presenting as a leukodystrophy in two siblings with Leigh syndrome.
Zafeiriou DI; Koletzko B; Mueller-Felber W; Paetzke I; Kueffer G; Jensen M
Brain Dev; 1995; 17(2):117-21. PubMed ID: 7625545
[TBL] [Abstract][Full Text] [Related]
2. Cytochrome oxidase deficiency presenting as birth asphyxia.
Willis TA; Davidson J; Gray RG; Poulton K; Ramani P; Whitehouse W
Dev Med Child Neurol; 2000 Jun; 42(6):414-7. PubMed ID: 10875529
[TBL] [Abstract][Full Text] [Related]
3. A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome c oxidase deficiency.
Santoro L; Carrozzo R; Malandrini A; Piemonte F; Patrono C; Villanova M; Tessa A; Palmeri S; Bertini E; Santorelli FM
Neuromuscul Disord; 2000 Aug; 10(6):450-3. PubMed ID: 10899453
[TBL] [Abstract][Full Text] [Related]
4. Cytochrome c oxidase partial deficiency-associated Leigh disease presenting as an extrapyramidal syndrome.
Cacić M; Wilichowski E; Mejaski-Bosnjak V; Fumić K; Lujić L; Marusić Della Marina B; Hanefeld F
J Child Neurol; 2001 Aug; 16(8):616-9. PubMed ID: 11510939
[TBL] [Abstract][Full Text] [Related]
5. A novel mutation in the SURF1 gene in a child with Leigh disease, peripheral neuropathy, and cytochrome-c oxidase deficiency.
Bruno C; Biancheri R; Garavaglia B; Biedi C; Rossi A; Lamba LD; Bado M; Greco M; Zeviani M; Minetti C
J Child Neurol; 2002 Mar; 17(3):233-6. PubMed ID: 12026244
[TBL] [Abstract][Full Text] [Related]
6. Syndrome of encephalopathy, petechiae, and ethylmalonic aciduria.
García-Silva MT; Ribes A; Campos Y; Garavaglia B; Arenas J
Pediatr Neurol; 1997 Sep; 17(2):165-70. PubMed ID: 9367300
[TBL] [Abstract][Full Text] [Related]
7. Leigh disease: clinical, neuroradiologic, and biochemical study of three new cases with cytochrome c oxidase deficiency.
Savasta S; Comi GP; Perini MP; Lupi A; Strazzer S; Rognoni F; Rossoni R
J Child Neurol; 2001 Aug; 16(8):608-13. PubMed ID: 11510937
[TBL] [Abstract][Full Text] [Related]
8. Deficiency in complex II of the respiratory chain, presenting as a leukodystrophy in two sisters with Leigh syndrome.
Burgeois M; Goutieres F; Chretien D; Rustin P; Munnich A; Aicardi J
Brain Dev; 1992 Nov; 14(6):404-8. PubMed ID: 1492653
[TBL] [Abstract][Full Text] [Related]
9. Cytochrome C oxidase deficiency in two siblings with Leigh encephalomyelopathy.
Miyabayashi S; Narisawa K; Iinuma K; Tada K; Sakai K; Kobayashi K; Kobayashi Y; Morinaga S
Brain Dev; 1984; 6(4):362-72. PubMed ID: 6093613
[TBL] [Abstract][Full Text] [Related]
10. Clinical and molecular survey in 124 Chinese patients with Leigh or Leigh-like syndrome.
Zhang Y; Yang YL; Sun F; Cai X; Qian N; Yuan Y; Wang ZX; Qi Y; Xiao JX; Wang XY; Zhang YH; Jiang YW; Qin J; Wu XR
J Inherit Metab Dis; 2007 Apr; 30(2):265. PubMed ID: 17323145
[TBL] [Abstract][Full Text] [Related]
11. Dysmyelinating leukodystrophies: "LACK Proper Myelin".
Hatten HP
Pediatr Radiol; 1991; 21(7):477-82. PubMed ID: 1771108
[TBL] [Abstract][Full Text] [Related]
12. Loss of the smallest subunit of cytochrome c oxidase, COX8A, causes Leigh-like syndrome and epilepsy.
Hallmann K; Kudin AP; Zsurka G; Kornblum C; Reimann J; Stüve B; Waltz S; Hattingen E; Thiele H; Nürnberg P; Rüb C; Voos W; Kopatz J; Neumann H; Kunz WS
Brain; 2016 Feb; 139(Pt 2):338-45. PubMed ID: 26685157
[TBL] [Abstract][Full Text] [Related]
13. Leigh syndrome, cytochrome C oxidase deficiency and hypsarrhythmia with infantile spasms.
Tsao CY; Luquette M; Rusin JA; Herr GM; Kien CL; Morrow G
Clin Electroencephalogr; 1997 Oct; 28(4):214-7. PubMed ID: 9343714
[TBL] [Abstract][Full Text] [Related]
14. A SURF1 gene mutation presenting as isolated leukodystrophy.
Rahman S; Brown RM; Chong WK; Wilson CJ; Brown GK
Ann Neurol; 2001 Jun; 49(6):797-800. PubMed ID: 11409433
[TBL] [Abstract][Full Text] [Related]
15. Clinical and magnetic resonance imaging findings in patients with Leigh syndrome and SURF1 mutations.
Sonam K; Khan NA; Bindu PS; Taly AB; Gayathri N; Bharath MM; Govindaraju C; Arvinda HR; Nagappa M; Sinha S; Thangaraj K
Brain Dev; 2014 Oct; 36(9):807-12. PubMed ID: 24262866
[TBL] [Abstract][Full Text] [Related]
16. Diagnosis and treatment in a case of juvenile subacute necrotizing encephalopathy Leigh without cytochrome c oxidase deficiency.
Westarp ME; Holzgraefe M; Gallenkamp U; Thomas R; Bechinger D
Eur Neurol; 1992; 32(4):206-11. PubMed ID: 1324178
[TBL] [Abstract][Full Text] [Related]
17. Leigh syndrome in an infant resulting from mitochondrial DNA depletion.
Absalon MJ; Harding CO; Fain DR; Li L; Mack KJ
Pediatr Neurol; 2001 Jan; 24(1):60-3. PubMed ID: 11182283
[TBL] [Abstract][Full Text] [Related]
18. Clinical and laboratory survey of 65 Chinese patients with Leigh syndrome.
Yang YL; Sun F; Zhang Y; Qian N; Yuan Y; Wang ZX; Qi Y; Xiao JX; Wang XY; Qi ZY; Zhang YH; Jiang YW; Bao XH; Qin J; Wu XR
Chin Med J (Engl); 2006 Mar; 119(5):373-7. PubMed ID: 16542579
[TBL] [Abstract][Full Text] [Related]
19. [The molecular background of Leigh syndrome].
Piekutowska-Abramczuk D
Neurol Neurochir Pol; 2008; 42(3):238-50. PubMed ID: 18651330
[TBL] [Abstract][Full Text] [Related]
20. Cytochrome C oxydase deficiency: SURF1 gene investigation in patients with Leigh syndrome.
Maalej M; Kammoun T; Alila-Fersi O; Kharrat M; Ammar M; Felhi R; Mkaouar-Rebai E; Keskes L; Hachicha M; Fakhfakh F
Biochem Biophys Res Commun; 2018 Mar; 497(4):1043-1048. PubMed ID: 29481804
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]