196 related articles for article (PubMed ID: 11803021)
1. Inborn errors of complex II--unusual human mitochondrial diseases.
Rustin P; Rötig A
Biochim Biophys Acta; 2002 Jan; 1553(1-2):117-22. PubMed ID: 11803021
[TBL] [Abstract][Full Text] [Related]
2. Phenotypic dichotomy in mitochondrial complex II genetic disorders.
Baysal BE; Rubinstein WS; Taschner PE
J Mol Med (Berl); 2001 Sep; 79(9):495-503. PubMed ID: 11692162
[TBL] [Abstract][Full Text] [Related]
3. Succinate dehydrogenase deficiency in human.
Brière JJ; Favier J; El Ghouzzi V; Djouadi F; Bénit P; Gimenez AP; Rustin P
Cell Mol Life Sci; 2005 Oct; 62(19-20):2317-24. PubMed ID: 16143825
[TBL] [Abstract][Full Text] [Related]
4. Mitochondrial myopathies.
DiMauro S; Bonilla E; Zeviani M; Servidei S; DeVivo DC; Schon EA
J Inherit Metab Dis; 1987; 10 Suppl 1():113-28. PubMed ID: 2824920
[TBL] [Abstract][Full Text] [Related]
5. [Complex II (succinate-ubiquinone reductase) deficiency].
Nonaka I
Ryoikibetsu Shokogun Shirizu; 2001; (36):132-4. PubMed ID: 11596343
[No Abstract] [Full Text] [Related]
6. Biochemical investigations and immunoblot analyses of two unrelated patients with an isolated deficiency in complex II of the mitochondrial respiratory chain.
Birch-Machin MA; Marsac C; Ponsot G; Parfait B; Taylor RW; Rustin P; Munnich A
Biochem Biophys Res Commun; 1996 Mar; 220(1):57-62. PubMed ID: 8602857
[TBL] [Abstract][Full Text] [Related]
7. [Optic atrophy and ataxia (complex II deficiency-mutation in Fp subunit gene of succinate dehydrogenase)].
Goto Y
Nihon Rinsho; 2002 Apr; 60 Suppl 4():376-7. PubMed ID: 12013890
[No Abstract] [Full Text] [Related]
8. Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency.
Alston CL; Davison JE; Meloni F; van der Westhuizen FH; He L; Hornig-Do HT; Peet AC; Gissen P; Goffrini P; Ferrero I; Wassmer E; McFarland R; Taylor RW
J Med Genet; 2012 Sep; 49(9):569-77. PubMed ID: 22972948
[TBL] [Abstract][Full Text] [Related]
9. The genetic basis of isolated mitochondrial complex II deficiency.
Fullerton M; McFarland R; Taylor RW; Alston CL
Mol Genet Metab; 2020; 131(1-2):53-65. PubMed ID: 33162331
[TBL] [Abstract][Full Text] [Related]
10. Succinate: quinone oxidoreductases: new insights from X-ray crystal structures.
Lancaster CR; Kröger A
Biochim Biophys Acta; 2000 Aug; 1459(2-3):422-31. PubMed ID: 11004459
[TBL] [Abstract][Full Text] [Related]
11. [Complex II deficiency due to Fp gene mutation].
Ito M
Nihon Rinsho; 2002 Apr; 60 Suppl 4():444-5. PubMed ID: 12013908
[No Abstract] [Full Text] [Related]
12. Mutations in SDHC cause autosomal dominant paraganglioma, type 3.
Niemann S; Müller U
Nat Genet; 2000 Nov; 26(3):268-70. PubMed ID: 11062460
[TBL] [Abstract][Full Text] [Related]
13. Succinate dehydrogenase and human diseases: new insights into a well-known enzyme.
Rustin P; Munnich A; Rötig A
Eur J Hum Genet; 2002 May; 10(5):289-91. PubMed ID: 12082502
[TBL] [Abstract][Full Text] [Related]
14. Succinate:quinone oxidoreductases from epsilon-proteobacteria.
Lancaster CR; Simon J
Biochim Biophys Acta; 2002 Jan; 1553(1-2):84-101. PubMed ID: 11803019
[TBL] [Abstract][Full Text] [Related]
15. [From gene to disease; from SDHD, a defect in the respiratory chain, to paragangliomas and pheochromocytomas].
Taschner PE; Bröcker-Vriends AH; van der Mey AG
Ned Tijdschr Geneeskd; 2002 Nov; 146(46):2188-90. PubMed ID: 12467161
[TBL] [Abstract][Full Text] [Related]
16. Cytopathies involving mitochondrial complex II.
Ackrell BA
Mol Aspects Med; 2002 Oct; 23(5):369-84. PubMed ID: 12231007
[TBL] [Abstract][Full Text] [Related]
17. Inborn errors of the Krebs cycle: a group of unusual mitochondrial diseases in human.
Rustin P; Bourgeron T; Parfait B; Chretien D; Munnich A; Rötig A
Biochim Biophys Acta; 1997 Aug; 1361(2):185-97. PubMed ID: 9300800
[TBL] [Abstract][Full Text] [Related]
18. A role for mitochondrial enzymes in inherited neoplasia and beyond.
Eng C; Kiuru M; Fernandez MJ; Aaltonen LA
Nat Rev Cancer; 2003 Mar; 3(3):193-202. PubMed ID: 12612654
[TBL] [Abstract][Full Text] [Related]
19. Comparative study and cDNA cloning of the flavoprotein subunit of mitochondrial complex II (succinate-ubiquinone oxidoreductase: fumarate reductase) from the dog heartworm, Dirofilaria immitis.
Kuramochi T; Kita K; Takamiya S; Kojima S; Hayasaki M
Comp Biochem Physiol B Biochem Mol Biol; 1995 Jul; 111(3):491-502. PubMed ID: 7613771
[TBL] [Abstract][Full Text] [Related]
20. Architecture of succinate dehydrogenase and reactive oxygen species generation.
Yankovskaya V; Horsefield R; Törnroth S; Luna-Chavez C; Miyoshi H; Léger C; Byrne B; Cecchini G; Iwata S
Science; 2003 Jan; 299(5607):700-4. PubMed ID: 12560550
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]