734 related articles for article (PubMed ID: 25652200)
1. Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease.
Gorman GS; Schaefer AM; Ng Y; Gomez N; Blakely EL; Alston CL; Feeney C; Horvath R; Yu-Wai-Man P; Chinnery PF; Taylor RW; Turnbull DM; McFarland R
Ann Neurol; 2015 May; 77(5):753-9. PubMed ID: 25652200
[TBL] [Abstract][Full Text] [Related]
2. Prevalence of mitochondrial DNA disease in adults.
Schaefer AM; McFarland R; Blakely EL; He L; Whittaker RG; Taylor RW; Chinnery PF; Turnbull DM
Ann Neurol; 2008 Jan; 63(1):35-9. PubMed ID: 17886296
[TBL] [Abstract][Full Text] [Related]
3. Mitochondrial DNA mutation analysis from exome sequencing-A more holistic approach in diagnostics of suspected mitochondrial disease.
Wagner M; Berutti R; Lorenz-Depiereux B; Graf E; Eckstein G; Mayr JA; Meitinger T; Ahting U; Prokisch H; Strom TM; Wortmann SB
J Inherit Metab Dis; 2019 Sep; 42(5):909-917. PubMed ID: 31059585
[TBL] [Abstract][Full Text] [Related]
4. Respiratory chain complex I deficiency caused by mitochondrial DNA mutations.
Swalwell H; Kirby DM; Blakely EL; Mitchell A; Salemi R; Sugiana C; Compton AG; Tucker EJ; Ke BX; Lamont PJ; Turnbull DM; McFarland R; Taylor RW; Thorburn DR
Eur J Hum Genet; 2011 Jul; 19(7):769-75. PubMed ID: 21364701
[TBL] [Abstract][Full Text] [Related]
5. Classical mitochondrial phenotypes without mtDNA mutations: the possible role of nuclear genes.
Pulkes T; Liolitsa D; Nelson IP; Hanna MG
Neurology; 2003 Oct; 61(8):1144-7. PubMed ID: 14581685
[TBL] [Abstract][Full Text] [Related]
6. Prevalence of rare mitochondrial DNA mutations in mitochondrial disorders.
Bannwarth S; Procaccio V; Lebre AS; Jardel C; Chaussenot A; Hoarau C; Maoulida H; Charrier N; Gai X; Xie HM; Ferre M; Fragaki K; Hardy G; Mousson de Camaret B; Marlin S; Dhaenens CM; Slama A; Rocher C; Paul Bonnefont J; Rötig A; Aoutil N; Gilleron M; Desquiret-Dumas V; Reynier P; Ceresuela J; Jonard L; Devos A; Espil-Taris C; Martinez D; Gaignard P; Le Quan Sang KH; Amati-Bonneau P; Falk MJ; Florentz C; Chabrol B; Durand-Zaleski I; Paquis-Flucklinger V
J Med Genet; 2013 Oct; 50(10):704-14. PubMed ID: 23847141
[TBL] [Abstract][Full Text] [Related]
7. The epidemiology of pathogenic mitochondrial DNA mutations.
Chinnery PF; Johnson MA; Wardell TM; Singh-Kler R; Hayes C; Brown DT; Taylor RW; Bindoff LA; Turnbull DM
Ann Neurol; 2000 Aug; 48(2):188-93. PubMed ID: 10939569
[TBL] [Abstract][Full Text] [Related]
8. Pathogenic mutations of nuclear genes associated with mitochondrial disorders.
Zhu X; Peng X; Guan MX; Yan Q
Acta Biochim Biophys Sin (Shanghai); 2009 Mar; 41(3):179-87. PubMed ID: 19280056
[TBL] [Abstract][Full Text] [Related]
9. Mitochondrial disease genetic diagnostics: optimized whole-exome analysis for all MitoCarta nuclear genes and the mitochondrial genome.
Falk MJ; Pierce EA; Consugar M; Xie MH; Guadalupe M; Hardy O; Rappaport EF; Wallace DC; LeProust E; Gai X
Discov Med; 2012 Dec; 14(79):389-99. PubMed ID: 23272691
[TBL] [Abstract][Full Text] [Related]
10. Novel reproductive technologies to prevent mitochondrial disease.
Craven L; Tang MX; Gorman GS; De Sutter P; Heindryckx B
Hum Reprod Update; 2017 Sep; 23(5):501-519. PubMed ID: 28651360
[TBL] [Abstract][Full Text] [Related]
11. Epidemiology of pediatric mitochondrial respiratory chain disorders in northwest Spain.
Castro-Gago M; Blanco-Barca MO; Campos-González Y; Arenas-Barbero J; Pintos-Martínez E; Eirís-Puñal J
Pediatr Neurol; 2006 Mar; 34(3):204-11. PubMed ID: 16504790
[TBL] [Abstract][Full Text] [Related]
12. Mutations causing mitochondrial disease: What is new and what challenges remain?
Lightowlers RN; Taylor RW; Turnbull DM
Science; 2015 Sep; 349(6255):1494-9. PubMed ID: 26404827
[TBL] [Abstract][Full Text] [Related]
13. Mitochondrial disease in childhood: mtDNA encoded.
Saneto RP; Sedensky MM
Neurotherapeutics; 2013 Apr; 10(2):199-211. PubMed ID: 23224691
[TBL] [Abstract][Full Text] [Related]
14. [Characteristics of molecular genetics and research progress on mitochondrial diseases].
Zhang M; Si Y; Zhao J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Oct; 33(5):717-25. PubMed ID: 27577231
[TBL] [Abstract][Full Text] [Related]
15. Genetic Counselling for Maternally Inherited Mitochondrial Disorders.
Poulton J; Finsterer J; Yu-Wai-Man P
Mol Diagn Ther; 2017 Aug; 21(4):419-429. PubMed ID: 28536827
[TBL] [Abstract][Full Text] [Related]
16. Nuclear genes involved in mitochondrial diseases caused by instability of mitochondrial DNA.
Rusecka J; Kaliszewska M; Bartnik E; Tońska K
J Appl Genet; 2018 Feb; 59(1):43-57. PubMed ID: 29344903
[TBL] [Abstract][Full Text] [Related]
17. Mitochondrial Diseases: A Diagnostic Revolution.
Schon KR; Ratnaike T; van den Ameele J; Horvath R; Chinnery PF
Trends Genet; 2020 Sep; 36(9):702-717. PubMed ID: 32674947
[TBL] [Abstract][Full Text] [Related]
18. Mitochondrial DNA mutations: an overview of clinical and molecular aspects.
Craigen WJ
Methods Mol Biol; 2012; 837():3-15. PubMed ID: 22215537
[TBL] [Abstract][Full Text] [Related]
19. Mitochondrial DNA mutations and depletion in pediatric medicine.
Spinazzola A
Semin Fetal Neonatal Med; 2011 Aug; 16(4):190-6. PubMed ID: 21652274
[TBL] [Abstract][Full Text] [Related]
20. Clinical features of mtDNA-related syndromes in adulthood.
Montano V; Gruosso F; Simoncini C; Siciliano G; Mancuso M
Arch Biochem Biophys; 2021 Jan; 697():108689. PubMed ID: 33227288
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]