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.
151 related articles for article (PubMed ID: 33380711)
1. Unmasking fibromyalgia as a mitochondrial disorder requires search for more than a single variant or single mtDNA deletions. Finsterer J Indian J Med Res; 2020 Oct; 152(4):429-430. PubMed ID: 33380711 [No Abstract] [Full Text] [Related]
2. A descriptive pilot study of mitochondrial mutations & clinical phenotype in fibromyalgia syndrome. Danda S; Thomas BM; Paramasivam G; Thomas R; Mathew J; Danda D Indian J Med Res; 2019 Jan; 149(1):47-50. PubMed ID: 31115374 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. [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]
6. Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion. Varga NÁ; Pentelényi K; Balicza P; Gézsi A; Reményi V; Hársfalvi V; Bencsik R; Illés A; Prekop C; Molnár MJ Behav Brain Funct; 2018 Feb; 14(1):4. PubMed ID: 29458409 [TBL] [Abstract][Full Text] [Related]
7. Comprehensive Mitochondrial Genome Analysis by Massively Parallel Sequencing. Palculict ME; Zhang VW; Wong LJ; Wang J Methods Mol Biol; 2016; 1351():3-17. PubMed ID: 26530670 [TBL] [Abstract][Full Text] [Related]
8. Molecular analysis of oxidative phosphorylation diseases for detection of mitochondrial DNA mutations. Shoffner JM Curr Protoc Hum Genet; 2001 May; Chapter 9():Unit 9.9. PubMed ID: 18428320 [TBL] [Abstract][Full Text] [Related]
9. Techniques and pitfalls in the detection of pathogenic mitochondrial DNA mutations. Moraes CT; Atencio DP; Oca-Cossio J; Diaz F J Mol Diagn; 2003 Nov; 5(4):197-208. PubMed ID: 14573777 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. The non-syndromic clinical spectrums of mtDNA 3243A>G mutation. Shen X; Du A Neurosciences (Riyadh); 2021 Apr; 26(2):128-133. PubMed ID: 33814365 [TBL] [Abstract][Full Text] [Related]
12. Single deletions in mitochondrial DNA--molecular mechanisms and disease phenotypes in clinical practice. Pitceathly RD; Rahman S; Hanna MG Neuromuscul Disord; 2012 Jul; 22(7):577-86. PubMed ID: 22578526 [TBL] [Abstract][Full Text] [Related]
13. Autosomal disorders of mitochondrial DNA maintenance. Van Goethem G Acta Neurol Belg; 2006 Jun; 106(2):66-72. PubMed ID: 16898256 [TBL] [Abstract][Full Text] [Related]
14. Diagnostic screening of mitochondrial DNA mutations in Australian adults 1990-2001. Marotta R; Chin J; Quigley A; Katsabanis S; Kapsa R; Byrne E; Collins S Intern Med J; 2004; 34(1-2):10-9. PubMed ID: 14748908 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. The clinical diagnosis of POLG disease and other mitochondrial DNA depletion disorders. Cohen BH; Naviaux RK Methods; 2010 Aug; 51(4):364-73. PubMed ID: 20558295 [TBL] [Abstract][Full Text] [Related]
17. Sequence homology at the breakpoint and clinical phenotype of mitochondrial DNA deletion syndromes. Sadikovic B; Wang J; El-Hattab AW; Landsverk M; Douglas G; Brundage EK; Craigen WJ; Schmitt ES; Wong LJ PLoS One; 2010 Dec; 5(12):e15687. PubMed ID: 21187929 [TBL] [Abstract][Full Text] [Related]
18. Further pitfalls in the diagnosis of mtDNA mutations: homoplasmic mt-tRNA mutations. Tuppen HA; Fattori F; Carrozzo R; Zeviani M; DiMauro S; Seneca S; Martindale JE; Olpin SE; Treacy EP; McFarland R; Santorelli FM; Taylor RW J Med Genet; 2008 Jan; 45(1):55-61. PubMed ID: 18178636 [TBL] [Abstract][Full Text] [Related]
19. A Heterozygous NDUFV1 Variant Aggravates Mitochondrial Complex I Deficiency in a Family with a Homoplasmic ND1 Variant. Baertling F; Sánchez-Caballero L; van den Brand MAM; Distelmaier F; Janssen MCH; Rodenburg RJT; Smeitink JAM; Nijtmans LGJ J Pediatr; 2018 May; 196():309-313.e3. PubMed ID: 29395179 [TBL] [Abstract][Full Text] [Related]
20. Diseases caused by nuclear genes affecting mtDNA stability. Suomalainen A; Kaukonen J Am J Med Genet; 2001; 106(1):53-61. PubMed ID: 11579425 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]