202 related articles for article (PubMed ID: 37988592)
21. Anatomic & metabolic brain markers of the m.3243A>G mutation: A multi-parametric 7T MRI study.
Haast RAM; Ivanov D; IJsselstein RJT; Sallevelt SCEH; Jansen JFA; Smeets HJM; de Coo IFM; Formisano E; Uludağ K
Neuroimage Clin; 2018; 18():231-244. PubMed ID: 29868447
[TBL] [Abstract][Full Text] [Related]
22. Phenotypes and genotypes of mitochondrial diseases with mtDNA variations in Chinese children: A multi-center study.
Shi Y; Chen G; Sun D; Hu C; Liu Z; Shen D; Wang J; Song T; Zhang W; Li J; Ren X; Han T; Ding C; Wang Y; Fang F
Mitochondrion; 2022 Jan; 62():139-150. PubMed ID: 34800692
[TBL] [Abstract][Full Text] [Related]
23. The clinical variability of maternally inherited diabetes and deafness is associated with the degree of heteroplasmy in blood leukocytes.
Laloi-Michelin M; Meas T; Ambonville C; Bellanné-Chantelot C; Beaufils S; Massin P; Vialettes B; Gin H; Timsit J; Bauduceau B; Bernard L; Bertin E; Blickle JF; Cahen-Varsaux J; Cailleba A; Casanova S; Cathebras P; Charpentier G; Chedin P; Crea T; Delemer B; Dubois-Laforgue D; Duchemin F; Ducluzeau PH; Bouhanick B; Dusselier L; Gabreau T; Grimaldi A; Guerci B; Jacquin V; Kaloustian E; Larger E; Lecleire-Collet A; Lorenzini F; Louis J; Mausset J; Murat A; Nadler-Fluteau S; Olivier F; Paquis-Flucklinger V; Paris-Bockel D; Raynaud I; Reznik Y; Riveline JP; Schneebeli S; Sonnet E; Sola-Gazagnes A; Thomas JL; Trabulsi B; Virally M; Guillausseau PJ;
J Clin Endocrinol Metab; 2009 Aug; 94(8):3025-30. PubMed ID: 19470619
[TBL] [Abstract][Full Text] [Related]
24. Intra-patient variability of heteroplasmy levels in urinary epithelial cells in carriers of the m.3243A>G mutation.
de Laat P; Rodenburg RJ; Smeitink JAM; Janssen MCH
Mol Genet Genomic Med; 2019 Feb; 7(2):e00523. PubMed ID: 30516030
[TBL] [Abstract][Full Text] [Related]
25. Quantitative Variation in m.3243A > G Mutation Produce Discrete Changes in Energy Metabolism.
McMillan RP; Stewart S; Budnick JA; Caswell CC; Hulver MW; Mukherjee K; Srivastava S
Sci Rep; 2019 Apr; 9(1):5752. PubMed ID: 30962477
[TBL] [Abstract][Full Text] [Related]
26. Mitochondrial diabetes and deafness: possible dysfunction of strial marginal cells of the inner ear.
Olmos PR; Borzone GR; Olmos JP; Diez A; Santos JL; Serrano V; Cataldo LR; Anabalón JL; Correa CH
J Otolaryngol Head Neck Surg; 2011 Apr; 40(2):93-103. PubMed ID: 21453644
[TBL] [Abstract][Full Text] [Related]
27. The heart in m.3243A>G carriers.
Finsterer J; Zarrouk-Mahjoub S
Herz; 2020 Jun; 45(4):356-361. PubMed ID: 30128910
[TBL] [Abstract][Full Text] [Related]
28. Obstetric complications in carriers of the m.3243A>G mutation, a retrospective cohort study on maternal and fetal outcome.
de Laat P; Fleuren LH; Bekker MN; Smeitink JA; Janssen MC
Mitochondrion; 2015 Nov; 25():98-103. PubMed ID: 26455484
[TBL] [Abstract][Full Text] [Related]
29. Whole mitochondrial genome screening of a family with maternally inherited diabetes and deafness (MIDD) associated with retinopathy: A putative haplotype associated to MIDD and a novel MT-CO2 m.8241T>G mutation.
Tabebi M; Charfi N; Kallabi F; Alila-Fersi O; Ben Mahmoud A; Tlili A; Keskes-Ammar L; Kamoun H; Abid M; Mnif M; Fakhfakh F
J Diabetes Complications; 2017 Jan; 31(1):253-259. PubMed ID: 27422531
[TBL] [Abstract][Full Text] [Related]
30. Prevalence and progression of diabetes in mitochondrial disease.
Whittaker RG; Schaefer AM; McFarland R; Taylor RW; Walker M; Turnbull DM
Diabetologia; 2007 Oct; 50(10):2085-9. PubMed ID: 17653689
[TBL] [Abstract][Full Text] [Related]
31. Forecasting stroke-like episodes and outcomes in mitochondrial disease.
Ng YS; Lax NZ; Blain AP; Erskine D; Baker MR; Polvikoski T; Thomas RH; Morris CM; Lai M; Whittaker RG; Gebbels A; Winder A; Hall J; Feeney C; Farrugia ME; Hirst C; Roberts M; Lawthom C; Chrysostomou A; Murphy K; Baird T; Maddison P; Duncan C; Poulton J; Nesbitt V; Hanna MG; Pitceathly RDS; Taylor RW; Blakely EL; Schaefer AM; Turnbull DM; McFarland R; Gorman GS
Brain; 2022 Apr; 145(2):542-554. PubMed ID: 34927673
[TBL] [Abstract][Full Text] [Related]
32. Case report: mitochondrial diabetes mellitus in a Chinese family due to m.3243A>G.
Bai W; Zhang Q; Fan Y; Han T; Gu N; Zhang Y; Liang F; Ma Y; Xiong H
J Pediatr Endocrinol Metab; 2023 Aug; 36(8):777-781. PubMed ID: 37459161
[TBL] [Abstract][Full Text] [Related]
33. Identification of eight genomic protective alleles for mitochondrial diabetes by Kinship-graph convolutional network.
Wang J; Yan D; Cui H; Zhang R; Ma X; Chen L; Hu C; Wu J
J Diabetes Investig; 2024 Jan; 15(1):52-62. PubMed ID: 38157301
[TBL] [Abstract][Full Text] [Related]
34. A case-comparison study of pregnant women with mitochondrial disease - what to expect?
Feeney CL; Lim AZ; Fagan E; Blain A; Bright A; Maddison J; Devine H; Stewart J; Taylor RW; Gorman GS; Turnbull DM; Nesbitt V; McFarland R
BJOG; 2019 Oct; 126(11):1380-1389. PubMed ID: 30801962
[TBL] [Abstract][Full Text] [Related]
35. A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with severe nephropathy.
Tabebi M; Mkaouar-Rebai E; Mnif M; Kallabi F; Ben Mahmoud A; Ben Saad W; Charfi N; Keskes-Ammar L; Kamoun H; Abid M; Fakhfakh F
Biochem Biophys Res Commun; 2015 Apr; 459(3):353-60. PubMed ID: 25701779
[TBL] [Abstract][Full Text] [Related]
36. Mutation-specific effects in germline transmission of pathogenic mtDNA variants.
Otten ABC; Sallevelt SCEH; Carling PJ; Dreesen JCFM; Drüsedau M; Spierts S; Paulussen ADC; de Die-Smulders CEM; Herbert M; Chinnery PF; Samuels DC; Lindsey P; Smeets HJM
Hum Reprod; 2018 Jul; 33(7):1331-1341. PubMed ID: 29850888
[TBL] [Abstract][Full Text] [Related]
37. Maternally-inherited diabetes with deafness (MIDD) and hyporeninemic hypoaldosteronism.
Mory PB; Santos MC; Kater CE; Moisés RS
Arq Bras Endocrinol Metabol; 2012 Nov; 56(8):574-7. PubMed ID: 23295301
[TBL] [Abstract][Full Text] [Related]
38. The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation--implications for diagnosis and management.
Nesbitt V; Pitceathly RD; Turnbull DM; Taylor RW; Sweeney MG; Mudanohwo EE; Rahman S; Hanna MG; McFarland R
J Neurol Neurosurg Psychiatry; 2013 Aug; 84(8):936-8. PubMed ID: 23355809
[TBL] [Abstract][Full Text] [Related]
39. Determining Mitochondrial 3243A>G Heteroplasmy Using an ARMS-ddPCR Strategy.
Xu P; Jia M; Yan J; Yuan X; Yu W; Zhou Z; Fang H; Gao F; Shen L
Am J Clin Pathol; 2022 May; 157(5):664-677. PubMed ID: 34698344
[TBL] [Abstract][Full Text] [Related]
40. The first concurrent detection of mitochondrial DNA m.3243A>G mutation, deletion, and depletion in a family with mitochondrial diabetes.
Tabebi M; Safi W; Felhi R; Alila Fersi O; Keskes L; Abid M; Mnif M; Fakhfakh F
Mol Genet Genomic Med; 2020 Jul; 8(7):e1292. PubMed ID: 32394641
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
