144 related articles for article (PubMed ID: 38311059)
1. Clinical Characteristics of Diabetes in People with Mitochondrial DNA 3243A>G Mutation in Korea.
Rho EH; Baek SI; Lee H; Seong MW; Chae JH; Park KS; Kwak SH
Diabetes Metab J; 2024 May; 48(3):482-486. PubMed ID: 38311059
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. The Mutations and Clinical Variability in Maternally Inherited Diabetes and Deafness: An Analysis of 161 Patients.
Yang M; Xu L; Xu C; Cui Y; Jiang S; Dong J; Liao L
Front Endocrinol (Lausanne); 2021; 12():728043. PubMed ID: 34899594
[TBL] [Abstract][Full Text] [Related]
4. De Novo Mutation of m.3243A>G together with m.16093T>C Associated with Atypical Clinical Features in a Pedigree with MIDD Syndrome.
Jiang Z; Zhang Y; Yan J; Li F; Geng X; Lu H; Wei X; Feng Y; Wang C; Jia W
J Diabetes Res; 2019; 2019():5184647. PubMed ID: 31143779
[TBL] [Abstract][Full Text] [Related]
5. Clinical features and heteroplasmy in blood, urine and saliva in 34 Dutch families carrying the m.3243A > G mutation.
de Laat P; Koene S; van den Heuvel LP; Rodenburg RJ; Janssen MC; Smeitink JA
J Inherit Metab Dis; 2012 Nov; 35(6):1059-69. PubMed ID: 22403016
[TBL] [Abstract][Full Text] [Related]
6. Multimodal imaging analysis of macular dystrophy in patient with maternally inherited diabetes and deafness (MIDD) with m.3243A>G mutation.
Oishi N; Kubota D; Nakamoto K; Takeda Y; Hayashi M; Gocho K; Yamaki K; Igarashi T; Takahashi H; Kameya S
Ophthalmic Genet; 2021 Jun; 42(3):304-311. PubMed ID: 33541179
[No Abstract] [Full Text] [Related]
7. [Mitochondrial DNA heteroplasmy of the m.3243A>G mutation in maternally inherited diabetes and deafness].
Cataldo LR; Olmos P; Valerie Smalley S; Díez A; Parada A; Gejman R; Fadic R; Santos JL
Rev Med Chil; 2013 Mar; 141(3):305-12. PubMed ID: 23900320
[TBL] [Abstract][Full Text] [Related]
8. HLA-DQ polymorphism and degree of heteroplasmy of the A3243G mitochondrial DNA mutation in maternally inherited diabetes and deafness.
van Essen EH; Roep BO; 't Hart LM; Jansen JJ; Van den Ouweland JM; Lemkes HH; Maassen JA
Diabet Med; 2000 Dec; 17(12):841-7. PubMed ID: 11168326
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. Increased Peripheral Blood Heteroplasmy of the mt.3243A>G Mutation Is Associated with Earlier End-Stage Kidney Disease: A Case Report and Review of the Literature.
Shand JAD; Potter HC; Pilmore HL; Cundy T; Murphy R
Nephron; 2020; 144(7):358-362. PubMed ID: 32434190
[TBL] [Abstract][Full Text] [Related]
13. MIDD or MELAS : that's not the question MIDD evolving into MELAS : a severe phenotype of the m.3243A>G mutation due to paternal co-inheritance of type 2 diabetes and a high heteroplasmy level.
de Wit HM; Westeneng HJ; van Engelen BG; Mudde AH
Neth J Med; 2012 Dec; 70(10):460-2. PubMed ID: 23230016
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation.
Murphy R; Turnbull DM; Walker M; Hattersley AT
Diabet Med; 2008 Apr; 25(4):383-99. PubMed ID: 18294221
[TBL] [Abstract][Full Text] [Related]
16. The clinical characteristics of patients with mitochondrial tRNA Leu(UUR)m.3243A > G mutation: Compared with type 1 diabetes and early onset type 2 diabetes.
Zhu J; Yang P; Liu X; Yan L; Rampersad S; Li F; Li H; Sheng C; Cheng X; Zhang M; Qu S
J Diabetes Complications; 2017 Aug; 31(8):1354-1359. PubMed ID: 28599824
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Prevalence of mitochondrial diabetes in southwestern Finland: a molecular epidemiological study.
Martikainen MH; Rönnemaa T; Majamaa K
Acta Diabetol; 2013 Oct; 50(5):737-41. PubMed ID: 22492248
[TBL] [Abstract][Full Text] [Related]
19. Chronological change of left ventricular global longitudinal strain in patients with maternally inherited diabetes and deafness: A case series.
Seo JS
Medicine (Baltimore); 2024 Mar; 103(10):e37447. PubMed ID: 38457558
[TBL] [Abstract][Full Text] [Related]
20. One mutation, three phenotypes: novel metabolic insights on MELAS, MIDD and myopathy caused by the m.3243A > G mutation.
Esterhuizen K; Lindeque JZ; Mason S; van der Westhuizen FH; Rodenburg RJ; de Laat P; Smeitink JAM; Janssen MCH; Louw R
Metabolomics; 2021 Jan; 17(1):10. PubMed ID: 33438095
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
