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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 12221518)

  • 1. A case of a de novo A3243G mutation in mitochondrial DNA in a patient with diabetes and deafness.
    Maassen JA; Biberoglu S; 't Hart LM; Bakker E; de Knijff P
    Arch Physiol Biochem; 2002 Jul; 110(3):186-8. PubMed ID: 12221518
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. A detailed investigation of maternally inherited diabetes and deafness (MIDD) including clinical characteristics, C-peptide secretion, HLA-DR and -DQ status and autoantibody pattern.
    Hosszúfalusi N; Karcagi V; Horváth R; Palik E; Várkonyi J; Rajczy K; Prohászka Z; Szentirmai C; Karádi I; Romics L; Pánczél P
    Diabetes Metab Res Rev; 2009 Feb; 25(2):127-35. PubMed ID: 19116951
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Diabetes mellitus, deafness, muscle weakness and hypocalcemia in a patient with an A3243G mutation of the mitochondrial DNA.
    Tanaka K; Takada Y; Matsunaka T; Yuyama S; Fujino S; Maguchi M; Yamashita S; Yuba I
    Intern Med; 2000 Mar; 39(3):249-52. PubMed ID: 10772130
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Maternally-inherited diabetes and deafness: report of two affected German families with the A3243G mitochondrial DNA mutation.
    Thorns C; Widjaja A; Boeck N; Skamira C; Zühlke H
    Exp Clin Endocrinol Diabetes; 1998; 106(5):384-8. PubMed ID: 9831303
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Involvement of nervous system in maternally inherited diabetes and deafness (MIDD) with the A3243G mutation of mitochondrial DNA.
    Lien LM; Lee HC; Wang KL; Chiu JC; Chiu HC; Wei YH
    Acta Neurol Scand; 2001 Mar; 103(3):159-65. PubMed ID: 11240563
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Maternally inherited diabetes and deafness (MIDD): unusual occult exocrine pancreatic manifestation in an affected German family.
    Schleiffer T; 't Hart LM; Schürfeld C; Kraatz K; Riemann JF
    Exp Clin Endocrinol Diabetes; 2000; 108(2):81-5. PubMed ID: 10826513
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Gastrointestinal tract symptoms in Maternally Inherited Diabetes and Deafness (MIDD).
    Narbonne H; Paquis-Fluckinger V; Valero R; Heyries L; Pellissier JF; Vialettes B
    Diabetes Metab; 2004 Feb; 30(1):61-6. PubMed ID: 15029099
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Heterogeneous phenotypic manifestations of maternally inherited deafness associated with the mitochondrial A3243G mutation. Case report.
    Hoptasz M; Szczuciński A; Losy J
    Neurol Neurochir Pol; 2014; 48(2):150-3. PubMed ID: 24821643
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Unusual occurrence of intestinal pseudo obstruction in a patient with maternally inherited diabetes and deafness (MIDD) and favorable outcome with coenzyme Q10.
    Bergamin CS; Rolim LC; Dib SA; Moisés RS
    Arq Bras Endocrinol Metabol; 2008 Nov; 52(8):1345-9. PubMed ID: 19169492
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A mother and a child with maternally inherited diabetes and deafness (MIDD) showing atrophy of the cerebrum, cerebellum and brainstem on magnetic resonance imaging (MRI).
    Kobayashi Z; Tsunemi T; Miake H; Tanaka S; Watabiki S; Morokuma Y
    Intern Med; 2005 Apr; 44(4):328-31. PubMed ID: 15897646
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [A new subtype of diabetes mellitus: maternally inherited diabetes and deafness (MIDD)].
    Maassen JA; Jansen JJ; van den Ouweland JM; Hart LM; van Essen EH; Lemkes HH
    Ned Tijdschr Geneeskd; 1998 Jan; 142(5):229-33. PubMed ID: 9557035
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation.
    Smith PR; Bain SC; Good PA; Hattersley AT; Barnett AH; Gibson JM; Dodson PM
    Ophthalmology; 1999 Jun; 106(6):1101-8. PubMed ID: 10366077
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Dilated cardiomyopathy, diabetes and deafness related to a mutation of mitochondrial DNA].
    Ferreira-Maldent N; Maillot F; Quilliet L; Guilmot JL; Charbonnier B
    Arch Mal Coeur Vaiss; 2007 Feb; 100(2):149-52. PubMed ID: 17474502
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Maternally inherited diabetes mellitus, deafness, chronic progressive external ophthalmoplegia and myopathy as the result of A3243G mutation of mtDNA].
    Gál A; Szabó A; Pentelényi K; Pál Z
    Orv Hetil; 2008 Aug; 149(34):1593-8. PubMed ID: 18708313
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Diabetes mellitus associated with the A3243G mutation of mitochondrial DNA. Apropos a case].
    Biarnés J; Barrientos A; Ricart W; Nunes V; Fernández-Castañer M; Soler J
    Med Clin (Barc); 1999 Jan; 112(3):99-101. PubMed ID: 10074618
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Family Phenotypic Heterogeneity Caused by Mitochondrial DNA Mutation A3243G.
    Alves D; Calmeiro ME; Macário C; Silva R
    Acta Med Port; 2017 Aug; 30(7-8):581-585. PubMed ID: 28926334
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pyrosequencing is an accurate and reliable method for the analysis of heteroplasmy of the A3243G mutation in patients with mitochondrial diabetes.
    Yan JB; Zhang R; Xiong C; Hu C; Lv Y; Wang CR; Jia WP; Zeng F
    J Mol Diagn; 2014 Jul; 16(4):431-9. PubMed ID: 24803323
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mitochondrial 3243 BP mutation: a case report.
    Rigoli L; Caruso RA; Zuccarello D; Rigoli M; Barberi I
    Diabetes Nutr Metab; 2001 Dec; 14(6):343-8. PubMed ID: 11853367
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.