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 *

105 related articles for article (PubMed ID: 12002277)

  • 1. A case of diabetes, deafness, cardiomyopathy, and central sleep apnea: novel mitochondrial DNA polymorphisms.
    Sakaue S; Ohmuro J; Mishina T; Miyazaki H; Yamaguchi E; Nishimura M; Fujita M; Nagashima K; Tagami S; Kawakami Y
    Tohoku J Exp Med; 2002 Mar; 196(3):203-11. PubMed ID: 12002277
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Comparison of electron microscopic findings and clinical presentation in three patients with mitochondrial cardiomyopathy caused by the mitochondrial DNA mutation m.3243A > G.
    Saku T; Takashio S; Tsuruta Y; Otsuka Y; Takae M; Kiyama T; Yamamoto E; Kaikita K; Hotta T; Matsumoto S; Kang D; Tsujita K; Komohara Y
    Med Mol Morphol; 2021 Jun; 54(2):181-186. PubMed ID: 33113037
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. [A pedigree with maternally transmitted diabetes mellitus, deafness and cardiomyopathy].
    Kuzuya N; Noda M; Fujii M; Kanazawa Y
    Nihon Rinsho; 1994 Oct; 52(10):2611-5. PubMed ID: 7983786
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus.
    Soini HK; Moilanen JS; Vilmi-Kerälä T; Finnilä S; Majamaa K
    BMC Med Genet; 2013 Jul; 14():73. PubMed ID: 23870133
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A familial case of mitochondrial disease resembling Alport syndrome.
    Fujii H; Mori Y; Kayamori K; Igari T; Ito E; Akashi T; Noguchi Y; Kitamura K; Okado T; Terada Y; Kanda E; Rai T; Uchida S; Sasaki S
    Clin Exp Nephrol; 2008 Apr; 12(2):159-163. PubMed ID: 18180872
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Diabetes, sensorineural deafness, and mitochondrial DNA mutation.
    Prisco F; Iafusco D
    Laryngoscope; 2006 Mar; 116(3):505-6; author reply 506. PubMed ID: 16540920
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. [Clinical characterizations of familial diabetes mellitus associated with mitochondrial gene mutation].
    Xiu L; Zhang Q; Yu B
    Zhonghua Yi Xue Za Zhi; 1997 Jun; 77(6):418-21. PubMed ID: 9772504
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cardiomyopathy and kidney disease in a patient with maternally inherited diabetes and deafness caused by the 3243A>G mutation of mitochondrial DNA.
    Azevedo O; Vilarinho L; Almeida F; Ferreira F; Guardado J; Ferreira M; Lourenço A; Medeiros R; Almeida J
    Cardiology; 2010; 115(1):71-4. PubMed ID: 19864902
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.
    van den Ouweland JM; Lemkes HH; Trembath RC; Ross R; Velho G; Cohen D; Froguel P; Maassen JA
    Diabetes; 1994 Jun; 43(6):746-51. PubMed ID: 7910800
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Role of mitochondrial variation in maternally inherited diabetes and deafness syndrome.
    Howes T; Madden C; Dasgupta S; Saeed S; Das V
    J Laryngol Otol; 2008 Nov; 122(11):1249-52. PubMed ID: 18950542
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Mitochondrial diabetes complicated by or associated with "MELAS" syndrome?].
    Drouet A; Guilloton L; Godinot C; Rochet D; Ribot C; Carrier H
    Rev Neurol (Paris); 2000 Oct; 156(10):892-5. PubMed ID: 11033519
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Electron Microscopic Findings Are an Important Aid for Diagnosing Mitochondrial Cardiomyopathy With Mitochondrial DNA Mutation 3243A>G.
    Takemura G; Onoue K; Kashimura T; Kanamori H; Okada H; Tsujimoto A; Miyazaki N; Nakano T; Sakaguchi Y; Saito Y
    Circ Heart Fail; 2016 Jul; 9(7):. PubMed ID: 27402860
    [No Abstract]   [Full Text] [Related]  

  • 15. Renal complications in a patient with A-to-G mutation of mitochondrial DNA at the 3243 position of leucine tRNA.
    Hirano M; Konishi K; Arata N; Iyori M; Saruta T; Kuramochi S; Akizuki M
    Intern Med; 2002 Feb; 41(2):113-8. PubMed ID: 11868597
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Frequency and clinical features of patients with sensorineural hearing loss associated with the A3243G mutation of the mitochondrial DNA in otorhinolaryngic clinics.
    Nagata H; Kumahara K; Tomemori T; Arimoto Y; Isoyama K; Yoshida K; Konno A
    J Hum Genet; 2001; 46(10):595-9. PubMed ID: 11587074
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Sensorineural hearing loss, diabetes, and mitochondrial DNA mutation in Taiwan.
    Tseng FY
    Laryngoscope; 2006 Mar; 116(3):506. PubMed ID: 16540924
    [No Abstract]   [Full Text] [Related]  

  • 19. Diabetes mellitus is one of the heterogeneous phenotypic features of a mitochondrial DNA point mutation within the tRNALeu(UUR) gene.
    Gerbitz KD; Paprotta A; Jaksch M; Zierz S; Drechsel J
    FEBS Lett; 1993 Apr; 321(2-3):194-6. PubMed ID: 8477849
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Cardiomyopathy showing progression from diffuse left ventricular hypertrophy to dilated phase associated with mitochondrial DNA point mutation A3243G: A case report].
    Ohmoto N; Fujiwara Y; Kibira S; Kobayashi M; Saito T; Miura M
    J Cardiol; 2003 Jan; 41(1):21-7. PubMed ID: 12564110
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.