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 *

99 related articles for article (PubMed ID: 9455926)

  • 1. Mitochondrial related diabetes: a clinical perspective.
    Walker M; Turnbull DM
    Diabet Med; 1997 Dec; 14(12):1007-9. PubMed ID: 9455926
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. Novel mitochondrial DNA mutation in tRNA(Lys) (8296A-->G) associated with diabetes.
    Kameoka K; Isotani H; Tanaka K; Azukari K; Fujimura Y; Shiota Y; Sasaki E; Majima M; Furukawa K; Haginomori S; Kitaoka H; Ohsawa N
    Biochem Biophys Res Commun; 1998 Apr; 245(2):523-7. PubMed ID: 9571188
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. Clinical aspects of mitochondrial diabetes.
    Vialettes B; Paquis-Flucklinger V; Bendahan D
    Diabetes Metab; 1997 Mar; 23 Suppl 2():52-6. PubMed ID: 9105784
    [TBL] [Abstract][Full Text] [Related]  

  • 6. New insights in the molecular pathogenesis of the maternally inherited diabetes and deafness syndrome.
    Maassen JA; Jahangir Tafrechi RS; Janssen GM; Raap AK; Lemkes HH; 't Hart LM
    Endocrinol Metab Clin North Am; 2006 Jun; 35(2):385-96, x-xi. PubMed ID: 16632100
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [From gene to disease; mutation in mitochondrial DNA and maternally inherited diabetes mellitus with deafness (MIDD)].
    Leys AM; de Jong PT
    Ned Tijdschr Geneeskd; 2001 Nov; 145(46):2250-2. PubMed ID: 11757250
    [No Abstract]   [Full Text] [Related]  

  • 8. [Mitochondrial myopathy/diabetes mellitus].
    Sakuta R
    Ryoikibetsu Shokogun Shirizu; 2001; (36):190-2. PubMed ID: 11596367
    [No Abstract]   [Full Text] [Related]  

  • 9. Mitochondrial DNA variations in patients with maternally inherited diabetes and deafness syndrome.
    Perucca-Lostanlen D; Narbonne H; Hernandez JB; Staccini P; Saunieres A; Paquis-Flucklinger V; Vialettes B; Desnuelle C
    Biochem Biophys Res Commun; 2000 Nov; 277(3):771-5. PubMed ID: 11062027
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [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]  

  • 12. [Mitochondrial diabetes with a focus on maternally inherited diabetes and deafness].
    Frederiksen AL; Kyvik KO; Andersen PH
    Ugeskr Laeger; 2004 Aug; 166(33):2785-8. PubMed ID: 15344856
    [No Abstract]   [Full Text] [Related]  

  • 13. [Mitochondrial myopathy, deafness and type 2 diabetes mellitus with tRNALeu(UUR) point mutation in mitochondrial DNA].
    Stratilová L; Zeman J; Hansíková H; Houstĕk J; Hermanská J; Dudková Z; Konrádová V; Hůlková H; Elleder M
    Cas Lek Cesk; 1998 Jul; 137(14):430-3. PubMed ID: 9748738
    [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. Progressive sensorineural hearing impairment in maternally inherited diabetes mellitus and deafness (MIDD).
    Hendrickx JJ; Mudde AH; 't Hart LM; Huygen PL; Cremers CW
    Otol Neurotol; 2006 Sep; 27(6):802-8. PubMed ID: 16788417
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dual developments in diabetes.
    Spielman RS; Nussbaum RL
    Nat Genet; 1992 May; 1(2):82-3. PubMed ID: 1302013
    [No Abstract]   [Full Text] [Related]  

  • 17. [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]  

  • 18. Absence of maternal A3243G mtDNA mutation and reversible hyperglycemia in a patient with MELAS syndrome.
    Liou CW; Huang CC; Tsai JL; Liu JY; Pang CY; Lee HC; Wang EK; Wei YH
    Acta Neurol Scand; 2000 Jan; 101(1):65-9. PubMed ID: 10660156
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Analysis of mitochondrial DNA gene tRNALeu(UUR) A3243G mutation in diabetic pedigrees].
    Wang CL; Li F; Hou QZ; Li HZ; Zhang Y; Ning G
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Feb; 26(1):74-7. PubMed ID: 19199257
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 5.