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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

210 related items for PubMed ID: 11033519

  • 1. [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
    [Abstract] [Full Text] [Related]

  • 2. [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 13; 137(14):430-3. PubMed ID: 9748738
    [Abstract] [Full Text] [Related]

  • 3. [Evolution until death of two members of a family with A3243G mutation and MELAS phenotype versus diabetes mellitus].
    Pérez López-Fraile MI, Barrena R, Montoya J, Marta E.
    Neurologia; 2006 Jul 13; 21(6):327-32. PubMed ID: 16799910
    [Abstract] [Full Text] [Related]

  • 4. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS) syndrome: an autopsy report.
    Prayson RA, Wang N.
    Arch Pathol Lab Med; 1998 Nov 13; 122(11):978-81. PubMed ID: 9822126
    [Abstract] [Full Text] [Related]

  • 5. Fundus changes in patients with the mitochondrial DNA point mutation at position 3243.
    Bonte C, Leys A, Matthijs G, Missotten L.
    Bull Soc Belge Ophtalmol; 1996 Nov 13; 261():9-12. PubMed ID: 9009357
    [Abstract] [Full Text] [Related]

  • 6. [MELAS associated with diabetes mellitus and point mutation in mitochondrial DNA].
    Onishi H, Inoue K, Osaka H, Nagatomo H, Ando N, Yamada Y, Suzuki K, Hanihara T, Kawamoto S, Okuda K.
    No To Shinkei; 1992 Mar 13; 44(3):259-64. PubMed ID: 1591103
    [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 Mar 13; 108(2):81-5. PubMed ID: 10826513
    [Abstract] [Full Text] [Related]

  • 8. 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 13; 101(1):65-9. PubMed ID: 10660156
    [Abstract] [Full Text] [Related]

  • 9. Mitochondrial 3243 BP mutation: a case report.
    Rigoli L, Caruso RA, Zuccarello D, Rigoli M, Barberi I.
    Diabetes Nutr Metab; 2001 Dec 13; 14(6):343-8. PubMed ID: 11853367
    [Abstract] [Full Text] [Related]

  • 10. Prevalence of A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene in Japanese patients with diabetes mellitus and end stage renal disease.
    Iwasaki N, Babazono T, Tsuchiya K, Tomonaga O, Suzuki A, Togashi M, Ujihara N, Sakka Y, Yokokawa H, Ogata M, Nihei H, Iwamoto Y.
    J Hum Genet; 2001 Dec 13; 46(6):330-4. PubMed ID: 11393536
    [Abstract] [Full Text] [Related]

  • 11. An infant with a mitochondrial A3243G mutation demonstrating the MELAS phenotype.
    Kanaumi T, Hirose S, Goto Y, Naitou E, Mitsudome A.
    Pediatr Neurol; 2006 Mar 13; 34(3):235-8. PubMed ID: 16504796
    [Abstract] [Full Text] [Related]

  • 12. Maternally inherited diabetes and deafness: a diabetic subtype associated with a mutation in mitochondrial DNA.
    Maassen JA, van den Ouweland JM, t Hart LM, Lemkes HH.
    Horm Metab Res; 1997 Feb 13; 29(2):50-5. PubMed ID: 9105898
    [Abstract] [Full Text] [Related]

  • 13. Diagnosis and management of MELAS.
    Thambisetty M, Newman NJ.
    Expert Rev Mol Diagn; 2004 Sep 13; 4(5):631-44. PubMed ID: 15347257
    [Abstract] [Full Text] [Related]

  • 14. Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
    Auré K, Fayet G, Leroy JP, Lacène E, Romero NB, Lombès A.
    Brain; 2006 May 13; 129(Pt 5):1249-59. PubMed ID: 16537564
    [Abstract] [Full Text] [Related]

  • 15. [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 17; 145(46):2250-2. PubMed ID: 11757250
    [No Abstract] [Full Text] [Related]

  • 16. MELAS A3243G mitochondrial DNA mutation and age related maculopathy.
    Jones M, Mitchell P, Wang JJ, Sue C.
    Am J Ophthalmol; 2004 Dec 17; 138(6):1051-3. PubMed ID: 15629304
    [Abstract] [Full Text] [Related]

  • 17. A novel mtDNA point mutation in tRNA(Val) is associated with hypertrophic cardiomyopathy and MELAS.
    Menotti F, Brega A, Diegoli M, Grasso M, Modena MG, Arbustini E.
    Ital Heart J; 2004 Jun 17; 5(6):460-5. PubMed ID: 15320572
    [Abstract] [Full Text] [Related]

  • 18. The role of complex I genes in MELAS: a novel heteroplasmic mutation 3380G>A in ND1 of mtDNA.
    Horváth R, Reilmann R, Holinski-Feder E, Ringelstein EB, Klopstock T.
    Neuromuscul Disord; 2008 Jul 17; 18(7):553-6. PubMed ID: 18590963
    [Abstract] [Full Text] [Related]

  • 19. 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 Jul 17; 115(1):71-4. PubMed ID: 19864902
    [Abstract] [Full Text] [Related]

  • 20. Clinical and genetic features in a MELAS child with a 3271T>C mutation.
    Chou HF, Liang WC, Zhang Q, Goto Y, Jong YJ.
    Pediatr Neurol; 2008 Feb 17; 38(2):143-6. PubMed ID: 18206799
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.