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: 11123121)

  • 1. Maternally inherited hypertrophic cardiomyopathy: a manifestation of mitochondrial DNA mutations--clinical course in two families.
    Dipchand AI; Tein I; Robinson B; Benson LN
    Pediatr Cardiol; 2001; 22(1):14-22. PubMed ID: 11123121
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Maternally inherited cardiomyopathy: clinical and molecular characterization of a large kindred harboring the A4300G point mutation in mitochondrial deoxyribonucleic acid.
    Casali C; d'Amati G; Bernucci P; DeBiase L; Autore C; Santorelli FM; Coviello D; Gallo P
    J Am Coll Cardiol; 1999 May; 33(6):1584-9. PubMed ID: 10334428
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy.
    Taylor RW; Giordano C; Davidson MM; d'Amati G; Bain H; Hayes CM; Leonard H; Barron MJ; Casali C; Santorelli FM; Hirano M; Lightowlers RN; DiMauro S; Turnbull DM
    J Am Coll Cardiol; 2003 May; 41(10):1786-96. PubMed ID: 12767666
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with maternally inherited cardiomyopathy.
    Silvestri G; Santorelli FM; Shanske S; Whitley CB; Schimmenti LA; Smith SA; DiMauro S
    Hum Mutat; 1994; 3(1):37-43. PubMed ID: 7906985
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel m.3395A>G missense mutation in the mitochondrial ND1 gene associated with the new tRNA(Ile) m.4316A>G mutation in a patient with hypertrophic cardiomyopathy and profound hearing loss.
    Chamkha I; Mkaouar-Rebai E; Aloulou H; Chabchoub I; Kifagi C; Fendri-Kriaa N; Kammoun T; Hachicha M; Fakhfakh F
    Biochem Biophys Res Commun; 2011 Jan; 404(1):504-10. PubMed ID: 21144833
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Combination of mtDNA mutations in a patient with a mitochondrial multisystem syndrome.
    De Joanna G; Santorelli FM; Casali C; Brescia-Morra V; Perretti A; Santoro L
    J Hum Genet; 2000; 45(2):109-11. PubMed ID: 10721677
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Cardiomyopathy associated with mitochondrial disorders].
    Matsushita T; Okada S
    Nihon Rinsho; 2000 Jan; 58(1):196-9. PubMed ID: 10885313
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mitochondrial DNA mutations in cardiomyopathy.
    Ito T; Hattori K; Obayashi T; Tanaka M; Sugiyama S; Ozawa T
    Jpn Circ J; 1992 Oct; 56(10):1045-53. PubMed ID: 1433821
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial DNA point mutation (T8993G).
    Pastores GM; Santorelli FM; Shanske S; Gelb BD; Fyfe B; Wolfe D; Willner JP
    Am J Med Genet; 1994 Apr; 50(3):265-71. PubMed ID: 8042671
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel mtDNA point mutation in maternally inherited cardiomyopathy.
    Casali C; Santorelli FM; D'Amati G; Bernucci P; DeBiase L; DiMauro S
    Biochem Biophys Res Commun; 1995 Aug; 213(2):588-93. PubMed ID: 7646516
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mitochondrial cardiomyopathy: molecular and biochemical analysis.
    Marin-Garcia J; Goldenthal MJ
    Pediatr Cardiol; 1997; 18(4):251-60. PubMed ID: 9175519
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A5814G mutation in mitochondrial DNA can cause mitochondrial myopathy and cardiomyopathy.
    Karadimas C; Tanji K; Geremek M; Chronopoulou P; Vu T; Krishna S; Sue CM; Shanske S; Bonilla E; DiMauro S; Lipson M; Bachman R
    J Child Neurol; 2001 Jul; 16(7):531-3. PubMed ID: 11453453
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Beta-myosin heavy chain gene mutations and hypertrophic cardiomyopathy in Austrian children.
    Greber-Platzer S; Marx M; Fleischmann C; Suppan C; Dobner M; Wimmer M
    J Mol Cell Cardiol; 2001 Jan; 33(1):141-8. PubMed ID: 11133230
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Molecular biology of mitochondrial DNA and mutations in mitochondrial cytopathy].
    Ito T
    Nihon Rinsho; 1993 Jun; 51(6):1425-8. PubMed ID: 8320824
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Maternally inherited mitochondrial cardiomyopathy associated with a C-to-T transition at nucleotide 3303 of mitochondrial DNA in the tRNA(Leu(UUR)) gene.
    Goldstein JD; Shanske S; Bruno C; Perszyk AA
    Pediatr Dev Pathol; 1999; 2(1):78-85. PubMed ID: 9841711
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fatal hypertrophic cardiomyopathy associated with an A8296G mutation in the mitochondrial tRNA(Lys) gene.
    Akita Y; Koga Y; Iwanaga R; Wada N; Tsubone J; Fukuda S; Nakamura Y; Kato H
    Hum Mutat; 2000 Apr; 15(4):382. PubMed ID: 10737988
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Mitochondrial DNA mutation associated with hypertension in tRNA(Ile) and tRNA(Gln) genes].
    Zhu C; Liu Y; Gao J; Yang J; Yin T; Lan Y; Li Z; Guan M; Li Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):619-22. PubMed ID: 25297595
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rapid progression of cardiomyopathy in mitochondrial diabetes.
    Momiyama Y; Atsumi Y; Ohsuzu F; Ui S; Morinaga S; Matsuoka K; Kimura M
    Jpn Circ J; 1999 Feb; 63(2):130-2. PubMed ID: 10084376
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical presentations of mitochondrial cardiomyopathies.
    Lev D; Nissenkorn A; Leshinsky-Silver E; Sadeh M; Zeharia A; Garty BZ; Blieden L; Barash V; Lerman-Sagie T
    Pediatr Cardiol; 2004; 25(5):443-50. PubMed ID: 15185043
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A family with diabetes and heart failure.
    Gerber B; Manser C; Wiesli P; Meier CA
    BMJ Case Rep; 2010 Oct; 2010():. PubMed ID: 22790282
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.