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 *

149 related articles for article (PubMed ID: 18202211)

  • 61. Quality of life, fatigue and mental health in patients with the m.3243A > G mutation and its correlates with genetic characteristics and disease manifestation.
    Verhaak C; de Laat P; Koene S; Tibosch M; Rodenburg R; de Groot I; Knoop H; Janssen M; Smeitink J
    Orphanet J Rare Dis; 2016 Mar; 11():25. PubMed ID: 26988355
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial disease.
    Scaglia F; Towbin JA; Craigen WJ; Belmont JW; Smith EO; Neish SR; Ware SM; Hunter JV; Fernbach SD; Vladutiu GD; Wong LJ; Vogel H
    Pediatrics; 2004 Oct; 114(4):925-31. PubMed ID: 15466086
    [TBL] [Abstract][Full Text] [Related]  

  • 63. CDC National Health Report: leading causes of morbidity and mortality and associated behavioral risk and protective factors--United States, 2005-2013.
    Johnson NB; Hayes LD; Brown K; Hoo EC; Ethier KA;
    MMWR Suppl; 2014 Oct; 63(4):3-27. PubMed ID: 25356673
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Mitochondrial diabetes and deafness: possible dysfunction of strial marginal cells of the inner ear.
    Olmos PR; Borzone GR; Olmos JP; Diez A; Santos JL; Serrano V; Cataldo LR; Anabalón JL; Correa CH
    J Otolaryngol Head Neck Surg; 2011 Apr; 40(2):93-103. PubMed ID: 21453644
    [TBL] [Abstract][Full Text] [Related]  

  • 65. 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]  

  • 66. Frequency of mitochondrial defects in patients with chronic intestinal pseudo-obstruction.
    Amiot A; Tchikviladzé M; Joly F; Slama A; Hatem DC; Jardel C; Messing B; Lombès A
    Gastroenterology; 2009 Jul; 137(1):101-9. PubMed ID: 19344718
    [TBL] [Abstract][Full Text] [Related]  

  • 67. A 3-year clinical follow-up of adult patients with 3243A>G in mitochondrial DNA.
    Majamaa-Voltti KA; Winqvist S; Remes AM; Tolonen U; Pyhtinen J; Uimonen S; Kärppä M; Sorri M; Peuhkurinen K; Majamaa K
    Neurology; 2006 May; 66(10):1470-5. PubMed ID: 16717204
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Mitochondrial cardiomyopathy due to m.3243A>G mitochondrial DNA mutation presenting in late adulthood: a case report.
    Chau EMC; Ma ESK; Chan AOO; Tsoi TH; Law WL
    Hong Kong Med J; 2020 Jun; 26(3):240-242. PubMed ID: 32554818
    [No Abstract]   [Full Text] [Related]  

  • 69. [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]  

  • 70. Fear of disease progression in carriers of the m.3243A > G mutation.
    Custers JAE; de Laat P; Koene S; Smeitink J; Janssen MCH; Verhaak C
    Orphanet J Rare Dis; 2018 Nov; 13(1):203. PubMed ID: 30424784
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Mitochondrial inheritance in depression, dysmotility and migraine?
    Burnett BB; Gardner A; Boles RG
    J Affect Disord; 2005 Sep; 88(1):109-16. PubMed ID: 16019080
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Pathogenic mitochondrial DNA mutations are common in the general population.
    Elliott HR; Samuels DC; Eden JA; Relton CL; Chinnery PF
    Am J Hum Genet; 2008 Aug; 83(2):254-60. PubMed ID: 18674747
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss.
    Kato T; Nishigaki Y; Noguchi Y; Ueno H; Hosoya H; Ito T; Kimura Y; Kitamura K; Tanaka M
    J Hum Genet; 2010 Mar; 55(3):147-54. PubMed ID: 20111055
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Novel mutation in the mitochondrial DNA tRNA glycine gene associated with sudden unexpected death.
    Santorelli FM; Schlessel JS; Slonim AE; DiMauro S
    Pediatr Neurol; 1996 Sep; 15(2):145-9. PubMed ID: 8888049
    [TBL] [Abstract][Full Text] [Related]  

  • 75. How the most common mitochondrial DNA mutation (m.3243A>G) vanishes from leukocytes: a mathematical model.
    Veitia RA
    Hum Mol Genet; 2018 May; 27(9):1565-1571. PubMed ID: 29474538
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Cause of Death in Children With Mitochondrial Diseases.
    Eom S; Lee HN; Lee S; Kang HC; Lee JS; Kim HD; Lee YM
    Pediatr Neurol; 2017 Jan; 66():82-88. PubMed ID: 27843091
    [TBL] [Abstract][Full Text] [Related]  

  • 77. What the Cardiologist Should Know About Mitochondrial Cardiomyopathy?
    St-Pierre G; Steinberg C; Dubois M; Sénéchal M
    Can J Cardiol; 2019 Feb; 35(2):221-224. PubMed ID: 30760430
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Retinal involvement in m.3243A>G carriers.
    Finsterer J; Zarrouk-Mahjoub S
    Ophthalmic Genet; 2018 Oct; 39(5):664-665. PubMed ID: 29979901
    [No Abstract]   [Full Text] [Related]  

  • 79. Acute decompensated heart failure associated with a heteroplasmic 3243A > G mitochondrial DNA point mutation.
    Auer J; Wallner M; Windpessl M; Schmidt WM; Bittner RE; Baradaran-Dilmaghani R; Berent R
    Eur Heart J; 2016 Jun; 37(21):1707. PubMed ID: 26941201
    [No Abstract]   [Full Text] [Related]  

  • 80. Quantification of gait in mitochondrial m.3243A > G patients: a validation study.
    Ramakers R; Koene S; Groothuis JT; de Laat P; Janssen MC; Smeitink J
    Orphanet J Rare Dis; 2017 May; 12(1):91. PubMed ID: 28506302
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.