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 *

287 related articles for article (PubMed ID: 25294199)

  • 1. [The complex clinical presentation of hereditary mitochondrial diseases].
    Frederiksen AL; Nielsen MF; Yderstræde K; Vissing J
    Ugeskr Laeger; 2014 Sep; 176(38):. PubMed ID: 25294199
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic Counselling for Maternally Inherited Mitochondrial Disorders.
    Poulton J; Finsterer J; Yu-Wai-Man P
    Mol Diagn Ther; 2017 Aug; 21(4):419-429. PubMed ID: 28536827
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Concise Review: Heteroplasmic Mitochondrial DNA Mutations and Mitochondrial Diseases: Toward iPSC-Based Disease Modeling, Drug Discovery, and Regenerative Therapeutics.
    Hatakeyama H; Goto Y
    Stem Cells; 2016 Apr; 34(4):801-8. PubMed ID: 26850516
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mitochondrial DNA mutations: an overview of clinical and molecular aspects.
    Craigen WJ
    Methods Mol Biol; 2012; 837():3-15. PubMed ID: 22215537
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Characteristics of molecular genetics and research progress on mitochondrial diseases].
    Zhang M; Si Y; Zhao J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Oct; 33(5):717-25. PubMed ID: 27577231
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mitochondrial disorders: genetics, counseling, prenatal diagnosis and reproductive options.
    Thorburn DR; Dahl HH
    Am J Med Genet; 2001; 106(1):102-14. PubMed ID: 11579429
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel mutation in mitochondrial DNA in a patient with diabetes, deafness and proteinuria.
    Adema AY; Janssen MC; van der Heijden JW
    Neth J Med; 2016 Dec; 74(10):455-457. PubMed ID: 27966441
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mitochondrial diseases.
    Molnar MJ; Kovacs GG
    Handb Clin Neurol; 2017; 145():147-155. PubMed ID: 28987165
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetics of mitochondrial respiratory chain deficiencies.
    Rötig A
    Rev Neurol (Paris); 2014 May; 170(5):309-22. PubMed ID: 24798924
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The spectrum of clinical presentation, diagnosis, and management of mitochondrial forms of diabetes.
    Karaa A; Goldstein A
    Pediatr Diabetes; 2015 Feb; 16(1):1-9. PubMed ID: 25330715
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mitochondrial DNA mutations in human disease.
    DiMauro S; Schon EA
    Am J Med Genet; 2001; 106(1):18-26. PubMed ID: 11579421
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Segregation of mitochondrial DNA (mtDNA) in human oocytes and in animal models of mtDNA disease: clinical implications.
    Poulton J; Marchington DR
    Reproduction; 2002 Jun; 123(6):751-5. PubMed ID: 12052229
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Techniques and pitfalls in the detection of pathogenic mitochondrial DNA mutations.
    Moraes CT; Atencio DP; Oca-Cossio J; Diaz F
    J Mol Diagn; 2003 Nov; 5(4):197-208. PubMed ID: 14573777
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial Heteroplasmy.
    Stefano GB; Bjenning C; Wang F; Wang N; Kream RM
    Adv Exp Med Biol; 2017; 982():577-594. PubMed ID: 28551808
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Origins of tissue and cell-type specificity in mitochondrial DNA (mtDNA) disease.
    Burr SP; Chinnery PF
    Hum Mol Genet; 2024 May; 33(R1):R3-R11. PubMed ID: 38779777
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Mitochondrial hearing impairment. Background, genetic predisposition and possibilities for diagnosis].
    Riemann K; Pfister M; Blin N; Kupka S
    HNO; 2004 Jun; 52(6):503-9. PubMed ID: 15241512
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Mitochondrial disorders].
    Munnich A; de Lonlay P; Rötig A; Rustin P
    Bull Acad Natl Med; 2009 Jan; 193(1):19-41; discussion 41-3. PubMed ID: 19718979
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A national perspective on prenatal testing for mitochondrial disease.
    Nesbitt V; Alston CL; Blakely EL; Fratter C; Feeney CL; Poulton J; Brown GK; Turnbull DM; Taylor RW; McFarland R
    Eur J Hum Genet; 2014 Nov; 22(11):1255-9. PubMed ID: 24642831
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial Mutations in Cardiac Disorders.
    Lee SR; Han J
    Adv Exp Med Biol; 2017; 982():81-111. PubMed ID: 28551783
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Autosomal disorders of mitochondrial DNA maintenance.
    Van Goethem G
    Acta Neurol Belg; 2006 Jun; 106(2):66-72. PubMed ID: 16898256
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.