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.
11. Mitochondrial hepatopathies in the newborn period. Fellman V; Kotarsky H Semin Fetal Neonatal Med; 2011 Aug; 16(4):222-8. PubMed ID: 21680270 [TBL] [Abstract][Full Text] [Related]
12. Mitochondrial disease criteria: diagnostic applications in children. Morava E; van den Heuvel L; Hol F; de Vries MC; Hogeveen M; Rodenburg RJ; Smeitink JA Neurology; 2006 Nov; 67(10):1823-6. PubMed ID: 17130416 [TBL] [Abstract][Full Text] [Related]
13. Deoxyguanosine kinase mutations and combined deficiencies of the mitochondrial respiratory chain in patients with hepatic involvement. Slama A; Giurgea I; Debrey D; Bridoux D; de Lonlay P; Levy P; Chretien D; Brivet M; Legrand A; Rustin P; Munnich A; Rötig A Mol Genet Metab; 2005 Dec; 86(4):462-5. PubMed ID: 16263314 [TBL] [Abstract][Full Text] [Related]
14. Hearing loss in mitochondrial disorders. Hsu CH; Kwon H; Perng CL; Bai RK; Dai P; Wong LJ Ann N Y Acad Sci; 2005 May; 1042():36-47. PubMed ID: 15965043 [TBL] [Abstract][Full Text] [Related]
15. [Mitochondrial disorders: a classification for the 21st century]. Andreu AL; Gonzalo-Sanz R Neurologia; 2004; 19(1):15-22. PubMed ID: 14762729 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. Phenotypic variations in 3 children with POLG1 mutations. Burusnukul P; de los Reyes EC J Child Neurol; 2009 Apr; 24(4):482-6. PubMed ID: 19189930 [TBL] [Abstract][Full Text] [Related]
18. [The mitochondrial genome and human mitochondrial diseases]. Sukernik RI; Derbeneva OA; Starikovskaia EB; Volod'ko NV; Mikhaĭlovskaia IE; Bychkov IIu; Lott M; Brown M; Wallace D Genetika; 2002 Feb; 38(2):161-70. PubMed ID: 11898607 [TBL] [Abstract][Full Text] [Related]
19. Renal disease and mitochondrial genetics. Rötig A J Nephrol; 2003; 16(2):286-92. PubMed ID: 12768079 [TBL] [Abstract][Full Text] [Related]