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.
5. Defects of intergenomic communication: autosomal disorders that cause multiple deletions and depletion of mitochondrial DNA. Hirano M; Marti R; Ferreiro-Barros C; Vilà MR; Tadesse S; Nishigaki Y; Nishino I; Vu TH Semin Cell Dev Biol; 2001 Dec; 12(6):417-27. PubMed ID: 11735376 [TBL] [Abstract][Full Text] [Related]
6. Defects of mitochondrial DNA. Zeviani M; Antozzi C Brain Pathol; 1992 Apr; 2(2):121-32. PubMed ID: 1341953 [TBL] [Abstract][Full Text] [Related]
7. Nucleus-driven mutations of human mitochondrial DNA. Zeviani M J Inherit Metab Dis; 1992; 15(4):456-71. PubMed ID: 1528006 [TBL] [Abstract][Full Text] [Related]
8. Defects of intergenomic communication: where do we stand? Hirano M; Vu TH Brain Pathol; 2000 Jul; 10(3):451-61. PubMed ID: 10885664 [TBL] [Abstract][Full Text] [Related]
10. Multiple mtDNA deletions features in autosomal dominant and recessive diseases suggest distinct pathogeneses. Carrozzo R; Hirano M; Fromenty B; Casali C; Santorelli FM; Bonilla E; DiMauro S; Schon EA; Miranda AF Neurology; 1998 Jan; 50(1):99-106. PubMed ID: 9443465 [TBL] [Abstract][Full Text] [Related]
11. Searching for genes affecting the structural integrity of the mitochondrial genome. Zeviani M; Amati P; Comi G; Fratta G; Mariotti C; Tiranti V Biochim Biophys Acta; 1995 May; 1271(1):153-8. PubMed ID: 7599202 [TBL] [Abstract][Full Text] [Related]
12. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a disease of two genomes. Hirano M; Nishigaki Y; Martí R Neurologist; 2004 Jan; 10(1):8-17. PubMed ID: 14720311 [TBL] [Abstract][Full Text] [Related]
13. Multiple mtDNA deletions with features of MNGIE. Vissing J; Ravn K; Danielsen ER; Dunø M; Wibrand F; Wevers RA; Schwartz M Neurology; 2002 Sep; 59(6):926-9. PubMed ID: 12297582 [TBL] [Abstract][Full Text] [Related]
14. Inherited Mendelian defects of nuclear-mitochondrial communication affecting the stability of mitochondrial DNA. Limongelli A; Tiranti V Mitochondrion; 2002 Nov; 2(1-2):39-46. PubMed ID: 16120307 [TBL] [Abstract][Full Text] [Related]
15. Diseases caused by nuclear genes affecting mtDNA stability. Suomalainen A; Kaukonen J Am J Med Genet; 2001; 106(1):53-61. PubMed ID: 11579425 [TBL] [Abstract][Full Text] [Related]
16. Progressive External Ophthalmoplegia in Polish Patients-From Clinical Evaluation to Genetic Confirmation. Kierdaszuk B; Kaliszewska M; Rusecka J; Kosińska J; Bartnik E; Tońska K; Kamińska AM; Kostera-Pruszczyk A Genes (Basel); 2020 Dec; 12(1):. PubMed ID: 33396418 [TBL] [Abstract][Full Text] [Related]
17. Cellular and molecular studies in muscle and cultures from patients with multiple mitochondrial DNA deletions. Carrozzo R; Davidson MM; Walker WF; Hirano M; Miranda AF J Neurol Sci; 1999 Nov; 170(1):24-31. PubMed ID: 10540032 [TBL] [Abstract][Full Text] [Related]
18. Mitochondrial diseases. Zeviani M; Taroni F Baillieres Clin Neurol; 1994 Aug; 3(2):315-34. PubMed ID: 7952850 [TBL] [Abstract][Full Text] [Related]
19. [Mitochondrial encephalomyopathies: pleomorphism of the mitochondrial DNA mutations and clinical features]. Sato T; Hirawake H Nihon Rinsho; 1993 Sep; 51(9):2364-72. PubMed ID: 8411714 [TBL] [Abstract][Full Text] [Related]