Search Results

Heart Diseases in Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke Syndrome

Author: Fayssoil, Abdallah

Source: Congestive Heart Failure, Volume 15, Number 6, November/December 2009 , pp. 284-287(4)

Publisher: Blackwell Publishing

Atorvastatin/lovastatin/niacin: Myotoxicity in a patient with an A3243G mutation: case report

Source: Reactions, Volume 1, Number 1236, 2009-01-24 , pp. 8-8(1)

Publisher: Adis International

A new phenotype of macular dystrophy associated with a mitochondrial A3243G mutation

Source: Clinical & Experimental Ophthalmology, Volume 36, Number 1, January/February 2008 , pp. 92-93(2)

Publisher: Blackwell Publishing

Valproic Acid Aggravates Epilepsy due to MELAS in a Patient with an A3243G Mutation of Mitochondrial DNA

Authors: Lin, Chih-Ming; Thajeb, Peterus

Source: Metabolic Brain Disease, Volume 22, Number 1, March 2007 , pp. 105-109(5)

Publisher: Springer

Early cardiac involvement in children carrying the A3243G mtDNA mutation

Authors: Wortmann, S B; Rodenburg, R J; Backx, A P; Schmitt, E; Smeitink, J A M; Morava, E

Source: Acta Pædiatrica, Volume 96, Number 3, March 2007 , pp. 450-451(2)

Publisher: Blackwell Publishing

Genetic, pathogenetic, and phenotypic implications of the mitochondrial A3243G tRNALeu(UUR) mutation

Author: Finsterer, J.

Source: Acta Neurologica Scandinavica, Volume 116, Number 1, July 2007 , pp. 1-14(14)

Publisher: Blackwell Publishing

Clinical and molecular survey in 124 Chinese patients with Leigh or Leigh-like syndrome

Authors: Zhang, Y.; Yang, Y.; Sun, F.; Cai, X.; Qian, N.; Yuan, Y.; Wang, Z.; Qi, Y.; Xiao, J.; Wang, X.; Jiang, Y.; Qin, J.; Wu, X.

Source: Journal of Inherited Metabolic Disease, Volume 30, Number 2, April 2007 , pp. 265-265(1)

Publisher: Springer

Alteration in the copy number of mitochondrial DNA in leukocytes of patients with mitochondrial encephalomyopathies

Authors: Liu, C.-S.; Cheng, W.-L.; Lee, C.-F.; Ma, Y.-S.; Lin, C.-Y.; Huang, C.-C.; Wei, Y.-H.

Source: Acta Neurologica Scandinavica, Volume 113, Number 5, May 2006 , pp. 334-341(8)

Publisher: Blackwell Publishing

Acquisition of the wobble modification in mitochondrial tRNA^Leu(CUN) bearing the G12300A mutation suppresses the MELAS molecular defect

Authors: Kirino, Yohei; Yasukawa, Takehiro; Marjavaara, Sanna K.; Jacobs, Howard T.; Holt, Ian J.; Watanabe, Kimitsuna; Suzuki, Tsutomu

Source: Human Molecular Genetics, Volume 15, Number 6, 15 March 2006 , pp. 897-904(8)

Publisher: Oxford University Press

Molecular mechanisms of mitochondrial diabetes (MIDD)

Authors: Maassen, Johannes; Janssen, George; 't Hart, Leen

Source: Annals of Medicine, Volume 37, Number 3, May 2005 , pp. 213-221(9)

Publisher: Informa Healthcare

Mitochondrial tRNA^Leu(UUR) mutation in a patient with steroid-resistant nephrotic syndrome and focal segmental glomerulosclerosis

Authors: Löwik, M. M.; Hol, F. A.; Steenbergen, E. J.; Wetzels, J. F. M.; van den Heuvel, L. P. W. J.

Source: Nephrology Dialysis Transplantation, Volume 20, Number 2, February 2005 , pp. 336-341(6)

Publisher: Oxford University Press

Case reports of dobutamine-induced myoclonia in severe renal failure: potential of emerging pharmacovigilance technologies

Authors: Hauben, Manfred; Reich, Lester

Source: Nephrology Dialysis Transplantation, Volume 20, Number 2, February 2005 , pp. 471-472(2)

Publisher: Oxford University Press

Study of Mitochondrial DNA Mutations in Patients With Migraine With Prolonged Aura

Authors: Rozen T.D.; Shanske S.; Otaegui D.; Lu J.; Young W.B.; Bradley K.; DiMauro S.; Silberstein S.D.

Source: Headache: The Journal of Head and Face Pain, Volume 44, Number 7, July 2004 , pp. 674-677(4)

Publisher: Blackwell Publishing

A non-syndromic hearing loss caused by very low levels of the mtDNA A3243G mutation

Authors: Mancuso, M.; Filosto, M.; Forli, F.; Rocchi, A.; Berrettini, S.; Siciliano, G.; Murri, L.

Source: Acta Neurologica Scandinavica, Volume 110, Number 1, July 2004 , pp. 72-74(3)

Publisher: Blackwell Publishing

Diagnostic screening of mitochondrial DNA mutations in Australian adults 1990–2001

Authors: Marotta R.; Chin J.; Quigley A.; Katsabanis S.; Kapsa R.; Byrne E.; Collins S.

Source: Internal Medicine Journal, Volume 34, Numbers 1-2, January 2004 , pp. 10-19(10)

Publisher: Blackwell Publishing

Clinical Heterogeneity, Tissue Distribution, and Intergenerational Segregation of mtDNA Mutation A3243G

Authors: M. Tesarova; H. Hansikova; J. Kytnarova; H. Houstkova; M. Bohm; L. Cerna; J. Zeman; J. Houstek

Source: Toxicology Mechanisms and Methods, Volume 14, Numbers 1-2, Numbers 1-2/January-April 2004 , pp. 79-84(6)

Publisher: Informa Healthcare

Towards Understanding Human Mitochondrial Leucine Aminoacylation Identity

Authors: Sohm B.; Frugier M.; Brule H.; Olszak K.; Przykorska A.; Florentz C.

Source: Journal of Molecular Biology, Volume 328, Number 5, 16 May 2003 , pp. 995-1010(16)

Publisher: Elsevier

Pelvic lymphocyst infection associated with maternally inherited diabetes mellitus

Authors: Ogawa D.; Shikata K.; Matsuda M.; Wada J.; Uchida H.; Asada M.; Makino H.

Source: Diabetes Research and Clinical Practice, Volume 61, Number 2, August 2003 , pp. 137-141(5)

Publisher: Elsevier

Search for Difference in Aminoacylation of Mitochondrial DNA-encoded Wild-type and Mutant Human tRNA^Leu (UUR)

Authors: Wang Zhen-Cheng; Wang Xue-Min; Jin You-Xin; Jiao Bing-Hua; Xu Feng; Miao Ming-Yong; Zhu Ke-Jun

Source: IUBMB Life, Volume 55, Number 3, March 2003 , pp. 139-144(6)

Publisher: Informa Healthcare

Article
Executive and visuospatial deficits in patients with chronic progressive external ophthalmoplegia and Kearns–Sayre syndrome

Authors: Bosbach S.; Kornblum C.; Schröder R.; Wagner M.

Source: Brain, Volume 126, Number 5, May 2003 , pp. 1231-1240(10)

Publisher: Oxford University Press