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Mitochondrial encephalopathy

Mitochondrial myopathy encephalopathy lactic acidosis and strokelike episodes
Networked: 215 relevant articles (1 outcomes, 10 trials/studies)

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Bio-Agent Context: Research Results

Experts

1. Kaufmann, Petra: 4 articles (02/2009 - 11/2007)
2. Zeviani, Massimo: 3 articles (10/2014 - 01/2006)
3. Taylor, Robert W: 3 articles (08/2013 - 01/2009)
4. Qi, Yu: 3 articles (04/2013 - 12/2008)
5. DiMauro, Salvatore: 3 articles (01/2013 - 02/2006)
6. Nakano, K: 3 articles (01/2003 - 04/2001)
7. Osawa, M: 3 articles (01/2003 - 04/2001)
8. Cisotto, Paola: 2 articles (10/2014 - 01/2006)
9. Zordan, Mauro A: 2 articles (10/2014 - 01/2006)
10. Costa, Rodolfo: 2 articles (10/2014 - 01/2006)

Related Diseases

1. Lactic Acidosis
2. Stroke (Strokes)
3. MELAS Syndrome (Syndrome, MELAS)
4. Mitochondrial Diseases (Mitochondrial Disease)
5. Leber Hereditary Optic Atrophy (Leber's Hereditary Optic Neuropathy)
03/01/2011 - "The aim of this paper is to describe the clinical features and molecular findings of a unique case of Leber's hereditary optic neuropathy (LHON)/mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) overlap syndrome presenting as nonischemic central retinal vein occlusion (CRVO). "
06/01/1991 - "It is argued that this rare disease, since the princeps description in 1964 only reported in England (1986) and the U.S.A (1986), is most likely a singular type of mitochondrial encephalopathy: it is associated with Leber's optic atrophy, and the NMR changes observed have been signalled in other mitochondrial encephalomyelopathies, such as Leigh's disease and MELAS."
04/01/2013 - "These trials have included patients with various mitochondrial disorders, a selected subcategory of mitochondrial disorders, or specific mitochondrial disorders (Leber hereditary optic neuropathy or mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes). "
03/01/1998 - "Mutations usually associated with either mitochondrial encephalopathy, lactic acidosis and stroke-like episode, myoclonic epilepsy with ragged red fibres, or those strongly linked to Leber's hereditary optic neuropathy (LHON) were not detected in patients or controls. "
09/01/2006 - "The ND1 subunit gene of the mitochondrial NADH-ubiquinone oxidoreductase (complex I) is a hot spot for mutations causing Leber hereditary optic neuropathy and several mutations causing the mitochondrial encephalopathy, lactic acidosis and stroke-like episodes syndrome (MELAS). "

Related Drugs and Biologics

1. Sympathomimetics (Sympathomimetic Amines)
2. Mitochondrial DNA (mtDNA)
3. Phosphorus
4. Noninsulin-dependent diabetes mellitus with deafness
5. Electron Transport Complex I (NADH-CoQ Reductase)
6. Lactic Acid
7. Lys Transfer RNA
8. Leu Transfer RNA
9. Transfer RNA (tRNA)
10. Prostaglandins D (PGD)

Related Therapies and Procedures

1. Cochlear Implants (Cochlear Implant)
2. Cochlear Implantation
3. Ketogenic Diet
4. Heart Transplantation (Grafting, Heart)
5. Transplantation (Transplant Recipients)