|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)|
12/01/2015 - "Spectral-domain optical coherence tomography in mitochondrial encephalopathy, lactic acidosis, and strokelike episodes."
01/01/2013 - "Five children were diagnosed with MELAS (mitochondrial encephalopathy, lactic acidosis, and strokelike episodes) and one with Leigh's syndrome (LS). "
09/01/2005 - "Two of them are males with severe lactic acidosis suggestive of a mitochondrial encephalopathy, and the third is a female who was less severely affected, suggesting skewed X-inactivation. "
08/01/2005 - "Imaging, performed with a combination of the MR diffusion tensor imaging, fiber tracking, and MR spectroscopy, suggested the diagnosis of an acute severe unusual mitochondrial encephalopathy, lactic acidosis, and strokelike event, which was confirmed by muscle biopsy, but fiber tracking showed unexpected unaltered white matter tracts."
05/01/1999 - "Pregnancy with mitochondrial encephalopathy, lactic acidosis, and strokelike episodes syndrome."
05/24/1995 - "This study examines the relationship of genotype to phenotype in 14 unselected patients who were found to harbour the A3243G transition in the mitochondrial transfer RNALeu(UUR) gene commonly associated with the syndrome of mitochondrial encephalopathy, lactic acidosis and strokes (MELAS). "
11/01/2015 - "Characteristically, giving rise to MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes), a phenotypic spectrum associated with this genetic variant is now apparent. "
09/01/2014 - "Mutation-free baby born from a mitochondrial encephalopathy, lactic acidosis and stroke-like syndrome carrier after blastocyst trophectoderm preimplantation genetic diagnosis."
05/01/2014 - "The acronym MELAS (mitochondrial encephalopathy with lactic acidosis and stroke-like episodes) belies the true scope of one of the most prevalent mitochondriopathies in adults. "
03/01/2014 - "the maternally inherited MTTL1 A3243G mutation in the mitochondrial genome causes MelaS (Mitochondrial encephalopathy lactic acidosis with Stroke-like episodes), a condition that is multisystemic but affects primarily the nervous system. "
|3.||MELAS Syndrome (Syndrome, MELAS)
01/01/1991 - "The muscular biopsy enables us to classify this case as a mitochondrial encephalopathy similar to the MELAS syndrome. "
10/01/2008 - "Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome."
07/01/2007 - "Among the syndromic manifestations the mitochondrial encephalopathy, lactacidosis, and stroke-like episode (MELAS) syndrome is the most frequent. "
01/01/1993 - "We conclude that these patients suffered from adult-onset mitochondrial encephalopathy, lactic acidosis and strokelike episodes (MELAS syndrome). "
11/01/1985 - "Mitochondrial encephalopathy, lactic acidosis, and strokelike syndrome (MELAS)"
|4.||Mitochondrial Diseases (Mitochondrial Disease)
10/01/2008 - "Since the initial description almost 25 years ago, the syndrome of mitochondrial encephalopathy, lactic acidosis, and strokelike episodes (MELAS) has been a useful model to study the complex interplay of factors that define mitochondrial disease. "
09/01/2013 - "The most common clinical presentation of mitochondrial diseases is encephalomyopathy, and epileptic seizures can frequently occur as a presenting sign of mitochondrial encephalopathy. "
03/01/2004 - "Initial brain imaging and a series of laboratory studies were performed which suggested mitochondrial disorders, especially mitochondrial encephalopathy, lactic acidosis, and strokelike episodes (MELAS) syndrome. "
01/01/2012 - "Ischemic stroke may be a complication of myopathy and needs to be delineated from stroke-like episodes, which are unique to mitochondrial disorders, particularly mitochondrial encephalopathy, lactacidosis and stroke-likeepisode syndrome. "
01/01/2012 - "Stroke-like episodes occur particularly in mitochondrial encephalopathy, lactacidosis and stroke-likeepisode syndrome but rarely also in Leigh-syndrome and other mitochondrial disorders. "
|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). "
|1.||Sympathomimetics (Sympathomimetic Amines)
|2.||Mitochondrial DNA (mtDNA)
|4.||Noninsulin-dependent diabetes mellitus with deafness
|5.||Electron Transport Complex I (NADH-CoQ Reductase)
|7.||Lys Transfer RNA
|8.||Leu Transfer RNA
|9.||Transfer RNA (tRNA)
|10.||Prostaglandins D (PGD)
|1.||Cochlear Implants (Cochlear Implant)
|4.||Heart Transplantation (Grafting, Heart)
|5.||Transplantation (Transplant Recipients)