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Abbreviation: MELAS
Appearance Frequency: 750 time(s)
Long forms: 17

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Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
(715 times)
Neurology
(276 times)
mtDNA (113 times)
MERRF (85 times)
CPEO (39 times)
1985 Mitochondrial encephalopathy, lactic acidosis, and strokelike syndrome (MELAS)
myopathy, lactic acidosis, and stroke-like episodes
(10 times)
Neurology
(5 times)
MERRF (6 times)
mtDNA (3 times)
KSS (2 times)
1991 MELAS of infantile onset: mitochondrial angiopathy or cytopathy?
mitochondrial encephalomyopathy and stroke-like episodes
(5 times)
Cell Biology
(2 times)
mtDNA (3 times)
CS (1 time)
DCA (1 time)
1992 Melas: an original case and clinical criteria for diagnosis.
mitochondrial disease
(3 times)
Neurology
(2 times)
PET (1 time)
1994 Hereditary and acquired risk factors for childhood stroke.
mitochondrial encephalopathy, lactic acidosis and cerebrovascular accident syndrome
(3 times)
Neurology
(2 times)
mtDNA (2 times)
2000 [Mitochondrial encephalomyelitis, lactic acidosis and cerebrovascular accidents (MELAS) in pediatric age with the A3243G mutation in the tRNALeu(UUR) gene of mitochondrial DNA].
mitochondrial encephalomyopathy and lactic acidosis
(2 times)
Genetics, Medical
(1 time)
MD (1 time)
mtDNA (1 time)
SLE (1 time)
2006 A novel mutation in the mitochondrial tRNA(Ser(AGY)) gene associated with mitochondrial myopathy, encephalopathy, and complex I deficiency.
myopathy, encephalopathy and stroke-like episodes
(2 times)
Cardiology
(1 time)
LVH (1 time)
2009 Manifestations of the mitochondrial A3243G mutation.
matter of the occipital, temporal, and frontal lobes
(1 time)
Neurology
(1 time)
LS (1 time)
mtDNA (1 time)
2010 Phenotypic patterns of MELAS/LS overlap syndrome associated with m.13513G>A mutation, and neuropathological findings in one autopsy case.
mellitus, encephalomyopathy and several stroke-like episodes associated with lactic acidosis
(1 time)
Neurology
(1 time)
MERRF (1 time)
1996 The T-C(8356) mitochondrial DNA mutation in a Japanese family.
10  mitochondrial encephalomyopathy, lactic acidosis, stroke-like episodes, and sensorineural hearing loss
(1 time)
Audiology
(1 time)
MERRF (1 time)
STL (1 time)
USH (1 time)
2002 Genes and syndromic hearing loss.
11  mitochondrial lactic acidosis and stroke-like syndrome
(1 time)
Drug Therapy
(1 time)
CLA (1 time)
PDH (1 time)
1999 Dichloroacetate and cerebral ischaemia therapeutics.
12  mutation in a family with lactic acidosis and stroke-like episodes
(1 time)
Cell Biology
(1 time)
--- 2011 New mitochondrial tRNA HIS mutation in a family with lactic acidosis and stroke-like episodes (MELAS).
13  mutation is also associated with a neurological syndrome
(1 time)
Endocrinology
(1 time)
MIDD (1 time)
1997 Maternally inherited diabetes and deafness: prevalence in a hospital diabetic population.
14  myoclonic epilepsy with lactic acidosis
(1 time)
Biochemistry
(1 time)
MERRF (1 time)
2016 [Genetic system for maintaining the mitochondrial human genome in yeast Yarrowia lipolytica].
15  myoclonus-epilepsy-lactic acidosis-stroke
(1 time)
Biochemistry
(1 time)
KSS (1 time)
LHON (1 time)
PDH (1 time)
1992 Nonviability of cells with oxidative defects in galactose medium: a screening test for affected patient fibroblasts.
16  myopathy, encephalopathy, lactic acidosis, early atherosclerosis and stroke-like episodes
(1 time)
Neurology
(1 time)
--- 1995 A congenital syndrome of mental deficiency, gait disturbance, sensorineural deafness and pigmentary retinopathy associated with premature atherosclerosis.
17  myopathy, Encephalopathy, Lactic Acidosis, Stroke-like episodes/Leigh overlap syndrome
(1 time)
Medicine
(1 time)
GC-MS (1 time)
iPSCs (1 time)
PCA (1 time)
2016 Metabolic Signature of MELAS/Leigh Overlap Syndrome in Patient-specific Induced Pluripotent Stem Cells Model.