Results 161 to 170 of about 5,347 (184)

[Ocular changes in MELAS syndrome].

Klinische Monatsblatter fur Augenheilkunde, 1991
The present paper reports on the clinical findings of a 34-year-old male patient with MELAS syndrome. MELAS syndrome (mitochondrial encephalomyopathy, lactic acidosis and strokelike episodes) belongs to a group of syndromes called mitochondrial encephalomyopathies that are characterized by changes of the mitochondrial respiratory chain and the ...
M, Küchle, P M, Brenner, A, Engelhardt, G O, Naumann   +3 more
openaire   +1 more source

[Arreflexic coma and MELAS syndrome].

Revista clinica espanola, 2009
MELAS is a progressive neurodegenerative and fatal disease characterized by mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes. It is the result of a mitochondrial DNA mutation. Although the incidence of MELAS is currently unknown, it is suspected that approximately 1 out of every 5,000 persons world-wide have some type of
N, Muñoz-Guillén, R, León-López, M J, Ferrer-Higueras, F J, Vargas-Vaserot, J M, Dueñas-Jurado   +4 more
openaire   +1 more source

Melas syndrome, case report

Journal of the Neurological Sciences, 2021
Serla Grabova, Gleni Halili, Jera Kruja
openaire   +1 more source

Phenotypic patterns of MELAS/LS overlap syndrome associated with m.13513G>A mutation, and neuropathological findings in one autopsy case

Neuropathology, 2010
Zhaoxia Wang, Yun Yuan
exaly  

The MELAS syndrome. Review of the literature: the role of the otologist

Clinical Otolaryngology, 2004
P D Karkos
exaly  

Clinical profile and outcome of cardiac involvement in MELAS syndrome

International Journal of Cardiology, 2019
Alice Brambilla, Silvia Favilli, Iacopo Olivotto   +2 more
exaly  

Melas Syndrome

2008
openaire   +1 more source

MELAS syndrome, cardiomyopathy, rhabdomyolysis, and autism associated with the A3260G mitochondrial DNA mutation

Biochemical and Biophysical Research Communications, 2010
Anne I Dipchand, David K Simon
exaly  

A Diabetic Subject With MELAS and Antiphospholipid Syndrome

Diabetes Care, 2003
Hung-Yuan Li, Wei-Shiung Yang, Tong-Yuan Tai   +2 more
exaly  

Prenatal diagnosis of a fetus harboring an intermediate load of the A3243G mtDNA mutation in a maternal carrier diagnosed with MELAS syndrome

Prenatal Diagnosis, 2004
Te-Yao Hsu, Chia-Wei Liou, Cheng-Feng Lee   +2 more
exaly