Results 191 to 200 of about 2,461,819 (231)

Cochlear implantation in patients with MELAS syndrome

European Archives of Oto-Rhino-Laryngology, 2004
MELAS syndrome (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes) is a rare congenital disorder of mitochondrial DNA (mt-DNA). Patients with this syndrome may present to the otolaryngologist with sensorineural hearing loss (SNHL) that is genetic in origin. Mitochondrial cytopathies can present with a variety of symptoms,
Karkos PD, Anari S, Johnson IJ
openaire   +3 more sources

Magnetic resonance spectroscopy in MELAS syndrome: correlation with CSF and plasma metabolite levels and change after glutamine supplementation

Neuroradiology, 2023
M. P. Guerrero-Molina, Á. Bernabéu-Sanz, A. Ramos-González, Montserrat Morales-Conejo, A. Delmiro, C. Domínguez-González, Joaquín Arenas, Miguel A. Martín, J. González de la Aleja   +8 more
semanticscholar   +1 more source

Clinical score for early diagnosis and treatment of stroke-like episodes in MELAS syndrome

Acta Neurologica Belgica, 2023
J. Naftali, Maor Mermelstein, Y. Landau, R. Barnea, S. Shelly, E. Auriel, S. Peretz   +6 more
semanticscholar   +1 more source

MELAS syndrome masquerading as herpes simplex encephalitis

Neurology, 1993
Herpes simplex encephalitis (HSE) is commonly treated empirically with acyclovir without confirmatory brain biopsy. Three consecutive adults with molecularly verified mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome presented with, and were treated for, apparent HSE.
D R, Johns, A G, Stein, R, Wityk
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Melas syndrome, case report

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

[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

MELAS syndrome with anti-Caspr2 autoantibody positivity: a case report

Acta Neurologica Belgica, 2022
W. Yuan, Xiao-fei Gao, Xiangming Yi, Chen Jinbo, Yuliang Wang   +4 more
semanticscholar   +1 more source

Melas syndrome

Drugs of the Future, 2009
null Agier, V., null Aure, K., null Lombes, A.   +2 more
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MELAS Syndrome

International Ophthalmology Clinics, 1993
E M, Stroh, J M, Winterkorn, A E, Jalkh, S, Lessell   +3 more
openaire   +2 more sources

Imaging findings in MELAS syndrome

2015
Clinical History Image Findings Discussion Find Diagnosis Differential ...
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