Results 91 to 100 of about 12,239 (244)
Cerebral hyperemia in MELAS. [PDF]
The pathophysiology of stroke-like episodes in MELAS (mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes) is uncertain. We studied a 24-year-old man with MELAS who had fluent aphasia and right hemianopia.
I Prohovnik +3 more
core +1 more source
Introducción: mutaciones en mtDNA causan citopatias mitocondriales, la más común de ellas es el síndrome MELAS; la transición A3243G en tRNA de leucina (tRNALeu) se presenta en 80% de pacientes.
María Victoria Parra Marín +4 more
doaj
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke (MELAS) syndrome is a progressive multisystemic neurodegenerative disorder. MELAS syndrome impairs oxidative phosphorylation and predisposes patients to lactic acidosis, particularly ...
Kwong Weng Loh +4 more
doaj +1 more source
Letter to the Editor With interest we read the article by Thomas et al. about a 44 year old female with MELAS syndrome due to the m.3243A > G mutation, which manifested cardiologically as hypertrophic cardiomyopathy and episodes of supraventricular tachycardia requiring atenolol [1]. We have the following comments and concerns.
Josef Finsterer, Sinda Zarrouk-Mahjoub
openaire +3 more sources
Demand Estimation with Text and Image Data
ABSTRACT We propose a demand estimation approach that leverages unstructured data to infer substitution patterns. Using pre‐trained deep learning models, we extract embeddings from product images and textual descriptions and incorporate them into a mixed logit demand model.
Giovanni Compiani +2 more
wiley +1 more source
Mitochondrial myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like episodes (MELAS) is a rare mitochondrial disorder. Diagnostic criteria for MELAS include typical manifestations of the disease: stroke-like episodes, encephalopathy, evidence of ...
Paulo José Lorenzoni +4 more
doaj +1 more source
Clinical manifestations of dual‐gene variants in retinitis pigmentosa
Abstract Purpose Retinitis pigmentosa (RP) is an inherited retinal disease (IRD), whereby each affected individual typically harbours pathogenic variants in a single causative gene, yet the disorder exhibits marked genetic heterogeneity, with more than 100 genes reported to underlie RP.
Lasse Wolfram +11 more
wiley +1 more source
Un Globicephalus melas (Traill) [PDF]
Aparición de un cetáceo en la playa de Rodiles (España), perteneciente a la especie "Globicephalus melas", descrito con el nombre de Delphinus melas por Traill en 1809. - Características del ejemplar aparecido. Nombres vulgares por los que se le conoce (
Buen y Lozano, Fernando de
core
Acute auditory agnosia as the presenting hearing disorder in MELAS. [PDF]
MELAS is commonly associated with peripheral hearing loss. Auditory agnosia is a rare cortical auditory impairment, usually due to bilateral temporal damage. We document, for the first time, auditory agnosia as the presenting hearing disorder in MELAS. A
Servidei, Serenella +4 more
core +1 more source

