Results 91 to 100 of about 12,239 (244)

Cerebral hyperemia in MELAS. [PDF]

open access: yes, 1994
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

Comportamiento de la mutación mtDNA A3243G en dos familias antioqueñas de pacientes diagnosticados con el síndrome MELAS

open access: yesIatreia, 2010
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  

Posterior Spinal Instrumented Fusion for Idiopathic Scoliosis in Patients with Multisystemic Neurodegenerative Disorder: A Report of Two Cases

open access: yesJournal of Orthopaedic Surgery, 2016
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

Arrhythmias in MELAS syndrome

open access: yesMolecular Genetics and Metabolism Reports, 2016
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

open access: yesThe RAND Journal of Economics, EarlyView.
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

When should MELAS (Mitochondrial myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like episodes) be the diagnosis?

open access: yesArquivos de Neuro-Psiquiatria
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

open access: yesActa Ophthalmologica, EarlyView.
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]

open access: yes, 1928
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]

open access: yes, 2008
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

Cardiopulmonary Exercise Testing (CPET) Guided Sub‐Anaerobic Threshold Rehabilitation in MELAS Syndrome: A Case Report

open access: yes
The Kaohsiung Journal of Medical Sciences, EarlyView.
Yu‐Lien Tsai   +3 more
wiley   +1 more source

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