Results 101 to 110 of about 12,239 (244)

Non‐Alzheimer Aβ deposits in the human CNS: Implications with hypoxia and related conditions

open access: yesBrain Pathology, EarlyView.
An Aβ deposit in a non‐Alzheimer's brain from an individual who experienced hypoxia/energy failure. Abstract We recently reported the deposition of Aβ in the frontal cortex of individuals who died of acute coronavirus disease 2019 (COVID‐19), or who did not have COVID‐19 but had respiratory distress, or infants with severe cardiac malformations.
Esma Karlovich   +5 more
wiley   +1 more source

Cellular pathophysiology of MELAS syndrome [PDF]

open access: yes, 2023
Programa de Doctorado en Biotecnología, Ingeniería y Tecnología QuímicaLínea de Investigación: Biología Celular, Molecular e Ingeniería GenéticaClave Programa: DBICódigo Línea: 108MELAS (Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke- like ...
Povea Cabello, Suleva
core  

Is there a role for cannabidiol in obesity, metabolic syndrome and binge eating?

open access: yesBritish Journal of Pharmacology, EarlyView.
Cannabidiol (CBD) is one of the most abundant phytocannabinoids isolated from the Cannabis sativa plant. CBD is a lipophilic, non‐intoxicating substance that differently from Δ9‐tetrahydrocannabinol (Δ9‐THC) does not present the typical profile of a drug of abuse.
Luca Botticelli   +7 more
wiley   +1 more source

MELAS en el Perú: reporte de caso. [PDF]

open access: yes, 2015
El síndrome de MELAS es una rara citopatía mitocondrial de difícil diagnóstico. Reportamos el caso de una niña de 10 años, que ingresó al Instituto Nacional de Ciencias Neurológicas de Lima, Perú, quien presentó episodios bruscos similares a accidentes ...
Escalante-Gavancho, Carlos   +4 more
core   +2 more sources

A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report

open access: yesJournal of Medical Case Reports, 2009
Introduction There are currently 23 missense point mutations and one 4 basepair deletion spanning different mitochondrial genes associated with mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS).
Abu-Amero Khaled K   +4 more
doaj   +1 more source

Globicephala melas subsp. melas Traill 1809

open access: yes, 2005
Published as part of Wilson, Don E. & Reeder, DeeAnn, 2005, Order Cetacea, pp. 723-743 in Mammal Species of the World: a Taxonomic and Geographic Reference (3 rd Edition), Volume 1, Baltimore :The Johns Hopkins University Press on page 728, DOI: 10.5281/zenodo ...
Wilson, Don E., Reeder, DeeAnn
openaire   +2 more sources

Comparative species distribution model framework for marine conservation and its application to loggerhead turtles in the Mediterranean

open access: yesConservation Biology, EarlyView.
Abstract Modeling species distributions in dynamic pelagic environments remains challenging, particularly for wide‐ranging and highly mobile species when there is limited guidance on model performance. This limitation constrains the effective use of species distribution models (SDMs) in marine conservation, where robust and transferable predictions are
E. Pasanisi   +32 more
wiley   +1 more source

Maria Adele Melas [PDF]

open access: yes, 1886
Photograph shows a studio portrait of Maria Adele ...
C. H. Savage (San Antonio, Tex.)
core  

MELAS syndrome as a unusual cause of hypoparathyroidism: clinical case

open access: yesОстеопороз и остеопатии, 2019
MELAS syndrome belongs to the group of progressive mitochondrial diseases associated with point mutations in mitochondrial DNA, and includes mitochondrial encephalomyopathy, lactic acidosis, stroke-like episodes, which can combined with endocrine ...
Diliara Sh. Umiarova   +4 more
doaj   +1 more source

MELAS or more [PDF]

open access: yesArquivos de Neuro-Psiquiatria, 2016
Josef Finsterer, Marlies Frank
openaire   +3 more sources

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