Results 81 to 90 of about 125,008 (257)
Four decades of retinal vessel segmentation research (1982–2025) are synthesized, spanning classical image processing, machine learning, and deep learning paradigms. A meta‐analysis of 428 studies establishes a unified taxonomy and highlights performance trends, generalization capabilities, and clinical relevance.
Avinash Bansal +6 more
wiley +1 more source
Abilities of the correction of the adaptive process at chronic cerebral ischemia
The management abilities of the adaptive process at chronic cerebral ischemia is the object of this study. The influence to a level of adaptive abilities at the different stages of chronic cerebral ischemia of complex natural adaptogen and modulate ...
E A Antipenko, A V Gustov, T V Mokina
doaj
Chronic ischemic cerebrovascular diseases: pathogenesis and treatment
The annual incidence of new cases of acute cerebral circulatory disorders is noted to be at least 700 per 100 000 population. Chronic brain ischemia leads to the development of encephalopathy with a wide spectrum of subjective and objective neurological ...
N. V. Pizova, D. S. Druzhinin
doaj +1 more source
Compound from Magnolia officinalis Ameliorates White Matter Injury by Promoting Oligodendrocyte Maturation in Chronic Cerebral Ischemia Models. [PDF]
Zhang Z +11 more
europepmc +1 more source
ABSTRACT Management of cerebral vasculopathy in sickle cell anemia (SCA) includes standard‐care, that is, chronic transfusion (CT) or hydroxyurea, and hematopoietic cell transplantation (HCT). DREPAGREFFE‐1 (December 2010/June 2013), a French multicenter trial, was the first prospective trial comparing standard‐care to match sibling donor (MSD)‐HCT in ...
Francoise Bernaudin +40 more
wiley +1 more source
Activated AMPK Protects Against Chronic Cerebral Ischemia in Bilateral Carotid Artery Stenosis Mice. [PDF]
Xie W, Zeng Y, Zheng Y, Cai B.
europepmc +1 more source
Expanding the Phenotype of TUFM‐Related Combined Oxidative Phosphorylation Deficiency 4
ABSTRACT Combined oxidative phosphorylation deficiency 4 (COXPD4) is a rare mitochondrial condition caused by biallelic deleterious variants in the nuclear‐encoded gene TUFM. To date, most individuals with COXPD4 have presented with encephalopathy, hypotonia, and abnormal brain imaging. Many of the reported individuals died in infancy. We aim to expand
Noémie Villeneuve‐Cloutier +2 more
wiley +1 more source
Vascular endothelium deploys caveolin-1 to regulate oligodendrogenesis after chronic cerebral ischemia in mice. [PDF]
Zhao Y +10 more
europepmc +1 more source
ABSTRACT Heterozygous germline variants in CBL disrupt its function as a negative regulator of the Ras/MAPK pathway, classically predisposing to Juvenile myelomonocytic leukemia (JMML) and moyamoya. We describe two affected siblings carrying a paternally inherited CBL variant (c.1210 T> C, p.
Michal Bar‐Hakim +12 more
wiley +1 more source
The purpose of the study was to investigate the efficacy of separate and combined administration of pentoxifylline, memantine and xavron in the pharmacological correction of cognitive impairment in rats under conditions of experimental chronic brain ...
O. Myronov
doaj +1 more source

