Results 61 to 70 of about 19,992,265 (173)
Abstract Objective To evaluate the effectiveness of objective audiological and vestibular assessments in detecting functional changes associated with vitamin B12 deficiency. Data Sources A comprehensive literature search was conducted in PubMed, Scopus, Web of Science, and EMBASE databases.
Nesmah Zainab +2 more
wiley +1 more source
Vitamin B12 (cobalamin) deficiency in gastroenterological diseases - review [PDF]
Introduction: Vitamin B12 is a water-soluble vitamin found primarily in animal-derived products such as red meat, dairy, and eggs. An essential substance for its absorption is the intrinsic factor, produced by the parietal cells of the stomach.
Dominika Opala +6 more
core +3 more sources
ABSTRACT Organophosphate esters (OPEs) are found ubiquitously in the environment and exposure to these chemicals has induced behavioral, developmental, and morphological impairments in several model organisms. Yet there is still a lack of understanding of how sub‐lethal exposure disrupts organism function at the molecular‐level, especially for Daphnia ...
Salwa Hajir +4 more
wiley +1 more source
Vitamin B12 (Cobalamin) Deficiency in the Older Adult
Vitamin B12 (Cobalamin) deficiency in the older adult occurs frequently and has the potential for serious neurological and hematological complications.
Orton, Christine
core +1 more source
Cobalamin D Deficiency Identified Through Newborn Screening [PDF]
Cobalamin D deficiency (cblD) is one of the least common cobalamin metabolism disorders. It may result in isolated homocystinuria, isolated methylmalonic aciduria, or combined methylmalonic aciduria and homocystinuria (cblD-combined). Only seven cases of
Abu-El-Haija, Aya +13 more
core +1 more source
Background Mutation of MMACHC gene causes cobalamin C disease (cblC), an inherited metabolic disorder, which presents as combined methylmalonic aciduria (MMA-uria) and hyperhomocysteinaemia in clinical. Renal complications may also be present in patients
Daorina Bao +9 more
doaj +1 more source
Clinical features and molecular genetics of autosomal recessive ataxia in the Turkish population
Background: Autosomal recessive cerebellar ataxias (ARCAs) are a heterogeneous group of inherited neurodegenerative disorders. The aim of this study was to present the clinical and genetic features of patients with ataxia complaints and those genetically
Faruk Incecik +2 more
doaj +1 more source
A total of 435 non‐redundant metagenome‐assembled genomes (MAGs) were obtained from fecal samples of Taihangshan macaque across all four seasons. The alpha diversity of the gut microbiome in spring and winter was significantly higher than in summer and autumn. Furthermore, marked differences were detected in functional pathways and carbohydrate enzymes
Yanyan Zhou +6 more
wiley +1 more source
Utkan Sevuk,1 Erkan Baysal,2 Nurettin Ay,3 Yakup Altas,2 Rojhat Altindag,2 Baris Yaylak,2 Vahhac Alp,3 Ertan Demirtas4 1Department of Cardiovascular Surgery, Diyarbakir Gazi Yasargil Education and Research Hospital, Diyarbakir, 2Department of Cardiology,
Altindag R +7 more
core
Neuropsychiatric sequelae of chronic nitrous oxide misuse in middle‐aged adults: A case series
Abstract Background and Objectives Chronic nitrous oxide (N2O) misuse causes heterogeneous neuropsychiatric toxicity. Methods We retrospectively reviewed three middle‐aged adults with chronic N2O misuse and neuropsychiatric presentations. Results Presentations included cognitive impairment, hallucinations, and variable neurologic dysfunction ...
Theodore Tsonis +3 more
wiley +1 more source

