Výsledky vyhledávání - "cognitive impairement"

Akademický článek

Movement Releated Cortical Potentials Obtained by Saccadic Eye Movements In Multiple Sclerosis

Autor: Tomris Ugur Egercioglu, Zahide Betül Gündüz, Osman Serhat Tokgöz, Zehra Akpınar

Publikováno v: Genel Tıp Dergisi, Vol 32, Iss 3, Pp 238-244 (2022)

Background Movement-related cortical potentials (MRCPs) are electrophysiological activities that reflect neurological mechanisms that occur in the cortex during the planning of and preparation for movement. We aimed to evaluate the MRCPs that occur d

Externí odkaz: https://doaj.org/article/2b10c4b1b68342aaa4fa9966631eb67f

Zobrazit plný text záznamu

Akademický článek

Brain CT can predict low lean mass in the elderly with cognitive impairment: a community-dwelling study

Autor: Yun-Ting Chen, Chiun-Chieh Yu, Yu-Ching Lin, Shan-Ho Chan, Yi-Yun Lin, Nai-Ching Chen, Wei-Che Lin

Publikováno v: BMC Geriatrics, Vol 22, Iss 1, Pp 1-13 (2022)

Abstract Background The coexistence of sarcopenia and dementia in aging populations is not uncommon, and they may share common risk factors and pathophysiological pathways. This study aimed to evaluate the relationship between brain atrophy and low l

Externí odkaz: https://doaj.org/article/24ae5927aaa54732891d0c06a89c2606

Zobrazit plný text záznamu

Akademický článek

COVID-19 infection could be a risk factor for dementia?

Autor: P. Costa, I. Pinto, P. Branco

Publikováno v: European Psychiatry, Vol 65, Pp S519-S519 (2022)

Introduction Since the COVID-19 pandemic start in early 2020, there have been reports of a high prevalence of neuropsychiatric symptoms. Cognitive impairment is being increasingly recognized as an acute and possibly long-term sequel of the disease. A

Externí odkaz: https://doaj.org/article/c94aa34452944152bafb2c697c038e9a

Zobrazit plný text záznamu

Causes, Types, Symptoms and Diagnosis of Methyl Melonic Acidemia (MMA), Common Symptoms of Methyl Malonic Acid (MMA) and Homocysteine (HMA -HCY0, Differential Diagnosis of Methyl Malonic Acidemia (MMA), Treatment of Methyl Melonyl Acidemia

Autor: Vinayasree. C, Mohan Naidu. K, Muralinath. E, Amrutham Sandeep, Venkat Naveen. A, Guruprasad. M, Sravani Pragna. K

Methylmalonic acidemia (MMA) is a rare inherited metabolic disorder manifested by impaired metabolism of certain amino acids and fatty acids. It occurs by a deficiency of the enzyme methylmalonyl-CoA mutase, which leads to the collection of toxic lev

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bd3cd6569dacfc79ce47c339bf54ed6

Zobrazit plný text záznamu

Types and Causes of Citrullinemia Type I, Type II, Symptoms of Citrullinemia Type I, Type II, Diagnosis of Citrullinemia, Clinical Evaluation of Citrullinemia and Treatment of Cutrullinemia

Autor: Vinayasree.C, Naidu.K, Mohan, Muralinath.E, Amrutham Sandeep, Venkat Naveen . A, Guruprasad.M, Sravani Pragna.K

Citrullinemia is a rare genetic disorder that affects the metabolism of the amino acid arginine. It is manifested by the collection of citrulline, a toxic substance, in the blood and tissues due to the deficiency or malfunctioning of an enzyme called

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f0ca18017d3caf6e26906d35158f61c

Zobrazit plný text záznamu

Causes, Symptoms, Intellectual Disability, Behavioural Issues, Skin Conditions, Microcephaly, Seizures, Management, Regular Monitoring, Nutrition a Supplementation, Support As Well As Counselling of Classical PKD and Symptoms, Treatment As Well As Management, Future Perspectives Of Non Classical PKD and Genetic Basis As Well As Management Strategies, Psychosocial Impact, Diagnosis As Well As Treatment of Variant Forms of PKU

Autor: Mohan Naidu.K, Muralinath.E, Amrutham Sandeep, Vinayasree.C, Venkat Naveen.A, Guruprasad.M, Sravani Pragna.K

Phenylketonuria (PKU) is a genetic disorder with an incidence of approximately 1 in 10,000 to 15,000 births worldwide. Phenylketonuria is an inherited metabolic disorder manifested by the lack of ability to metabolize phenylalanine, an amino acid fou

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29d4174770d360355bfb3334f8ac49c1

Zobrazit plný text záznamu

Akademický článek

Screening for Cognitive Impairment in Multiple Sclerosis with MOCA Test

Autor: Selma Aksoy, Emin Timer, Sibel Mumcu, Mücella Akgün, Elif Kırak, Dilek Necioğlu Örken

Publikováno v: Türk Nöroloji Dergisi, Vol 19, Iss 2, Pp 52-55 (2013)

OBJECTIVE: Cognitive dysfunction is currently recognized as a significant cause of disability in multiple sclerosis (MS). The Montreal Cognitive Assessment (MOCA) is screening device used to evaluate executive functions, visuo-spatial abilities, lang

Externí odkaz: https://doaj.org/article/f31f65768b47438c98c7be58ad5bada7

Zobrazit plný text záznamu

Blood based biomarkers for the identification of Alzheimer’s disease using proteomics approaches

Autor: Virk, Gurjeet Kaur

Alzheimer's disease (AD) is a multifactorial neurodegenerative disease characterised by dysregulation of various cellular and molecular processes. Apart from environmental and lifestyle effects, genetic variations of the apolipoprotein E (APOE) gene

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d62886a84c2f03ae4553517a38d6cc5d

Zobrazit plný text záznamu

Akademický článek

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Syndrome de Korsakoff révélateur d’une sclérose en plaques active

Autor: Marion Tailland, Morgan Dornadic, Eric Thouvenot

Publikováno v: Revue Neurologique
Revue Neurologique, Elsevier Masson, 2020, 176, pp.S119. ⟨10.1016/j.neurol.2020.01.329⟩

International audience; Les atteintes cognitives sévères dans la sclérose en plaques (SEP) sont rarement inaugurales et les amnésies sont exceptionnelles.Observation : une patiente de 26 ans, droitière, sans antécédent, a été hospitalisée p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f0d3498103b880f119feff42db9c387
https://hal.umontpellier.fr/hal-03339732

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání