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Publikationstyp
Academic Journals (260)
Electronic Resources (30)
Books (6)
eBooks (4)
Conference Materials (1)
Thema
human (30)
cognitive dysfunction (21)
cognition (20)
multiple sclerosis (18)
humans (15)
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Treffer 1 - 25 von 313, Suchdauer: 1.13s
  • 15
    Analysis of SOD2 rs4880 Genetic Variant in Patients with Alzheimer’s Disease

    von Siokas V. ; Stamati P. ; Pateraki G. ; et al.

    Current Issues in Molecular Biology ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85140639107&doi=10.3390%2fcimb44100302&partnerID=40&md5=54e2e6a35f7ffd5b8a34b1bf197dc88e

    Schlagworte: manganese superoxide dismutase; aged; Alzheimer disease; Article; case control study; cohort analysis; controlled study; dominant inheritance; female; genetic association; genetic model; genetic variability; genotype; human; human cell; major clinical study; male; missense mutation; molecular pathology; mutational analysis; recessive inheritance; sex difference; SOD2 gene; MDPI

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  • 17
    Lack of an association between SCFD1 rs10139154 polymorphism and amyotrophic lateral sclerosis

    von Siokas V. ; Aloizou A.-M. ; Liampas I. ; et al.

    Molecular Medicine Reports ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85125572199&doi=10.3892%2fmmr.2022.12662&partnerID=40&md5=4b6afe201a96672fc8cabb8f9321b003

    Schlagworte: adult; amyotrophic lateral sclerosis; Article; case control study; chromosome 14q; controlled study; female; gene; gene frequency; gene locus; genetic association; genetic model; genetic polymorphism; genetic susceptibility; genetic variability; genome-wide association study; genotype; human; major clinical study; male; middle aged; onset age; risk assessment; risk factor; sec1 family domain containing 1 gene; single nucleotide polymorphism; degenerative disease; genetics; Humans; Neurodegenerative Diseases

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  • 19
    Transcranial magnetic stimulation (TMS) and repetitive TMS in multiple sclerosis

    von Aloizou A.-M. ; Pateraki G. ; Anargyros K. ; et al.

    Reviews in the Neurosciences ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85102030452&doi=10.1515%2frevneuro-2020-0140&partnerID=40&md5=dddecc2cc9a09aabcee357f903823093

    Schlagworte: 4 aminobutyric acid A receptor; biological marker; natalizumab; Article; cerebellum disease; clinical feature; cognitive defect; comparative effectiveness; cortical excitability; disease association; Expanded Disability Status Scale; fatigue; human; kinesiotherapy; major depression; multiple sclerosis; neuropathology; observational study; open study; phase 2 clinical trial (topic); pilot study; quality of life; randomized controlled trial (topic); repetitive transcranial magnetic stimulation; sham procedure; spasticity; transcranial magnetic stimulation; treatment outcome; urinary tract disease; electroencephalography

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  • 21
    The Impact of Primary Progressive Aphasia on Picture Naming and General Language Ability

    von Peristeri E. ; Messinis L. ; Kosmidis M.H. ; et al.

    Cognitive and Behavioral Neurology ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85115370491&doi=10.1097%2fWNN.0000000000000275&partnerID=40&md5=8e351bd356093907c84239962aa6cd87

    Schlagworte: adult; age; aged; Article; atrophy; Boston diagnostic aphasia examination; cerebrospinal fluid analysis; clinical article; cognition; controlled study; diffusion weighted imaging; dorsolateral prefrontal cortex; education; Expanded Disability Status Scale; female; gender; Greek (citizen); human; human experiment; image analysis; image segmentation; inferior frontal gyrus; language ability; language network; language test; male; Mini Mental State Examination; neurologic examination; neuropsychological test; normal human

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  • 24
    Lack of association between TREM2 rs75932628 variant and amyotrophic lateral sclerosis

    von Siokas V. ; Aloizou A.-M. ; Liampas I. ; et al.

    Molecular Biology Reports ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85103893173&doi=10.1007%2fs11033-021-06312-1&partnerID=40&md5=138c1865fa53587cb805d7f2d45d6a5b

    Schlagworte: triggering receptor expressed on myeloid cells 2; immunoglobulin receptor; membrane protein; TREM2 protein; human; adult; amyotrophic lateral sclerosis; Article; clinical evaluation; controlled study; female; genetic association; genetic trait; genetic variability; genotype; major clinical study; male; risk assessment; sensitivity analysis; single nucleotide polymorphism; TREM2 gene; cohort analysis; genetic association study; genetic predisposition; genetics; meta analysis (topic); middle aged; publishing; Cohort Studies; Genetic Association Studies

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