Results 121 to 130 of about 7,658,238 (373)

Cutaneous Phosphorylated Alpha‐Synuclein in Lewy Body Dementia

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To determine the test performance of cutaneous phosphorylated alpha‐synuclein (P‐SYN) in dementia with Lewy bodies (DLB), individuals with reduced Montreal Cognitive Assessment (MoCA) and healthy controls. Methods This is the first subgroup analysis of the Synuclein‐One study, a prospective, blinded study evaluating P‐SYN detection ...
Christopher H. Gibbons   +31 more
wiley   +1 more source

Bułgarska misja Tadeusza S. Grabowskiego, 
wysłannika odradzającej się Polski 
i dwujęzyczne wydanie 
Ankiety bułgarskiej w sprawie polskiej (1915–1916)

open access: yesPostscriptum Polonistyczne, 2020
Years 2011 and 2015 are two anniversaries both linked with the name of Tadeusz Grabowski – 130th anniversary of the Polish professor and diplomat and 100th anniversary of the Bulgarian questionnaire on the Polish issue (1915–1916) – an important document
Albena Popowa
doaj  

The Young Schema Questionnaire Short Form 3 (YSQ-S3): does the new four-domains model show the best fit?

open access: diamond, 2020
Matteo Aloi   +4 more
openalex   +2 more sources

Remote Monitoring in Myasthenia Gravis: Exploring Symptom Variability

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Myasthenia gravis (MG) is a rare, autoimmune disorder characterized by fluctuating muscle weakness and potential life‐threatening crises. While continuous specialized care is essential, access barriers often delay timely interventions. To address this, we developed MyaLink, a telemedical platform for MG patients.
Maike Stein   +13 more
wiley   +1 more source

Diagnostic Utility of the ATG9A Ratio in AP‐4–Associated Hereditary Spastic Paraplegia

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Adaptor protein complex 4–associated hereditary spastic paraplegia (AP‐4‐HSP), a childhood‐onset neurogenetic disorder and frequent mimic of cerebral palsy, is caused by biallelic variants in the adaptor protein complex 4 (AP‐4) subunit genes (AP4B1 [for SPG47], AP4M1 [for SPG50], AP4E1 [for SPG51], and AP4S1 [for SPG52]).
Habibah A. P. Agianda   +12 more
wiley   +1 more source

German Translation of the Four-Item Mentalising Index (FIMI-G)

open access: yesMeasurement Instruments for the Social Sciences
Mentalising can be defined as the social-cognitive ability to understand and infer the mental non-emotional states of oneself and others. Recently, the Four-Item Mentalising Index (FIMI), a self-report scale, was developed to efficiently measure ...
Alex Bertrams, Max Blaise, Ann Krispenz
doaj   +1 more source

Knowledge, attitudes and sexual behavior concerning AIDS among college students in Guangzhou, China: a cross-sectional questionnaire survey

open access: yesFrontiers in Public Health
BackgroundDespite global efforts to control human immunodeficiency virus (HIV) among adolescents, the number of new infections among adolescents continues to increase.
Yanjun Yang, Shaomin Wu, Yuan Tang
doaj   +1 more source

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