Výsledky vyhľadávania - "Djamshidian‐Tehrani, Atbin"
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Update on treatments for nonmotor symptoms of Parkinson's disease—an evidence‐based medicine review
ISSN: 0885-3185, 1531-8257, 1531-8257Vydavateľské údaje: Hoboken, USA John Wiley & Sons, Inc 01.02.2019Vydané v Movement disorders (01.02.2019)“…ABSTRACT Objective To update evidence‐based medicine recommendations for treating nonmotor symptoms in Parkinson's disease (PD). Background The International…”
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Movement disorders in systemic diseases
ISSN: 1557-9875, 1557-9875Vydavateľské údaje: United States 01.02.2015Vydané v Neurologic clinics (01.02.2015)“…Movement disorders, classically involving dysfunction of the basal ganglia commonly occur in neurodegenerative and structural brain disorders. At times,…”
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Dopaminagonisten spielen eine Schlüsselrolle
ISSN: 1437-062X, 2195-5166Vydavateľské údaje: 01.09.2018Vydané v InFo Neurologie + Psychiatrie (01.09.2018)Získať plný text
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Extending the Spectrum of Nonmotor Symptoms with Olfaction in Premotor Huntington’s Disease: A Pilot Study
ISSN: 1660-2854, 1660-2862, 1660-2862Vydavateľské údaje: Basel, Switzerland 01.11.2021Vydané v Neuro-degenerative diseases (01.11.2021)“…Objective: The aim of this pilot study was to investigate change of olfactory functions in Huntington’s disease (HD). Background: HD is a neurodegenerative…”
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Postural orthostatic tachycardia syndrome is the most frequent cardiovascular autonomic disorder following COVID-19 infection or vaccination
ISSN: 0340-5354, 1432-1459, 1432-1459Vydavateľské údaje: Berlin/Heidelberg Springer Berlin Heidelberg 01.12.2025Vydané v Journal of neurology (01.12.2025)“…Background Cardiovascular autonomic disorders (CAD) were described following COVID-19 infection and vaccination, but previous reports were limited in size and…”
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Tit for Tat: Costly Punishment in Manifest Huntington’s Disease
ISSN: 1660-2854, 1660-2862, 1660-2862Vydavateľské údaje: Basel, Switzerland 01.04.2022Vydané v Neuro-degenerative diseases (01.04.2022)“…Objective: We aimed to investigate costly punishment in patients with Huntington’s disease (HD). Background: HD is an autosomal dominant neurodegenerative…”
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