Results 21 to 30 of about 429 (89)
Neurosyphilis-associated movement disorder: A literature review
Annals of Movement Disorders, 2020 Syphilis is a well-known “great simulator/mimicker” of other diseases. Over the last decades, the clinical features of neurosyphilis have changed with an increasing percentage of atypical manifestations.
Jamir Pitton Rissardo +1 more
doaj +1 more source
Chinese Medical Journal, 2022 . Background:. Intensive phototherapy (IPT) and exchange transfusion (ET) are the main treatments for extreme hyperbilirubinemia. However, there is no reliable evidence on determining the thresholds for these treatments.
Meng Zhang +17 more
doaj +1 more source
Uraga grahonmada: Extrapyramidal movement disorder?/Tourette syndrome-plus?
Indian Journal of Health Sciences and Biomedical Research KLEU, 2018 Uraga/Sarpa/Bhujaga grahonmada (UG) is one among the 18 types of bhootonmada. Bhootonmada denotes a category of psychiatric/neuropsychiatric conditions assumed to be caused by affliction of evil spirits (bhuta/graha).
Prasad Mamidi, Kshama Gupta
doaj +1 more source
Frontiers in Veterinary Science, 2015 Dystonia is defined as a neurological syndrome characterized by involuntary sustained or intermittent muscle contractions causing twisting, often repetitive movements and postures.
Angelika eRichter +3 more
doaj +1 more source
Diagnosis of multiple sclerosis and Fahr's Disease in a young woman: A case report (PP-15) [PDF]
Neurology Letters, 2023 Fahr’s disease is a progressive and idiopathic basal ganglia calcification with normal metabolism of calcium and phosphore with motor and psychiatric sings and symptoms.
Mohammadreza Malek Zadeh +2 more
doaj
MUTATIONS IN THE ARX GENE: CLINICAL, ELECTROENCEPHALOGRAPHIC AND NEUROIMAGING FEATURES IN 3 PATIENTS
Русский журнал детской неврологии, 2017 The Aristaless-related homeobox (ARX) gene is a member of the paired-type homeodomain transcription factor family with critical roles in embryonic development, particularly in the developing brain.
I. V. Ivanova +5 more
doaj +1 more source
Zaporožskij Medicinskij Žurnal, 2019 Diagnostics and differential diagnostics of inherited metabolic diseases in children have still been complicated. The diagnostic difficulties are due to the fact that the diseases are orphan and their recognition is not always timely. Objective.
M. A. Trishchynska, V. O. Svystilnyk
doaj +1 more source
Instrumented assessment of motor function in dyskinetic cerebral palsy: a systematic review
Journal of NeuroEngineering and Rehabilitation, 2020 Background In this systematic review we investigate which instrumented measurements are available to assess motor impairments, related activity limitations and participation restrictions in children and young adults with dyskinetic cerebral palsy. We aim
Helga Haberfehlner +7 more
doaj +1 more source
Paroxysmal Nonkinesigenic Dyskinesia with Tremor
Case Reports in Neurological Medicine, 2013 Introduction. Paroxysmal nonkinesigenic dyskinesia (PNKD) consists of episodes of chorea, athetosis, or dystonia which are not triggered by movement, with complete remission between episodes.
Robert Fekete
doaj +1 more source
Biomechanical analysis of countermovement jump in people with cerebral palsy
European Journal of Human Movement, 2010 The main purpose of the study was to evaluate the patterns of the developed ground reaction forces in the two – legged countermovement jumping, performed by persons affected by tetraparesis with ataxia, tetraparesis with athetosis, tetraparesis with ...
K. Gianikellis +3 more
doaj