Results 181 to 190 of about 988,752 (341)

Effectiveness of the Rapid Eye Movement Sequential Therapy Program in Reducing Post-Traumatic Stress Disorders in Individuals with Obsessive-Compulsive Disorder: A Sample of Mothers of Children with Special Needs Referred from Psychological Clinics in Kha

Bakhita Muhammad Zain Ali Muhammad
openalex   +2 more sources

Global Survey on Telemedicine Utilization for Movement Disorders During the COVID‐19 Pandemic [PDF]

, 2020
Anhar Hassan, Zoltán Mari, Emilia Gatto, Adriana Cardozo, Jinyoung Youn, Njideka Okubadejo, Jawad A. Bajwa, Ali Shalash, Shinsuke Fujioka, Zakiyah Aldaajani, Esther Cubo, the International Telemedicine Study Group   +11 more
openalex   +1 more source

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

Annals 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, Hyo‐Min Kim, Nicole Battaglia, Joshua Rong, Amy Tam, Enrique Gonzalez Saez‐Diez, Cornelius F. Boerkoel, Afshin Saffari, Vicente Quiroz, Luca Schierbaum, Zainab Zaman, Katerina Bernardi, Darius Ebrahimi‐Fakhari   +12 more
wiley   +1 more source

Movement Disorders in Toxoplasmosis: A Systematic Review. [PDF]

Tremor Other Hyperkinet Mov (N Y)
Garg RK, Pandey S, Agarwal M, Singhal S.
europepmc   +1 more source

Clinically Relevant Outcome Measures in Women With Adrenoleukodystrophy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Adrenoleukodystrophy is a rare inherited peroxisomal disease caused by pathogenic variants in the ABCD1 gene located on the X chromosome. Although the most severe central nervous system and adrenal complications typically affect only men with adrenoleukodystrophy, the majority of women develop myeloneuropathy symptoms in adulthood.
Chenwei Yan, Elizabeth I. Pierpont, Amena S. Fine, Reena V. Kartha   +3 more
wiley   +1 more source

Cerebellar ataxias and functional movement disorders: navigating clinical overlap. [PDF]

BMJ Neurol Open
Erdlenbruch F, Thieme A, Depienne C, Timmann D, Popkirov S.   +4 more
europepmc   +1 more source

Neuropsychiatry of movement disorders [PDF]

, 1999
Black, Kevin J, Mink, Jonathan W
core   +2 more sources

Polysomnographic features prior to dream enactment behaviors in isolated rapid eye movement sleep behavior disorder

Shumpei Date, Yukiyoshi Sumi, Koichi Fujiwara, Makoto Imai, Keiko Ogawa, Hiroshi Kadotani   +5 more
openalex   +1 more source

Single‐Event Multilevel Surgery to Correct Movement Disorders in Children with Cerebral Palsy [PDF]

, 2018
Jane M. Wick, Jing Feng, Ellen M. Raney, Michael D. Aiona   +3 more
openalex   +1 more source

Meningovascular Inflammation in Cerebral Amyloid Angiopathy‐Related Cortical Superficial Siderosis

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT The role of inflammation in cortical superficial siderosis (cSS), a marker of cerebral amyloid angiopathy (CAA) linked to high hemorrhage risk, is unclear. We examined 15 patients with cSS using 3 T post‐contrast vessel wall MRI (VWI) and CSF analysis.
Philipp Arndt, Eya Khadhraoui, Sebastian J. Müller, Katja Neumann, Hendrik Mattern, Sven G. Meuth, Valentina Perosa, Andreas Charidimou, Stefanie Schreiber   +8 more
wiley   +1 more source