Results 161 to 170 of about 464,707 (350)
Where Do We Go From Here?: A Roundtable Discussion of Buffy+ Studies and Whether, How, or Why to Forge a Path Forward [PDF]
Slayage, 2021 Halfyard, Janet K. +4 more
doaj
The Image of Psychiatric Nurses in Motion Pictures
, 1981 Philip A. Kalisch, Beatrice J. Kalisch
openalex +1 more source
Liouville’s theorem, and two pictures of motion in classical mechanics [PDF]
, 2009 L. D. Faddeev, O. Yakubovskiĭ
openalex +1 more source
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective To provide a comprehensive clinical and genetic characterization of individuals with arthrogryposis multiplex congenita (AMC), focusing on the distribution of genetic etiologies across the neuromuscular spectrum and comparing myogenic and neurogenic subtypes. Methods A total of 105 individuals with AMC were clinically and genetically
Florencia Pérez‐Vidarte +13 more
wiley +1 more source
Projecting Motion Pictures [PDF]
American Journal of Public Health and the Nations Health, 1951 openaire +3 more sources
Phenotyping Healthcare Use 2–3 Decades Before the First Multiple Sclerosis Demyelinating Event
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Phenotype hospital, physician, and emergency department (ED) visits by diagnoses and specialty up to 29 years pre‐multiple sclerosis (MS) onset versus a matched population without MS. Methods We identified people with MS (PwMS) using population‐based administrative data from Ontario, Canada (1991–2020).
Helen Tremlett +8 more
wiley +1 more source
"You can't beat evil by doing evil":Buffy, Discursive Challenges, and Nuclear Weapons [PDF]
Slayage, 2022 Broadhead, Lee-Anne
doaj
Genetic Diversity and Expanded Phenotypes in Dystonia: Insights From Large‐Scale Exome Sequencing
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Dystonia is one of the most prevalent movement disorders, characterized by significant clinical and etiological heterogeneity. Despite considerable heritability (~25%), the etiology in most patients remains elusive. Moreover, understanding correlations between clinical manifestations and genetic variants has become increasingly ...
Mirja Thomsen +47 more
wiley +1 more source