Results 341 to 350 of about 512,984 (398)

Transient C5 Palsy After Full-Endoscopic Posterior Cervical Foraminotomy. [PDF]

Case Rep Orthop
Bergamaschi JPM, Lugão AF, de Assis RR, de Oliveira Teixeira K, de Araújo FF, Soares TQ, Depieri GV, Dowling Á, de Oliveira RC, Wirth F, da Silva Forti F, Defino HLA.   +11 more
europepmc   +1 more source

Neonatal Septic Shoulder Joint Masquerading as Brachial Plexus Palsy: A Case Report and Review of the Literature. [PDF]

Case Rep Pediatr
Townson A, Pang C, Theocharidou L, Bostock S, Loh CYY.   +4 more
europepmc   +1 more source

Clinical efficacy of neurofacilitation technology combined with rehabilitation training based on cerebral blood flow velocity and cerebral metabolism in children with cerebral palsy. [PDF]

Front Med (Lausanne)
Zhao W, Bai Y, Wang B, Fan Y, Yu W, Song P.   +5 more
europepmc   +1 more source

Cerebral palsy

Nature Reviews Disease Primers, 2016
Cerebral palsy is the most common cause of childhood-onset, lifelong physical disability in most countries, affecting about 1 in 500 neonates with an estimated prevalence of 17 million people worldwide. Cerebral palsy is not a disease entity in the traditional sense but a clinical description of children who share features of a non-progressive brain ...
Kerr Graham, Peter L Rosenbaum, Nigel Paneth   +2 more
exaly   +6 more sources

State of the Evidence Traffic Lights 2019: Systematic Review of Interventions for Preventing and Treating Children with Cerebral Palsy

Current Neurology and Neuroscience Reports, 2020
Purpose of Review Cerebral palsy is the most common physical disability of childhood, but the rate is falling, and severity is lessening. We conducted a systematic overview of best available evidence (2012–2019), appraising evidence using GRADE and the ...
Iona Novak, Catherine Morgan, Michael Fahey   +2 more
exaly   +2 more sources

Distribution patterns of tau pathology in progressive supranuclear palsy

Acta Neuropathologica, 2020
Progressive supranuclear palsy (PSP) is a 4R-tauopathy predominated by subcortical pathology in neurons, astrocytes, and oligodendroglia associated with various clinical phenotypes. In the present international study, we addressed the question of whether
Gabor G Kovacs, Edward B Lee, David Coughlin   +2 more
exaly   +2 more sources

Mutations disrupting neuritogenesis genes confer risk for cerebral palsy

Nature Genetics, 2020
Sheng Chih Jin, Sara A Lewis, Xue Zeng
exaly   +2 more sources