Results 171 to 180 of about 71,305 (285)

Expanding the clinical phenotype of DYNC1H1 -associated mutations: a Chinese family with autosomal dominant complex hereditary spastic paraplegia. [PDF]

BMC Med Genomics
Yuan X, Zhang S, Tang Y.
europepmc   +1 more source

Three‐year outcomes of repeated botulinum neurotoxin A injections to the lower extremities in young children with spastic cerebral palsy in GMFCS levels I to III

Developmental Medicine &Child Neurology, EarlyView.
In this study, we followed a group of children 2 to 6 years old with spastic cerebral palsy functioning in GMFCS levels I–III, over 3 years. Sixty‐five received BoNT‐A and 59 did not. Repeated BoNT‐A injections over 3 years were not associated with improvements in gross motor function or passive ankle dorsiflexion. Daily step counts, favouring the BoNT‐
Darcy Fehlings, Emma Bohn, Lauren Switzer, Charles H. Goldsmith, Unni Narayanan, Peter L. Rosenbaum, F. Virginia Wright, Gary Foster, CP‐BoNT‐A Study Group, Timothy Carey, Mark Mason, Ronit Mesterman   +11 more
wiley   +1 more source

Evaluation of the Wisconsin Gait Scale in Patients With Multiple Sclerosis and Spastic Hemiplegia. [PDF]

Med Sci Monit
Guzik A, Wolan-Nieroda A, Kiper P, Cieślik B, Federico S, Luque-Moreno C, Drużbicki M.   +6 more
europepmc   +1 more source

Structural validity of the Pain Interference Questionnaire and Fear of Pain Questionnaire for children and young people with cerebral palsy

Developmental Medicine &Child Neurology, EarlyView.
This paper examined the structural validity and internal consistency of two newly adapted pain assessment tools for children and young people with cerebral palsy and chronic pain ‐ The Pain Interference Questionnaire for Cerebral Palsy and the Fear of Pain Questionnaire Adapted for Cerebral Palsy. Plain language summary: https://onlinelibrary.wiley.com/
Meredith G. Smith, Rachel J. Gibson, Remo N. Russo, Nadine Smith, Adrienne R. Harvey   +4 more
wiley   +1 more source

Effects of crank length on the cardiovascular response in a rat model of motorized cycling. [PDF]

Spinal Cord
States GJR, Shum-Siu A, Burke DA, Magnuson DSK.   +3 more
europepmc   +1 more source

A 17‐year‐old male with chronic epilepsy status post remote functional hemispherectomy

Brain Pathology, EarlyView.
Claire Voyles, Elliot Stalter, Melissa M. Blessing, Osorio Lopes Abath Neto   +3 more
wiley   +1 more source

Gastroenterological disorders and hepatic disease in adults with cerebral palsy: A systematic review

Developmental Medicine &Child Neurology, EarlyView.
Abstract Aim To describe the incidence, prevalence, and prognostic factors for gastroenterological disorders and hepatic disease in adults with cerebral palsy (CP), and to examine the effectiveness of any screening or interventions. Method Six databases were searched for articles published in any language since 1990 meeting eligibility criteria ...
Christina M. Marciniak, Jennifer M. Ryan, Alejandra Camacho‐Soto, Emily Capellari, Jessica Burke, Maram Sofiany, Zoë Post, Eric C. Sung, Michael D. Brown, the Adult Cerebral Palsy Clinical Practice Guidelines Working Group, Jennifer M Ryan, Rachel Byrne, Emily Capellari, Donna Riccio Omichinski, Mark Peterson, Jan Willem Gorter, Ashley Harris Whaley, Christine Imms, Christina M. Marciniak   +18 more
wiley   +1 more source

Diagnostic Yield and Genotype-Phenotype Correlations of Clinical Exome Sequencing in Hereditary Spastic Paraparesis: Experience From Eastern Spain. [PDF]

Eur J Neurol
Carretero-Vilarroig L, Sivera R, Baviera R, Espinós C, Muelas N, Vazquez-Costa JF, Aller E, Bataller L, Jaijo T.   +8 more
europepmc   +1 more source

Microscopic and molecular aspects of skeletal muscle alterations in cerebral palsy

Developmental Medicine &Child Neurology, EarlyView.
Cerebral palsy, caused by non‐progressive brain injury, is frequently accompanied by skeletal muscle alterations. This review synthesizes current evidence from muscle biopsy studies, revealing cellular and molecular adaptations in muscle tissue. Abstract Cerebral palsy (CP), the most prevalent childhood‐onset motor disability, frequently entails ...
Sebastian Edman, Oscar Horwath, Eva Pontén, Sudarshan Dayanidhi, Ferdinand von Walden   +4 more
wiley   +1 more source

RAB3A variants in ataxia and other neurodegenerative disorders. [PDF]

Brain
Percetti M, Monfrini E, Del Bo R, Canesi M, Cavallieri F, Di Rauso G, Fioravanti V, Del Prete E, Frosini D, Palermo G, Ceravolo R, Sacilotto G, Di Fonzo A.   +12 more
europepmc   +1 more source