Results 101 to 110 of about 446,708 (245)

Reliability and stability of cerebral palsy classification scales for individuals with STXBP1‐ and SYNGAP1‐related disorders

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
Aim To determine the interrater reliability and stability of the Gross Motor Function Classification System (GMFCS), Manual Ability Classification System (MACS)/Mini‐MACS, and Communication Function Classification System (CFCS) in individuals with STXBP1‐ and SYNGAP1‐related disorders.
Samuel R. Pierce   +6 more
wiley   +1 more source

Cost-effectiveness of Prednisolone to Treat Bell Palsy in Children: An Economic Evaluation Alongside a Randomized Controlled Trial. [PDF]

open access: yesNeurology, 2023
Xiong X   +11 more
europepmc   +1 more source

The F‐words for childhood development in community‐based physical activity programmes for children with physical disabilities: A scoping review

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
This scoping review identifies intervention ingredients that address the F‐words for childhood development in community‐based physical activity programs for children with physical disabilities. An electronic database and hand search of the international literature was conducted.
Belinda Munroe   +5 more
wiley   +1 more source

Genetic testing in paediatric neurological disorders

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
In this study 390 paediatric patients with neurological disorders underwent genetic testing via exome sequencing, commercial panel, in‐house epilepsy, and movement disorder gene panels. Exome sequencing provides the highest diagnostic yield, and severe developmental delay and hypotonia predicted pathogenic variants in the exome sequencing cohort ...
Wafa Bani Uraba   +15 more
wiley   +1 more source

Transient Inverse Bell’s Phenomenon Following Frontalis Sling–Suspension Ptosis Surgery: A Rare Ophthalmic Phenomenon

open access: yesInternational Medical Case Reports Journal, 2019
Triptesh Raj Pandey,1 Ben Limbu,2 Purnima Rajkarnikar Sthapit,2 Hom Bahadur Gurung,2 Rohit Saiju2 1Mechi Netralaya & Ophthalmic Research Center (P) Ltd., Jhapa, Nepal; 2Tilganga Institute of Ophthalmology, Kathmandu, NepalCorrespondence: Triptesh Raj
Pandey TR   +4 more
doaj  

Physical therapy interventions for children and adolescents with myelomeningocele: A systematic review

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
Abstract Aim To systematically review the current evidence on physical therapy interventions for children and adolescents with myelomeningocele, the most complex and common presentation of spina bifida, to explore intervention components and the outcomes according to International Classification of Functioning, Disability and Health (ICF) domains, and ...
Lorena Costa Ferreira   +3 more
wiley   +1 more source

BELL\u27S PALSY AMONG INFANTS - OUR EXPERIENCES IN A TERTIARY CARE HOSPITAL OF EASTERN INDIA [PDF]

open access: yes, 2017
Objectiv:The most common etiology of unilateral facial palsy is Bell\u27s palsy, also called as idiopathic facial palsy. Bell\u27s palsy in infant is rare and an uncommon clinical entity and often taken as pediatric emergency by parents.
Sahu, Mahesh Chandra   +2 more
core   +1 more source

International consensus recommendations for identifying malnutrition in children with neurological impairment

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
Abstract Children with neurological impairment (CNI) are at increased risk of malnutrition because of functional, medical, and socioeconomic challenges. However, difficulties in obtaining reliable anthropometric measurements and differences in body composition limit the usefulness of conventional nutritional indicators.
Sarah Vermilyea   +19 more
wiley   +1 more source

RCC1 neuropathy mimics childhood axonal Guillain–Barré syndrome with variable clinical severity and survival

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
We present 10 patients who presented with acute onset axonal neuropathy following infection, mimicking childhood axonal Guillain–Barré syndrome. We review phenotypes, undertake survival analysis, and assess function of novel RCC1 variants in vitro. Abstract Aim To assess the phenotype and genotype of 10 new patients with biallelic RCC1 variants who ...
Han Zhang   +28 more
wiley   +1 more source

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