Results 261 to 270 of about 121,621 (353)

Genetic testing in cerebral palsy with clinical and neuroimaging variables

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
Abstract Aim To optimize genetic testing in children with cerebral palsy (CP) by using clinical and magnetic resonance imaging (MRI) variables. Method In this mixed methods study, we surveyed current approaches to genetic testing by Australian clinicians involved in the diagnosis of CP.
Esther M. Tantsis   +46 more
wiley   +1 more source

Targeted Long-Read Sequencing as a Single Assay Improves the Diagnosis of Spastic-Ataxia Disorders. [PDF]

open access: yesAnn Clin Transl Neurol
Rudaks LI   +20 more
europepmc   +1 more source

Mobility device use in children with cerebral palsy

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
Abstract Aims To quantify the number and types of mobility devices used by children with cerebral palsy (CP) and explore the relationships between Gross Motor Functional Classification System (GMFCS) level, age, insurance, income, and number and types of devices. Method This was a secondary analysis of a cohort from a larger randomized controlled trial.
Elizabeth Maus   +2 more
wiley   +1 more source

Respiratory admissions and impact of COVID‐19 lockdowns for children with severe cerebral palsy

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
In a population cohort of children with severe cerebral palsy, there was a reduced frequency of hospitalization for respiratory illness during periods of restricted social contact, implemented to reduce transmission of COVID‐19. This mirrored trends in the wider population and underlines the importance of community viral transmission in these children.
Susan M. Reid   +9 more
wiley   +1 more source

The effect of traditional Thai massage vs routine physical therapy on gait pattern in spastic cerebral palsy: A cross-over randomized controlled trial. [PDF]

open access: yesPLoS One
Lertwiram P   +8 more
europepmc   +1 more source

Early detection of infants with neurodevelopmental concerns indicative of cerebral palsy in a lower middle‐income country (India)

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
In this prospective sub‐study testing the predictive validity of General Movements Assessment (GMA) and/or Hammersmith Infant Neurological Examination (HINE), 785 infants with birth/infant‐detectable risk factors, aged 12 to 40 weeks corrected age were recruited. GMA and HINE were reliable and accurate tools for screening high‐risk populations in India,
Katherine A. Benfer   +13 more
wiley   +1 more source

Heterotopic calcification in a child presenting as acute on chronic myelopathy. [PDF]

open access: yesChilds Nerv Syst
Zeoli T   +4 more
europepmc   +1 more source

Modified sports intervention for improving participation goals and activity competence in ambulant children with cerebral palsy: A randomized controlled trial

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
This study evaluates the effectiveness of a modified sports intervention for improving participation goals and activity competence in ambulant children with cerebral palsy. Abstract Aim To evaluate the effectiveness of a modified sports intervention (Sports Stars Brazil) on leisure‐time physical activity participation goals, motor skill performance and
Ricardo R. Sousa Junior   +7 more
wiley   +1 more source

The Spastic Paraplegia-Centers of Excellence Research Network (SP-CERN): Clinical Trial Readiness for Hereditary Spastic Paraplegia. [PDF]

open access: yesNeurol Genet
Schierbaum L   +23 more
europepmc   +1 more source

Rare dysfunctional SCN2A variants are associated with malformation of cortical development

open access: yesEpilepsia, Volume 66, Issue 3, Page 914-928, March 2025.
Abstract Objective SCN2A encodes the voltage‐gated sodium (Na+) channel α subunit NaV1.2, which is important for the generation and forward and back propagation of action potentials in neurons. Genetic variants in SCN2A are associated with a spectrum of neurodevelopmental disorders.
Jérôme Clatot   +19 more
wiley   +1 more source

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