Results 191 to 200 of about 89,317 (316)

Predictors for Development of Asphyxiated Neonates Treated With Therapeutic Hypothermia

open access: yesActa Paediatrica, Volume 114, Issue 7, Page 1553-1561, July 2025.
ABSTRACT Aim To describe the long‐term neurodevelopmental outcomes of asphyxiated neonates treated with hypothermia in association with neonatal magnetic resonance imaging (MRI) findings. Methods We evaluated, retrospectively, clinical and radiological single‐centre data at 0, 2, and 5 years of age of 53 asphyxiated neonates born between 2005 and 2015.
Fabienne Kühne   +7 more
wiley   +1 more source

Potentiating microglial efferocytosis by MFG‐E8 improves survival and neurological outcome after successful cardiopulmonary resuscitation in mice

open access: yesBrain Pathology, Volume 35, Issue 4, July 2025.
Schematic representation of the effects of rmMFG‐E8 on post‐CA/CPR brain injury. Ischemic/reperfusion injury caused by CA/RCA results in elevated apoptotic cell death in various cells and decreased apoptotic cell clearance by phagocytes, such as microglia.
Kunxue Zhang   +9 more
wiley   +1 more source

Prediction of cerebral palsy and cognitive delay among high‐risk children in a developing nation: A successful early detection programme

open access: yesDevelopmental Medicine &Child Neurology, Volume 67, Issue 7, Page 892-900, July 2025.
201 infants at risk for developmental disorders were assessed using two General Movements Assessments (GMA) and one Hammersmith Infant Neurological Examination (HINE), integrated into routine follow up care. Developmental outcome was assessed with a neurologic examination at 2 years, and the Bayley Scales of Infant and Toddler Development at 2 ‐ 3.5 ...
Gemunu Hewawitharana   +12 more
wiley   +1 more source

Cognitive and Adaptive Functioning of CTNNB1 Syndrome Patients: A Comparison With Autism Spectrum Disorder and Cerebral Palsy

open access: yesJournal of Intellectual Disability Research, Volume 69, Issue 7, Page 558-568, July 2025.
ABSTRACT Background The CTNNB1 syndrome is a neurodevelopmental disorder considered an ultra‐rare disease, first discovered in 2012. Given its comorbidity of symptoms with more prevalent diseases, such as ASD or CP, many CTNNB1 syndrome patients had previously received those diagnosis. Therefore, the aim of this study is to establish differences on the
Mercè Pallarès‐Sastre   +6 more
wiley   +1 more source

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