[HTML][HTML] Cerebral palsy and related neuromotor disorders: Overview of genetic and genomic studies

JM Friedman, P van Essen… - Molecular genetics and …, 2022 - Elsevier
Cerebral palsy (CP) is a debilitating condition characterized by abnormal movement or
posture, beginning early in development. Early family and twin studies and more recent …

Glutamate transport and preterm brain injury

S Pregnolato, E Chakkarapani, AR Isles… - Frontiers in …, 2019 - frontiersin.org
Preterm birth complications are the leading cause of child death worldwide and a top global
health priority. Among the survivors, the risk of life-long disabilities is high, including cerebral …

Familial risk of cerebral palsy: population based cohort study

MC Tollånes, AJ Wilcox, RT Lie, D Moster - Bmj, 2014 - bmj.com
Objective To investigate risks of recurrence of cerebral palsy in family members with various
degrees of relatedness to elucidate patterns of hereditability. Design Population based …

Cerebral palsy and the placenta: A review of the maternal-placental-fetal origins of cerebral palsy.

EM Chin, N Gorny, M Logan, AH Hoon - Experimental Neurology, 2022 - Elsevier
Accumulating evidence from clinical and neuropathological study has identified a number of
seemingly disparate associations carrying a predisposition for cerebral palsy (CP). We …

[HTML][HTML] Systematic review of cerebral palsy registries/surveillance groups: relationships between registry characteristics and knowledge dissemination

DS Hurley, T Sukal-Moulton… - … journal of physical …, 2015 - ncbi.nlm.nih.gov
The aims of this study were to provide a comprehensive summary of the body of research
disseminated by Cerebral Palsy (CP) registries and surveillance programs from January …

The association of apolipoprotein E gene polymorphisms with cerebral palsy in Chinese infants

Y Xu, H Wang, Y Sun, Q Shang, M Chen, T Li… - Molecular Genetics and …, 2014 - Springer
Abstract Apolipoprotein E (APOE, protein; ApoE, gene) is a lipid transport protein abundantly
present in brain cells. Previous studies have suggested that there is an association between …

Genetic variation, magnesium sulfate exposure, and adverse neurodevelopmental outcomes following preterm birth

EAS Clark, SJ Weiner, DJ Rouse… - American journal of …, 2018 - thieme-connect.com
Objective To evaluate the association of magnesium sulfate (MgSO 4) exposure and
candidate gene polymorphisms with adverse neurodevelopmental outcomes following …

Relationship Between TNF-α and the Risk of Cerebral Palsy: A Systematic Review and Meta-Analysis

B Wang, F Wang, D Wu, X Xu, L Yang, J Zhu… - Frontiers in …, 2022 - frontiersin.org
Objective We performed a meta-analysis to investigate the relationship between blood tumor
necrosis factor-alpha (TNF-α) levels and the risk of cerebral palsy (CP) in children. Methods …

[HTML][HTML] Биомаркеры детского церебрального паралича

ТА Камилова, АС Голота, ДА Вологжанин… - Физическая и …, 2021 - cyberleninka.ru
Детский церебральный паралич (ДЦП)-неврологическое расстройство, связанное с
непрогрессирующим повреждением или пороком развития в развивающемся мозге …

Genetic Predisposition to Adverse Neurodevelopmental Outcome of Extremely Low Birth Weight Infants

MW Varner, EA Thom, CM Cotten… - American journal of …, 2024 - thieme-connect.com
Objective This study aimed to evaluate whether there are genetic variants associated with
adverse neurodevelopmental outcomes in extremely low birth weight (ELBW) infants. Study …