Results 151 to 160 of about 4,545,027 (267)
Missing Children Clearinghouse annual report
, 2005 Description based on: 2005; title from PDF cover (viewed on July 17, 2007).; Harvested from the web on 7/17 ...
Ohio Missing Children Clearinghouse. +1 more
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Use of WHO Growth Standards Rather Than Locally Specific Linear Growth Curves Promotes Equity in Pediatric Growth Research for Children Younger Than 5 Years. [PDF]
Nutr RevFinaret AB, Taylor-Forde P.
europepmc +1 more source
MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objectives The study aimed to characterize the clinical features, etiologies, and outcomes of isolated, first‐time pediatric ON in the post‐MOG‐IgG era. Methods This was a single‐center retrospective cohort study at Texas Children's Hospital of patients diagnosed with first‐time ON between 2018–2024, with follow‐up data collected through 2025.
Chaitanya Aduru +13 more
wiley +1 more source
, 2019 January 28, 2019. Presentation date and committee name taken from Kansas Legislature website.<br>Presentation before the Kansas Legislature, House Appropriations Committee, by Kansas Department for Children and Families, Family Services Division ...
Kansas. Department for Children and Families. Family Services Division. Economic and Employment Services.
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Children With Idiopathic Toe Walking Display Different Cortical Activation Patterns When Interpreting Tactile Sensation. [PDF]
Dev PsychobiolDonne JH +4 more
europepmc +1 more source
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Variants in SLC6A1, encoding the GABA transporter 1 (GAT‐1), cause epilepsy, autism spectrum disorder, and developmental delay via loss of GABA uptake, impaired trafficking, and ER retention. We previously found that 4‐Phenylbutyrate (PBA), an FDA‐approved drug, restores GABA uptake and reduces seizures in SLC6A1‐related disorders ...
Melissa B. DeLeeuw +5 more
wiley +1 more source
The Impact of Intergroup Collaboration on In-Group Bias Between Rohingya Refugee and Bangladeshi Host Community Children. [PDF]
Dev SciCorbit J, MacIntosh T, Muhammad S.
europepmc +1 more source
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Facioscapulohumeral muscular dystrophy (FSHD) is one of the most debilitating and common muscular dystrophies. Despite its severity, no approved therapy exists for FSHD patients. However, several therapeutic candidates are currently under development, and some have recently entered clinical trials, marking the need for reliable ...
Mustafa Bilal Bayazit +11 more
wiley +1 more source
, 2006 This research records what 3,322 children from eight countries in the Southeast Asia and the Pacific region told researchers about everyday, common violence - both physical and emotional - used as punishment against them. It used a systematic, scientific
Beazley, H S +7 more
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A 17 Year Old With Developmental Delay Presenting With Increasing Confusion and Imbalance
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Methylmalonic acidemia is an autosomal recessive genetic disorder primarily caused by defects in methylmalonyl‐CoA mutase and cobalamin (vitamin B12) metabolism. These defects disrupt the tricarboxylic acid cycle and oxidative phosphorylation, leading to the abnormal accumulation of metabolic products such as methylmalonic acid, propionic acid,
Wei Zhao, Yingli Zhang, Hongliang Zheng
wiley +1 more source