Results 51 to 60 of about 562,551 (304)

Neuropsychomotor developmental delay: conceptual map, term definitions, uses and limitations

Revista Paulista de Pediatria, 2015
OBJECTIVE: To retrieve the origin of the term neuropsychomotor developmental delay" (NPMD), its conceptual evolution over time, and to build a conceptual map based on literature review. DATA SOURCE: A literature search was performed in the SciELO Brazil,
Lílian de Fátima Dornelas, Neuza Maria de Castro Duarte, Lívia de Castro Magalhães   +2 more
doaj   +1 more source

83569 Receipt of Pharmacologic Weaning Therapy and Developmental Delay

Journal of Clinical and Translational Science, 2021
IMPACT: This study evaluates the long term effects of pharmacologic weaning therapy for opiate exposed infants. OBJECTIVES/GOALS: Infants born to chronic opioid users often suffer from neonatal abstinence syndrome (NAS), a condition characterized by ...
Angela G. Campbell, Pengyue Zhang, Sami Gharbi, Sarah Wiehe   +3 more
doaj   +1 more source

Developmental changes in the engagement of episodic retrieval processes and their relationship with working memory during the period of middle childhood. [PDF]

, 2011
We examined the development of children’s engagement of the episodic retrieval processes of recollection and familiarity and their relationship with working memory (WM).
Atkinson, Baddeley, Baddeley, Baddeley, Baddeley, Billingsley, Brainerd, Cannon, Curtis, Cycowicz, Cycowicz, Defeyter, Drummey, Dunn, D’Esposito, Ferneyhough, Fray, Gardiner, Ghetti, Goodman, Halliday, Holliday, Jacoby, Jacoby, Kim, Knott, Luciana, Mandler, Marshall, Milner, Miyake, Morris, Petrides, Ranganath, Rhodes, Rhodes, Rhodes, Rhodes, Rhodes, Robbins, Roderer, Rybash, Shah, Sluzenski, Snodgrass, Tulving, Welsh, Yonelinas   +47 more
core   +1 more source

The Fate (Outcome) of Clinically Apparent Single Lesion and Oligofocal Nephroblastomatosis Treated According to SIOP/GPOH Protocols for Wilms Tumor

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background The management of clinically apparent single lesions or oligofocal nephroblastomatosis, a facultative precursor of nephroblastoma, remains debated. Methods We retrospectively analyzed 37 patients with clinically apparent single or oligofocal nephroblastomatosis (two to three lesions per kidney) among 2347 patients registered between
Nils Welter, Jens‐Peter Schenk, Jenny Wegert, Manfred Gessler, Leo Kager, Stefan Wagenpfeil, Marina Müller, Jean‐Michel Wolff, Joerg Fuchs, Steven W. Warmann, Clemens‐Magnus Meier, Jochen Hubertus, Christian Rübe, Christian Vokuhl, Patrick Melchior, Lena Tschirner, Norbert Graf, Rhoikos Furtwängler   +17 more
wiley   +1 more source

Riskfactors of developmental delay in children under 5 years old in Tabriz, Iran: A case-control study [PDF]

Journal of Holistic Nursing and Midwifery
Introduction: Developmental Delay (DD) refers to a child’s inability to attain developmental milestones compared to healthy peers. Although evidence shows that DD has irreparable impacts on children's lives, several aspects continue to remain unknown ...
Monireh Hamed-Biabani, Somayeh Abdolalipour, Khadijeh Khalili-Azar, Seifollah Heidarabadi, Mojgan Mirghafourvand   +4 more
doaj  

WIC Improves Child Health and School Readiness [PDF]

, 2010
New research by Children's HealthWatch demonstrates that young children who participate in the Special Supplemental Nutrition program for Women, Infants, and Children (WIC) are more likely to be in excellent or good health and have a reduced risk of ...
Annie Gayman, Deborah A. Frank, Elizabeth L. March, John T. Cook, Sharon Coleman, Stephanie Ettinger de Cuba   +5 more
core  

Phonological Priming In Young Children Who Stutter: Holistic Versus Incremental Processing [PDF]

, 2007
Purpose: To investigate the holistic versus incremental phonological encoding processes of young children who stutter (CWS; N = 26) and age- and gender-matched children who do not stutter (CWNS; N = 26) via a picture-naming auditory priming paradigm ...
Byrd, Courtney T., Conture, Edward G., Ohde, Ralph N.   +2 more
core   +2 more sources

Germline TP53 Mutations Causing Diamond–Blackfan Anemia: A French Report

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Diamond–Blackfan anemia is a rare congenital erythroblastopenia typically caused by mutations in ribosomal protein genes. Recently, gain‐of‐function mutations in TP53 have been identified as a novel cause of Diamond–Blackfan anemia. We report two French patients who both harbored a heterozygous TP53 deletion (NM_000546.5: c.1077delA; p ...
Rafael Moisan, Lydie Da Costa, Ludivine David Nguyen, Heloise Chosseler, Audrey Riquet, Benedicte Bruno, Melissa Barbati   +6 more
wiley   +1 more source

Assessment of Development of Children in Diyala Province

Diyala Journal of Medicine
Background: Developmental assessment is a systematic and comprehensive process that evaluates a child's progress across multiple domains of development to identify potential developmental delays or disabilities.
Haider Asad Mohammad, Najdat Sh. Mahmood, Jalil I. Alezzi   +2 more
doaj   +1 more source

Expanding the mutational spectrum of ZTTK syndrome: A de novo variant with global developmental delay and malnutrition in a Chinese patient

Molecular Genetics & Genomic Medicine, 2023
Background Zhu‐Tokita‐Takenouchi‐Kim (ZTTK, OMIM 617140) syndrome is a severe multisystem developmental disorder characterized by intellectual disability, developmental delay, cortical malformations, epilepsy, visual problems, musculoskeletal ...
Shuo Tang, Jieyu You, Li Liu, Hongjuan Ouyang, Na Jiang, Jiaqi Duan, Canlin Li, Yanhong Luo, Wenting Zhang, Meizheng Zhan, Chenxi Liu, Gui‐Zhen Lyu, Victor Wei Zhang, Hongmei Zhao   +13 more
doaj   +1 more source