Results 151 to 160 of about 630,387 (212)

Children, Cell Phones, and Reading Comprehension. [PDF]

Behav Sci (Basel)
Greenfield PM, Hanna M, Burgos-Calvillo R, Rhinehart L.   +3 more
europepmc   +1 more source

Sleep Disturbances in Adults With Tuberous Sclerosis Complex: Influences of Treatment and Clinical Features

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Tuberous sclerosis complex (TSC) is a genetic condition with multisystem neurocutaneous signs, including hamartomas, epilepsy, and neuropsychological difficulties. Although sleep disorders are increasingly recognized in TSC, they remain poorly described in adults.
Kirstin A. Risgaard, Laura Farach, Hope Northrup, Sarah L. Wilson, Deborah Pearson, Syed Hashmi, Kate Richardson   +6 more
wiley   +1 more source

A Data-Driven Approach to the Issue of 'Catching Up With Monolinguals'. [PDF]

Int J Lang Commun Disord
De Cat C, Gusnanto A, Serratrice L, Prévost P, Tuller L, Unsworth S.   +5 more
europepmc   +1 more source

Assessment of Growth in Cardio‐Facio‐Cutaneous Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cardio‐facio‐cutaneous (CFC) syndrome is a rare, multiple congenital anomaly disorder in which individuals commonly experience faltering growth; however, systematic analysis of growth parameters in this disorder has not been performed. We recruited 69 participants with CFC through CFC International and collected data on assessing height ...
Kari Johnston, Sandesh C. S. Nagamani, Bradley S. Miller, Katherine A. Rauen, Richard D. Boyce, Salma Musaad, Pilar L. Magoulas   +6 more
wiley   +1 more source

Pediatric Literacy Promotion for Latino Families by Texts and Referrals: A 3-Arm RCT. [PDF]

Pediatrics
Jimenez ME, Hemler JR, Strickland PO, Bator A, Lima D, Azcona N, Perez Y, Ayala J, Alas KM, Dillon J, Fasano RM, Ramachandran U, Pai S, Devine KA, Cortes SP, Crabtree BF, Hudson SV, Mackie TI, Mendelsohn AL.   +18 more
europepmc   +1 more source

Genetic Variation in ADHD‐Related Risk Genes in an Indigenous Population of the Amazon

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Attention‐Deficit/Hyperactivity Disorder (ADHD) is a highly heritable neurodevelopmental disorder; however, its genetic architecture remains poorly explored in Indigenous populations. This study aimed to analyze and characterize genetic variation in 11 genes (ADGRL3, CDH8, DCC, DUSP6, FOXP1, FOXP2, MEF2C, PCDH7, SEMA6D, SORCS3, and ST3GAL3 ...
Hirlesson Paixão de Matos, Natasha Monte, Kaio Evandro Cardoso Aguiar, Rita de Cássia Calderaro, Aline Pasquini Santos, Juliana Carla Gomes Rodrigues, André Maurício Ribeiro‐Dos‐Santos, Sandro José De Souza, Ândrea Ribeiro‐Dos‐Santos, João Farias Guerreiro, Sidney Emanuel Batista Dos Santos, Ney Pereira Carneiro Dos Santos   +11 more
wiley   +1 more source

Assessment tools for patients with stroke-related sarcopenia: a scoping review. [PDF]

Front Med (Lausanne)
Liang Y, Xie L, Qiao W, Guo R, Wan H, Jing J.   +5 more
europepmc   +1 more source

Milestone Attainment in Young Children With Arthrogryposis Multiplex Congenita: Developmental Profile and Associated Factors

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Evidence on developmental milestones in children with arthrogryposis multiplex congenita (AMC) under the age of five is scarce. This multisite cross‐sectional study described developmental status and examined factors associated with milestone attainment in 143 children aged 0–66 months from a pediatric AMC Registry.
Ahlam Zidan, Sophia C. Pasia, Emmanouil Rampakakis, Reggie Hamdy, Frank Rauch, Lauren C. Hyer, Joel Lerman, Haluk Altiok, Krister Freese, Cary Mielke, Sarah B. Nossov, Philip F. Giampietro, Thania Ordaz‐Robles, Noémi Dahan‐Oliel   +13 more
wiley   +1 more source

Expanding Access to Primary Care Research for Non-English-Speaking Primary Care Providers, Researchers, and Policy Makers. [PDF]

Ann Fam Med
Garcia-Huidobro D, Chen PH, Hegazy NN, Inoue M, McCarthy E, Prasad R, Batista SRR, Rodriguez T, Schuers M, Steiner M, Sunjaya A, Capurro D.   +11 more
europepmc   +1 more source