Results 11 to 20 of about 2,416 (97)

Paternal perinatal mental health and early child development: An outcome-wide analysis. [PDF]

Infant Ment Health J
Abstract Paternal mental health (PMH) has been shown to associate with child development as early as infancy. However, the moderating effects of certain contextual factors remain poorly understood. Using data from the French SEPAGES cohort, an outcome‐wide analytic approach was used to investigate the relationship between PMH during pregnancy (n = 166),
Scarlett H, Benarous X, Consoli A, Montreuil T, Lyon-Caen S, Philippat C, Waerden JV.   +6 more
europepmc   +2 more sources

Pais, educadores e testes: estão de acordo na avaliação de aptidões de crianças pré-escolares? Parents, teachers and tests: do they agree in the assessment of oreschoolers'abilities?

Psicologia: Reflexão e Crítica, 2012
O presente estudo pretende contribuir para o esclarecimento de questões relativas ao acordo entre pais e educadores quando avaliam o desenvolvimento infantil e com o grau em que estas avaliações estão relacionadas com aptidões cognitivas das crianças ...
Maria João Seabra-Santos, Maria Filomena Fonseca Gaspar   +1 more
doaj   +1 more source

Status cognitivo-comportamental de prematuros de baixo peso ao nascimento em idade pré-escolar que vivem em país em desenvolvimento Cognitive and behavioral status of low birth weight preterm children raised in a developing country at preschool age

Jornal de Pediatria, 2009
OBJETIVO: Avaliar o desenvolvimento cognitivo e comportamental em idade pré-escolar de crianças prematuras com baixo peso ao nascimento que vivem em um país em desenvolvimento.
Júlia L. do Espírito Santo, Mirna W. Portuguez, Magda L. Nunes   +2 more
doaj   +1 more source

Fatores prognósticos para o desenvolvimento cognitivo de prematuros de muito baixo peso Prognostic factors for cognitive development of very low birth weight premature children

Revista de Saúde Pública, 2003
OBJETIVO: Crianças prematuras, de muito baixo peso, podem apresentar alterações em seu desenvolvimento cognitivo. No Brasil, pouco se conhece sobre a evolução dessas crianças na idade pré-escolar.
Maria Dalva Barbosa Baker Méio, Claudia S Lopes, Denise Streit Morsch   +2 more
doaj   +1 more source

Distinct Neuropsychiatric Profiles Associated With 17p11.2 Deletions and RAI1 Variants in Smith–Magenis Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Smith–Magenis syndrome (SMS) results from either a recurrent 17p11.2 deletion or pathogenic variants in the retinoic acid induced 1 gene (RAI1). While neurodevelopmental impairment and behavioral dysregulation are well recognized, systematic genotype‐stratified analyses across psychiatric domains remain limited.
Albin Blanc, Christophe Nemos, Céline Bonnet, Mathilde Renaud, Sandra Chapuis, Pauline Boiroux, Marie‐Noëlle Babinet, Caroline Demily   +7 more
wiley   +1 more source

Cognitive and behavioral clinical outcome assessments in children with developmental and epileptic encephalopathies: Issues and instruments

Epilepsia, EarlyView.
Abstract Children with developmental and epileptic encephalopathies (DEEs) face cognitive and behavioral challenges that may have a greater impact than seizures on their quality of life (QoL). The need to assess these nonseizure outcomes for evaluating treatments is increasingly recognized.
Cinzia Correale, Nicola Specchio, Jenny Downs, J. Helen Cross, Simona Cappelletti, Andrea Palacio‐Navarro, Sam Geuens, Kette Valente, Andreas Brunklaus, Colin Reilly   +9 more
wiley   +1 more source

Associations Between Comorbidities, Developmental Status, and Disease Severity in Children With Autism Spectrum Disorder: A Multicenter Cross-Sectional Study in China. [PDF]

Autism Res
ABSTRACT Children with autism spectrum disorder (ASD) frequently present with co‐occurring conditions that can influence autism symptom severity and complicate clinical management. However, studies with clinician‐confirmed diagnoses in non‐Western populations remain limited.
Pang D, Duan G, Shang Q, Zhang H, Wang B, Ding H, Kang H, Zhao Y, Lu Y, Tian G, Zhang L, Jiang W, Wang G, Liang C, Zhang L, Li B, Li Z, Song C, Yang Y, Wang Y, Yue K, Lang Y, Liu J, Zhang X, Xu Y, Zhu C.   +25 more
europepmc   +2 more sources

Beyond seizures: A multidimensional approach to non‐seizure issues in Lennox–Gastaut syndrome. Insights from Italian experts

Epilepsia Open, EarlyView.
Abstract Non‐seizure issues (NSIs), including cognition, behavior/psychiatric symptoms, adaptive and social functioning, sleep, autonomic, and motor impairments, often shape day‐to‐day outcomes in Lennox–Gastaut syndrome (LGS) more than seizures, yet clinicians lack LGS‐specific, feasible assessment pathways.
Giancarlo Di Gennaro, Domenica Immacolata Battaglia, Paolo Bonanni, Gian Marco Duma, Antonietta Coppola, Edoardo Ferlazzo, Dario Pruna, Carlo Di Bonaventura   +7 more
wiley   +1 more source

Cognitive assessment in children with intestinal failure on and weaned off parenteral nutrition

Journal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objectives Children with intestinal failure (IF) are vulnerable to adverse cognitive outcomes. We assessed intelligence quotient (IQ) and identified associated factors. Methods Multicentre international cross‐sectional study in children with IF and weaned children, treated at Erasmus MC Sophia Children's Hospital, Amsterdam UMC Emma Children's
Rozemarijn A. L. Duister, Lotte E. Vlug, Marjolein Spoel, Merit M. Tabbers, Theodoric Wong, Caroline Godber, Vikki Langford, Aksa Jamil, Gemma Kavanagh, Lotte Bosman, Petra Mazer, Edmond H. H. M. Rings, René M.H. Wijnen, Barbara A. E. de Koning, Jeroen S. Legerstee   +14 more
wiley   +1 more source

Missense Variants in the A Isoform of FGF13 as a Novel Cause of Paroxysmal Dyskinesia

Movement Disorders, EarlyView.
Abstract Background Pathogenic variants within the unique N‐terminal inactivation particle of FGF13 isoform A (FGF13A) have so far been associated only with an X‐linked dominant epileptic encephalopathy (DEE). Objective The aim was to expand the clinical and molecular spectrum of FGF13A‐related disorder.
Cyril Mignot, Matthildi Athina Papathanasiou Terzi, Claudia Ravelli, Elisabeth Bosch, Xueqin Lin, Adeline Trauffler, Roseline Caumes, Andrew E. Fry, Clementine Fort, Gaelle Gauthe, Regina Trollmann, Thomas Wirth, Mathieu Anheim, Aurélie Méneret, Emmanuel Roze, Jean‐Madeleine de Sainte Agathe, Hailan He, Eleni Panagiotakaki, Gaëtan Lesca, André Reis, Diane Doummar, Thomas Smol, Georgia Vasileiou   +22 more
wiley   +1 more source