Results 121 to 130 of about 59,438 (255)

Diagnostic tests for autism spectrum disorder (ASD) in preschool children. [PDF]

Cochrane Database Syst Rev
Brignell A, Chan K, Chellew T, Maddumahewa CV, Wong N, Hooft L, Alshawsh M, Williams K.   +7 more
europepmc   +1 more source

Development and validation of the new French ORALQUEST scale for evaluating feeding difficulties in young children

Journal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objective Feeding difficulties are common in children with and without somatic conditions. Our objective was to develop a parent‐report questionnaire (ORALQUEST) designed to be administered by a professional and to assess feeding difficulties in children aged 9 months to 6 years. Methods The questionnaire explores four domains: eating behavior,
Béatrice Thouvenin, Redha Ould‐Ammar, Lisa Ouss, Pascale Gavelle, Giulia Disnan, Aurélie Royer, Nancy Vegas, Catherine du Fraysseix, Pauline Adnot, Valeria Barbieri, Christine Hassler, Caroline Elie, Caroline Barry, Véronique Abadie   +13 more
wiley   +1 more source

Fundamental Motor Skills and Motor Competence in Children and Adolescents with Autism Spectrum Disorder (ASD): A Narrative Review. [PDF]

Children (Basel)
Asonitou K, Kottara M, Charitou S, Koutsouki D.   +3 more
europepmc   +1 more source

Constipation outcomes in children with and without autism spectrum disorder: Insights from a tertiary motility service

Journal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objectives Autism spectrum disorder (ASD) is commonly associated with gastrointestinal comorbidities, particularly chronic constipation. Despite high clinical burden and frequent tertiary referrals, comparative data describing clinical characteristics, management and outcomes between children with and without ASD—and across ASD severity levels—
Umair Khalid, Rishi Bolia, Joshua Bunt, Ray Lang, Nikhil Thapar   +4 more
wiley   +1 more source

Management of an Autism Spectrum Disorder (ASD) Patient With Respiratory Failure in the Intensive Care Unit: A Case Report on the Role of Dexmedetomidine. [PDF]

Case Rep Crit Care
Ciccozzi A, Murgia F, Piroli A, Paladini A, Ciccone C, Leonardis F, Fionda D, Ciccone A, Marinangeli F.   +8 more
europepmc   +1 more source

FXTAS and the Spectrum of FMR1 Premutation‐Associated Phenotypes in Latin America: A Scoping Review

Movement Disorders Clinical Practice, EarlyView.
Abstract Background Fragile X–associated tremor/ataxia syndrome (FXTAS) is a late‐onset neurodegenerative disorder caused by FMR1 premutation expansions (55–200 CGG repeats). Although well described in populations of predominantly European ancestry, FXTAS remains poorly characterized in Latin America due to limited awareness, restricted access to ...
Amy Schmidmajer, Salomón Páez‐García, Santiago Martínez, Jacobo Ramírez‐Triana, Kevin O'Hara‐Veintimilla, Andrés Ricaurte‐Fajardo, Catalina Cerquera‐Cleves   +6 more
wiley   +1 more source

Feasibility and preliminary efficacy of an infant preemptive intervention for prodromes of autism spectrum disorder (ASD) delivered within an Italian tertiary hospital. [PDF]

Front Child Adolesc Psychiatry
Colombi C, Chericoni N, Conti E, Colombino I, Guainai G, Riva B, Apicella F, Calderoni S, Guzzetta A.   +8 more
europepmc   +1 more source

Movement Disorders in Developmental and Epileptic Encephalopathies

Movement Disorders Clinical Practice, EarlyView.
Abstract Background Monogenic developmental and epileptic encephalopathies (DEE) frequently feature co‐occurring movement disorders. Gene discovery has expanded epilepsy‐dyskinesia syndromes (EDS) from classic associations such as stereotypies in Rett syndrome to PRRT2‐related infantile seizures with paroxysmal dyskinesia and crouched gait in SCN1A ...
Shekeeb Mohammad, Darius Ebrahimi‐Fakhari, Hugo Morales‐Briceno   +2 more
wiley   +1 more source

SYNESTHESIA AND THE AUTISM SPECTRUM DISORDER (ASD)

, 2018
Introdução: A sinestesia, que possui uma prevalência de 4%, é uma condição neurológica em que um único estímulo elicia experiências adicionais a outro sentido sensorial, que pode ser: visual, auditivo, olfativo, gustativo e tátil. Essa condição não está incluída no Manual Diagnóstico e Estatístico de Transtornos Mentais 5ª edição (DSM-5), entretanto ...
Tomasi, Maria Cecilia, Brandes, Jaciara Muller, Lopes, Juliana, Klostermann, Henrique Sartori, Cyrino, Luiz Arthur Rangel   +4 more
openaire   +1 more source

NKX2‐1 Downstream Regulatory Structural Variants Explain a Substantial Proportion of Molecular Diagnoses in Patients With Benign Hereditary Chorea

Movement Disorders, EarlyView.
Abstract Background NKX2‐1–related disorders (NKX2‐1‐RDs) classically present with a triad of neurological, endocrine, and pulmonary manifestations, including benign hereditary chorea. However, in a fraction of patients, NKX2‐1 coding variants are not detected, and variants outside the NKX2‐1 locus have been reported.
Robin Wijngaard, Lucy Dougherty‐de Miguel, German Demidov, Galuh Astuti, Amaia Lasa‐Aranzasti, Ana Cueto‐González, Marta Correa‐Vela, Carlos Lázaro‐Hernández, Charlotte A. Haaxma, Clara D.M. van Karnebeek, David Gómez‐Andrés, Ignacio Iglesias‐Serrano, Jiddeke M. van de Kamp, Jolanda Schieving, Laura Trujillano, Marc Engelen, Beatriz Muñoz‐Cabello, Roderick P.P.W.M. Maas, Thatjana Gardeitchik, Victoria Gonzalez, Annemarie de Vreugd, Cristina Pérez‐Sanchez, Elisabet Lloveras, Erik‐Jan Kamsteeg, Maartje Pennings, Natalia Rey‐Viñets, Javier Sánchez, Ronald van Beek, Antonio Moreno‐Galdó, Lisenka E.L.M. Vissers, Kornelia Neveling, Anna Marcé‐Grau, Machteld M. Oud, Belén Pérez‐Dueñas   +33 more
wiley   +1 more source