Results 231 to 240 of about 1,168,154 (292)

Genetic testing in paediatric neurological disorders

Developmental Medicine &Child Neurology, EarlyView.
In this study 390 paediatric patients with neurological disorders underwent genetic testing via exome sequencing, commercial panel, in‐house epilepsy, and movement disorder gene panels. Exome sequencing provides the highest diagnostic yield, and severe developmental delay and hypotonia predicted pathogenic variants in the exome sequencing cohort ...
Wafa Bani Uraba, Byoung Chan Lee, Shekeeb S. Mohammad, Katrina Fisk, Michael Buckley, Russell C. Dale, Tony Roscioli, Paediatric Neurogenomic Working Group, Manoj P. Menezes, Sachin Gupta, Christopher Troedson, Esther Tantsis, Richard Webster, Bruce Bennetts, Deepak Gill, Kavitha Kothur   +15 more
wiley   +1 more source

Neonatal Assessment Visual European Grid accuracy in detecting infants born preterm at risk of neurological impairment

Developmental Medicine &Child Neurology, EarlyView.
NAVEG: a screening tool for detecting preterm newborn at risk of neurolocal impairment, key findings and diagnostic accuracy. Abstract Aim To analyse the factorial structure of the Neonatal Assessment Visual European Grid (NAVEG), its diagnostic accuracy, the discriminative capacity of its individual items, and total score in detecting infants born ...
Elisa Fazzi, Laura Malerba, Jessica Galli, Salvatore Aversa, Lotfi B. Merabet, Francesco Risso, Andrea Rossi, NAVEG Group, Patrizia Accorsi, Anna Alessandrini, Sabina Bettelli, Nicole D'adda, Erika Loi, Michela Gritti, Paola Martelli, Paola Mattei, Giuseppe Nascimbeni, Federica Tansini, Francesco Semeraro, Vania Spinoni, Serena Micheletti, Giulia Balboni   +21 more
wiley   +1 more source

Autism spectrum disorder assessment in cerebral palsy and other early‐onset motor conditions: A scoping review

Developmental Medicine &Child Neurology, EarlyView.
Abstract Aim To map diagnostic procedures and standardized instruments reportedly used to identify autism spectrum disorder (ASD) in people with cerebral palsy or other early‐onset motor conditions (EOMC) including Rett syndrome and muscular dystrophy.
Olga Laporta‐Hoyos, Marina Fernández‐Andújar, Lee Reid, Marta Oporto‐Alonso, Júlia Ballester‐Plané, América Carrascal‐Zuluaga, María Gutiérrez‐del Hoyo, Jacqui Ferraiolo, Magnus Påhlman, Kate Himmelmann, Somer Bishop, Roser Pueyo   +11 more
wiley   +1 more source

Perinatal complications, mode of delivery, and neurological morbidity in children with COL4A1/A2 variants

Developmental Medicine &Child Neurology, EarlyView.
Abstract Aim To characterize reported perinatal complications and childhood neurological diagnoses among children with COL4A1/2 variants and explore associations between mode of delivery and selected neurological outcomes. Method This was a retrospective cross‐sectional patient registry study using surveys collected through the Gould Syndrome ...
Shraddha Pandey, Dawn Gano, Danielle Boyce, Rachel Vassar   +3 more
wiley   +1 more source

Maternal depression as a mediator of preterm birth and child development

Developmental Medicine &Child Neurology, EarlyView.
Abstract Aim To assess the causal pathway between preterm birth and infant neurodevelopmental delay, with maternal depression as the mediator using a counterfactual mediation framework. Method A prospective cohort of 1253 mother–infant pairs were enrolled and followed up until 6 months in Nepal.
Ashish KC, Miriam Sophia Meier, Jaya Chandna, Lea Kreyenbaum, Carin Andrews, Omkar Basnet   +5 more
wiley   +1 more source

Extremely preterm infant admissions within the SafeBoosC-III consortium during the COVID-19 lockdown

, 2020
Rasmussen MI, Lühr Hansen M, Pichler G, Dempsey E, Pellicer A, EL-Khuffash A, Shashidhar A, Piris-Borregas S, Alsina M, Cetinkaya M, Chalak L, Ozkan H, Baserga M, Sirc J, Fuchs H, Ergenekon E, Arruza L, Mathur A, Stocker M, Vaccarello OO, Szczapa T, Sarafidis K, Krolak-Olejnik B, Memisoglu A, Reigstad H, Rafińska-Ważny E, Hatzidaki E, Peng Z, Gkentzi D, Viellevoye R, De Buyst J, Mastretta E, Wang P, Hahn GH, Bender L, Cornette L, Tkaczyk J, Rio Rd, Fumagalli M, Papathoma E, Wilinska M, Naulers G, Sadowska-Krawczenko I, Lecart C, Couce ML, Fredly S, Heuchan AM, Karen T, Greisen G.   +48 more
europepmc   +1 more source

International consensus recommendations for identifying malnutrition in children with neurological impairment

Developmental Medicine &Child Neurology, EarlyView.
Abstract Children with neurological impairment (CNI) are at increased risk of malnutrition because of functional, medical, and socioeconomic challenges. However, difficulties in obtaining reliable anthropometric measurements and differences in body composition limit the usefulness of conventional nutritional indicators.
Sarah Vermilyea, Jodi Wolff, Gina Rempel, Jessie M. Hulst, Koen Huysentruyt, Mandy Neudecker, Denise Kennedy, Valérie Marchand, Erika Ochoa‐Ortiz, Richard D. Stevenson, Promoting International Collaboration for Nutrition in Neurological Impairment in Children (PICNNIC) Working Group, Lucinda Lourens, Mark Conaway, Tejas S. Desai, Mercedes Ruiz Brunner, Nathalia Sanchez Vargas, Valeria Martinez Tenorio, Kristie L. Bell, Claudio Romano, Richard Grossberg   +19 more
wiley   +1 more source

Definition of childhood visual impairment: A systematic overview of reviews and authoritative sources across clinical, research, and policy contexts

Developmental Medicine &Child Neurology, EarlyView.
Abstract Aims To identify, synthesize, and compare current terminologies and definitions of cerebral visual impairment (CVI) in children across clinical, research, educational, and policy settings. Method We conducted a systematic overview of systematic reviews and authoritative documents registered in PROSPERO (CRD420251025233) and reported in ...
Martina Micai, Letizia Gila, Francesca Fulceri, Angela Caruso, Mara Sabbioni, Els Ortibus, Elisa Maria Fazzi, Corinna Bauer, John Ravencroft, Maria Luisa Scattoni   +9 more
wiley   +1 more source

Ηip dysplasia in children with spina bifida after prenatal surgical closure

Developmental Medicine &Child Neurology, EarlyView.
Neonatal hip morphology following prenatal closure remains poorly characterized. This study is the first to compare the prevalence of sonographically detectable hip dysplasia in children who underwent prenatal closure for spina bifida with that of the general infant population.
Domenic Grisch, Aurelia Hof, Charlotte Vlachopoulos, Spina Bifida Study Group Zurich, Barbara Casanova, Ruth Etter, Patrice Grehten, Sandra Fernandez‐Diaz, Cornelia Hagmann, Maya Horst Luethy, Raimund Kottke, Niklaus Krayenbuehl, Markus A. Landolt, Bea Latal Hajnal, Andrea Lehmann, Luca Mazzone, Andreas Meyer‐Heim, Carolin Meyer zu Spradow, Theres Moehrlen, Ueli Moehrlen, Svea Muehlberg, Timothy Müller, Beth Padden, Susanne Polentarutti, Antonin Prouza, Evelyne Riesen, Brigitte Seliner, Mithula Shellvarajah, Selma Sirin, Alexandra Wattinger, Noemi Zweifel, Lukas Kandler, Nicole Ochsenbein, Nele Struebing, Max Antonio Thomasius, Ladina Vonzun, Britta K. Krautwurst, Christos Tsagkaris, Thomas Dreher   +38 more
wiley   +1 more source

Vitamin D deficiency in early pregnancy and the risk of developing cerebral palsy: A case–control study

Developmental Medicine &Child Neurology, EarlyView.
Abstract Aim To investigate whether maternal deficiency of vitamin D in early pregnancy increases the risk of cerebral palsy (CP) in offspring. Method This registry and biobank‐based case–control study consisted of mother–child pairs from Scania, Sweden. Cases (n = 322) were identified from a nationwide CP‐register born between 1995 and 2014.
Ebba Bergman, Lars Rylander, Christian Lindh, Jesse D. Thacher   +3 more
wiley   +1 more source