Results 71 to 80 of about 46,879 (178)

Genetic Diagnoses Among Congenital Anomaly Cases in Europe: Data From the EUROCAT Network

Paediatric and Perinatal Epidemiology, EarlyView.
ABSTRACT Background Surveillance of congenital anomaly prevalence over time can identify new teratogens. Anomalies with a genetic cause are excluded from the monitoring. Objectives We examined temporal changes in the proportion of genetic diagnoses among cases with a congenital anomaly.
Jorieke E. H. Bergman, Annie Perraud, Ester Garne, Ingeborg Barisic, David Tucker, Elisa Ballardini, Lea Bruneau, Clara Cavero‐Carbonell, Ianis Cousin, Miriam Gatt, Katya Kovacheva, Anna Latos‐Bielenska, Mary O'Mahony, Isabelle Monier, Isabelle Perthus, Riccardo Pertile, Anke Rissmann, Florence Rouget, Michelle Santoro, Joanna Sichitiu, Christine Verellen‐Dumoulin, Wladimir Wertelecki, Diana Wellesley, Joan K. Morris   +23 more
wiley   +1 more source

Prevalence of psychiatric and cognitive disorders in patients with Pierre-Robin sequence - a statistical analysis

European Psychiatry
Introduction The Pierre-Robin sequence (PRS), characterized by micrognathia, glossoptosis, and cleft palate, has long been a subject of clinical interest.
G. Pereira Bernd, V. Dall Agnol Bouvier, T. Brusa da Costa Linn, I. Cho de Almeida, B. de Oliveira de Marchi, L. Guinter Muccillo, C. G. Menezes Chaves Barcellos, C. Paz Portinho, M. V. Martins Collares   +8 more
doaj   +1 more source

Risk factors for obstructive sleep apnea syndrome in children: state of the art [PDF]

, 2019
The obstructive sleep apnea syndrome (OSAS) represents only part of a large group of pathologies of variable entity called respiratory sleep disorders (RSD) which include simple snoring and increased upper airway resistance syndrome (UARS).
Bellini, Chiara, Cammaroto, G., Colizza, A., de Vincentiis, M., De Vito, A., Firinu, E., Gobbi, R., Greco, A., Gulotta, G., Iannella, G., Magliulo, G., Meccariello, G., Pace, A., Pelucchi, S., Polimeni, A., Vicini, C., Visconti, I. C.   +16 more
core   +2 more sources

Feeding difficulty in an infant with stickler's syndrome

Contemporary Clinical Dentistry, 2019
Stickler syndrome or hereditary progressive arthro-ophthalmopathy is an autosomal dominant condition characterized by ocular manifestations, arthritic changes, orofacial features, and deafness, in variable degrees.
Parvathy Vijay, Parvathy Kumaran, Arun Mamachan Xavier, R Balagopal Varma, J Suresh Kumar   +4 more
doaj   +1 more source

Remembering Courtney Cazden, 1925–2025

Reading Research Quarterly, Volume 61, Issue 2, April/May/June 2026.
ABSTRACT Here we remember and honor Courtney B. Cazden (1925–2025), whose scholarship, mentorship, and moral clarity profoundly shaped the study of language, literacy, and learning. Drawing on our shared experiences as colleagues, collaborators, students, and friends, we reflect on Courtney's enduring contributions to classroom discourse analysis ...
Kris D. Gutiérrez, Allan Luke, Mary Kalantzis, Bill Cope, Sarah Michaels, James Paul Gee   +5 more
wiley   +1 more source

Диагностика синдромов Пьера Робена и сонного апноэ у ребенка с органической церебральной задержкой развития [PDF]

, 2018
В работе рассматривается клинический случай диагностики врожденной патологии челюстно-лицевой области (синдром или «последовательность» Пьера Робена) и синдрома сонного апноэ тяжелой степени выявленные на этапе развития легочной гипертензии и сердечной ...
Васильева, Л.И., Ивчина, Н.А., Калашникова, О.С.   +2 more
core  

Neuromuscular Block and Video Laryngoscope to Facilitate Intubation—A Survey of Current Practice in Denmark and Sweden

Acta Anaesthesiologica Scandinavica, Volume 70, Issue 4, April 2026.
ABSTRACT Background Neuromuscular blocking agents (NMBA) provide optimal conditions for tracheal intubation. A high dose of opioid can be used as an alternative but may give suboptimal conditions for intubation. The use of a video laryngoscope for intubation might eliminate this potential difference.
Åse Lodenius, Louise Holland‐Bill, Emil Ørskov Ipsen, Maria Cronhjort, Arash Afshari, Matias Vested, Andreas Creutzburg, Lars Hyldborg Lundstrøm, Helene Korvenius Nedergaard, Anders Kehlet Nørskov, ROCVIDEO Survey Collaborator Group, Mette Schytt Price, Christian Jessen, Mathias Sinkbæk Thomsen, Mikkel Schjødt Heide Jensen, Torben Krabbe Laustrup, Karina Baekby Houborg, Fabian Spies, Line Agger Kolstrup, Anni Nørgaard Jeppesen, Hanna Poulsen, Jannie Bisgaard, Hansjörg Selter, Cecilie Harries Klementsen, Hayan El‐Hallak, Daniel Hägi‐Pedersen, Jakob Hessel Andersen, Anders Lolle, Jacqueline Møller Mistry, Peter Martin Hansen, Kirsten Lerche Licht, Wojciech Jan Pietrzyk, Michael Leth Jørgensen, Christina Borgen, Anders Karlsen, Karsten Kindberg, Kim Wildgaard, Laila Mulla Reich, Simon Strøyer, Robin Lohse, Mette Lea Mortensen, Rune Lundsgaard, Mark Søgaard Niegsch, Erik Wikström, Anna Bandert, Carl Olsson, Malin Bohlin, Mälarsjukhuset Eskilstuna, Nanny Hareide, Olof Brattström, Karin Bursell, Lars Mattsson, Pontus Weinar, Katrin Ögren, Åsa Eriksson Nordesjö, Björn Ahlström, Petter Huitfeldt, Jakob Boethius, Tomi Myrberg, Jakob Walldén, Ulf A. Karlsson, Simon Näverlo, Jonas Rudenstam, Sofia Hannu, Pauline Koch, Thorey Steinarsdóttir, Gustaf Rosin, Anna Borglund Hemph, Jacob Broms, Liselott Wickerts, Anna Wennmo, Hanna Smeds, Mark Larsson, Jelena Paegle, Jonas Graf, Pierre Sundin, Katalin Rockstroh, Sebastian Felixson, Jim Runesson, Johan Berkius, Helena Krook, Louise Walther Sturesson, Fredrik Sjövall, Nikolaus Groll, Olof Nilsson, Johanna Broman, Susanne Gustafsson Liljenthal, Isabella Görloff Nordenskjöld, Martina Jarnlo Klarén, Andreas Ekman   +89 more
wiley   +1 more source

Management of a Dentigerous Cyst in a Child with Robin Sequence

Archives of Plastic Surgery, 2017
This is a brief clinical report describing an 18-month-old female with Robin sequence found to have an incidental mandibular cystic lesion on a head computed tomography scan in the preoperative workup before performing mandibular distraction.
Shayda Mirhaidari, Ananth Murthy
doaj   +1 more source

Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex

Journal of Developmental Biology, 2020
The phenotype currently accepted as Pierre Robin syndrome/sequence/anomalad/complex (PR) is characterized by mandibular dysmorphology, glossoptosis, respiratory obstruction, and in some cases, cleft palate. A causative sequence of developmental events is
Susan M. Motch Perrine, Meng Wu, Greg Holmes, Bryan C. Bjork, Ethylin Wang Jabs, Joan T. Richtsmeier   +5 more
doaj   +1 more source

Cubature formulas, geometrical designs, reproducing kernels, and Markov operators

, 2005
Cubature formulas and geometrical designs are described in terms of reproducing kernels for Hilbert spaces of functions on the one hand, and Markov operators associated to orthogonal group representations on the other hand.
De La Harpe, Pierre, Pache, Claude
core   +3 more sources