Results 251 to 260 of about 825,443 (336)

Obstetric outcome in women with congenital heart disease: A nationwide cohort in Sweden. [PDF]

Acta Obstet Gynecol Scand
Wedlund F, Widing E, von Wowern E, Christensson C, Lindstedt S, Sörensson P, Trzebiatowska-Krzynska A, Mandalenakis Z, Bay A, Johansson B, Hlebowicz J.   +10 more
europepmc   +1 more source

Incomplete Form of Shone Complex in an Adult Congenital Heart Disease Patient

, 2019
Beatrice Chia-Hui Shih, Jae Hong Lim, Jooncheol Min, Eung Re Kim, Jae Gun Kwak, Woong‐Han Kim   +5 more
openalex   +2 more sources

Recanalization of Thrombosed Atrial Flow Regulator in Failing Fontan: A Bridge to Transplant

Catheterization and Cardiovascular Interventions, EarlyView.
ABSTRACT We report the case of a 10‐year‐old boy (41 kg, 133 cm) with hypoplastic left heart syndrome (mitral and aortic atresia), who underwent staged palliation: Norwood‐Sano at 6 days, Glenn at 7 months, and Fontan completion at 3 years using a 16 mm non‐fenestrated extracardiac Gore‐Tex conduit.
Raymond N. Haddad, Estibaliz Valdeolmillos, Emre Belli, Sébastien Hascoët   +3 more
wiley   +1 more source

The impact of congenital heart disease on the timing of Alzheimer's disease in Down syndrome. [PDF]

Alzheimers Dement (Amst)
Clina JG, Helsel BC, Hartley SL, White DA, Fleming-Batayneh VL, Handen B, Christian B, Head E, Mapstone M, Hom CL, Ances B, Burns J, Rosas HD, Lai F, McHale SK, Lee JH, Schmitt FA, Harp J, Lott IT, Zaman S, Ptomey LT, Alzheimer Biomarker Consortium–Down Syndrome (ABC‐DS) Investigators.   +21 more
europepmc   +1 more source

Retrospective, Multicenter Study of Lacosamide to Treat Neonatal Seizures

Annals of the Child Neurology Society, EarlyView.
ABSTRACT Objective Most antiseizure medications (ASMs) are prescribed off label for neonates. Lacosamide's efficacy in infants and availability in intravenous formulation suggest potential utility for neonates. We evaluated the safety and efficacy of lacosamide for neonatal seizures. Methods This 10‐center, retrospective study of neonates with seizures
Alexandra Santana Almansa, Jessica R. Landers, Nicholas S. Abend, Giulia M. Benedetti, Catherine J. Chu, Andrew T. Knox, Shavonne Massey, Steffany Moen, Andrea C. Pardo, Arnold Sansevere, Renée A. Shellhaas, Cameron Thomas, Tammy Tsuchida, Sonya Wang, Bo Zhang, Janet S. Soul   +15 more
wiley   +1 more source

Anesthetic Considerations in Congenital Myasthenic Syndrome: A Case Report. [PDF]

Cureus
Knio ZO, Dean J, O'Brien J.
europepmc   +1 more source

Lesions Associated With Autism Symptoms Map to a Cerebellar Brain Network in Tuberous Sclerosis Complex

Annals of the Child Neurology Society, EarlyView.
ABSTRACT Objective Autism spectrum disorder (ASD) affects 1 in 36 individuals in the United States and is characterized by impaired social communication and restrictive/repetitive behaviors. Individuals with tuberous sclerosis complex (TSC) have a high incidence of ASD (40%) and exhibit congenital brain lesions (tubers), offering a unique lesion‐based ...
Wendy Xiao Herman, Gillian N. Miller, Mustafa Sahin, Jurriaan M. Peters, Simon K. Warfield, Darcy A. Krueger, E. Martina Bebin, Hope Northrup, Joyce Y. Wu, Michael D. Fox, Alexander L. Cohen   +10 more
wiley   +1 more source

Hope in Miniature: The First Case of Implantation of a "Tiny Pacemaker" in Italy as a Successful Treatment for Congenital Atrioventricular Block in a Low Birth Weight Child. [PDF]

Case Rep Cardiol
Paola F, Raul L, Giovanni M, Luisa P, Paolo F.   +4 more
europepmc   +1 more source

Epilepsy Phenotypic Spectrum of NUS1‐Related Disorder: A Case Series

Annals of the Child Neurology Society, EarlyView.
ABSTRACT Background Epilepsy with myoclonic and atonic seizures (EMAtS), also known as Doose syndrome, accounts for 1%–2% of childhood epilepsies, and various genes have been implicated in causing this epilepsy syndrome. NUS1 encodes for Nogo‐B receptor (NgBR), which stabilizes the dehydrodolichyl‐diphosphate synthase complex in the endoplasmic ...
Saumel Ahmadi, Natalie Fulton, Michael Morrissey, Rebekah Landre, Stuart Tomko, Fumihiko Urano, Réjean M Guerriero   +6 more
wiley   +1 more source

Syndromic Congenital Heart Disease Diagnosed in Adulthood: A Reminder of the Phenotypic Variability of Alagille Syndrome. [PDF]

Case Rep Cardiol
Campbell MK, Hallam J, Casella SL, Shah S.   +3 more
europepmc   +1 more source