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Alfred Peter Born

Showing results (51-60 of 60) with videos related to

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Journal of Clinical Medicine|January 8, 2025
A Prospective Study on the Feasibility and Effect of an Optimized Perioperative Care Protocol in Pediatric Neuromuscular Scoliosis SurgeryMarie Mostue Naume, Christina Engel Hoei-Hansen, Alfred Peter Born, et al.
Clinical Epidemiology|April 26, 2022
Validation of Pediatric Idiopathic Generalized Epilepsy Diagnoses from the Danish National Patient Register During 1994‒2019Magnus Spangsberg Boesen, Melita Cacic Hribljan, Søren Kirchhoff Christensen, et al.
Journal of Neurology|May 20, 2022
School performance and psychiatric comorbidity in juvenile absence epilepsy and juvenile myoclonic epilepsy: a Danish population-based cohort studyMagnus Spangsberg Boesen, Malene Landbo Børresen, Søren Kirchhoff Christensen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 30, 2022
School performance and psychiatric comorbidity in childhood absence epilepsy: A Danish cohort studyMagnus Spangsberg Boesen, Malene Landbo Børresen, Søren Kirchhoff Christensen, et al.
Circulation. Genomic and Precision Medicine|November 12, 2025
Exploring <i>RBFOX2</i> Haploinsufficiency: A New Genetic Link to Hypoplastic Left Heart SyndromeClément Sauvestre, Amel Bouchatal, Claire Beneteau, et al.
British Journal of Clinical Pharmacology|March 5, 2025
Paracetamol and its metabolites in children and adults with spinal muscular atrophy - a population pharmacokinetic modelQiaolin Zhao, Marie Mostue Naume, Brenda C M de Winter, et al.
Neuromuscular Disorders : NMD|December 5, 2023
Acetaminophen treatment in children and adults with spinal muscular atrophy: a lower tolerance and higher risk of hepatotoxicityMarie Mostue Naume, Qiaolin Zhao, Sissel Sundell Haslund-Krog, et al.
Nature Medicine|December 8, 2025
Intrathecal onasemnogene abeparvovec in treatment-naive patients with spinal muscular atrophy: a phase 3, randomized controlled trialCrystal M Proud, Dũng Chí Vũ, Jo M Wilmshurst, et al.
Journal of Inherited Metabolic Disease|October 18, 2015
Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patientsRosalba Carrozzo, Daniela Verrigni, Magnhild Rasmussen, et al.
Neurology. Genetics|February 12, 2020
Defining and expanding the phenotype of <i>QARS</i>-associated developmental epileptic encephalopathyKatrine M Johannesen, Diana Mitter, Robert Janowski, et al.
Pageof 6

Showing results (51-60 of 60) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
Journal of Clinical Medicine|January 8, 2025
A Prospective Study on the Feasibility and Effect of an Optimized Perioperative Care Protocol in Pediatric Neuromuscular Scoliosis SurgeryMarie Mostue Naume, Christina Engel Hoei-Hansen, Alfred Peter Born, et al.
Clinical Epidemiology|April 26, 2022
Validation of Pediatric Idiopathic Generalized Epilepsy Diagnoses from the Danish National Patient Register During 1994‒2019Magnus Spangsberg Boesen, Melita Cacic Hribljan, Søren Kirchhoff Christensen, et al.
Journal of Neurology|May 20, 2022
School performance and psychiatric comorbidity in juvenile absence epilepsy and juvenile myoclonic epilepsy: a Danish population-based cohort studyMagnus Spangsberg Boesen, Malene Landbo Børresen, Søren Kirchhoff Christensen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 30, 2022
School performance and psychiatric comorbidity in childhood absence epilepsy: A Danish cohort studyMagnus Spangsberg Boesen, Malene Landbo Børresen, Søren Kirchhoff Christensen, et al.
Circulation. Genomic and Precision Medicine|November 12, 2025
Exploring <i>RBFOX2</i> Haploinsufficiency: A New Genetic Link to Hypoplastic Left Heart SyndromeClément Sauvestre, Amel Bouchatal, Claire Beneteau, et al.
British Journal of Clinical Pharmacology|March 5, 2025
Paracetamol and its metabolites in children and adults with spinal muscular atrophy - a population pharmacokinetic modelQiaolin Zhao, Marie Mostue Naume, Brenda C M de Winter, et al.
Neuromuscular Disorders : NMD|December 5, 2023
Acetaminophen treatment in children and adults with spinal muscular atrophy: a lower tolerance and higher risk of hepatotoxicityMarie Mostue Naume, Qiaolin Zhao, Sissel Sundell Haslund-Krog, et al.
Nature Medicine|December 8, 2025
Intrathecal onasemnogene abeparvovec in treatment-naive patients with spinal muscular atrophy: a phase 3, randomized controlled trialCrystal M Proud, Dũng Chí Vũ, Jo M Wilmshurst, et al.
Journal of Inherited Metabolic Disease|October 18, 2015
Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patientsRosalba Carrozzo, Daniela Verrigni, Magnhild Rasmussen, et al.
Neurology. Genetics|February 12, 2020
Defining and expanding the phenotype of <i>QARS</i>-associated developmental epileptic encephalopathyKatrine M Johannesen, Diana Mitter, Robert Janowski, et al.
Pageof 6