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Allan Bayat

Showing results (21-30 of 130) with videos related to

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Genes|August 6, 2021
Epilepsy Syndromes in the First Year of Life and Usefulness of Genetic Testing for Precision TherapyAllan Bayat, Michael Bayat, Guido Rubboli, et al.
Ugeskrift for Laeger|May 18, 2010
[Foetal akinesia-hypokinesia deformation sequence]Allan Bayat, Astrid Petersen, Margrethe Møller, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 18, 2008
Incidence of fetal akinesia-hypokinesia deformation sequence: a population-based studyAllan Bayat, Astrid Petersen, Margrethe Møller, et al.
JIMD Reports|November 5, 2014
Mild Lesch-Nyhan Disease in a Boy with a Null Mutation in HPRT1: An Exception to the Known Genotype-Phenotype CorrelationAllan Bayat, Mette Christensen, Flemming Wibrand, et al.
American Journal of Medical Genetics. Part A|April 7, 2022
Novel truncating variants in FGD1 detected in two Danish families with Aarskog-Scott syndrome and myopathic featuresAllan Bayat, Bjørg Krett, Morten Dunø, et al.
Clinical Dysmorphology|April 29, 2017
Familial craniofacial abnormality and polymicrogyria associated with a microdeletion affecting the NFIA geneAllan Bayat, Maria Kirchhoff, Camilla G Madsen, et al.
Ugeskrift for Laeger|July 5, 2022
[Genetic factors provide individualised targeted treatment of epilepsy]Katrine M Johannesen, Allan Bayat, Trine Bjørg Hammer, et al.
Journal of Neurology|August 24, 2024
POLG-related mitochondrial disease mimicking autoimmune encephalitisMichael Bayat, Thomas Harbo, Maryam Anzabi, et al.
Danish Medical Journal|June 8, 2013
Nitrous oxide provides safe and effective analgesia for minor paediatric procedures--a systematic reviewRie S Pedersen, Allan Bayat, Nick Phaff Steen, et al.
Epilepsia|September 26, 2023
Solving the unsolved genetic epilepsies: Current and future perspectivesKatrine M Johannesen, Zeynep Tümer, Sarah Weckhuysen, et al.
Pageof 13

Showing results (21-30 of 130) with videos related to

Sort By:
Pageof 13
Genes|August 6, 2021
Epilepsy Syndromes in the First Year of Life and Usefulness of Genetic Testing for Precision TherapyAllan Bayat, Michael Bayat, Guido Rubboli, et al.
Ugeskrift for Laeger|May 18, 2010
[Foetal akinesia-hypokinesia deformation sequence]Allan Bayat, Astrid Petersen, Margrethe Møller, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 18, 2008
Incidence of fetal akinesia-hypokinesia deformation sequence: a population-based studyAllan Bayat, Astrid Petersen, Margrethe Møller, et al.
JIMD Reports|November 5, 2014
Mild Lesch-Nyhan Disease in a Boy with a Null Mutation in HPRT1: An Exception to the Known Genotype-Phenotype CorrelationAllan Bayat, Mette Christensen, Flemming Wibrand, et al.
American Journal of Medical Genetics. Part A|April 7, 2022
Novel truncating variants in FGD1 detected in two Danish families with Aarskog-Scott syndrome and myopathic featuresAllan Bayat, Bjørg Krett, Morten Dunø, et al.
Clinical Dysmorphology|April 29, 2017
Familial craniofacial abnormality and polymicrogyria associated with a microdeletion affecting the NFIA geneAllan Bayat, Maria Kirchhoff, Camilla G Madsen, et al.
Ugeskrift for Laeger|July 5, 2022
[Genetic factors provide individualised targeted treatment of epilepsy]Katrine M Johannesen, Allan Bayat, Trine Bjørg Hammer, et al.
Journal of Neurology|August 24, 2024
POLG-related mitochondrial disease mimicking autoimmune encephalitisMichael Bayat, Thomas Harbo, Maryam Anzabi, et al.
Danish Medical Journal|June 8, 2013
Nitrous oxide provides safe and effective analgesia for minor paediatric procedures--a systematic reviewRie S Pedersen, Allan Bayat, Nick Phaff Steen, et al.
Epilepsia|September 26, 2023
Solving the unsolved genetic epilepsies: Current and future perspectivesKatrine M Johannesen, Zeynep Tümer, Sarah Weckhuysen, et al.
Pageof 13