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Allan Bayat

Showing results (31-40 of 130) with videos related to

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Acta Ophthalmologica|February 19, 2020
Prevalence and causes of infantile nystagmus in a large population-based Danish cohortKaren Hvid, Kamilla Rothe Nissen, Allan Bayat, et al.
Journal of Medical Genetics|September 10, 2025
Mixed functional consequences of the N651D <i>GRIA3</i> variant: a case of early-onset developmental and epileptic encephalopathy with parkinsonismCarmen Fons, Yu-Han Ge, Laura Kristine Rasmussen, et al.
Molecular Syndromology|July 14, 2020
Novel Clinical and Radiological Findings in a Family with Autosomal Recessive OmodysplasiaAllan Bayat, Morton Dunø, Maria Kirchhoff, et al.
European Journal of Medical Genetics|May 21, 2021
Expansion of the CCDC22 associated Ritscher-Schinzel/3C syndrome and review of the literature: Should the minimal diagnostic criteria be revised?Cathrine E Gjerulfsen, Rikke S Møller, Christina D Fenger, et al.
American Journal of Medical Genetics. Part A|July 29, 2021
5q11.2 deletion syndrome revisited-Further narrowing of the smallest region of overlap for the main clinical characteristics of the syndromeAllan Bayat, Michael Bayat, Chantal Broers, et al.
American Journal of Medical Genetics. Part A|March 21, 2016
Further delineation of facioaudiosymphalangism syndrome: Description of a family with a novel NOG mutation and without hearing lossAllan Bayat, Igor Fijalkowski, Tobias Andersen, et al.
Basic & Clinical Pharmacology & Toxicology|February 8, 2026
Pharmacokinetics of Perampanel in Danish Paediatric Patients With Epilepsy Based on Therapeutic Drug MonitoringSara Angelucci, Morten Baltzer Houlind, Maja Stjerne Hansen, et al.
Clinical Genetics|June 19, 2024
Unraveling GRIA1 neurodevelopmental disorders: Lessons learned from the p.(Ala636Thr) variantNicolai Kohring Tvergaard, Tinatin Tkemaladze, Tommy Stödberg, et al.
American Journal of Medical Genetics. Part A|January 16, 2026
A Growth Chart for KBG SyndromeKaren J Low, Elena Martinez-Cayuelas, Berta Almoguera, et al.
Ugeskrift for Laeger|September 6, 2022
[Genetic testing in autism spectrum disorder]Janni Majgaard Jensen, Ulla Schierup Nielsen, Allan Bayat, et al.
Pageof 13

Showing results (31-40 of 130) with videos related to

Sort By:
Pageof 13
Acta Ophthalmologica|February 19, 2020
Prevalence and causes of infantile nystagmus in a large population-based Danish cohortKaren Hvid, Kamilla Rothe Nissen, Allan Bayat, et al.
Journal of Medical Genetics|September 10, 2025
Mixed functional consequences of the N651D <i>GRIA3</i> variant: a case of early-onset developmental and epileptic encephalopathy with parkinsonismCarmen Fons, Yu-Han Ge, Laura Kristine Rasmussen, et al.
Molecular Syndromology|July 14, 2020
Novel Clinical and Radiological Findings in a Family with Autosomal Recessive OmodysplasiaAllan Bayat, Morton Dunø, Maria Kirchhoff, et al.
European Journal of Medical Genetics|May 21, 2021
Expansion of the CCDC22 associated Ritscher-Schinzel/3C syndrome and review of the literature: Should the minimal diagnostic criteria be revised?Cathrine E Gjerulfsen, Rikke S Møller, Christina D Fenger, et al.
American Journal of Medical Genetics. Part A|July 29, 2021
5q11.2 deletion syndrome revisited-Further narrowing of the smallest region of overlap for the main clinical characteristics of the syndromeAllan Bayat, Michael Bayat, Chantal Broers, et al.
American Journal of Medical Genetics. Part A|March 21, 2016
Further delineation of facioaudiosymphalangism syndrome: Description of a family with a novel NOG mutation and without hearing lossAllan Bayat, Igor Fijalkowski, Tobias Andersen, et al.
Basic & Clinical Pharmacology & Toxicology|February 8, 2026
Pharmacokinetics of Perampanel in Danish Paediatric Patients With Epilepsy Based on Therapeutic Drug MonitoringSara Angelucci, Morten Baltzer Houlind, Maja Stjerne Hansen, et al.
Clinical Genetics|June 19, 2024
Unraveling GRIA1 neurodevelopmental disorders: Lessons learned from the p.(Ala636Thr) variantNicolai Kohring Tvergaard, Tinatin Tkemaladze, Tommy Stödberg, et al.
American Journal of Medical Genetics. Part A|January 16, 2026
A Growth Chart for KBG SyndromeKaren J Low, Elena Martinez-Cayuelas, Berta Almoguera, et al.
Ugeskrift for Laeger|September 6, 2022
[Genetic testing in autism spectrum disorder]Janni Majgaard Jensen, Ulla Schierup Nielsen, Allan Bayat, et al.
Pageof 13