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Erwin Brosens

Showing results (11-20 of 72) with videos related to

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International Journal of Molecular Sciences|December 18, 2020
Spliceosome Mutations in Uveal MelanomaJosephine Q N Nguyen, Wojtek Drabarek, Serdar Yavuzyigitoglu, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|August 29, 2013
Increased incidence of hypertrophic pyloric stenosis in esophageal atresia patientsNicole Wilhelmina Gerarda van Beelen, Daphne S Mous, Erwin Brosens, et al.
Fetal Diagnosis and Therapy|September 15, 2025
Prenatal Assessment of Fetal Vertebrae and Ribs by Three-Dimensional Ultrasound and the Association with Fetal and Neonatal OutcomePauline C Schut, Titia E Cohen-Overbeek, Tom J M van Dooren, et al.
Ophthalmology Science|January 8, 2024
8q Gain Has No Additional Predictive Value in <i>SF3B1</i><sup>MUT</sup> Uveal Melanoma but Is Predictive for a Worse Prognosis in Patients with <i>BAP1</i><sup>MUT</sup> Uveal MelanomaJosephine Q N Nguyen, Wojtek Drabarek, Jolanda Vaarwater, et al.
International Journal of Molecular Sciences|January 5, 2021
Genetics of Ocular Melanoma: Insights into Genetics, Inheritance and TestingNatasha M van Poppelen, Daniël P de Bruyn, Tolga Bicer, et al.
Ophthalmology Science|October 17, 2022
High C-Reactive Protein Levels Are Related to Better Survival in Patients with Uveal MelanomaNikki Meijer, Daniël P de Bruyn, Annelies de Klein, et al.
European Journal of Human Genetics : EJHG|November 11, 2011
Copy number detection in discordant monozygotic twins of Congenital Diaphragmatic Hernia (CDH) and Esophageal Atresia (EA) cohortsDanielle Veenma, Erwin Brosens, Elisabeth de Jong, et al.
Frontiers in Pediatrics|December 13, 2021
Case Report and Review of the Literature: Congenital Diaphragmatic Hernia and Craniosynostosis, a Coincidence or Common Cause?Linda Gaillard, Anne Goverde, Quincy C C van den Bosch, et al.
Genes|October 23, 2021
Heritability and De Novo Mutations in Oesophageal Atresia and Tracheoesophageal Fistula AetiologyErwin Brosens, Rutger W W Brouwer, Hannie Douben, et al.
Cancers|August 27, 2021
MiRNAs Correlate with HLA Expression in Uveal Melanoma: Both Up- and Downregulation Are Related to Monosomy 3Zahra Souri, Annemijn P A Wierenga, Emine Kiliç, et al.
Pageof 8

Showing results (11-20 of 72) with videos related to

Sort By:
Pageof 8
International Journal of Molecular Sciences|December 18, 2020
Spliceosome Mutations in Uveal MelanomaJosephine Q N Nguyen, Wojtek Drabarek, Serdar Yavuzyigitoglu, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|August 29, 2013
Increased incidence of hypertrophic pyloric stenosis in esophageal atresia patientsNicole Wilhelmina Gerarda van Beelen, Daphne S Mous, Erwin Brosens, et al.
Fetal Diagnosis and Therapy|September 15, 2025
Prenatal Assessment of Fetal Vertebrae and Ribs by Three-Dimensional Ultrasound and the Association with Fetal and Neonatal OutcomePauline C Schut, Titia E Cohen-Overbeek, Tom J M van Dooren, et al.
Ophthalmology Science|January 8, 2024
8q Gain Has No Additional Predictive Value in <i>SF3B1</i><sup>MUT</sup> Uveal Melanoma but Is Predictive for a Worse Prognosis in Patients with <i>BAP1</i><sup>MUT</sup> Uveal MelanomaJosephine Q N Nguyen, Wojtek Drabarek, Jolanda Vaarwater, et al.
International Journal of Molecular Sciences|January 5, 2021
Genetics of Ocular Melanoma: Insights into Genetics, Inheritance and TestingNatasha M van Poppelen, Daniël P de Bruyn, Tolga Bicer, et al.
Ophthalmology Science|October 17, 2022
High C-Reactive Protein Levels Are Related to Better Survival in Patients with Uveal MelanomaNikki Meijer, Daniël P de Bruyn, Annelies de Klein, et al.
European Journal of Human Genetics : EJHG|November 11, 2011
Copy number detection in discordant monozygotic twins of Congenital Diaphragmatic Hernia (CDH) and Esophageal Atresia (EA) cohortsDanielle Veenma, Erwin Brosens, Elisabeth de Jong, et al.
Frontiers in Pediatrics|December 13, 2021
Case Report and Review of the Literature: Congenital Diaphragmatic Hernia and Craniosynostosis, a Coincidence or Common Cause?Linda Gaillard, Anne Goverde, Quincy C C van den Bosch, et al.
Genes|October 23, 2021
Heritability and De Novo Mutations in Oesophageal Atresia and Tracheoesophageal Fistula AetiologyErwin Brosens, Rutger W W Brouwer, Hannie Douben, et al.
Cancers|August 27, 2021
MiRNAs Correlate with HLA Expression in Uveal Melanoma: Both Up- and Downregulation Are Related to Monosomy 3Zahra Souri, Annemijn P A Wierenga, Emine Kiliç, et al.
Pageof 8