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Heiko Reutter

Showing results (31-40 of 209) with videos related to

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Pediatric Surgery International|July 1, 2008
Investigation of FGF10 as a candidate gene in patients with anorectal malformations and exstrophy of the cloacaVictoria Krüger, Mercedeh Khoshvaghti, Heiko Reutter, et al.
Genes|December 20, 2018
Towards a Central Role of <i>ISL1</i> in the Bladder Exstrophy⁻Epispadias Complex (BEEC): Computational Characterization of Genetic Variants and Structural ModellingAmit Sharma, Tikam Chand Dakal, Michael Ludwig, et al.
Genes|August 27, 2021
The Genomic Architecture of Bladder Exstrophy Epispadias ComplexGlenda M Beaman, Raimondo M Cervellione, David Keene, et al.
Early Human Development|January 17, 2015
Antioxidative status and oxidative stress in the fetal circulation at birth: the effects of time of delivery and presence of laborDavid Katzer, Andreas Mueller, Lars Welzing, et al.
Journal of Medical Case Reports|July 18, 2018
Extracorporeal membrane oxygenation support in a newborn with lower urinary tract obstruction and pulmonary hypoplasia: a case reportEva Gatzweiler, Bernd Hoppe, Oliver Dewald, et al.
BMC Pediatrics|February 4, 2026
Documented rituals in pediatric intensive care: a decade of sacramental and symbolic practices in a pluralistic clinical settingSteven Hébert, Heiko Reutter, Gregor Hanslik, et al.
Journal of Medical Case Reports|November 13, 2018
Congenital intrahepatic portocaval shunts and hypoglycemia due to secondary hyperinsulinism: a case report and review of the literatureAlexander Weigert, Jeanette Bierwolf, Heiko Reutter, et al.
Health Science Reports|March 25, 2024
Familial congenital lower urinary tract obstruction (LUTO) suggested by screening for lower urinary tract dysfunction in parents of patients: A descriptive studyFabian Ebach, Pauline Wagner, Raimund Stein, et al.
Molecular Medicine Reports|December 20, 2017
Whole exome sequencing identifies a mutation in EYA1 and GLI3 in a patient with branchio‑otic syndrome and esophageal atresia: Coincidence or a digenic mode of inheritance?Franziska Kause, Heiko Reutter, Florian Marsch, et al.
Zeitschrift Fur Geburtshilfe Und Neonatologie|February 8, 2024
[SARS-CoV-2 Infection in Pregnancy and Incidence of Congenital Malformations - is there a Correlation? Analysis of 8032 Pregnancies from the CRONOS Registry]Anna Hofbauer, Holm Schneider, Sven Kehl, et al.
Pageof 21

Showing results (31-40 of 209) with videos related to

Sort By:
Pageof 21
Pediatric Surgery International|July 1, 2008
Investigation of FGF10 as a candidate gene in patients with anorectal malformations and exstrophy of the cloacaVictoria Krüger, Mercedeh Khoshvaghti, Heiko Reutter, et al.
Genes|December 20, 2018
Towards a Central Role of <i>ISL1</i> in the Bladder Exstrophy⁻Epispadias Complex (BEEC): Computational Characterization of Genetic Variants and Structural ModellingAmit Sharma, Tikam Chand Dakal, Michael Ludwig, et al.
Genes|August 27, 2021
The Genomic Architecture of Bladder Exstrophy Epispadias ComplexGlenda M Beaman, Raimondo M Cervellione, David Keene, et al.
Early Human Development|January 17, 2015
Antioxidative status and oxidative stress in the fetal circulation at birth: the effects of time of delivery and presence of laborDavid Katzer, Andreas Mueller, Lars Welzing, et al.
Journal of Medical Case Reports|July 18, 2018
Extracorporeal membrane oxygenation support in a newborn with lower urinary tract obstruction and pulmonary hypoplasia: a case reportEva Gatzweiler, Bernd Hoppe, Oliver Dewald, et al.
BMC Pediatrics|February 4, 2026
Documented rituals in pediatric intensive care: a decade of sacramental and symbolic practices in a pluralistic clinical settingSteven Hébert, Heiko Reutter, Gregor Hanslik, et al.
Journal of Medical Case Reports|November 13, 2018
Congenital intrahepatic portocaval shunts and hypoglycemia due to secondary hyperinsulinism: a case report and review of the literatureAlexander Weigert, Jeanette Bierwolf, Heiko Reutter, et al.
Health Science Reports|March 25, 2024
Familial congenital lower urinary tract obstruction (LUTO) suggested by screening for lower urinary tract dysfunction in parents of patients: A descriptive studyFabian Ebach, Pauline Wagner, Raimund Stein, et al.
Molecular Medicine Reports|December 20, 2017
Whole exome sequencing identifies a mutation in EYA1 and GLI3 in a patient with branchio‑otic syndrome and esophageal atresia: Coincidence or a digenic mode of inheritance?Franziska Kause, Heiko Reutter, Florian Marsch, et al.
Zeitschrift Fur Geburtshilfe Und Neonatologie|February 8, 2024
[SARS-CoV-2 Infection in Pregnancy and Incidence of Congenital Malformations - is there a Correlation? Analysis of 8032 Pregnancies from the CRONOS Registry]Anna Hofbauer, Holm Schneider, Sven Kehl, et al.
Pageof 21