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Alina C Hilger

Showing results (1-10 of 50) with videos related to

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Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|February 19, 2026
Genetics of CAKUTAlina C Hilger, Rik Westland, Julia Hoefele
Annals of Translational Medicine|December 7, 2019
Expanding the knowledge on development of CAKUT: molecular genetics and beyondGabriel C Dworschak, Heiko Reutter, Alina C Hilger
Pediatric Nephrology (Berlin, Germany)|February 10, 2016
Underlying genetic factors of the VATER/VACTERL association with special emphasis on the "Renal" phenotypeHeiko Reutter, Alina C Hilger, Friedhelm Hildebrandt, et al.
Molecular and Cellular Pediatrics|October 5, 2021
Exome sequencing implicates a novel heterozygous missense variant in DSTYK in autosomal dominant lower urinary tract dysfunction and mild hereditary spastic paraparesisClara Vidic, Marcin Zaniew, Szymon Jurga, 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.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 26, 2016
PLAGL1 epimutation and bladder exstrophy: Coincidence or concurrent etiology?Julia Kolarova, Susanne Bens, Ole Ammerpohl, et al.
Pediatric Nephrology (Berlin, Germany)|November 13, 2025
Early diagnosis and intervention in congenital lower urinary tract obstruction: time to revise our approach?Jaap Mulder, Stefan Kohl, Federica Fontanella, et al.
Molecular and Cellular Pediatrics|March 28, 2023
Modelling human lower urinary tract malformations in zebrafishCaroline M Kolvenbach, Gabriel C Dworschak, Johanna M Rieke, et al.
Asia Pacific Journal of Clinical Nutrition|December 10, 2017
Low maternal folate concentrations and maternal MTHFR C677T polymorphism are associated with an increased risk for neural tube defects in offspring: a case-control study among Pakistani case and control mothersNuzhat Nauman, Samina Jalali, Sajjad Shami, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|December 19, 2015
Whole-Exome Sequencing in Nine Monozygotic Discordant TwinsRong Zhang, Holger Thiele, Peter Bartmann, et al.
Pageof 5

Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|February 19, 2026
Genetics of CAKUTAlina C Hilger, Rik Westland, Julia Hoefele
Annals of Translational Medicine|December 7, 2019
Expanding the knowledge on development of CAKUT: molecular genetics and beyondGabriel C Dworschak, Heiko Reutter, Alina C Hilger
Pediatric Nephrology (Berlin, Germany)|February 10, 2016
Underlying genetic factors of the VATER/VACTERL association with special emphasis on the "Renal" phenotypeHeiko Reutter, Alina C Hilger, Friedhelm Hildebrandt, et al.
Molecular and Cellular Pediatrics|October 5, 2021
Exome sequencing implicates a novel heterozygous missense variant in DSTYK in autosomal dominant lower urinary tract dysfunction and mild hereditary spastic paraparesisClara Vidic, Marcin Zaniew, Szymon Jurga, 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.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 26, 2016
PLAGL1 epimutation and bladder exstrophy: Coincidence or concurrent etiology?Julia Kolarova, Susanne Bens, Ole Ammerpohl, et al.
Pediatric Nephrology (Berlin, Germany)|November 13, 2025
Early diagnosis and intervention in congenital lower urinary tract obstruction: time to revise our approach?Jaap Mulder, Stefan Kohl, Federica Fontanella, et al.
Molecular and Cellular Pediatrics|March 28, 2023
Modelling human lower urinary tract malformations in zebrafishCaroline M Kolvenbach, Gabriel C Dworschak, Johanna M Rieke, et al.
Asia Pacific Journal of Clinical Nutrition|December 10, 2017
Low maternal folate concentrations and maternal MTHFR C677T polymorphism are associated with an increased risk for neural tube defects in offspring: a case-control study among Pakistani case and control mothersNuzhat Nauman, Samina Jalali, Sajjad Shami, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|December 19, 2015
Whole-Exome Sequencing in Nine Monozygotic Discordant TwinsRong Zhang, Holger Thiele, Peter Bartmann, et al.
Pageof 5