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Michael Ludwig

Showing results (91-100 of 239) with videos related to

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Pediatric Nephrology (Berlin, Germany)|June 30, 2006
Hypercalciuria in patients with CLCN5 mutationsMichael Ludwig, Boris Utsch, Bernd Balluch, et al.
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.
Scandinavian Journal of Urology and Nephrology|December 17, 2003
Exclusion of WTAP and HOXA13 as candidate genes for isolated hypospadiasBoris Utsch, Ali Kaya, Atila Ozburun, 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.
Fertility and Sterility|February 19, 2008
Neuromotor development and mental health at 5.5 years of age of singletons born at term after intracytoplasmatic sperm injection ICSI: results of a prospective controlled single-blinded study in GermanyAnnika Ludwig, Alexander Katalinic, Ute Thyen, et al.
Human Genetics|February 14, 2007
Reproduction abnormalities and twin pregnancies in parents of sporadic patients with oculo-auriculo-vertebral spectrum/Goldenhar syndromeDagmar Wieczorek, Michael Ludwig, Stefan Boehringer, et al.
Kidney & Blood Pressure Research|July 30, 2003
Four additional CLCN5 exons encode a widely expressed novel long CLC-5 isoform but fail to explain Dent's phenotype in patients without mutations in the short variantMichael Ludwig, Siegfried Waldegger, Matti Nuutinen, et al.
Fertility and Sterility|March 7, 2003
Sperm to zona pellucida binding depends on the use of a gonadotropin-releasing hormone agonist or a gonadotropin-releasing hormone antagonistAnnika K Schröder, Beate Schöpper, Safaa Al-Hasani, 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.
Clinical Nutrition ESPEN|May 14, 2025
Fasting orders and malnutrition risk in hospitals: The impact of mandatory fasting on hunger perception in nutritionally at-risk patientsTrixi Braasch, Ildiko Hoffmann, Ulrich Wesemann, et al.
Pageof 24

Showing results (91-100 of 239) with videos related to

Sort By:
Pageof 24
Pediatric Nephrology (Berlin, Germany)|June 30, 2006
Hypercalciuria in patients with CLCN5 mutationsMichael Ludwig, Boris Utsch, Bernd Balluch, et al.
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.
Scandinavian Journal of Urology and Nephrology|December 17, 2003
Exclusion of WTAP and HOXA13 as candidate genes for isolated hypospadiasBoris Utsch, Ali Kaya, Atila Ozburun, 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.
Fertility and Sterility|February 19, 2008
Neuromotor development and mental health at 5.5 years of age of singletons born at term after intracytoplasmatic sperm injection ICSI: results of a prospective controlled single-blinded study in GermanyAnnika Ludwig, Alexander Katalinic, Ute Thyen, et al.
Human Genetics|February 14, 2007
Reproduction abnormalities and twin pregnancies in parents of sporadic patients with oculo-auriculo-vertebral spectrum/Goldenhar syndromeDagmar Wieczorek, Michael Ludwig, Stefan Boehringer, et al.
Kidney & Blood Pressure Research|July 30, 2003
Four additional CLCN5 exons encode a widely expressed novel long CLC-5 isoform but fail to explain Dent's phenotype in patients without mutations in the short variantMichael Ludwig, Siegfried Waldegger, Matti Nuutinen, et al.
Fertility and Sterility|March 7, 2003
Sperm to zona pellucida binding depends on the use of a gonadotropin-releasing hormone agonist or a gonadotropin-releasing hormone antagonistAnnika K Schröder, Beate Schöpper, Safaa Al-Hasani, 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.
Clinical Nutrition ESPEN|May 14, 2025
Fasting orders and malnutrition risk in hospitals: The impact of mandatory fasting on hunger perception in nutritionally at-risk patientsTrixi Braasch, Ildiko Hoffmann, Ulrich Wesemann, et al.
Pageof 24