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Michael Ludwig

Showing results (171-180 of 239) with videos related to

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Journal of Neurochemistry|October 23, 2002
Characterization of the dehydroepiandrosterone (DHEA) metabolism via oxysterol 7alpha-hydroxylase and 17-ketosteroid reductase activity in the human brainStephan Steckelbroeck, Matthias Watzka, Dieter Lütjohann, et al.
Zeitschrift Fur Gastroenterologie|May 20, 2026
Ultrasound-Based Hepatorenal Index (HRI): Measurement Principles, Normal Values, and Clinical ApplicationNils Daum, Yi Dong, Michael Ludwig, et al.
The Journal of Steroid Biochemistry and Molecular Biology|August 29, 2003
Characterisation of estrogenic 17beta-hydroxysteroid dehydrogenase (17beta-HSD) activity in the human brainStephan Steckelbroeck, Matthias Watzka, Annette Reissinger, et al.
Clinical Nephrology|August 27, 2015
Dent disease in children: diagnostic and therapeutic considerationsMaria Szczepanska, Marcin Zaniew, Florian Recker, et al.
The Journal of Clinical Endocrinology and Metabolism|September 13, 2003
Nonsupplemented luteal phase characteristics after the administration of recombinant human chorionic gonadotropin, recombinant luteinizing hormone, or gonadotropin-releasing hormone (GnRH) agonist to induce final oocyte maturation in in vitro fertilization patients after ovarian stimulation with recombinant follicle-stimulating hormone and GnRH antagonist cotreatmentNicole G M Beckers, Nicholas S Macklon, Marinus J Eijkemans, et al.
Human Mutation|March 21, 2012
Deep intronic APC mutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposisIsabel Spier, Sukanya Horpaopan, Stefanie Vogt, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 19, 2015
Array-based molecular karyotyping in fetal brain malformations: Identification of novel candidate genes and chromosomal regionsSophia K Krutzke, Hartmut Engels, Andrea Hofmann, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 31, 2010
Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian familyHeiko Reutter, Franz Rüschendorf, Manuel Mattheisen, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 6, 2013
Candidate gene association study implicates p63 in the etiology of nonsyndromic bladder-exstrophy-epispadias complexLihong Qi, Mei Wang, Garima Yagnik, et al.
Medical Ultrasonography|January 21, 2026
Ultrasound measurements and normal values of the liver: a comprehensive review and practical guideKathleen Möller, Michael Ludwig, Christian Jenssen, et al.
Pageof 24

Showing results (171-180 of 239) with videos related to

Sort By:
Pageof 24
Journal of Neurochemistry|October 23, 2002
Characterization of the dehydroepiandrosterone (DHEA) metabolism via oxysterol 7alpha-hydroxylase and 17-ketosteroid reductase activity in the human brainStephan Steckelbroeck, Matthias Watzka, Dieter Lütjohann, et al.
Zeitschrift Fur Gastroenterologie|May 20, 2026
Ultrasound-Based Hepatorenal Index (HRI): Measurement Principles, Normal Values, and Clinical ApplicationNils Daum, Yi Dong, Michael Ludwig, et al.
The Journal of Steroid Biochemistry and Molecular Biology|August 29, 2003
Characterisation of estrogenic 17beta-hydroxysteroid dehydrogenase (17beta-HSD) activity in the human brainStephan Steckelbroeck, Matthias Watzka, Annette Reissinger, et al.
Clinical Nephrology|August 27, 2015
Dent disease in children: diagnostic and therapeutic considerationsMaria Szczepanska, Marcin Zaniew, Florian Recker, et al.
The Journal of Clinical Endocrinology and Metabolism|September 13, 2003
Nonsupplemented luteal phase characteristics after the administration of recombinant human chorionic gonadotropin, recombinant luteinizing hormone, or gonadotropin-releasing hormone (GnRH) agonist to induce final oocyte maturation in in vitro fertilization patients after ovarian stimulation with recombinant follicle-stimulating hormone and GnRH antagonist cotreatmentNicole G M Beckers, Nicholas S Macklon, Marinus J Eijkemans, et al.
Human Mutation|March 21, 2012
Deep intronic APC mutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposisIsabel Spier, Sukanya Horpaopan, Stefanie Vogt, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 19, 2015
Array-based molecular karyotyping in fetal brain malformations: Identification of novel candidate genes and chromosomal regionsSophia K Krutzke, Hartmut Engels, Andrea Hofmann, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 31, 2010
Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian familyHeiko Reutter, Franz Rüschendorf, Manuel Mattheisen, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 6, 2013
Candidate gene association study implicates p63 in the etiology of nonsyndromic bladder-exstrophy-epispadias complexLihong Qi, Mei Wang, Garima Yagnik, et al.
Medical Ultrasonography|January 21, 2026
Ultrasound measurements and normal values of the liver: a comprehensive review and practical guideKathleen Möller, Michael Ludwig, Christian Jenssen, et al.
Pageof 24