Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Michael Ludwig

Showing results (71-80 of 239) with videos related to

Pageof 24
Sort By:
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 9, 2005
CLCN5 mutation (R347X) associated with hypokalaemic metabolic alkalosis in a Turkish child: an unusual presentation of Dent's diseaseNesrin Besbas, Fatih Ozaltin, Nikola Jeck, et al.
Journal of Pediatric Genetics|August 11, 2017
Role of the LF-SINE-Derived Distal <i>ISL1</i> Enhancer in Patients with Classic Bladder ExstrophyRong Zhang, Michael Knapp, Franziska Kause, et al.
European Journal of Human Genetics : EJHG|October 23, 2008
Low frequency of imprinting defects in ICSI children born small for gestational ageDeniz Kanber, Karin Buiting, Michael Zeschnigk, et al.
Orphanet Journal of Rare Diseases|November 3, 2009
The exstrophy-epispadias complexAnne-Karoline Ebert, Heiko Reutter, Michael Ludwig, et al.
Journal of Microscopy|December 14, 2021
Reconstruction of calcium silicate hydrates using multiple 2D and 3D imaging techniques: Light microscopy, μ-CT, SEM, FIB-nT combined with EDXFlorian Kleiner, Christiane Rößler, Franziska Vogt, et al.
Collegium Antropologicum|November 8, 2011
A boy with Dent-2 diseaseKristina Vrljicak, Danica Batinić, Danko Milosević, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|June 22, 2016
Liddle syndrome in a Turkish family with heterogeneous phenotypesBahar Büyükkaragöz, Aysun Caltik Yilmaz, Deniz Karcaaltincaba, et al.
Pediatric Nephrology (Berlin, Germany)|May 16, 2009
Vitamin A responsive night blindness in Dent's diseaseSidharth Kumar Sethi, Michael Ludwig, Madhulika Kabra, et al.
Journal of Agricultural and Food Chemistry|September 30, 2008
Influence of processing on quality parameters of strawberriesAnnetta Hartmann, Claus-Dieter Patz, Wilfried Andlauer, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|September 13, 2003
Unilateral follicular aspiration and in-vitro maturation before contralateral oocyte retrieval: a method to prevent ovarian hyperstimulation syndromeAnnika K Schröder, Beate Schöpper, Saafa Al-Hasani, et al.
Pageof 24

Showing results (71-80 of 239) with videos related to

Sort By:
Pageof 24
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 9, 2005
CLCN5 mutation (R347X) associated with hypokalaemic metabolic alkalosis in a Turkish child: an unusual presentation of Dent's diseaseNesrin Besbas, Fatih Ozaltin, Nikola Jeck, et al.
Journal of Pediatric Genetics|August 11, 2017
Role of the LF-SINE-Derived Distal <i>ISL1</i> Enhancer in Patients with Classic Bladder ExstrophyRong Zhang, Michael Knapp, Franziska Kause, et al.
European Journal of Human Genetics : EJHG|October 23, 2008
Low frequency of imprinting defects in ICSI children born small for gestational ageDeniz Kanber, Karin Buiting, Michael Zeschnigk, et al.
Orphanet Journal of Rare Diseases|November 3, 2009
The exstrophy-epispadias complexAnne-Karoline Ebert, Heiko Reutter, Michael Ludwig, et al.
Journal of Microscopy|December 14, 2021
Reconstruction of calcium silicate hydrates using multiple 2D and 3D imaging techniques: Light microscopy, μ-CT, SEM, FIB-nT combined with EDXFlorian Kleiner, Christiane Rößler, Franziska Vogt, et al.
Collegium Antropologicum|November 8, 2011
A boy with Dent-2 diseaseKristina Vrljicak, Danica Batinić, Danko Milosević, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|June 22, 2016
Liddle syndrome in a Turkish family with heterogeneous phenotypesBahar Büyükkaragöz, Aysun Caltik Yilmaz, Deniz Karcaaltincaba, et al.
Pediatric Nephrology (Berlin, Germany)|May 16, 2009
Vitamin A responsive night blindness in Dent's diseaseSidharth Kumar Sethi, Michael Ludwig, Madhulika Kabra, et al.
Journal of Agricultural and Food Chemistry|September 30, 2008
Influence of processing on quality parameters of strawberriesAnnetta Hartmann, Claus-Dieter Patz, Wilfried Andlauer, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|September 13, 2003
Unilateral follicular aspiration and in-vitro maturation before contralateral oocyte retrieval: a method to prevent ovarian hyperstimulation syndromeAnnika K Schröder, Beate Schöpper, Saafa Al-Hasani, et al.
Pageof 24