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Peter Zimmer

Showing results (141-150 of 151) with videos related to

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Journal of Pediatric Gastroenterology and Nutrition|May 11, 2017
No Need for Routine Endoscopy in Children With Celiac Disease on a Gluten-free DietSibylle Koletzko, Renata Auricchio, Jernej Dolinsek, et al.
Human Molecular Genetics|November 17, 2018
SPINT2 (HAI-2) missense variants identified in congenital sodium diarrhea/tufting enteropathy affect the ability of HAI-2 to inhibit prostasin but not matriptaseLasse Holt-Danborg, Julia Vodopiutz, Annika W Nonboe, et al.
Plos One|September 9, 2022
Current and projected incidence trends of pediatric-onset inflammatory bowel disease in Germany based on the Saxon Pediatric IBD Registry 2000-2014 -a 15-year evaluation of trendsIvana Kern, Olaf Schoffer, Thomas Richter, et al.
Plos One|January 4, 2021
Incidence trends of pediatric onset inflammatory bowel disease in the years 2000-2009 in Saxony, Germany-first results of the Saxon Pediatric IBD RegistryIvana Kern, Olaf Schoffer, Wieland Kiess, et al.
Human Molecular Genetics|December 20, 2018
Impact of Fgf10 deficiency on pulmonary vasculature formation in a mouse model of bronchopulmonary dysplasiaCho-Ming Chao, Alena Moiseenko, Djuro Kosanovic, et al.
Trials|October 1, 2020
Application of two different nasal CPAP levels for the treatment of respiratory distress syndrome in preterm infants-"The OPTTIMMAL-Trial"-Optimizing PEEP To The IMMAture Lungs: study protocol of a randomized controlled trialMarkus Waitz, Corinna Engel, Rolf Schloesser, et al.
The Journal of Pathology|October 23, 2016
Fgf10 deficiency is causative for lethality in a mouse model of bronchopulmonary dysplasiaCho-Ming Chao, Faady Yahya, Alena Moiseenko, et al.
Human Molecular Genetics|September 12, 2015
Reduced sodium/proton exchanger NHE3 activity causes congenital sodium diarrheaAndreas R Janecke, Peter Heinz-Erian, Jianyi Yin, et al.
Journal of Pediatric Gastroenterology and Nutrition|October 30, 2012
Research progress reported at the 50th Anniversary of the Discovery of Congenital Sucrase-Isomaltase Deficiency WorkshopMark Gilger, Bruce Hamaker, Buford L Nichols, et al.
Nature Genetics|August 20, 2013
Variants in CPA1 are strongly associated with early onset chronic pancreatitisHeiko Witt, Sebastian Beer, Jonas Rosendahl, et al.
Pageof 16

Showing results (141-150 of 151) with videos related to

Sort By:
Pageof 16
Journal of Pediatric Gastroenterology and Nutrition|May 11, 2017
No Need for Routine Endoscopy in Children With Celiac Disease on a Gluten-free DietSibylle Koletzko, Renata Auricchio, Jernej Dolinsek, et al.
Human Molecular Genetics|November 17, 2018
SPINT2 (HAI-2) missense variants identified in congenital sodium diarrhea/tufting enteropathy affect the ability of HAI-2 to inhibit prostasin but not matriptaseLasse Holt-Danborg, Julia Vodopiutz, Annika W Nonboe, et al.
Plos One|September 9, 2022
Current and projected incidence trends of pediatric-onset inflammatory bowel disease in Germany based on the Saxon Pediatric IBD Registry 2000-2014 -a 15-year evaluation of trendsIvana Kern, Olaf Schoffer, Thomas Richter, et al.
Plos One|January 4, 2021
Incidence trends of pediatric onset inflammatory bowel disease in the years 2000-2009 in Saxony, Germany-first results of the Saxon Pediatric IBD RegistryIvana Kern, Olaf Schoffer, Wieland Kiess, et al.
Human Molecular Genetics|December 20, 2018
Impact of Fgf10 deficiency on pulmonary vasculature formation in a mouse model of bronchopulmonary dysplasiaCho-Ming Chao, Alena Moiseenko, Djuro Kosanovic, et al.
Trials|October 1, 2020
Application of two different nasal CPAP levels for the treatment of respiratory distress syndrome in preterm infants-"The OPTTIMMAL-Trial"-Optimizing PEEP To The IMMAture Lungs: study protocol of a randomized controlled trialMarkus Waitz, Corinna Engel, Rolf Schloesser, et al.
The Journal of Pathology|October 23, 2016
Fgf10 deficiency is causative for lethality in a mouse model of bronchopulmonary dysplasiaCho-Ming Chao, Faady Yahya, Alena Moiseenko, et al.
Human Molecular Genetics|September 12, 2015
Reduced sodium/proton exchanger NHE3 activity causes congenital sodium diarrheaAndreas R Janecke, Peter Heinz-Erian, Jianyi Yin, et al.
Journal of Pediatric Gastroenterology and Nutrition|October 30, 2012
Research progress reported at the 50th Anniversary of the Discovery of Congenital Sucrase-Isomaltase Deficiency WorkshopMark Gilger, Bruce Hamaker, Buford L Nichols, et al.
Nature Genetics|August 20, 2013
Variants in CPA1 are strongly associated with early onset chronic pancreatitisHeiko Witt, Sebastian Beer, Jonas Rosendahl, et al.
Pageof 16