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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 Diet
Sibylle 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 matriptase
Lasse 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 trends
Ivana 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 Registry
Ivana 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 dysplasia
Cho-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 trial
Markus 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 dysplasia
Cho-Ming Chao, Faady Yahya, Alena Moiseenko, et al.
Human Molecular Genetics
|
September 12, 2015
Reduced sodium/proton exchanger NHE3 activity causes congenital sodium diarrhea
Andreas 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 Workshop
Mark Gilger, Bruce Hamaker, Buford L Nichols, et al.
Nature Genetics
|
August 20, 2013
Variants in CPA1 are strongly associated with early onset chronic pancreatitis
Heiko Witt, Sebastian Beer, Jonas Rosendahl, et al.
Page
of 16
Search research articles
Search
Showing results (141-150 of 151) with videos related to
Sort By:
Page
of 16
Journal of Pediatric Gastroenterology and Nutrition
|
May 11, 2017
No Need for Routine Endoscopy in Children With Celiac Disease on a Gluten-free Diet
Sibylle 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 matriptase
Lasse 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 trends
Ivana 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 Registry
Ivana 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 dysplasia
Cho-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 trial
Markus 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 dysplasia
Cho-Ming Chao, Faady Yahya, Alena Moiseenko, et al.
Human Molecular Genetics
|
September 12, 2015
Reduced sodium/proton exchanger NHE3 activity causes congenital sodium diarrhea
Andreas 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 Workshop
Mark Gilger, Bruce Hamaker, Buford L Nichols, et al.
Nature Genetics
|
August 20, 2013
Variants in CPA1 are strongly associated with early onset chronic pancreatitis
Heiko Witt, Sebastian Beer, Jonas Rosendahl, et al.
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of 16