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Andreas Entenmann

Showing results (31-40 of 38) with videos related to

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Scientific Reports|June 4, 2020
Targeted metabolomic analysis of serum amino acids in the adult Fontan patient with a dominant left ventricleMiriam Michel, Karl-Otto Dubowy, Andreas Entenmann, et al.
Pediatric Transplantation|June 29, 2021
Influence of early biliary complications on survival rates after pediatric liver transplantation-A positive outlookValeria Berchtold, Franka Messner, Annemarie Weissenbacher, et al.
Therapeutic Advances in Chronic Disease|May 20, 2020
Targeted metabolomic analysis of serum phospholipid and acylcarnitine in the adult Fontan patient with a dominant left ventricleMiriam Michel, Karl-Otto Dubowy, Manuela Zlamy, 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.
Zeitschrift Fur Gastroenterologie|February 11, 2026
[Use of teduglutide in short bowel syndrome in infants, children and adolescents: Position paper of the working group "Chronic intestinal failure" of the Society for Paediatric Gastroenterology and Nutrition (GPGE)]Carsten Posovszky, Jan de Laffolie, Stephan Henning, et al.
Human Mutation|February 10, 2017
Deficiency of the sphingosine-1-phosphate lyase SGPL1 is associated with congenital nephrotic syndrome and congenital adrenal calcificationsAndreas R Janecke, Ruijuan Xu, Elisabeth Steichen-Gersdorf, et al.
International Journal of Hyperthermia : the Official Journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group|September 21, 2020
Stereotactic radiofrequency ablation of a variety of liver masses in childrenBenjamin Hetzer, Georg-Friedrich Vogel, Andreas Entenmann, et al.
American Journal of Human Genetics|July 19, 2016
Biallelic IARS Mutations Cause Growth Retardation with Prenatal Onset, Intellectual Disability, Muscular Hypotonia, and Infantile HepatopathyRobert Kopajtich, Kei Murayama, Andreas R Janecke, et al.
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Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Scientific Reports|June 4, 2020
Targeted metabolomic analysis of serum amino acids in the adult Fontan patient with a dominant left ventricleMiriam Michel, Karl-Otto Dubowy, Andreas Entenmann, et al.
Pediatric Transplantation|June 29, 2021
Influence of early biliary complications on survival rates after pediatric liver transplantation-A positive outlookValeria Berchtold, Franka Messner, Annemarie Weissenbacher, et al.
Therapeutic Advances in Chronic Disease|May 20, 2020
Targeted metabolomic analysis of serum phospholipid and acylcarnitine in the adult Fontan patient with a dominant left ventricleMiriam Michel, Karl-Otto Dubowy, Manuela Zlamy, 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.
Zeitschrift Fur Gastroenterologie|February 11, 2026
[Use of teduglutide in short bowel syndrome in infants, children and adolescents: Position paper of the working group "Chronic intestinal failure" of the Society for Paediatric Gastroenterology and Nutrition (GPGE)]Carsten Posovszky, Jan de Laffolie, Stephan Henning, et al.
Human Mutation|February 10, 2017
Deficiency of the sphingosine-1-phosphate lyase SGPL1 is associated with congenital nephrotic syndrome and congenital adrenal calcificationsAndreas R Janecke, Ruijuan Xu, Elisabeth Steichen-Gersdorf, et al.
International Journal of Hyperthermia : the Official Journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group|September 21, 2020
Stereotactic radiofrequency ablation of a variety of liver masses in childrenBenjamin Hetzer, Georg-Friedrich Vogel, Andreas Entenmann, et al.
American Journal of Human Genetics|July 19, 2016
Biallelic IARS Mutations Cause Growth Retardation with Prenatal Onset, Intellectual Disability, Muscular Hypotonia, and Infantile HepatopathyRobert Kopajtich, Kei Murayama, Andreas R Janecke, et al.
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