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Dominic Lenz

Showing results (1-10 of 38) with videos related to

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Plos One|July 8, 2021
The drug development pipeline for glioblastoma-A cross sectional assessment of the FDA Orphan Drug Product designation databasePascal Johann, Dominic Lenz, Markus Ries
Trends in Molecular Medicine|December 10, 2022
Common mechanisms in pediatric acute liver failureJake P Mann, Dominic Lenz, Zania Stamataki, et al.
Journal of Inherited Metabolic Disease|January 27, 2024
Disorders of vesicular trafficking presenting with recurrent acute liver failure: NBAS, RINT1, and SCYL1 deficiencyBianca Peters, Tal Dattner, Lea D Schlieben, et al.
JIMD Reports|May 8, 2023
Pregnancy, delivery, and postpartum period in infantile liver failure syndrome type 2 due to variants in <i>NBAS</i>Bianca Peters, Felix Wiemers, Dominic Lenz, et al.
Malaria Journal|July 20, 2011
Assessment of LED fluorescence microscopy for the diagnosis of Plasmodium falciparum infections in GabonDominic Lenz, Peter G Kremsner, Bertrand Lell, et al.
Frontiers in Pediatrics|March 6, 2024
Distinct neonatal hyperammonemia and liver synthesis dysfunction: case report of a severe MEGDHEL syndromeIna Kirchberg, Elke Lainka, Andrea Gangfuß, et al.
Stem Cell Research|April 9, 2019
Generation of an induced pluripotent stem cell (iPSC) line, DHMCi005-A, from a patient with CALFAN syndrome due to mutations in SCYL1Dominic Lenz, Christian Staufner, Selina Wächter, et al.
Stem Cell Research|February 18, 2019
Generation of an iPSC line from a patient with infantile liver failure syndrome 2 due to mutations in NBAS: DHMCi004-ADominic Lenz, Christian Staufner, Selina Wächter, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|May 13, 2022
Severe acute hepatitis and acute liver failure of unknown origin in children: a questionnaire-based study within 34 paediatric liver centres in 22 European countries and Israel, April 2022Ruben H de Kleine, Willem S Lexmond, Gustav Buescher, et al.
Molecular Genetics and Metabolism|March 10, 2026
Transaldolase deficiency - natural disease course towards adulthoodViktoria Bea Horvath, Konstantinos Tsiakas, Heiko Brennenstuhl, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
Plos One|July 8, 2021
The drug development pipeline for glioblastoma-A cross sectional assessment of the FDA Orphan Drug Product designation databasePascal Johann, Dominic Lenz, Markus Ries
Trends in Molecular Medicine|December 10, 2022
Common mechanisms in pediatric acute liver failureJake P Mann, Dominic Lenz, Zania Stamataki, et al.
Journal of Inherited Metabolic Disease|January 27, 2024
Disorders of vesicular trafficking presenting with recurrent acute liver failure: NBAS, RINT1, and SCYL1 deficiencyBianca Peters, Tal Dattner, Lea D Schlieben, et al.
JIMD Reports|May 8, 2023
Pregnancy, delivery, and postpartum period in infantile liver failure syndrome type 2 due to variants in <i>NBAS</i>Bianca Peters, Felix Wiemers, Dominic Lenz, et al.
Malaria Journal|July 20, 2011
Assessment of LED fluorescence microscopy for the diagnosis of Plasmodium falciparum infections in GabonDominic Lenz, Peter G Kremsner, Bertrand Lell, et al.
Frontiers in Pediatrics|March 6, 2024
Distinct neonatal hyperammonemia and liver synthesis dysfunction: case report of a severe MEGDHEL syndromeIna Kirchberg, Elke Lainka, Andrea Gangfuß, et al.
Stem Cell Research|April 9, 2019
Generation of an induced pluripotent stem cell (iPSC) line, DHMCi005-A, from a patient with CALFAN syndrome due to mutations in SCYL1Dominic Lenz, Christian Staufner, Selina Wächter, et al.
Stem Cell Research|February 18, 2019
Generation of an iPSC line from a patient with infantile liver failure syndrome 2 due to mutations in NBAS: DHMCi004-ADominic Lenz, Christian Staufner, Selina Wächter, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|May 13, 2022
Severe acute hepatitis and acute liver failure of unknown origin in children: a questionnaire-based study within 34 paediatric liver centres in 22 European countries and Israel, April 2022Ruben H de Kleine, Willem S Lexmond, Gustav Buescher, et al.
Molecular Genetics and Metabolism|March 10, 2026
Transaldolase deficiency - natural disease course towards adulthoodViktoria Bea Horvath, Konstantinos Tsiakas, Heiko Brennenstuhl, et al.
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