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Georg F Hoffmann

Showing results (221-230 of 381) with videos related to

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Klinische Padiatrie|September 25, 2023
High Throughput Newborn Screening for Sickle Cell Disease - Application of Two-Tiered Testing with a qPCR-Based Primary screenJoachim Janda, Sebastian Hegert, Jessica Bzdok, et al.
American Journal of Physiology. Renal Physiology|March 8, 2018
Endothelial progenitor cells accelerate endothelial regeneration in an in vitro model of Shigatoxin-2a-induced injury via soluble growth factorsChristian Patry, Christian Betzen, Farnoosh Fathalizadeh, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 26, 2010
Anserine inhibits carnosine degradation but in human serum carnosinase (CN1) is not correlated with histidine dipeptide concentrationVerena Peters, Erwin E W Jansen, Cornelis Jakobs, et al.
Amino Acids|June 18, 2015
Carnosine metabolism in diabetes is altered by reactive metabolitesVerena Peters, Barbara Lanthaler, Albert Amberger, et al.
Orphanet Journal of Rare Diseases|August 20, 2016
Clinical course of 63 patients with neonatal onset urea cycle disorders in the years 2001-2013Caroline Unsinn, Anibh Das, Vassili Valayannopoulos, et al.
Molecular Genetics and Metabolism|September 19, 2024
Severity-adjusted evaluation of initial dialysis on short-term health outcomes in urea cycle disordersMatthias Zielonka, Stefan Kölker, Sven F Garbade, et al.
Molecular Genetics and Metabolism|February 1, 2024
Impact of supplementation with L-citrulline/arginine after liver transplantation in individuals with Urea Cycle DisordersRoland Posset, Sven F Garbade, Florian Gleich, et al.
JIMD Reports|June 21, 2018
A Homozygous Splice Site Mutation in SLC25A42, Encoding the Mitochondrial Transporter of Coenzyme A, Causes Metabolic Crises and Epileptic EncephalopathyArcangela Iuso, Bader Alhaddad, Corina Weigel, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 10, 2016
CNDP1 genotype and renal survival in pediatric nephropathiesVerena Peters, Moustafa Kebbewar, Bart Janssen, et al.
Pediatric Research|September 27, 2005
Quantitative acylcarnitine profiling in peripheral blood mononuclear cells using in vitro loading with palmitic and 2-oxoadipic acids: biochemical confirmation of fatty acid oxidation and organic acid disordersAndrea Schulze-Bergkamen, Jürgen G Okun, Ute Spiekerkötter, et al.
Pageof 39

Showing results (221-230 of 381) with videos related to

Sort By:
Pageof 39
Klinische Padiatrie|September 25, 2023
High Throughput Newborn Screening for Sickle Cell Disease - Application of Two-Tiered Testing with a qPCR-Based Primary screenJoachim Janda, Sebastian Hegert, Jessica Bzdok, et al.
American Journal of Physiology. Renal Physiology|March 8, 2018
Endothelial progenitor cells accelerate endothelial regeneration in an in vitro model of Shigatoxin-2a-induced injury via soluble growth factorsChristian Patry, Christian Betzen, Farnoosh Fathalizadeh, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 26, 2010
Anserine inhibits carnosine degradation but in human serum carnosinase (CN1) is not correlated with histidine dipeptide concentrationVerena Peters, Erwin E W Jansen, Cornelis Jakobs, et al.
Amino Acids|June 18, 2015
Carnosine metabolism in diabetes is altered by reactive metabolitesVerena Peters, Barbara Lanthaler, Albert Amberger, et al.
Orphanet Journal of Rare Diseases|August 20, 2016
Clinical course of 63 patients with neonatal onset urea cycle disorders in the years 2001-2013Caroline Unsinn, Anibh Das, Vassili Valayannopoulos, et al.
Molecular Genetics and Metabolism|September 19, 2024
Severity-adjusted evaluation of initial dialysis on short-term health outcomes in urea cycle disordersMatthias Zielonka, Stefan Kölker, Sven F Garbade, et al.
Molecular Genetics and Metabolism|February 1, 2024
Impact of supplementation with L-citrulline/arginine after liver transplantation in individuals with Urea Cycle DisordersRoland Posset, Sven F Garbade, Florian Gleich, et al.
JIMD Reports|June 21, 2018
A Homozygous Splice Site Mutation in SLC25A42, Encoding the Mitochondrial Transporter of Coenzyme A, Causes Metabolic Crises and Epileptic EncephalopathyArcangela Iuso, Bader Alhaddad, Corina Weigel, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 10, 2016
CNDP1 genotype and renal survival in pediatric nephropathiesVerena Peters, Moustafa Kebbewar, Bart Janssen, et al.
Pediatric Research|September 27, 2005
Quantitative acylcarnitine profiling in peripheral blood mononuclear cells using in vitro loading with palmitic and 2-oxoadipic acids: biochemical confirmation of fatty acid oxidation and organic acid disordersAndrea Schulze-Bergkamen, Jürgen G Okun, Ute Spiekerkötter, et al.
Pageof 39