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Georg F Hoffmann

Showing results (21-30 of 381) with videos related to

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The New England Journal of Medicine|March 10, 2006
Congenital glutamine deficiency with glutamine synthetase mutationsStefan Kölker, Georg F Hoffmann, Jürgen G Okun
Journal of Inherited Metabolic Disease|March 20, 2021
Genomic newborn screening: Proposal of a two-stage approachChristian P Schaaf, Stefan Kölker, Georg F Hoffmann
International Journal of Food Sciences and Nutrition|October 24, 2008
Vitamin D deficiency in healthy children in a sunny country: associated factorsAbdulbari Bener, Mariam Al-Ali, Georg F Hoffmann
Molecular Genetics and Metabolism Reports|March 18, 2021
Maternal vitamin deficiency mimicking multiple acyl-CoA dehydrogenase deficiency on newborn screeningGwendolyn Gramer, Georg F Hoffmann, Julia B Hennermann
Molecular Genetics and Metabolism|April 1, 2019
Clinical and biochemical footprints of inherited metabolic diseases. I. Movement disordersCarlos R Ferreira, Georg F Hoffmann, Nenad Blau
Journal of Inherited Metabolic Disease|February 15, 2014
50 years of newborn screeningGeorg F Hoffmann, Martin Lindner, J Gerard Loeber
Deutsches Arzteblatt International|December 10, 2009
Principles of pediatric emergency careJochen Meyburg, Michael Bernhard, Georg F Hoffmann, et al.
American Journal of Medical Genetics. Part A|March 28, 2013
Prenatal presentation and diagnostic evaluation of suspected Smith-Lemli-Opitz (RSH) syndromeDorothea Haas, Gisela Haege, Georg F Hoffmann, et al.
BMJ Open|July 18, 2018
Publication status of completed registered studies in paediatric appendicitis: a cross-sectional analysisThomas Breil, Michael Boettcher, Georg F Hoffmann, et al.
Molecular Genetics and Metabolism|November 28, 2017
DNAJC12 deficiency: A new strategy in the diagnosis of hyperphenylalaninemiasNenad Blau, Aurora Martinez, Georg F Hoffmann, et al.
Pageof 39

Showing results (21-30 of 381) with videos related to

Sort By:
Pageof 39
The New England Journal of Medicine|March 10, 2006
Congenital glutamine deficiency with glutamine synthetase mutationsStefan Kölker, Georg F Hoffmann, Jürgen G Okun
Journal of Inherited Metabolic Disease|March 20, 2021
Genomic newborn screening: Proposal of a two-stage approachChristian P Schaaf, Stefan Kölker, Georg F Hoffmann
International Journal of Food Sciences and Nutrition|October 24, 2008
Vitamin D deficiency in healthy children in a sunny country: associated factorsAbdulbari Bener, Mariam Al-Ali, Georg F Hoffmann
Molecular Genetics and Metabolism Reports|March 18, 2021
Maternal vitamin deficiency mimicking multiple acyl-CoA dehydrogenase deficiency on newborn screeningGwendolyn Gramer, Georg F Hoffmann, Julia B Hennermann
Molecular Genetics and Metabolism|April 1, 2019
Clinical and biochemical footprints of inherited metabolic diseases. I. Movement disordersCarlos R Ferreira, Georg F Hoffmann, Nenad Blau
Journal of Inherited Metabolic Disease|February 15, 2014
50 years of newborn screeningGeorg F Hoffmann, Martin Lindner, J Gerard Loeber
Deutsches Arzteblatt International|December 10, 2009
Principles of pediatric emergency careJochen Meyburg, Michael Bernhard, Georg F Hoffmann, et al.
American Journal of Medical Genetics. Part A|March 28, 2013
Prenatal presentation and diagnostic evaluation of suspected Smith-Lemli-Opitz (RSH) syndromeDorothea Haas, Gisela Haege, Georg F Hoffmann, et al.
BMJ Open|July 18, 2018
Publication status of completed registered studies in paediatric appendicitis: a cross-sectional analysisThomas Breil, Michael Boettcher, Georg F Hoffmann, et al.
Molecular Genetics and Metabolism|November 28, 2017
DNAJC12 deficiency: A new strategy in the diagnosis of hyperphenylalaninemiasNenad Blau, Aurora Martinez, Georg F Hoffmann, et al.
Pageof 39