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Georg F Hoffmann

Showing results (1-10 of 381) with videos related to

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Journal of Inherited Metabolic Disease|February 15, 2019
Neurometabolic Hereditary Diseases of AdultsGeorg F Hoffmann
The New England Journal of Medicine|June 29, 2007
Mevalonate kinase deficiency and autoinflammatory disordersDorothea Haas, Georg F Hoffmann
Molecular Genetics and Metabolism|February 17, 2010
Liver, liver cell and stem cell transplantation for the treatment of urea cycle defectsJochen Meyburg, Georg F Hoffmann
Pediatric Nephrology (Berlin, Germany)|August 5, 2004
Pathophysiology, diagnosis, and treatment of methylmalonic aciduria-recent advances and new challengesFriederike Hörster, Georg F Hoffmann
Transplantation|November 16, 2005
Liver transplantation for inborn errors of metabolismJochen Meyburg, Georg F Hoffmann
Handbook of Clinical Neurology|April 30, 2013
Defects in amino acid catabolism and the urea cycleGeorg F Hoffmann, Stefan Kölker
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Second-tier strategies in newborn screening - potential and limitationsGwendolyn Gramer, Georg F Hoffmann
Current Medical Science|October 30, 2020
Vitamin B<sub>12</sub> Deficiency in Newborns and their Mothers-Novel Approaches to Early Detection, Treatment and Prevention of a Global Health IssueGwendolyn Gramer, Georg F Hoffmann
European Journal of Pediatrics|June 3, 2005
Ernst Moro (1874-1951)--a great pediatric career started at the rise of university-based pediatric research but was curtailed in the shadows of Nazi lawsAngela Weirich, Georg F Hoffmann
Orphanet Journal of Rare Diseases|May 26, 2006
Mevalonate kinase deficiencies: from mevalonic aciduria to hyperimmunoglobulinemia D syndromeDorothea Haas, Georg F Hoffmann
Pageof 39

Showing results (1-10 of 381) with videos related to

Sort By:
Pageof 39
Journal of Inherited Metabolic Disease|February 15, 2019
Neurometabolic Hereditary Diseases of AdultsGeorg F Hoffmann
The New England Journal of Medicine|June 29, 2007
Mevalonate kinase deficiency and autoinflammatory disordersDorothea Haas, Georg F Hoffmann
Molecular Genetics and Metabolism|February 17, 2010
Liver, liver cell and stem cell transplantation for the treatment of urea cycle defectsJochen Meyburg, Georg F Hoffmann
Pediatric Nephrology (Berlin, Germany)|August 5, 2004
Pathophysiology, diagnosis, and treatment of methylmalonic aciduria-recent advances and new challengesFriederike Hörster, Georg F Hoffmann
Transplantation|November 16, 2005
Liver transplantation for inborn errors of metabolismJochen Meyburg, Georg F Hoffmann
Handbook of Clinical Neurology|April 30, 2013
Defects in amino acid catabolism and the urea cycleGeorg F Hoffmann, Stefan Kölker
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Second-tier strategies in newborn screening - potential and limitationsGwendolyn Gramer, Georg F Hoffmann
Current Medical Science|October 30, 2020
Vitamin B<sub>12</sub> Deficiency in Newborns and their Mothers-Novel Approaches to Early Detection, Treatment and Prevention of a Global Health IssueGwendolyn Gramer, Georg F Hoffmann
European Journal of Pediatrics|June 3, 2005
Ernst Moro (1874-1951)--a great pediatric career started at the rise of university-based pediatric research but was curtailed in the shadows of Nazi lawsAngela Weirich, Georg F Hoffmann
Orphanet Journal of Rare Diseases|May 26, 2006
Mevalonate kinase deficiencies: from mevalonic aciduria to hyperimmunoglobulinemia D syndromeDorothea Haas, Georg F Hoffmann
Pageof 39