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Journal of Inherited Metabolic Disease
|
February 15, 2019
Neurometabolic Hereditary Diseases of Adults
Georg F Hoffmann
The New England Journal of Medicine
|
June 29, 2007
Mevalonate kinase deficiency and autoinflammatory disorders
Dorothea Haas, Georg F Hoffmann
Molecular Genetics and Metabolism
|
February 17, 2010
Liver, liver cell and stem cell transplantation for the treatment of urea cycle defects
Jochen Meyburg, Georg F Hoffmann
Pediatric Nephrology (Berlin, Germany)
|
August 5, 2004
Pathophysiology, diagnosis, and treatment of methylmalonic aciduria-recent advances and new challenges
Friederike Hörster, Georg F Hoffmann
Transplantation
|
November 16, 2005
Liver transplantation for inborn errors of metabolism
Jochen Meyburg, Georg F Hoffmann
Handbook of Clinical Neurology
|
April 30, 2013
Defects in amino acid catabolism and the urea cycle
Georg F Hoffmann, Stefan Kölker
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 5, 2024
Second-tier strategies in newborn screening - potential and limitations
Gwendolyn 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 Issue
Gwendolyn 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 laws
Angela Weirich, Georg F Hoffmann
Orphanet Journal of Rare Diseases
|
May 26, 2006
Mevalonate kinase deficiencies: from mevalonic aciduria to hyperimmunoglobulinemia D syndrome
Dorothea Haas, Georg F Hoffmann
Page
of 39
Search research articles
Search
Showing results (1-10 of 381) with videos related to
Sort By:
Page
of 39
Journal of Inherited Metabolic Disease
|
February 15, 2019
Neurometabolic Hereditary Diseases of Adults
Georg F Hoffmann
The New England Journal of Medicine
|
June 29, 2007
Mevalonate kinase deficiency and autoinflammatory disorders
Dorothea Haas, Georg F Hoffmann
Molecular Genetics and Metabolism
|
February 17, 2010
Liver, liver cell and stem cell transplantation for the treatment of urea cycle defects
Jochen Meyburg, Georg F Hoffmann
Pediatric Nephrology (Berlin, Germany)
|
August 5, 2004
Pathophysiology, diagnosis, and treatment of methylmalonic aciduria-recent advances and new challenges
Friederike Hörster, Georg F Hoffmann
Transplantation
|
November 16, 2005
Liver transplantation for inborn errors of metabolism
Jochen Meyburg, Georg F Hoffmann
Handbook of Clinical Neurology
|
April 30, 2013
Defects in amino acid catabolism and the urea cycle
Georg F Hoffmann, Stefan Kölker
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
|
June 5, 2024
Second-tier strategies in newborn screening - potential and limitations
Gwendolyn 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 Issue
Gwendolyn 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 laws
Angela Weirich, Georg F Hoffmann
Orphanet Journal of Rare Diseases
|
May 26, 2006
Mevalonate kinase deficiencies: from mevalonic aciduria to hyperimmunoglobulinemia D syndrome
Dorothea Haas, Georg F Hoffmann
Page
of 39