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European Journal of Pediatrics
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October 24, 2000
PAH gene mutation analysis in clinical practice--comments on mutation analysis anticipates dietary requirements in phenylketonuria
J Zschocke, G F Hoffmann
Der Radiologe
|
May 29, 2012
[Erich von Baeyer: the turbulent life of an outstanding German-American radiologist]
A Weirich, G F Hoffmann
Journal of Inherited Metabolic Disease
|
July 17, 1999
Glutaric aciduria type I: from clinical, biochemical and molecular diversity to successful therapy
G F Hoffmann, J Zschocke
Pediatric Research
|
January 1, 1995
Leukotrienes: biosynthesis, metabolism, and pathophysiologic significance
E Mayatepek, G F Hoffmann
Journal of Inherited Metabolic Disease
|
January 1, 1994
SSIEM Award. Impaired metabolism of leukotrienes in inherited metabolic disorders
E Mayatepek, G F Hoffmann
Journal of Inherited Metabolic Disease
|
April 9, 2008
Liver cell transplantation for the treatment of inborn errors of metabolism
J Meyburg, G F Hoffmann
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 15, 1991
O-(2,3,4,5,6-pentafluorobenzyl)oxime-trimethylsilyl ester derivatives for sensitive identification and quantitation of aldehydes, ketones, and oxoacids in biological fluids
G F Hoffmann, L Sweetman
Pediatric Radiology
|
August 26, 1998
Subdural haematoma in a child with glutaric aciduria type I
M Köhler, G F Hoffmann
European Journal of Pediatrics
|
December 10, 1997
Glutaric aciduria type 1 (glutaryl-CoA-dehydrogenase deficiency): advances and unanswered questions. Report from an international meeting
A Superti-Furga, G F Hoffmann
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
December 24, 1997
MRI in Smith-Lemli-Opitz syndrome type 1
J M Penzien, G F Hoffmann
Page
of 22
Search research articles
Search
Showing results (11-20 of 214) with videos related to
Sort By:
Page
of 22
European Journal of Pediatrics
|
October 24, 2000
PAH gene mutation analysis in clinical practice--comments on mutation analysis anticipates dietary requirements in phenylketonuria
J Zschocke, G F Hoffmann
Der Radiologe
|
May 29, 2012
[Erich von Baeyer: the turbulent life of an outstanding German-American radiologist]
A Weirich, G F Hoffmann
Journal of Inherited Metabolic Disease
|
July 17, 1999
Glutaric aciduria type I: from clinical, biochemical and molecular diversity to successful therapy
G F Hoffmann, J Zschocke
Pediatric Research
|
January 1, 1995
Leukotrienes: biosynthesis, metabolism, and pathophysiologic significance
E Mayatepek, G F Hoffmann
Journal of Inherited Metabolic Disease
|
January 1, 1994
SSIEM Award. Impaired metabolism of leukotrienes in inherited metabolic disorders
E Mayatepek, G F Hoffmann
Journal of Inherited Metabolic Disease
|
April 9, 2008
Liver cell transplantation for the treatment of inborn errors of metabolism
J Meyburg, G F Hoffmann
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 15, 1991
O-(2,3,4,5,6-pentafluorobenzyl)oxime-trimethylsilyl ester derivatives for sensitive identification and quantitation of aldehydes, ketones, and oxoacids in biological fluids
G F Hoffmann, L Sweetman
Pediatric Radiology
|
August 26, 1998
Subdural haematoma in a child with glutaric aciduria type I
M Köhler, G F Hoffmann
European Journal of Pediatrics
|
December 10, 1997
Glutaric aciduria type 1 (glutaryl-CoA-dehydrogenase deficiency): advances and unanswered questions. Report from an international meeting
A Superti-Furga, G F Hoffmann
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
December 24, 1997
MRI in Smith-Lemli-Opitz syndrome type 1
J M Penzien, G F Hoffmann
Page
of 22