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Child Psychiatry and Human Development
|
May 20, 2014
Health-related quality of life in adolescents with inflammatory bowel disease depends on disease activity and psychiatric comorbidity
G Engelmann, D Erhard, M Petersen, et al.
Neuropediatrics
|
August 30, 2000
Combined D-2- and L-2-hydroxyglutaric aciduria with neonatal onset encephalopathy: a third biochemical variant of 2-hydroxyglutaric aciduria?
A C Muntau, W Röschinger, A Merkenschlager, et al.
Bone Marrow Transplantation
|
August 11, 2001
Successful HLA-identical bone marrow transplantation in a patient with PNP deficiency using busulfan and fludarabine for conditioning
C F Classen, A S Schulz, M Sigl-Kraetzig, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
November 1, 1991
[Macrocephaly as the initial manifestation of glutaryl-CoA-dehydrogenase deficiency (glutaric aciduria type I)]
F K Trefz, G F Hoffmann, E Mayatepek, et al.
Neuropediatrics
|
June 15, 2006
The first case of 3-methylcrotonyl-CoA carboxylase (MCC) deficiency responsive to biotin
D Friebel, M von der Hagen, E R Baumgartner, et al.
Human Genetics
|
November 9, 2000
Mutation analysis in glycogen storage disease type 1 non-a
A R Janecke, M Lindner, M Erdel, et al.
Clinical Chemistry
|
December 10, 1999
Biochemical and molecular genetic characteristics of the severe form of tyrosine hydroxylase deficiency
C Bräutigam, G C Steenbergen-Spanjers, G F Hoffmann, et al.
Clinical Chemistry
|
September 11, 1998
Biochemical hallmarks of tyrosine hydroxylase deficiency
C Bräutigam, R A Wevers, R J Jansen, et al.
Journal of Inherited Metabolic Disease
|
October 25, 2008
Tetrahydrobiopterin deficiency in human rabies
R E Willoughby, T Opladen, T Maier, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Macrocephaly: an important indication for organic acid analysis
G F Hoffmann, F K Trefz, P G Barth, et al.
Page
of 22
Search research articles
Search
Showing results (161-170 of 214) with videos related to
Sort By:
Page
of 22
Child Psychiatry and Human Development
|
May 20, 2014
Health-related quality of life in adolescents with inflammatory bowel disease depends on disease activity and psychiatric comorbidity
G Engelmann, D Erhard, M Petersen, et al.
Neuropediatrics
|
August 30, 2000
Combined D-2- and L-2-hydroxyglutaric aciduria with neonatal onset encephalopathy: a third biochemical variant of 2-hydroxyglutaric aciduria?
A C Muntau, W Röschinger, A Merkenschlager, et al.
Bone Marrow Transplantation
|
August 11, 2001
Successful HLA-identical bone marrow transplantation in a patient with PNP deficiency using busulfan and fludarabine for conditioning
C F Classen, A S Schulz, M Sigl-Kraetzig, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
November 1, 1991
[Macrocephaly as the initial manifestation of glutaryl-CoA-dehydrogenase deficiency (glutaric aciduria type I)]
F K Trefz, G F Hoffmann, E Mayatepek, et al.
Neuropediatrics
|
June 15, 2006
The first case of 3-methylcrotonyl-CoA carboxylase (MCC) deficiency responsive to biotin
D Friebel, M von der Hagen, E R Baumgartner, et al.
Human Genetics
|
November 9, 2000
Mutation analysis in glycogen storage disease type 1 non-a
A R Janecke, M Lindner, M Erdel, et al.
Clinical Chemistry
|
December 10, 1999
Biochemical and molecular genetic characteristics of the severe form of tyrosine hydroxylase deficiency
C Bräutigam, G C Steenbergen-Spanjers, G F Hoffmann, et al.
Clinical Chemistry
|
September 11, 1998
Biochemical hallmarks of tyrosine hydroxylase deficiency
C Bräutigam, R A Wevers, R J Jansen, et al.
Journal of Inherited Metabolic Disease
|
October 25, 2008
Tetrahydrobiopterin deficiency in human rabies
R E Willoughby, T Opladen, T Maier, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Macrocephaly: an important indication for organic acid analysis
G F Hoffmann, F K Trefz, P G Barth, et al.
Page
of 22