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European Journal of Pediatrics
|
August 1, 1997
Assessment of energy expenditure in metabolic disorders
O A Bodamer, G F Hoffmann, G H Visser, et al.
Journal of Chromatography
|
July 23, 1993
Quantitative organic acid analysis in cerebrospinal fluid and plasma: reference values in a pediatric population
G F Hoffmann, C K Seppel, B Holmes, et al.
The Journal of Pediatrics
|
June 1, 1986
Fetal growth, major malformations, and minor anomalies in infants born to women receiving valproic acid
E Jäger-Roman, A Deichl, S Jakob, et al.
Pediatric Research
|
February 1, 1997
Hypoparathyroidism and deafness associated with pleioplasmic large scale rearrangements of the mitochondrial DNA: a clinical and molecular genetic study of four children with Kearns-Sayre syndrome
E Wilichowski, A Grüters, K Kruse, et al.
Journal of Inherited Metabolic Disease
|
July 13, 2004
Sedation with 4-hydroxybutyric acid: a potential pitfall in the diagnosis of SSADH deficiency
N I Wolf, D Haas, G F Hoffmann, 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.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
February 2, 2006
Intraoperative MRI for interventional neurosurgical procedures and tumor resection control in children
Paul Kremer, V Tronnier, H H Steiner, 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.
Klinische Padiatrie
|
July 21, 2005
[Optimizing epilepsy therapy in children and adolescents with lamotrigine]
H Siemes, U Brandl, C Helmstädter, et al.
The Journal of Pediatrics
|
December 5, 1997
Creatine deficiency syndrome caused by guanidinoacetate methyltransferase deficiency: diagnostic tools for a new inborn error of metabolism
A Schulze, T Hess, R Wevers, et al.
Page
of 10
Search research articles
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Showing results (81-90 of 96) with videos related to
Sort By:
Page
of 10
European Journal of Pediatrics
|
August 1, 1997
Assessment of energy expenditure in metabolic disorders
O A Bodamer, G F Hoffmann, G H Visser, et al.
Journal of Chromatography
|
July 23, 1993
Quantitative organic acid analysis in cerebrospinal fluid and plasma: reference values in a pediatric population
G F Hoffmann, C K Seppel, B Holmes, et al.
The Journal of Pediatrics
|
June 1, 1986
Fetal growth, major malformations, and minor anomalies in infants born to women receiving valproic acid
E Jäger-Roman, A Deichl, S Jakob, et al.
Pediatric Research
|
February 1, 1997
Hypoparathyroidism and deafness associated with pleioplasmic large scale rearrangements of the mitochondrial DNA: a clinical and molecular genetic study of four children with Kearns-Sayre syndrome
E Wilichowski, A Grüters, K Kruse, et al.
Journal of Inherited Metabolic Disease
|
July 13, 2004
Sedation with 4-hydroxybutyric acid: a potential pitfall in the diagnosis of SSADH deficiency
N I Wolf, D Haas, G F Hoffmann, 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.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
February 2, 2006
Intraoperative MRI for interventional neurosurgical procedures and tumor resection control in children
Paul Kremer, V Tronnier, H H Steiner, 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.
Klinische Padiatrie
|
July 21, 2005
[Optimizing epilepsy therapy in children and adolescents with lamotrigine]
H Siemes, U Brandl, C Helmstädter, et al.
The Journal of Pediatrics
|
December 5, 1997
Creatine deficiency syndrome caused by guanidinoacetate methyltransferase deficiency: diagnostic tools for a new inborn error of metabolism
A Schulze, T Hess, R Wevers, et al.
Page
of 10