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Archives of Disease in Childhood
|
June 12, 1998
Abuse or metabolic disorder?
G F Hoffmann, E R Naughten
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
May 21, 2010
Early onset epilepsy and inherited metabolic disorders: diagnosis and management
Asuri N Prasad, G F Hoffmann
Croatian Medical Journal
|
July 27, 2001
Inborn errors of metabolism at the turn of the millennium
I Barić, K Fumić, G F Hoffmann
Journal of Inherited Metabolic Disease
|
November 5, 1997
Enhanced excretion of urinary leukotriene E4 in mevalonic aciduria is not caused by an impaired peroxisomal degradation of cysteinyl leukotrienes
E Mayatepek, B Tiepelmann, G F Hoffmann
Journal of Inherited Metabolic Disease
|
May 4, 2005
Disorders of intermediary metabolism: toxic leukoencephalopathies
F Hörster, R Surtees, G F Hoffmann
Neuropediatrics
|
January 22, 2003
White matter disease in cerebral organic acid disorders: clinical implications and suggested pathomechanisms
S Kölker, E Mayatepek, G F Hoffmann
Journal of Inherited Metabolic Disease
|
April 8, 2006
Acrodermatitis acidaemia secondary to 'overtreatment' and protein deficiency
G F Hoffmann, R Happle, S Kölker
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 25, 2000
Analysis of leukotrienes in cerebrospinal fluid of a reference population and patients with inborn errors of metabolism: further evidence for a pathognomonic profile in LTC(4)-synthesis deficiency
E Mayatepek, R Zelezny, G F Hoffmann
Journal of Inherited Metabolic Disease
|
December 22, 1999
Urinary excretion of Krebs cycle metabolites in a 13-year-old girl
J Zschocke, G Koch, G F Hoffmann
Journal of Inherited Metabolic Disease
|
August 1, 1998
D-2-hydroxyglutaric aciduria: evidence of clinical and biochemical heterogeneity
L Wagner, G F Hoffmann, C Jakobs
Page
of 22
Search research articles
Search
Showing results (21-30 of 214) with videos related to
Sort By:
Page
of 22
Archives of Disease in Childhood
|
June 12, 1998
Abuse or metabolic disorder?
G F Hoffmann, E R Naughten
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
May 21, 2010
Early onset epilepsy and inherited metabolic disorders: diagnosis and management
Asuri N Prasad, G F Hoffmann
Croatian Medical Journal
|
July 27, 2001
Inborn errors of metabolism at the turn of the millennium
I Barić, K Fumić, G F Hoffmann
Journal of Inherited Metabolic Disease
|
November 5, 1997
Enhanced excretion of urinary leukotriene E4 in mevalonic aciduria is not caused by an impaired peroxisomal degradation of cysteinyl leukotrienes
E Mayatepek, B Tiepelmann, G F Hoffmann
Journal of Inherited Metabolic Disease
|
May 4, 2005
Disorders of intermediary metabolism: toxic leukoencephalopathies
F Hörster, R Surtees, G F Hoffmann
Neuropediatrics
|
January 22, 2003
White matter disease in cerebral organic acid disorders: clinical implications and suggested pathomechanisms
S Kölker, E Mayatepek, G F Hoffmann
Journal of Inherited Metabolic Disease
|
April 8, 2006
Acrodermatitis acidaemia secondary to 'overtreatment' and protein deficiency
G F Hoffmann, R Happle, S Kölker
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 25, 2000
Analysis of leukotrienes in cerebrospinal fluid of a reference population and patients with inborn errors of metabolism: further evidence for a pathognomonic profile in LTC(4)-synthesis deficiency
E Mayatepek, R Zelezny, G F Hoffmann
Journal of Inherited Metabolic Disease
|
December 22, 1999
Urinary excretion of Krebs cycle metabolites in a 13-year-old girl
J Zschocke, G Koch, G F Hoffmann
Journal of Inherited Metabolic Disease
|
August 1, 1998
D-2-hydroxyglutaric aciduria: evidence of clinical and biochemical heterogeneity
L Wagner, G F Hoffmann, C Jakobs
Page
of 22