Search research articles
Contact Us
Filters
Showing results (121-130 of 214) with videos related to
Page
of 22
Sort By:
The Journal of Biological Chemistry
|
October 23, 1997
Identification of an active site alanine in mevalonate kinase through characterization of a novel mutation in mevalonate kinase deficiency
D D Hinson, K L Chambliss, G F Hoffmann, et al.
Neurology
|
August 23, 2006
Presymptomatic treatment of neonatal guanidinoacetate methyltransferase deficiency
A Schulze, G F Hoffmann, P Bachert, et al.
European Journal of Pediatrics
|
January 1, 1994
Neurological manifestations of organic acid disorders
G F Hoffmann, K M Gibson, F K Trefz, et al.
European Journal of Pediatrics
|
May 1, 1996
Atypical vitamin B12-unresponsive methylmalonic aciduria in sibship with severe progressive encephalomyelopathy: a new genetic disease?
E Mayatepek, G F Hoffmann, R Baumgartner, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Mevalonate kinase assay using DEAE-cellulose column chromatography for first-trimester prenatal diagnosis and complementation analysis in mevalonic aciduria
G F Hoffmann, S U Brendel, S R Scharfschwerdt, et al.
Neuropediatrics
|
August 30, 2002
Clinical and laboratory findings in twins with neonatal epileptic encephalopathy mimicking aromatic L-amino acid decarboxylase deficiency
C Bräutigam, K Hyland, R Wevers, et al.
Der Nervenarzt
|
September 24, 2002
[CDG (congenital disorders of glycosylation). Differential hereditary ataxia in adulthood diagnosis]
S Bubel, V Peters, C Klein, et al.
Archives of Disease in Childhood
|
April 20, 1999
Glutaric aciduria and suspected child abuse
A A Morris, G F Hoffmann, E R Naughten, et al.
Neurology
|
June 30, 2005
Late-onset neurologic disease in glutaryl-CoA dehydrogenase deficiency
S Külkens, I Harting, S Sauer, et al.
Neuropediatrics
|
March 1, 2002
A new subtype of a congenital disorder of glycosylation (CDG) with mild clinical manifestations
B Assmann, R Hackler, V Peters, et al.
Page
of 22
Search research articles
Search
Showing results (121-130 of 214) with videos related to
Sort By:
Page
of 22
The Journal of Biological Chemistry
|
October 23, 1997
Identification of an active site alanine in mevalonate kinase through characterization of a novel mutation in mevalonate kinase deficiency
D D Hinson, K L Chambliss, G F Hoffmann, et al.
Neurology
|
August 23, 2006
Presymptomatic treatment of neonatal guanidinoacetate methyltransferase deficiency
A Schulze, G F Hoffmann, P Bachert, et al.
European Journal of Pediatrics
|
January 1, 1994
Neurological manifestations of organic acid disorders
G F Hoffmann, K M Gibson, F K Trefz, et al.
European Journal of Pediatrics
|
May 1, 1996
Atypical vitamin B12-unresponsive methylmalonic aciduria in sibship with severe progressive encephalomyelopathy: a new genetic disease?
E Mayatepek, G F Hoffmann, R Baumgartner, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Mevalonate kinase assay using DEAE-cellulose column chromatography for first-trimester prenatal diagnosis and complementation analysis in mevalonic aciduria
G F Hoffmann, S U Brendel, S R Scharfschwerdt, et al.
Neuropediatrics
|
August 30, 2002
Clinical and laboratory findings in twins with neonatal epileptic encephalopathy mimicking aromatic L-amino acid decarboxylase deficiency
C Bräutigam, K Hyland, R Wevers, et al.
Der Nervenarzt
|
September 24, 2002
[CDG (congenital disorders of glycosylation). Differential hereditary ataxia in adulthood diagnosis]
S Bubel, V Peters, C Klein, et al.
Archives of Disease in Childhood
|
April 20, 1999
Glutaric aciduria and suspected child abuse
A A Morris, G F Hoffmann, E R Naughten, et al.
Neurology
|
June 30, 2005
Late-onset neurologic disease in glutaryl-CoA dehydrogenase deficiency
S Külkens, I Harting, S Sauer, et al.
Neuropediatrics
|
March 1, 2002
A new subtype of a congenital disorder of glycosylation (CDG) with mild clinical manifestations
B Assmann, R Hackler, V Peters, et al.
Page
of 22