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Journal of Lipid Research
|
October 1, 1992
Phytanic acid alpha-oxidation: accumulation of 2-hydroxyphytanic acid and absence of 2-oxophytanic acid in plasma from patients with peroxisomal disorders
H J ten Brink, D S Schor, R M Kok, et al.
Journal of Inherited Metabolic Disease
|
May 11, 1999
Muscle strength in children with medium-chain acyl-CoA dehydrogenase deficiency
J W Custers, B T Poll-The, M Duran, et al.
European Journal of Pediatrics
|
December 29, 2000
Neurotransmitters in 3-phosphoglycerate dehydrogenase deficiency
T J de Koning, M Duran, L Dorland, et al.
AJNR. American Journal of Neuroradiology
|
January 19, 2006
Sequential MR imaging changes in nonketotic hyperglycinemia
J Mourmans, C B L M Majoie, P G Barth, et al.
Biochimica Et Biophysica Acta
|
April 12, 1996
Non-rhizomelic and rhizomelic chondrodysplasia punctata within a single complementation group
A M Motley, H F Tabak, J A Smeitink, et al.
Clinical Chemistry
|
March 25, 1998
Simultaneous analysis of plasma free fatty acids and their 3-hydroxy analogs in fatty acid beta-oxidation disorders
C G Costa, L Dorland, U Holwerda, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
Cerebrospinal fluid organic acids in biotinidase deficiency
M Duran, E R Baumgartner, T M Suormala, et al.
Lancet (London, England)
|
June 19, 1993
Sudden infant death associated with defective oxidative phosphorylation
J A Smeitink, J C Fischer, W Ruitenbeek, et al.
Pediatric Research
|
November 1, 1994
Rate-dependent distal renal tubular acidosis and carnitine palmitoyltransferase I deficiency
A J Bergman, R A Donckerwolcke, M Duran, et al.
Journal of Inherited Metabolic Disease
|
December 16, 2000
Hyperketonaemia in glycerol kinase deficiency
D R Sjarif, L Dorland, W Sperl, et al.
Page
of 13
Search research articles
Search
Showing results (41-50 of 127) with videos related to
Sort By:
Page
of 13
Journal of Lipid Research
|
October 1, 1992
Phytanic acid alpha-oxidation: accumulation of 2-hydroxyphytanic acid and absence of 2-oxophytanic acid in plasma from patients with peroxisomal disorders
H J ten Brink, D S Schor, R M Kok, et al.
Journal of Inherited Metabolic Disease
|
May 11, 1999
Muscle strength in children with medium-chain acyl-CoA dehydrogenase deficiency
J W Custers, B T Poll-The, M Duran, et al.
European Journal of Pediatrics
|
December 29, 2000
Neurotransmitters in 3-phosphoglycerate dehydrogenase deficiency
T J de Koning, M Duran, L Dorland, et al.
AJNR. American Journal of Neuroradiology
|
January 19, 2006
Sequential MR imaging changes in nonketotic hyperglycinemia
J Mourmans, C B L M Majoie, P G Barth, et al.
Biochimica Et Biophysica Acta
|
April 12, 1996
Non-rhizomelic and rhizomelic chondrodysplasia punctata within a single complementation group
A M Motley, H F Tabak, J A Smeitink, et al.
Clinical Chemistry
|
March 25, 1998
Simultaneous analysis of plasma free fatty acids and their 3-hydroxy analogs in fatty acid beta-oxidation disorders
C G Costa, L Dorland, U Holwerda, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
Cerebrospinal fluid organic acids in biotinidase deficiency
M Duran, E R Baumgartner, T M Suormala, et al.
Lancet (London, England)
|
June 19, 1993
Sudden infant death associated with defective oxidative phosphorylation
J A Smeitink, J C Fischer, W Ruitenbeek, et al.
Pediatric Research
|
November 1, 1994
Rate-dependent distal renal tubular acidosis and carnitine palmitoyltransferase I deficiency
A J Bergman, R A Donckerwolcke, M Duran, et al.
Journal of Inherited Metabolic Disease
|
December 16, 2000
Hyperketonaemia in glycerol kinase deficiency
D R Sjarif, L Dorland, W Sperl, et al.
Page
of 13