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Journal of Inherited Metabolic Disease
|
April 23, 2003
Plasma pipecolic acid is frequently elevated in non-peroxisomal disease
J C M Baas, R van de Laar, L Dorland, et al.
Journal of Medicinal Chemistry
|
March 19, 1993
Non-nucleoside inhibitors of HIV-1 reverse transcriptase: molecular modeling and X-ray structure investigations
W Schäfer, W G Friebe, H Leinert, et al.
Neuropediatrics
|
July 13, 1999
Pontocerebellar hypoplasia associated with respiratory-chain defects
T J de Koning, L S de Vries, F Groenendaal, et al.
Neurology
|
December 11, 2002
Biochemical markers predicting survival in peroxisome biogenesis disorders
J Gootjes, P A W Mooijer, C Dekker, et al.
The Journal of Pediatrics
|
May 1, 1988
de Toni-Fanconi-Debré syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiency
H Ogier, A Lombes, H R Scholte, et al.
Structure (London, England : 1993)
|
November 15, 1996
Enzyme flexibility, solvent and 'weak' interactions characterize thrombin-ligand interactions: implications for drug design
R A Engh, H Brandstetter, G Sucher, et al.
Annals of Neurology
|
August 26, 1998
Beneficial effects of L-serine and glycine in the management of seizures in 3-phosphoglycerate dehydrogenase deficiency
T J de Koning, M Duran, L Dorland, et al.
Pediatric Research
|
November 1, 1992
In vivo study of phytanic acid alpha-oxidation in classic Refsum's disease and chondrodysplasia punctata
H J ten Brink, D S Schor, R M Kok, et al.
Journal of Medical Genetics
|
August 27, 1998
Clinical heterogeneity and novel mutations in the glycerol kinase gene in three families with isolated glycerol kinase deficiency
D R Sjarif, R J Sinke, M Duran, et al.
Journal of Inherited Metabolic Disease
|
October 8, 1998
Recurrent nonimmune hydrops fetalis associated with carbohydrate-deficient glycoprotein syndrome
T J de Koning, M Toet, L Dorland, et al.
Page
of 17
Search research articles
Search
Showing results (91-100 of 169) with videos related to
Sort By:
Page
of 17
Journal of Inherited Metabolic Disease
|
April 23, 2003
Plasma pipecolic acid is frequently elevated in non-peroxisomal disease
J C M Baas, R van de Laar, L Dorland, et al.
Journal of Medicinal Chemistry
|
March 19, 1993
Non-nucleoside inhibitors of HIV-1 reverse transcriptase: molecular modeling and X-ray structure investigations
W Schäfer, W G Friebe, H Leinert, et al.
Neuropediatrics
|
July 13, 1999
Pontocerebellar hypoplasia associated with respiratory-chain defects
T J de Koning, L S de Vries, F Groenendaal, et al.
Neurology
|
December 11, 2002
Biochemical markers predicting survival in peroxisome biogenesis disorders
J Gootjes, P A W Mooijer, C Dekker, et al.
The Journal of Pediatrics
|
May 1, 1988
de Toni-Fanconi-Debré syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiency
H Ogier, A Lombes, H R Scholte, et al.
Structure (London, England : 1993)
|
November 15, 1996
Enzyme flexibility, solvent and 'weak' interactions characterize thrombin-ligand interactions: implications for drug design
R A Engh, H Brandstetter, G Sucher, et al.
Annals of Neurology
|
August 26, 1998
Beneficial effects of L-serine and glycine in the management of seizures in 3-phosphoglycerate dehydrogenase deficiency
T J de Koning, M Duran, L Dorland, et al.
Pediatric Research
|
November 1, 1992
In vivo study of phytanic acid alpha-oxidation in classic Refsum's disease and chondrodysplasia punctata
H J ten Brink, D S Schor, R M Kok, et al.
Journal of Medical Genetics
|
August 27, 1998
Clinical heterogeneity and novel mutations in the glycerol kinase gene in three families with isolated glycerol kinase deficiency
D R Sjarif, R J Sinke, M Duran, et al.
Journal of Inherited Metabolic Disease
|
October 8, 1998
Recurrent nonimmune hydrops fetalis associated with carbohydrate-deficient glycoprotein syndrome
T J de Koning, M Toet, L Dorland, et al.
Page
of 17