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Neuromuscular Disorders : NMD
|
January 1, 1992
Neonatal seizures and severe hypotonia in a male infant suffering from a defect in peroxisomal beta-oxidation
L Van Maldergem, M Espeel, R J Wanders, et al.
Progress in Clinical and Biological Research
|
January 1, 1988
Aberration in de novo ether lipid biosynthesis in peroxisomal disorders
H van den Bosch, C G Schalkwijk, G Schrakamp, et al.
European Journal of Pediatrics
|
January 1, 1991
3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment
M Duran, R J Wanders, J P de Jager, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1998
Molecular basis of rhizomelic chondrodysplasia punctata type I: high frequency of the Leu-292 stop mutation in 38 patients
P Brites, A Motley, E Hogenhout, et al.
Neurology
|
November 18, 1998
Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann disease
M R Baumgartner, N M Verhoeven, C Jakobs, et al.
Biochimica Et Biophysica Acta
|
March 19, 1987
Catalase in cultured skin fibroblasts from patients with the cerebro-hepato-renal (Zellweger) syndrome: normal maturation in peroxisome-deficient cells
R J Wanders, A Strijland, C W van Roermund, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation
|
March 21, 1998
Warm flush at 37 degrees C following cold storage attenuates reperfusion injury in preserved rat livers
B A van Wagensveld, M E Reinders, T M van Gulik, et al.
European Journal of Pediatrics
|
September 15, 1999
Cerebral palsy and pyruvate dehydrogenase deficiency: identification of two new mutations in the E1alpha gene
W Lissens, P Vreken, P G Barth, et al.
European Journal of Cancer (Oxford, England : 1990)
|
January 1, 1995
Meta-iodobenzylguanidine (MIBG) inhibits malate and succinate driven mitochondrial ATP synthesis in the human neuroblastoma cell line SK-N-BE(2c)
J Cornelissen, R J Wanders, C Van den Bogert, et al.
Journal of Lipid Research
|
November 4, 2000
Pristanic acid and phytanic acid: naturally occurring ligands for the nuclear receptor peroxisome proliferator-activated receptor alpha
A W Zomer, B van Der Burg, G A Jansen, et al.
Page
of 50
Search research articles
Search
Showing results (361-370 of 497) with videos related to
Sort By:
Page
of 50
Neuromuscular Disorders : NMD
|
January 1, 1992
Neonatal seizures and severe hypotonia in a male infant suffering from a defect in peroxisomal beta-oxidation
L Van Maldergem, M Espeel, R J Wanders, et al.
Progress in Clinical and Biological Research
|
January 1, 1988
Aberration in de novo ether lipid biosynthesis in peroxisomal disorders
H van den Bosch, C G Schalkwijk, G Schrakamp, et al.
European Journal of Pediatrics
|
January 1, 1991
3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment
M Duran, R J Wanders, J P de Jager, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1998
Molecular basis of rhizomelic chondrodysplasia punctata type I: high frequency of the Leu-292 stop mutation in 38 patients
P Brites, A Motley, E Hogenhout, et al.
Neurology
|
November 18, 1998
Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann disease
M R Baumgartner, N M Verhoeven, C Jakobs, et al.
Biochimica Et Biophysica Acta
|
March 19, 1987
Catalase in cultured skin fibroblasts from patients with the cerebro-hepato-renal (Zellweger) syndrome: normal maturation in peroxisome-deficient cells
R J Wanders, A Strijland, C W van Roermund, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation
|
March 21, 1998
Warm flush at 37 degrees C following cold storage attenuates reperfusion injury in preserved rat livers
B A van Wagensveld, M E Reinders, T M van Gulik, et al.
European Journal of Pediatrics
|
September 15, 1999
Cerebral palsy and pyruvate dehydrogenase deficiency: identification of two new mutations in the E1alpha gene
W Lissens, P Vreken, P G Barth, et al.
European Journal of Cancer (Oxford, England : 1990)
|
January 1, 1995
Meta-iodobenzylguanidine (MIBG) inhibits malate and succinate driven mitochondrial ATP synthesis in the human neuroblastoma cell line SK-N-BE(2c)
J Cornelissen, R J Wanders, C Van den Bogert, et al.
Journal of Lipid Research
|
November 4, 2000
Pristanic acid and phytanic acid: naturally occurring ligands for the nuclear receptor peroxisome proliferator-activated receptor alpha
A W Zomer, B van Der Burg, G A Jansen, et al.
Page
of 50