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Journal of Lipid Research
|
August 18, 2000
Simvastatin. A new therapeutic approach for Smith-Lemli-Opitz syndrome
P E Jira, R A Wevers, J de Jong, et al.
Neurology
|
February 5, 1999
Spinal muscular atrophy-like picture, cardiomyopathy, and cytochrome c oxidase deficiency
M E Rubio-Gozalbo, J A Smeitink, W Ruitenbeek, et al.
Journal of the Neurological Sciences
|
April 1, 1995
Immunophenotyping of congenital myopathies: disorganization of sarcomeric, cytoskeletal and extracellular matrix proteins
P F van der Ven, P H Jap, H J ter Laak, et al.
Biochimica Et Biophysica Acta
|
April 6, 2016
Computational modelling of placental amino acid transfer as an integrated system
N Panitchob, K L Widdows, I P Crocker, et al.
Clinical Neurology and Neurosurgery
|
January 1, 1981
Congenital fibre type disproportion
H J ter Laak, H H Jaspar, F J Gabreëls, et al.
European Journal of Pediatrics
|
December 1, 1990
Isolated and combined deficiencies of NADH dehydrogenase (complex I) in muscle tissue of children with mitochondrial myopathies
G C Korenke, H A Bentlage, W Ruitenbeek, et al.
Acta Physiologica (Oxford, England)
|
October 27, 2015
Deficiency or inhibition of lysophosphatidic acid receptor 1 protects against hyperoxia-induced lung injury in neonatal rats
X Chen, F J Walther, R van Boxtel, et al.
Brain & Development
|
May 30, 2007
Cerebral hemodynamics and oxygenation after serial CSF drainage in infants with PHVD
Adriana A E M van Alfen-van der Velden, Jeroen C W Hopman, John H G M Klaessens, et al.
Pediatric Nephrology (Berlin, Germany)
|
April 8, 2021
Transplantation outcomes in patients with primary hyperoxaluria: a systematic review
Elisabeth L Metry, Liza M M van Dijk, Hessel Peters-Sengers, et al.
British Journal of Clinical Pharmacology
|
August 7, 2023
Alkaline phosphatase to treat ischaemia-reperfusion injury in living-donor kidney transplantation: APhIRI I feasibility pilot study
Thei S Steenvoorden, Robert E van Duin, Janneke A J Rood, et al.
Page
of 34
Search research articles
Search
Showing results (241-250 of 340) with videos related to
Sort By:
Page
of 34
Journal of Lipid Research
|
August 18, 2000
Simvastatin. A new therapeutic approach for Smith-Lemli-Opitz syndrome
P E Jira, R A Wevers, J de Jong, et al.
Neurology
|
February 5, 1999
Spinal muscular atrophy-like picture, cardiomyopathy, and cytochrome c oxidase deficiency
M E Rubio-Gozalbo, J A Smeitink, W Ruitenbeek, et al.
Journal of the Neurological Sciences
|
April 1, 1995
Immunophenotyping of congenital myopathies: disorganization of sarcomeric, cytoskeletal and extracellular matrix proteins
P F van der Ven, P H Jap, H J ter Laak, et al.
Biochimica Et Biophysica Acta
|
April 6, 2016
Computational modelling of placental amino acid transfer as an integrated system
N Panitchob, K L Widdows, I P Crocker, et al.
Clinical Neurology and Neurosurgery
|
January 1, 1981
Congenital fibre type disproportion
H J ter Laak, H H Jaspar, F J Gabreëls, et al.
European Journal of Pediatrics
|
December 1, 1990
Isolated and combined deficiencies of NADH dehydrogenase (complex I) in muscle tissue of children with mitochondrial myopathies
G C Korenke, H A Bentlage, W Ruitenbeek, et al.
Acta Physiologica (Oxford, England)
|
October 27, 2015
Deficiency or inhibition of lysophosphatidic acid receptor 1 protects against hyperoxia-induced lung injury in neonatal rats
X Chen, F J Walther, R van Boxtel, et al.
Brain & Development
|
May 30, 2007
Cerebral hemodynamics and oxygenation after serial CSF drainage in infants with PHVD
Adriana A E M van Alfen-van der Velden, Jeroen C W Hopman, John H G M Klaessens, et al.
Pediatric Nephrology (Berlin, Germany)
|
April 8, 2021
Transplantation outcomes in patients with primary hyperoxaluria: a systematic review
Elisabeth L Metry, Liza M M van Dijk, Hessel Peters-Sengers, et al.
British Journal of Clinical Pharmacology
|
August 7, 2023
Alkaline phosphatase to treat ischaemia-reperfusion injury in living-donor kidney transplantation: APhIRI I feasibility pilot study
Thei S Steenvoorden, Robert E van Duin, Janneke A J Rood, et al.
Page
of 34