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Showing results (241-250 of 340) with videos related to

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Journal of Lipid Research|August 18, 2000
Simvastatin. A new therapeutic approach for Smith-Lemli-Opitz syndromeP E Jira, R A Wevers, J de Jong, et al.
Neurology|February 5, 1999
Spinal muscular atrophy-like picture, cardiomyopathy, and cytochrome c oxidase deficiencyM 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 proteinsP 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 systemN Panitchob, K L Widdows, I P Crocker, et al.
Clinical Neurology and Neurosurgery|January 1, 1981
Congenital fibre type disproportionH 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 myopathiesG 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 ratsX 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 PHVDAdriana 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 reviewElisabeth 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 studyThei S Steenvoorden, Robert E van Duin, Janneke A J Rood, et al.
Pageof 34

Showing results (241-250 of 340) with videos related to

Sort By:
Pageof 34
Journal of Lipid Research|August 18, 2000
Simvastatin. A new therapeutic approach for Smith-Lemli-Opitz syndromeP E Jira, R A Wevers, J de Jong, et al.
Neurology|February 5, 1999
Spinal muscular atrophy-like picture, cardiomyopathy, and cytochrome c oxidase deficiencyM 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 proteinsP 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 systemN Panitchob, K L Widdows, I P Crocker, et al.
Clinical Neurology and Neurosurgery|January 1, 1981
Congenital fibre type disproportionH 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 myopathiesG 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 ratsX 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 PHVDAdriana 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 reviewElisabeth 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 studyThei S Steenvoorden, Robert E van Duin, Janneke A J Rood, et al.
Pageof 34