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Sengers

Showing results (131-140 of 340) with videos related to

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The Journal of Physiology|February 26, 2026
A primary cell-based fluidic co-culture model to investigate drug transport across the human placentaBarbara Fuenzalida, Nadja Koechli, Edgar Ontsouka, et al.
Archives of Neurology|March 1, 1991
Successful treatment of pure myopathy, associated with complex I deficiency, with riboflavin and carnitineP L Bernsen, F J Gabreëls, W Ruitenbeek, et al.
European Journal of Pediatrics|November 1, 1988
Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approachJ M Trijbels, R C Sengers, W Ruitenbeek, et al.
Acta Neuropathologica|February 7, 1998
Infantile motor neuron disease with autonomic dysfunction and bunina bodiesB A Semmekrot, P Wesseling, J F Bruinenberg, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 24, 1997
Multicore myopathy with restrictive cardiomyopathyM A Willemsen, A M van Oort, H J ter Laak, et al.
Neuropediatrics|April 29, 1998
Systemic infantile complex I deficiency with fatal outcome in two brothersM E Rubio-Gozalbo, W Ruitenbeek, U Wendel, et al.
Biological Reviews of the Cambridge Philosophical Society|January 31, 2026
Placental crises: disruptive selection and maternal under-investment as the foundations of mammalian placental evolution and dysfunctionDavis Laundon, Neil J Gostling, Ian G Reddin, et al.
Tijdschrift Voor Kindergeneeskunde|February 1, 1985
[Congenital hydrocephalus, oligophrenia, dwarfism, centripetal obesity and hypogonadism; an X-linked recessive hereditary illness?]R C Sengers, B C Hamel, B J Otten, et al.
Klinische Padiatrie|September 1, 1988
[Encephalomyelopathy, cardiomyopathy, cataract and changes in the retinal pigment epithelium resulting from a cytochrome c oxidase deficiency]L Sieverding, A A Schmaltz, J Apitz, et al.
European Journal of Pediatrics|March 1, 1993
Problems with the biochemical diagnosis in mitochondrial (encephalo-)myopathiesJ M Trijbels, H R Scholte, W Ruitenbeek, et al.
Pageof 34

Showing results (131-140 of 340) with videos related to

Sort By:
Pageof 34
The Journal of Physiology|February 26, 2026
A primary cell-based fluidic co-culture model to investigate drug transport across the human placentaBarbara Fuenzalida, Nadja Koechli, Edgar Ontsouka, et al.
Archives of Neurology|March 1, 1991
Successful treatment of pure myopathy, associated with complex I deficiency, with riboflavin and carnitineP L Bernsen, F J Gabreëls, W Ruitenbeek, et al.
European Journal of Pediatrics|November 1, 1988
Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approachJ M Trijbels, R C Sengers, W Ruitenbeek, et al.
Acta Neuropathologica|February 7, 1998
Infantile motor neuron disease with autonomic dysfunction and bunina bodiesB A Semmekrot, P Wesseling, J F Bruinenberg, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 24, 1997
Multicore myopathy with restrictive cardiomyopathyM A Willemsen, A M van Oort, H J ter Laak, et al.
Neuropediatrics|April 29, 1998
Systemic infantile complex I deficiency with fatal outcome in two brothersM E Rubio-Gozalbo, W Ruitenbeek, U Wendel, et al.
Biological Reviews of the Cambridge Philosophical Society|January 31, 2026
Placental crises: disruptive selection and maternal under-investment as the foundations of mammalian placental evolution and dysfunctionDavis Laundon, Neil J Gostling, Ian G Reddin, et al.
Tijdschrift Voor Kindergeneeskunde|February 1, 1985
[Congenital hydrocephalus, oligophrenia, dwarfism, centripetal obesity and hypogonadism; an X-linked recessive hereditary illness?]R C Sengers, B C Hamel, B J Otten, et al.
Klinische Padiatrie|September 1, 1988
[Encephalomyelopathy, cardiomyopathy, cataract and changes in the retinal pigment epithelium resulting from a cytochrome c oxidase deficiency]L Sieverding, A A Schmaltz, J Apitz, et al.
European Journal of Pediatrics|March 1, 1993
Problems with the biochemical diagnosis in mitochondrial (encephalo-)myopathiesJ M Trijbels, H R Scholte, W Ruitenbeek, et al.
Pageof 34