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F J Gabreels

Showing results (1-10 of 11) with videos related to

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Neuropediatrics|August 1, 1980
Evaluation of diagnosis and non-surgical therapy in 24 children with a pontine tumourW O Renier, F J Gabreels
European Journal of Human Genetics : EJHG|July 6, 2000
A de novo missense mutation in a critical domain of the X-linked DDP gene causes the typical deafness-dystonia-optic atrophy syndromeL Tranebjaerg, B C Hamel, F J Gabreels, et al.
Epilepsy Research|December 1, 1994
Immunoglobulin treatment in epilepsy, a review of the literatureB G van Engelen, W O Renier, C M Weemaes, et al.
Epilepsia|January 1, 1988
Anomalies of the cerebral cortex in a case of epilepsia partialis continuaW I Verhagen, W O Renier, H ter Laak, et al.
American Journal of Medical Genetics|April 20, 1999
Psychometric assessment of families with X-linked mental retardationT van Roosmalen, A P Smits, G H Thoonen, et al.
Epilepsy Research|June 1, 1994
Cerebrospinal fluid examinations in cryptogenic West and Lennox-Gastaut syndrome before and after intravenous immunoglobulin administrationB G van Engelen, W O Renier, C M Weemaes, et al.
Clinical Chemistry|June 1, 1992
Age-related changes of neuron-specific enolase, S-100 protein, and myelin basic protein concentrations in cerebrospinal fluidB G van Engelen, K J Lamers, F J Gabreels, et al.
Plastic and Reconstructive Surgery|March 1, 1996
Peripheral nerve elongation by laser Doppler flowmetry-monitored expansion: an experimental basis for future application in the management of peripheral nerve defectsL P van der Wey, T W Polder, D F Stegeman, 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.
Journal of Autoimmunity|December 1, 1994
Coxsackie B1 virus-induced murine myositis: a correlative study of muscular lesions and serological changesP J Jongen, F W Heessen, I Bergmann, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Neuropediatrics|August 1, 1980
Evaluation of diagnosis and non-surgical therapy in 24 children with a pontine tumourW O Renier, F J Gabreels
European Journal of Human Genetics : EJHG|July 6, 2000
A de novo missense mutation in a critical domain of the X-linked DDP gene causes the typical deafness-dystonia-optic atrophy syndromeL Tranebjaerg, B C Hamel, F J Gabreels, et al.
Epilepsy Research|December 1, 1994
Immunoglobulin treatment in epilepsy, a review of the literatureB G van Engelen, W O Renier, C M Weemaes, et al.
Epilepsia|January 1, 1988
Anomalies of the cerebral cortex in a case of epilepsia partialis continuaW I Verhagen, W O Renier, H ter Laak, et al.
American Journal of Medical Genetics|April 20, 1999
Psychometric assessment of families with X-linked mental retardationT van Roosmalen, A P Smits, G H Thoonen, et al.
Epilepsy Research|June 1, 1994
Cerebrospinal fluid examinations in cryptogenic West and Lennox-Gastaut syndrome before and after intravenous immunoglobulin administrationB G van Engelen, W O Renier, C M Weemaes, et al.
Clinical Chemistry|June 1, 1992
Age-related changes of neuron-specific enolase, S-100 protein, and myelin basic protein concentrations in cerebrospinal fluidB G van Engelen, K J Lamers, F J Gabreels, et al.
Plastic and Reconstructive Surgery|March 1, 1996
Peripheral nerve elongation by laser Doppler flowmetry-monitored expansion: an experimental basis for future application in the management of peripheral nerve defectsL P van der Wey, T W Polder, D F Stegeman, 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.
Journal of Autoimmunity|December 1, 1994
Coxsackie B1 virus-induced murine myositis: a correlative study of muscular lesions and serological changesP J Jongen, F W Heessen, I Bergmann, et al.
Pageof 2