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W Robberecht

Showing results (51-60 of 83) with videos related to

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Genetic Counseling (Geneva, Switzerland)|November 5, 1999
A novel 7.4 kb mitochondrial deletion in a patient with congenital progressive external ophthalmoplegia, muscle weakness and mental retardationM Tabaku, E Legius, W Robberecht, et al.
Acta Neurologica Belgica|January 1, 1995
Neurocysticercosis: a poorly understood diseaseM Vantomme, R Swartenbroekx, B Dhaen, et al.
Journal of Neurophysiology|August 7, 2002
Na(+) entry through AMPA receptors results in voltage-gated k(+) channel blockade in cultured rat spinal cord motoneuronsP Van Damme, L Van Den Bosch, E Van Houtte, et al.
Neuroradiology|January 1, 1992
MRI of herpes simplex encephalitisP Demaerel, G Wilms, W Robberecht, et al.
Magnetic Resonance in Medicine|July 13, 2011
Response of mouse brain perfusion to hypo- and hyperventilation measured by arterial spin labelingW Wouter Oosterlinck, T Dresselaers, V Geldhof, et al.
Annals of Neurology|April 18, 1998
Increased sensitivity of fibroblasts from amyotrophic lateral sclerosis patients to oxidative stressT Aguirre, L Van Den Bosch, K Goetschalckx, et al.
Archives of Neurology|January 1, 1996
Familial juvenile focal amyotrophy of the upper extremity (Hirayama disease). Superoxide dismutase 1 genotype and activityW Robberecht, T Aguirre, L Van den Bosch, et al.
Neuropathology and Applied Neurobiology|September 15, 2007
Vascular endothelial growth factor counteracts the loss of phospho-Akt preceding motor neurone degeneration in amyotrophic lateral sclerosisM Dewil, D Lambrechts, R Sciot, et al.
Surgical Neurology|September 1, 1996
Lymphocytic infundibulohypophysitis presenting in the postpartum period: case reportT Van Havenbergh, W Robberecht, G Wilms, et al.
Annals of Neurology|June 1, 1994
Deletion in the CMT1A locus on chromosome 17p11.2 in hereditary neuropathy with liability to pressure palsiesD Verhalle, A Löfgren, E Nelis, et al.
Pageof 9

Showing results (51-60 of 83) with videos related to

Sort By:
Pageof 9
Genetic Counseling (Geneva, Switzerland)|November 5, 1999
A novel 7.4 kb mitochondrial deletion in a patient with congenital progressive external ophthalmoplegia, muscle weakness and mental retardationM Tabaku, E Legius, W Robberecht, et al.
Acta Neurologica Belgica|January 1, 1995
Neurocysticercosis: a poorly understood diseaseM Vantomme, R Swartenbroekx, B Dhaen, et al.
Journal of Neurophysiology|August 7, 2002
Na(+) entry through AMPA receptors results in voltage-gated k(+) channel blockade in cultured rat spinal cord motoneuronsP Van Damme, L Van Den Bosch, E Van Houtte, et al.
Neuroradiology|January 1, 1992
MRI of herpes simplex encephalitisP Demaerel, G Wilms, W Robberecht, et al.
Magnetic Resonance in Medicine|July 13, 2011
Response of mouse brain perfusion to hypo- and hyperventilation measured by arterial spin labelingW Wouter Oosterlinck, T Dresselaers, V Geldhof, et al.
Annals of Neurology|April 18, 1998
Increased sensitivity of fibroblasts from amyotrophic lateral sclerosis patients to oxidative stressT Aguirre, L Van Den Bosch, K Goetschalckx, et al.
Archives of Neurology|January 1, 1996
Familial juvenile focal amyotrophy of the upper extremity (Hirayama disease). Superoxide dismutase 1 genotype and activityW Robberecht, T Aguirre, L Van den Bosch, et al.
Neuropathology and Applied Neurobiology|September 15, 2007
Vascular endothelial growth factor counteracts the loss of phospho-Akt preceding motor neurone degeneration in amyotrophic lateral sclerosisM Dewil, D Lambrechts, R Sciot, et al.
Surgical Neurology|September 1, 1996
Lymphocytic infundibulohypophysitis presenting in the postpartum period: case reportT Van Havenbergh, W Robberecht, G Wilms, et al.
Annals of Neurology|June 1, 1994
Deletion in the CMT1A locus on chromosome 17p11.2 in hereditary neuropathy with liability to pressure palsiesD Verhalle, A Löfgren, E Nelis, et al.
Pageof 9