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B G van Engelen

Showing results (71-80 of 113) with videos related to

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Annals of the Rheumatic Diseases|October 15, 1998
Postural changes, dysphagia, and systemic sclerosisP Barrera, A A den Broeder, F H van den Hoogen, 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.
Neurology|June 21, 2008
Sporadic late-onset nemaline myopathy effectively treated by melphalan and stem cell transplantN C Voermans, M Minnema, M Lammens, et al.
American Journal of Medical Genetics. Part A|March 13, 2012
Myopathy in a 20-year-old female patient with D4ST-1 deficient Ehlers-Danlos syndrome due to a homozygous CHST14 mutationN C Voermans, M Kempers, M Lammens, et al.
Neuromuscular Disorders : NMD|July 19, 2000
Cerebrotendinous xanthomatosis. Controversies about nerve and muscle: observations in ten patientsA Verrips, B G van Engelen, H ter Laak, et al.
Human Immunology|January 5, 2002
Decreased immunoglobulin class switching in Nijmegen Breakage syndrome due to the DNA repair defectB G van Engelen, J A Hiel, F J Gabreëls, et al.
Journal of the Neurological Sciences|April 1, 1995
White matter abnormalities in congenital muscular dystrophyQ H Leyten, F J Gabreëls, W O Renier, et al.
Journal of Neurology|November 29, 2005
Recurrent neuropathy associated with Ehlers-Danlos syndromeN C Voermans, G Drost, A van Kampen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1992
A case of bilateral alternating hemifacial spasmsJ B van de Biezenbos, M W Horstink, C J van de Vlasakker, et al.
Clinical Neuropathology|February 24, 2010
Clinical features, lectin staining, and a novel GNE frameshift mutation in hereditary inclusion body myopathyN C Voermans, M Guillard, R Doedée, et al.
Pageof 12

Showing results (71-80 of 113) with videos related to

Sort By:
Pageof 12
Annals of the Rheumatic Diseases|October 15, 1998
Postural changes, dysphagia, and systemic sclerosisP Barrera, A A den Broeder, F H van den Hoogen, 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.
Neurology|June 21, 2008
Sporadic late-onset nemaline myopathy effectively treated by melphalan and stem cell transplantN C Voermans, M Minnema, M Lammens, et al.
American Journal of Medical Genetics. Part A|March 13, 2012
Myopathy in a 20-year-old female patient with D4ST-1 deficient Ehlers-Danlos syndrome due to a homozygous CHST14 mutationN C Voermans, M Kempers, M Lammens, et al.
Neuromuscular Disorders : NMD|July 19, 2000
Cerebrotendinous xanthomatosis. Controversies about nerve and muscle: observations in ten patientsA Verrips, B G van Engelen, H ter Laak, et al.
Human Immunology|January 5, 2002
Decreased immunoglobulin class switching in Nijmegen Breakage syndrome due to the DNA repair defectB G van Engelen, J A Hiel, F J Gabreëls, et al.
Journal of the Neurological Sciences|April 1, 1995
White matter abnormalities in congenital muscular dystrophyQ H Leyten, F J Gabreëls, W O Renier, et al.
Journal of Neurology|November 29, 2005
Recurrent neuropathy associated with Ehlers-Danlos syndromeN C Voermans, G Drost, A van Kampen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1992
A case of bilateral alternating hemifacial spasmsJ B van de Biezenbos, M W Horstink, C J van de Vlasakker, et al.
Clinical Neuropathology|February 24, 2010
Clinical features, lectin staining, and a novel GNE frameshift mutation in hereditary inclusion body myopathyN C Voermans, M Guillard, R Doedée, et al.
Pageof 12