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J E Hoogendijk

Showing results (11-20 of 44) with videos related to

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Journal of Neuroscience Research|November 15, 1996
Inherited demyelinating peripheral neuropathies: relating myelin packing abnormalities to P0 molecular defectsD A Kirschner, K Szumowski, A A Gabreëls-Festen, et al.
Muscle & Nerve|April 1, 1992
Conduction block in hereditary motor and sensory neuropathy type IJ E Hoogendijk, M de Visser, L J Bour, et al.
Neurology|September 1, 1990
Genetic linkage of hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease) to markers of chromosomes 1 and 17J C Defesche, J E Hoogendijk, M de Visser, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 4, 1998
Absence of characteristic features in two patients with inclusion body myositisM F van der Meulen, J E Hoogendijk, G H Jansen, et al.
Clinical Chemistry|September 1, 1993
Quantitative measurement of duplicated DNA as a diagnostic test for Charcot-Marie-Tooth disease type 1aG W Hensels, E A Janssen, J E Hoogendijk, et al.
Muscle & Nerve|January 1, 1994
Hereditary motor and sensory neuropathy type I: clinical and neurographical features of the 17p duplication subtypeJ E Hoogendijk, M De Visser, P A Bolhuis, et al.
Neuromuscular Disorders : NMD|June 19, 2001
Rimmed vacuoles and the added value of SMI-31 staining in diagnosing sporadic inclusion body myositisM F van der Meulen, J E Hoogendijk, K G Moons, et al.
Acta Neuropathologica|January 1, 1993
Chronic inflammatory demyelinating polyneuropathy or hereditary motor and sensory neuropathy? Diagnostic value of morphological criteriaA A Gabreëls-Festen, F J Gabreëls, J E Hoogendijk, et al.
Acta Neuropathologica|January 1, 1995
Charcot-Marie-Tooth disease type 1A: morphological phenotype of the 17p duplication versus PMP22 point mutationsA A Gabreëls-Festen, P A Bolhuis, J E Hoogendijk, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 1, 2002
[Three patients with divergent presentations of idiopathic inflammatory myopathy]I M Bronner, M F G van der Meulen, W H J P Linssen, et al.
Pageof 5

Showing results (11-20 of 44) with videos related to

Sort By:
Pageof 5
Journal of Neuroscience Research|November 15, 1996
Inherited demyelinating peripheral neuropathies: relating myelin packing abnormalities to P0 molecular defectsD A Kirschner, K Szumowski, A A Gabreëls-Festen, et al.
Muscle & Nerve|April 1, 1992
Conduction block in hereditary motor and sensory neuropathy type IJ E Hoogendijk, M de Visser, L J Bour, et al.
Neurology|September 1, 1990
Genetic linkage of hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease) to markers of chromosomes 1 and 17J C Defesche, J E Hoogendijk, M de Visser, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 4, 1998
Absence of characteristic features in two patients with inclusion body myositisM F van der Meulen, J E Hoogendijk, G H Jansen, et al.
Clinical Chemistry|September 1, 1993
Quantitative measurement of duplicated DNA as a diagnostic test for Charcot-Marie-Tooth disease type 1aG W Hensels, E A Janssen, J E Hoogendijk, et al.
Muscle & Nerve|January 1, 1994
Hereditary motor and sensory neuropathy type I: clinical and neurographical features of the 17p duplication subtypeJ E Hoogendijk, M De Visser, P A Bolhuis, et al.
Neuromuscular Disorders : NMD|June 19, 2001
Rimmed vacuoles and the added value of SMI-31 staining in diagnosing sporadic inclusion body myositisM F van der Meulen, J E Hoogendijk, K G Moons, et al.
Acta Neuropathologica|January 1, 1993
Chronic inflammatory demyelinating polyneuropathy or hereditary motor and sensory neuropathy? Diagnostic value of morphological criteriaA A Gabreëls-Festen, F J Gabreëls, J E Hoogendijk, et al.
Acta Neuropathologica|January 1, 1995
Charcot-Marie-Tooth disease type 1A: morphological phenotype of the 17p duplication versus PMP22 point mutationsA A Gabreëls-Festen, P A Bolhuis, J E Hoogendijk, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 1, 2002
[Three patients with divergent presentations of idiopathic inflammatory myopathy]I M Bronner, M F G van der Meulen, W H J P Linssen, et al.
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