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P De Jonghe

Showing results (1-10 of 116) with videos related to

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Journal of the Peripheral Nervous System : JPNS|January 21, 2000
Report of the 8th annual symposium of the European Charcot-Marie-Tooth Consortium, Antwerpen, Belgium, July 2-4, 1999V Timmerman, P De Jonghe, C Van Broeckhoven
Neuromuscular Disorders : NMD|May 11, 2006
136th ENMC International Workshop: Charcot-Marie-Tooth disease type 1A (CMT1A)8-10 April 2005, Naarden, The NetherlandsM M Reilly, P de Jonghe, D Pareyson
Nature Genetics|November 4, 2000
Of giant axons and curly hairV Timmerman, P De Jonghe, C Van Broeckhoven
Neuromuscular Disorders : NMD|September 21, 2000
Diagnostic guidelines for hereditary neuralgic amyotrophy or heredofamilial neuritis with brachial plexus predilection. On behalf of the European CMT ConsortiumG Kuhlenbäumer, F Stögbauer, V Timmerman, et al.
Acta Neurologica Belgica|December 1, 2000
Molecular genetics of inherited peripheral neuropathies: who are the actors?J Meuleman, V Timmerman, E Nelis, et al.
Acta Neuropathologica|January 1, 1982
Neuropathology of citrullinaemiaJ J Martin, J P Farriaux, P De Jonghe
Acta Neurologica Belgica|July 1, 1979
Cerebral manifestations of Whipple's diseaseP De Jonghe, J J Martin, H Budka, et al.
Neuromuscular Disorders : NMD|October 12, 2001
Axon damage in CMT due to mutation in myelin protein P0C O Hanemann, A A Gabreëls-Festen, P De Jonghe
Annales De La Societe Belge De Medecine Tropicale|June 1, 1980
Cerebral cysticercosis. Light- and electron microscopy report on one caseD Peeters, C Ceuterick, P De Jonghe, et al.
The Cochrane Database of Systematic Reviews|February 7, 2008
Treatment for Charcot-Marie-Tooth diseaseP Young, P De Jonghe, F Stögbauer, et al.
Pageof 12

Showing results (1-10 of 116) with videos related to

Sort By:
Pageof 12
Journal of the Peripheral Nervous System : JPNS|January 21, 2000
Report of the 8th annual symposium of the European Charcot-Marie-Tooth Consortium, Antwerpen, Belgium, July 2-4, 1999V Timmerman, P De Jonghe, C Van Broeckhoven
Neuromuscular Disorders : NMD|May 11, 2006
136th ENMC International Workshop: Charcot-Marie-Tooth disease type 1A (CMT1A)8-10 April 2005, Naarden, The NetherlandsM M Reilly, P de Jonghe, D Pareyson
Nature Genetics|November 4, 2000
Of giant axons and curly hairV Timmerman, P De Jonghe, C Van Broeckhoven
Neuromuscular Disorders : NMD|September 21, 2000
Diagnostic guidelines for hereditary neuralgic amyotrophy or heredofamilial neuritis with brachial plexus predilection. On behalf of the European CMT ConsortiumG Kuhlenbäumer, F Stögbauer, V Timmerman, et al.
Acta Neurologica Belgica|December 1, 2000
Molecular genetics of inherited peripheral neuropathies: who are the actors?J Meuleman, V Timmerman, E Nelis, et al.
Acta Neuropathologica|January 1, 1982
Neuropathology of citrullinaemiaJ J Martin, J P Farriaux, P De Jonghe
Acta Neurologica Belgica|July 1, 1979
Cerebral manifestations of Whipple's diseaseP De Jonghe, J J Martin, H Budka, et al.
Neuromuscular Disorders : NMD|October 12, 2001
Axon damage in CMT due to mutation in myelin protein P0C O Hanemann, A A Gabreëls-Festen, P De Jonghe
Annales De La Societe Belge De Medecine Tropicale|June 1, 1980
Cerebral cysticercosis. Light- and electron microscopy report on one caseD Peeters, C Ceuterick, P De Jonghe, et al.
The Cochrane Database of Systematic Reviews|February 7, 2008
Treatment for Charcot-Marie-Tooth diseaseP Young, P De Jonghe, F Stögbauer, et al.
Pageof 12