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D J Verlaan

Showing results (1-10 of 9) with videos related to

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Neurology|November 24, 2004
No CCM2 mutations in a cohort of 31 sporadic casesD J Verlaan, S B Laurent, G A Rouleau, et al.
Neurogenetics|January 11, 2007
Large germline deletions and duplication in isolated cerebral cavernous malformation patientsU Felbor, S Gaetzner, D J Verlaan, et al.
Neurology|March 27, 2002
Cerebral cavernous malformations: mutations in Krit1D J Verlaan, W J Davenport, H Stefan, et al.
Neurology|December 29, 2005
CCM3 mutations are uncommon in cerebral cavernous malformationsD J Verlaan, J Roussel, S B Laurent, et al.
Neurology|April 14, 2004
CCM1 mutation screen of sporadic cases with cerebral cavernous malformationsD J Verlaan, S B Laurent, U Sure, et al.
Journal of Medical Genetics|June 3, 2006
A new locus for autosomal dominant intracranial aneurysm, ANIB4, maps to chromosome 5p15.2-14.3D J Verlaan, M-P Dubé, J St-Onge, et al.
Neurosurgical Review|September 18, 2009
Inherited cavernous malformations of the central nervous system: clinical and genetic features in 19 Swiss familiesC Graeni, F Stepper, M Sturzenegger, et al.
Der Nervenarzt|February 11, 2005
[Familial cavernous malformations of the central nervous system. A clinical and genetic study of 15 German families]A M Siegel, H Bertalanffy, J J Dichgans, et al.
Lancet (London, England)|May 6, 2008
Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association studyJ B Richards, F Rivadeneira, M Inouye, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Neurology|November 24, 2004
No CCM2 mutations in a cohort of 31 sporadic casesD J Verlaan, S B Laurent, G A Rouleau, et al.
Neurogenetics|January 11, 2007
Large germline deletions and duplication in isolated cerebral cavernous malformation patientsU Felbor, S Gaetzner, D J Verlaan, et al.
Neurology|March 27, 2002
Cerebral cavernous malformations: mutations in Krit1D J Verlaan, W J Davenport, H Stefan, et al.
Neurology|December 29, 2005
CCM3 mutations are uncommon in cerebral cavernous malformationsD J Verlaan, J Roussel, S B Laurent, et al.
Neurology|April 14, 2004
CCM1 mutation screen of sporadic cases with cerebral cavernous malformationsD J Verlaan, S B Laurent, U Sure, et al.
Journal of Medical Genetics|June 3, 2006
A new locus for autosomal dominant intracranial aneurysm, ANIB4, maps to chromosome 5p15.2-14.3D J Verlaan, M-P Dubé, J St-Onge, et al.
Neurosurgical Review|September 18, 2009
Inherited cavernous malformations of the central nervous system: clinical and genetic features in 19 Swiss familiesC Graeni, F Stepper, M Sturzenegger, et al.
Der Nervenarzt|February 11, 2005
[Familial cavernous malformations of the central nervous system. A clinical and genetic study of 15 German families]A M Siegel, H Bertalanffy, J J Dichgans, et al.
Lancet (London, England)|May 6, 2008
Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association studyJ B Richards, F Rivadeneira, M Inouye, et al.
Pageof 1