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M D Ferrari

Showing results (241-250 of 246) with videos related to

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Clinical Genetics|April 11, 2008
CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraineA H Stam, K R J Vanmolkot, H P H Kremer, et al.
Annals of Neurology|January 27, 2006
Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutationK R J Vanmolkot, H Stroink, J B Koenderink, et al.
Neurology|December 7, 2007
Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraineB de Vries, T Freilinger, K R J Vanmolkot, et al.
American Journal of Human Genetics|July 5, 2001
Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3R A Ophoff, J DeYoung, S K Service, et al.
Cephalalgia : an International Journal of Headache|August 30, 2014
Candidate-gene association study searching for genetic factors involved in migraine chronificationM A Louter, J Fernandez-Morales, B de Vries, et al.
Rhinology|February 21, 2020
European Position Paper on Rhinosinusitis and Nasal Polyps 2020W J Fokkens, V J Lund, C Hopkins, et al.
Pageof 25

Showing results (241-250 of 246) with videos related to

Sort By:
Pageof 25
You have reached the last page of results.This site can display upto 246 results.
Clinical Genetics|April 11, 2008
CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraineA H Stam, K R J Vanmolkot, H P H Kremer, et al.
Annals of Neurology|January 27, 2006
Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutationK R J Vanmolkot, H Stroink, J B Koenderink, et al.
Neurology|December 7, 2007
Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraineB de Vries, T Freilinger, K R J Vanmolkot, et al.
American Journal of Human Genetics|July 5, 2001
Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3R A Ophoff, J DeYoung, S K Service, et al.
Cephalalgia : an International Journal of Headache|August 30, 2014
Candidate-gene association study searching for genetic factors involved in migraine chronificationM A Louter, J Fernandez-Morales, B de Vries, et al.
Rhinology|February 21, 2020
European Position Paper on Rhinosinusitis and Nasal Polyps 2020W J Fokkens, V J Lund, C Hopkins, et al.
Pageof 25