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Showing results (731-740 of 819) with videos related to

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Journal of the Neurological Sciences|June 12, 2016
Spreading depolarization-modulating drugs and delayed cerebral ischemia after subarachnoid hemorrhage: A hypothesis-generating retrospective clinical studyArend M Hamming, Inge A Mulder, Celine S Gathier, et al.
Cephalalgia : an International Journal of Headache|January 31, 2015
Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data setBoukje de Vries, Verneri Anttila, Tobias Freilinger, et al.
Frontiers in Neuroscience|November 22, 2021
Sex Differences in Risk Profile, Stroke Cause and Outcome in Ischemic Stroke Patients With and Without MigraineKatie M Linstra, Hendrikus J A van Os, Ynte M Ruigrok, et al.
Circulation|December 7, 2011
Migraine mutations increase stroke vulnerability by facilitating ischemic depolarizationsKatharina Eikermann-Haerter, Jeong Hyun Lee, Izumi Yuzawa, et al.
Brain and Behavior|February 18, 2019
Circle of Willis variations in migraine patients with ischemic strokeArend M Hamming, Marianne A A van Walderveen, Inge A Mulder, et al.
Cephalalgia : an International Journal of Headache|February 18, 2009
First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsyM-J Castro, A H Stam, C Lemos, et al.
Neuroscience|August 23, 2005
Gene dosage-dependent transmitter release changes at neuromuscular synapses of CACNA1A R192Q knockin mice are non-progressive and do not lead to morphological changes or muscle weaknessS Kaja, R C G van de Ven, L A M Broos, et al.
Proteomics|April 15, 2010
Quantitative cortical synapse proteomics of a transgenic migraine mouse model with mutated Ca(V)2.1 calcium channelsOleg I Klychnikov, Ka Wan Li, Igor A Sidorov, et al.
Human Mutation|April 3, 2007
The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. OnlineKaate R J Vanmolkot, Elena Babini, Boukje de Vries, et al.
European Journal of Endocrinology|October 23, 2019
Activity and safety of temozolomide in advanced adrenocortical carcinoma patientsDeborah Cosentini, Giuseppe Badalamenti, Salvatore Grisanti, et al.
Pageof 82

Showing results (731-740 of 819) with videos related to

Sort By:
Pageof 82
Journal of the Neurological Sciences|June 12, 2016
Spreading depolarization-modulating drugs and delayed cerebral ischemia after subarachnoid hemorrhage: A hypothesis-generating retrospective clinical studyArend M Hamming, Inge A Mulder, Celine S Gathier, et al.
Cephalalgia : an International Journal of Headache|January 31, 2015
Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data setBoukje de Vries, Verneri Anttila, Tobias Freilinger, et al.
Frontiers in Neuroscience|November 22, 2021
Sex Differences in Risk Profile, Stroke Cause and Outcome in Ischemic Stroke Patients With and Without MigraineKatie M Linstra, Hendrikus J A van Os, Ynte M Ruigrok, et al.
Circulation|December 7, 2011
Migraine mutations increase stroke vulnerability by facilitating ischemic depolarizationsKatharina Eikermann-Haerter, Jeong Hyun Lee, Izumi Yuzawa, et al.
Brain and Behavior|February 18, 2019
Circle of Willis variations in migraine patients with ischemic strokeArend M Hamming, Marianne A A van Walderveen, Inge A Mulder, et al.
Cephalalgia : an International Journal of Headache|February 18, 2009
First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsyM-J Castro, A H Stam, C Lemos, et al.
Neuroscience|August 23, 2005
Gene dosage-dependent transmitter release changes at neuromuscular synapses of CACNA1A R192Q knockin mice are non-progressive and do not lead to morphological changes or muscle weaknessS Kaja, R C G van de Ven, L A M Broos, et al.
Proteomics|April 15, 2010
Quantitative cortical synapse proteomics of a transgenic migraine mouse model with mutated Ca(V)2.1 calcium channelsOleg I Klychnikov, Ka Wan Li, Igor A Sidorov, et al.
Human Mutation|April 3, 2007
The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. OnlineKaate R J Vanmolkot, Elena Babini, Boukje de Vries, et al.
European Journal of Endocrinology|October 23, 2019
Activity and safety of temozolomide in advanced adrenocortical carcinoma patientsDeborah Cosentini, Giuseppe Badalamenti, Salvatore Grisanti, et al.
Pageof 82