[HTML][HTML] Mechanism underlying unaltered cortical inhibitory synaptic transmission in contrast with enhanced excitatory transmission in CaV2. 1 knockin migraine mice
D Vecchia, A Tottene… - Neurobiology of …, 2014 - Elsevier
Familial hemiplegic migraine type 1 (FHM1), a monogenic subtype of migraine with aura, is
caused by gain-of-function mutations in Ca V 2.1 (P/Q-type) calcium channels. In FHM1 …
caused by gain-of-function mutations in Ca V 2.1 (P/Q-type) calcium channels. In FHM1 …
Mechanism underlying unaltered cortical inhibitory synaptic transmission in contrast with enhanced excitatory transmission in CaV2. 1 knockin migraine mice.
D Vecchia, A Tottene… - NEUROBIOLOGY OF …, 2014 - research.unipd.it
Familial hemiplegic migraine type 1 (FHM1), a monogenic subtype of migraine with aura, is
caused by gain-of-function mutations in Ca (V) 2.1 (P/Q-type) calcium channels. In FHM1 …
caused by gain-of-function mutations in Ca (V) 2.1 (P/Q-type) calcium channels. In FHM1 …
[PDF][PDF] Mechanism underlying unaltered cortical inhibitory synaptic transmission in contrast with enhanced excitatory transmission in CaV2. 1 knockin migraine mice
D Vecchia, A Tottene… - Neurobiology of …, 2014 - researchgate.net
Dania Vecchia a, Angelita Tottene a, Arn MJM van den Maagdenberg b, Daniela Pietrobon
a,⁎ a Department of Biomedical Sciences, University of Padova and CNR Institute of …
a,⁎ a Department of Biomedical Sciences, University of Padova and CNR Institute of …
Mechanism underlying unaltered cortical inhibitory synaptic transmission in contrast with enhanced excitatory transmission in CaV2. 1 knockin migraine mice
D Vecchia, A Tottene… - Neurobiology of …, 2014 - pubmed.ncbi.nlm.nih.gov
Familial hemiplegic migraine type 1 (FHM1), a monogenic subtype of migraine with aura, is
caused by gain-of-function mutations in CaV2. 1 (P/Q-type) calcium channels. In FHM1 …
caused by gain-of-function mutations in CaV2. 1 (P/Q-type) calcium channels. In FHM1 …
[引用][C] Mechanism underlying unaltered cortical inhibitory synaptic transmission in contrast with enhanced excitatory transmission in Ca (V) 2.1 knockin migraine mice
D Vecchia, A Tottene… - Neurobiology …, 2014 - scholarlypublications …
Mechanism underlying unaltered cortical inhibitory synaptic transmission in contrast with
enhanced excitatory transmission in Ca(V)2.1 knockin migraine mice | Scholarly …
enhanced excitatory transmission in Ca(V)2.1 knockin migraine mice | Scholarly …
Mechanism underlying unaltered cortical inhibitory synaptic transmission in contrast with enhanced excitatory transmission in CaV2. 1 knockin migraine mice
D Vecchia, A Tottene… - Neurobiology of …, 2014 - infona.pl
Familial hemiplegic migraine type 1 (FHM1), a monogenic subtype of migraine with aura, is
caused by gain-of-function mutations in CaV2. 1 (P/Q-type) calcium channels. In FHM1 …
caused by gain-of-function mutations in CaV2. 1 (P/Q-type) calcium channels. In FHM1 …
Mechanism underlying unaltered cortical inhibitory synaptic transmission in contrast with enhanced excitatory transmission in CaV2. 1 knockin migraine mice.
D Vecchia, A Tottene… - Neurobiology of …, 2014 - europepmc.org
Familial hemiplegic migraine type 1 (FHM1), a monogenic subtype of migraine with aura, is
caused by gain-of-function mutations in Ca V 2.1 (P/Q-type) calcium channels. In FHM1 …
caused by gain-of-function mutations in Ca V 2.1 (P/Q-type) calcium channels. In FHM1 …
[PDF][PDF] Mechanism underlying unaltered cortical inhibitory synaptic transmission in contrast with enhanced excitatory transmission in CaV2. 1 knockin migraine mice
D Vecchia, A Tottene… - Neurobiology of …, 2014 - core.ac.uk
Dania Vecchia a, Angelita Tottene a, Arn MJM van den Maagdenberg b, Daniela Pietrobon
a,⁎ a Department of Biomedical Sciences, University of Padova and CNR Institute of …
a,⁎ a Department of Biomedical Sciences, University of Padova and CNR Institute of …
[HTML][HTML] Mechanism underlying unaltered cortical inhibitory synaptic transmission in contrast with enhanced excitatory transmission in CaV2. 1 knockin migraine mice
D Vecchia, A Tottene… - Neurobiology of …, 2014 - ncbi.nlm.nih.gov
Familial hemiplegic migraine type 1 (FHM1), a monogenic subtype of migraine with aura, is
caused by gain-of-function mutations in Ca V 2.1 (P/Q-type) calcium channels. In FHM1 …
caused by gain-of-function mutations in Ca V 2.1 (P/Q-type) calcium channels. In FHM1 …
Mechanism underlying unaltered cortical inhibitory synaptic transmission in contrast with enhanced excitatory transmission in CaV2. 1 knockin migraine mice.
D Vecchia, A Tottene… - Neurobiology of …, 2014 - europepmc.org
Familial hemiplegic migraine type 1 (FHM1), a monogenic subtype of migraine with aura, is
caused by gain-of-function mutations in Ca V 2.1 (P/Q-type) calcium channels. In FHM1 …
caused by gain-of-function mutations in Ca V 2.1 (P/Q-type) calcium channels. In FHM1 …