[HTML][HTML] Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2

L Leo, L Gherardini, V Barone, M De Fusco… - PLoS …, 2011 - journals.plos.org
Familial hemiplegic migraine type 2 (FHM2) is an autosomal dominant form of migraine with
aura that is caused by mutations of the α2-subunit of the Na, K-ATPase, an isoform almost …

[HTML][HTML] Increased Susceptibility to Cortical Spreading Depression in the Mouse Model of Familial Hemiplegic Migraine Type 2

L Leo, L Gherardini, V Barone, M De Fusco… - PLoS …, 2011 - ncbi.nlm.nih.gov
Familial hemiplegic migraine type 2 (FHM2) is an autosomal dominant form of migraine with
aura that is caused by mutations of the α2-subunit of the Na, K-ATPase, an isoform almost …

Increased Susceptibility to Cortical Spreading Depression in the Mouse Model of Familial Hemiplegic Migraine Type 2

L Leo, L Gherardini, V Barone, M De Fusco… - PLoS …, 2011 - search.proquest.com
Familial hemiplegic migraine type 2 (FHM2) is an autosomal dominant form of migraine with
aura that is caused by mutations of the α2-subunit of the Na, K-ATPase, an isoform almost …

Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2.

L Leo, L Gherardini, V Barone, M De Fusco… - Plos Genetics, 2011 - europepmc.org
Familial hemiplegic migraine type 2 (FHM2) is an autosomal dominant form of migraine with
aura that is caused by mutations of the α2-subunit of the Na, K-ATPase, an isoform almost …

[引用][C] Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2

L Leo, L Gherardini, V Barone, M De Fusco… - PLOS …, 2011 - iris.unisr.it
Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic
migraine type 2 IRIS IRIS Home Sfoglia Macrotipologie & tipologie Autore Titolo Riviste Serie IT …

Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2

L Leo, L Gherardini, V Barone, M De Fusco… - PLOS …, 2011 - research.unipd.it
Familial hemiplegic migraine type 2 (FHM2) is an autosomal dominant form of migraine with
aura that is caused by mutations of the a2-subunit of the Na, K-ATPase, an isoform almost …

[PDF][PDF] Increased Susceptibility to Cortical Spreading Depression in the Mouse Model of

L Leo, L Gherardini, V Barone, M De Fusco… - 2011 - core.ac.uk
Familial hemiplegic migraine type 2 (FHM2) is an autosomal dominant form of migraine with
aura that is caused by mutations of the o2-subunit of the Na, K-ATPase, an isoform almost …

Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2

L Leo, L Gherardini, V Barone, M De Fusco… - PLoS …, 2011 - pubmed.ncbi.nlm.nih.gov
Familial hemiplegic migraine type 2 (FHM2) is an autosomal dominant form of migraine with
aura that is caused by mutations of the α2-subunit of the Na, K-ATPase, an isoform almost …

[PDF][PDF] Increased Susceptibility to Cortical Spreading Depression in the Mouse Model of

L Leo, L Gherardini, V Barone, M De Fusco… - 2011 - academia.edu
Familial hemiplegic migraine type 2 (FHM2) is an autosomal dominant form of migraine with
aura that is caused by mutations of the o2-subunit of the Na, K-ATPase, an isoform almost …

Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2

L Leo, L Gherardini, V Barone, M De Fusco… - PLoS …, 2011 - go.gale.com
Familial hemiplegic migraine type 2 (FHM2) is an autosomal dominant form of migraine with
aura that is caused by mutations of the [alpha] 2-subunit of the Na, K-ATPase, an isoform …