Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 17

1.

Defective glutamate and K+ clearance by cortical astrocytes in familial hemiplegic migraine type 2.

Capuani C, Melone M, Tottene A, Bragina L, Crivellaro G, Santello M, Casari G, Conti F, Pietrobon D.

EMBO Mol Med. 2016 Aug 1;8(8):967-86. doi: 10.15252/emmm.201505944. Print 2016 Aug.

2.

Abnormal cortical synaptic transmission in CaV2.1 knockin mice with the S218L missense mutation which causes a severe familial hemiplegic migraine syndrome in humans.

Vecchia D, Tottene A, van den Maagdenberg AM, Pietrobon D.

Front Cell Neurosci. 2015 Feb 17;9:8. doi: 10.3389/fncel.2015.00008. eCollection 2015.

3.

Mechanism underlying unaltered cortical inhibitory synaptic transmission in contrast with enhanced excitatory transmission in CaV2.1 knockin migraine mice.

Vecchia D, Tottene A, van den Maagdenberg AM, Pietrobon D.

Neurobiol Dis. 2014 Sep;69:225-34. doi: 10.1016/j.nbd.2014.05.035. Epub 2014 Jun 5.

4.

Role of different voltage-gated Ca2+ channels in cortical spreading depression: specific requirement of P/Q-type Ca2+ channels.

Tottene A, Urbani A, Pietrobon D.

Channels (Austin). 2011 Mar-Apr;5(2):110-4. Epub 2011 Mar 1.

PMID:
21150292
5.

High cortical spreading depression susceptibility and migraine-associated symptoms in Ca(v)2.1 S218L mice.

van den Maagdenberg AM, Pizzorusso T, Kaja S, Terpolilli N, Shapovalova M, Hoebeek FE, Barrett CF, Gherardini L, van de Ven RC, Todorov B, Broos LA, Tottene A, Gao Z, Fodor M, De Zeeuw CI, Frants RR, Plesnila N, Plomp JJ, Pietrobon D, Ferrari MD.

Ann Neurol. 2010 Jan;67(1):85-98. doi: 10.1002/ana.21815.

PMID:
20186955
6.

Enhanced excitatory transmission at cortical synapses as the basis for facilitated spreading depression in Ca(v)2.1 knockin migraine mice.

Tottene A, Conti R, Fabbro A, Vecchia D, Shapovalova M, Santello M, van den Maagdenberg AM, Ferrari MD, Pietrobon D.

Neuron. 2009 Mar 12;61(5):762-73. doi: 10.1016/j.neuron.2009.01.027.

7.

Specific kinetic alterations of human CaV2.1 calcium channels produced by mutation S218L causing familial hemiplegic migraine and delayed cerebral edema and coma after minor head trauma.

Tottene A, Pivotto F, Fellin T, Cesetti T, van den Maagdenberg AM, Pietrobon D.

J Biol Chem. 2005 May 6;280(18):17678-86. Epub 2005 Mar 2.

8.

A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression.

van den Maagdenberg AM, Pietrobon D, Pizzorusso T, Kaja S, Broos LA, Cesetti T, van de Ven RC, Tottene A, van der Kaa J, Plomp JJ, Frants RR, Ferrari MD.

Neuron. 2004 Mar 4;41(5):701-10.

9.

Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons.

Tottene A, Fellin T, Pagnutti S, Luvisetto S, Striessnig J, Fletcher C, Pietrobon D.

Proc Natl Acad Sci U S A. 2002 Oct 1;99(20):13284-9. Epub 2002 Sep 16.

10.

Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity.

Fletcher CF, Tottene A, Lennon VA, Wilson SM, Dubel SJ, Paylor R, Hosford DA, Tessarollo L, McEnery MW, Pietrobon D, Copeland NG, Jenkins NA.

FASEB J. 2001 May;15(7):1288-90. No abstract available.

PMID:
11344116
11.

Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2.

Guida S, Trettel F, Pagnutti S, Mantuano E, Tottene A, Veneziano L, Fellin T, Spadaro M, Stauderman K, Williams M, Volsen S, Ophoff R, Frants R, Jodice C, Frontali M, Pietrobon D.

Am J Hum Genet. 2001 Mar;68(3):759-64. Epub 2001 Feb 1.

13.

Isoforms of alpha1E voltage-gated calcium channels in rat cerebellar granule cells--detection of major calcium channel alpha1-transcripts by reverse transcription-polymerase chain reaction.

Schramm M, Vajna R, Pereverzev A, Tottene A, Klöckner U, Pietrobon D, Hescheler J, Schneider T.

Neuroscience. 1999;92(2):565-75.

PMID:
10408605
14.

Anomalous L-type calcium channels of rat spinal motoneurons.

Hivert B, Luvisetto S, Navangione A, Tottene A, Pietrobon D.

J Gen Physiol. 1999 May;113(5):679-94.

15.

Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine.

Hans M, Luvisetto S, Williams ME, Spagnolo M, Urrutia A, Tottene A, Brust PF, Johnson EC, Harpold MM, Stauderman KA, Pietrobon D.

J Neurosci. 1999 Mar 1;19(5):1610-9.

16.

Functional diversity of P-type and R-type calcium channels in rat cerebellar neurons.

Tottene A, Moretti A, Pietrobon D.

J Neurosci. 1996 Oct 15;16(20):6353-63.

17.

Three novel types of voltage-dependent calcium channels in rat cerebellar neurons.

Forti L, Tottene A, Moretti A, Pietrobon D.

J Neurosci. 1994 Sep;14(9):5243-56.

Supplemental Content

Loading ...
Support Center