Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 177

1.

RNA expression profiling in brains of familial hemiplegic migraine type 1 knock-in mice.

de Vries B, Eising E, Broos LA, Koelewijn SC, Todorov B, Frants RR, Boer JM, Ferrari MD, Hoen PA, van den Maagdenberg AM.

Cephalalgia. 2014 Mar;34(3):174-82. doi: 10.1177/0333102413502736. Epub 2013 Aug 28.

PMID:
23985897
2.

A hyperexcitability phenotype in mouse trigeminal sensory neurons expressing the R192Q Cacna1a missense mutation of familial hemiplegic migraine type-1.

Hullugundi SK, Ansuini A, Ferrari MD, van den Maagdenberg AM, Nistri A.

Neuroscience. 2014 Apr 25;266:244-54. doi: 10.1016/j.neuroscience.2014.02.020. Epub 2014 Feb 27.

PMID:
24583041
3.

Differential cerebellar GABAA receptor expression in mice with mutations in CaV2.1 (P/Q-type) calcium channels.

Kaja S, Payne AJ, Nielsen EØ, Thompson CL, van den Maagdenberg AM, Koulen P, Snutch TP.

Neuroscience. 2015 Sep 24;304:198-208. doi: 10.1016/j.neuroscience.2015.07.044. Epub 2015 Jul 21.

4.

Familial hemiplegic migraine type-1 mutated cav2.1 calcium channels alter inhibitory and excitatory synaptic transmission in the lateral superior olive of mice.

Inchauspe CG, Pilati N, Di Guilmi MN, Urbano FJ, Ferrari MD, van den Maagdenberg AM, Forsythe ID, Uchitel OD.

Hear Res. 2015 Jan;319:56-68. doi: 10.1016/j.heares.2014.11.006. Epub 2014 Dec 4.

PMID:
25481823
5.

Enhanced subcortical spreading depression in familial hemiplegic migraine type 1 mutant mice.

Eikermann-Haerter K, Yuzawa I, Qin T, Wang Y, Baek K, Kim YR, Hoffmann U, Dilekoz E, Waeber C, Ferrari MD, van den Maagdenberg AM, Moskowitz MA, Ayata C.

J Neurosci. 2011 Apr 13;31(15):5755-63. doi: 10.1523/JNEUROSCI.5346-10.2011.

6.

Immunohistochemical characterization of calcitonin gene-related peptide in the trigeminal system of the familial hemiplegic migraine 1 knock-in mouse.

Mathew R, Andreou AP, Chami L, Bergerot A, van den Maagdenberg AM, Ferrari MD, Goadsby PJ.

Cephalalgia. 2011 Oct;31(13):1368-80. doi: 10.1177/0333102411418847. Epub 2011 Sep 5.

PMID:
21893556
7.

Differential trigeminovascular nociceptive responses in the thalamus in the familial hemiplegic migraine 1 knock-in mouse: a Fos protein study.

Park J, Moon H, Akerman S, Holland PR, Lasalandra MP, Andreou AP, Ferrari MD, van den Maagdenberg AM, Goadsby PJ.

Neurobiol Dis. 2014 Apr;64:1-7. doi: 10.1016/j.nbd.2013.12.004. Epub 2013 Dec 17.

PMID:
24355314
8.

Cortical Spreading Depression Causes Unique Dysregulation of Inflammatory Pathways in a Transgenic Mouse Model of Migraine.

Eising E, Shyti R, 't Hoen PAC, Vijfhuizen LS, Huisman SMH, Broos LAM, Mahfouz A, Reinders MJT, Ferrari MD, Tolner EA, de Vries B, van den Maagdenberg AMJM.

Mol Neurobiol. 2017 May;54(4):2986-2996. doi: 10.1007/s12035-015-9681-5. Epub 2016 Mar 31.

9.

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
10.

Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group.

Terwindt GM, Ophoff RA, Haan J, Vergouwe MN, van Eijk R, Frants RR, Ferrari MD.

Neurology. 1998 Apr;50(4):1105-10.

PMID:
9566402
11.

Activity-dependent calcium, oxygen, and vascular responses in a mouse model of familial hemiplegic migraine type 1.

Khennouf L, Gesslein B, Lind BL, van den Maagdenberg AM, Lauritzen M.

Ann Neurol. 2016 Aug;80(2):219-32. doi: 10.1002/ana.24707. Epub 2016 Jul 26.

PMID:
27314908
12.

Trigeminal ganglion neuron subtype-specific alterations of Ca(V)2.1 calcium current and excitability in a Cacna1a mouse model of migraine.

Fioretti B, Catacuzzeno L, Sforna L, Gerke-Duncan MB, van den Maagdenberg AM, Franciolini F, Connor M, Pietrobon D.

J Physiol. 2011 Dec 1;589(Pt 23):5879-95. doi: 10.1113/jphysiol.2011.220533. Epub 2011 Oct 17.

13.

Large-scale mass spectrometry imaging investigation of consequences of cortical spreading depression in a transgenic mouse model of migraine.

Carreira RJ, Shyti R, Balluff B, Abdelmoula WM, van Heiningen SH, van Zeijl RJ, Dijkstra J, Ferrari MD, Tolner EA, McDonnell LA, van den Maagdenberg AM.

J Am Soc Mass Spectrom. 2015 Jun;26(6):853-61. doi: 10.1007/s13361-015-1136-8. Epub 2015 Apr 16.

14.

Familial hemiplegic migraine type 1 mutations W1684R and V1696I alter G protein-mediated regulation of Ca(V)2.1 voltage-gated calcium channels.

Garza-López E, Sandoval A, González-Ramírez R, Gandini MA, Van den Maagdenberg A, De Waard M, Felix R.

Biochim Biophys Acta. 2012 Aug;1822(8):1238-46. doi: 10.1016/j.bbadis.2012.04.008. Epub 2012 Apr 20.

15.

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.

16.

CaV2.1 voltage activated calcium channels and synaptic transmission in familial hemiplegic migraine pathogenesis.

Uchitel OD, Inchauspe CG, Urbano FJ, Di Guilmi MN.

J Physiol Paris. 2012 Jan;106(1-2):12-22. doi: 10.1016/j.jphysparis.2011.10.004. Epub 2011 Nov 2. Review.

PMID:
22074995
17.

The familial hemiplegic migraine type 1 mutation K1336E affects direct G protein-mediated regulation of neuronal P/Q-type Ca2+ channels.

Garza-López E, González-Ramírez R, Gandini MA, Sandoval A, Felix R.

Cephalalgia. 2013 Apr;33(6):398-407. doi: 10.1177/0333102412475236. Epub 2013 Feb 19.

PMID:
23430985
18.

Severe and progressive neurotransmitter release aberrations in familial hemiplegic migraine type 1 Cacna1a S218L knock-in mice.

Kaja S, Van de Ven RC, Broos LA, Frants RR, Ferrari MD, Van den Maagdenberg AM, Plomp JJ.

J Neurophysiol. 2010 Sep;104(3):1445-55. doi: 10.1152/jn.00012.2010. Epub 2010 Jul 14.

19.

Presynaptic CaV2.1 calcium channels carrying familial hemiplegic migraine mutation R192Q allow faster recovery from synaptic depression in mouse calyx of Held.

Inchauspe CG, Urbano FJ, Di Guilmi MN, Ferrari MD, van den Maagdenberg AM, Forsythe ID, Uchitel OD.

J Neurophysiol. 2012 Dec;108(11):2967-76. doi: 10.1152/jn.01183.2011. Epub 2012 Sep 5.

20.

Synaptic gain-of-function effects of mutant Cav2.1 channels in a mouse model of familial hemiplegic migraine are due to increased basal [Ca2+]i.

Di Guilmi MN, Wang T, Inchauspe CG, Forsythe ID, Ferrari MD, van den Maagdenberg AM, Borst JG, Uchitel OD.

J Neurosci. 2014 May 21;34(21):7047-58. doi: 10.1523/JNEUROSCI.2526-13.2014.

Supplemental Content

Support Center