Ferrari MD - Search Results

1

Genetics of migraine: an update with special attention to genetic comorbidity.

Stam AH, van den Maagdenberg AM, Haan J, Terwindt GM, Ferrari MD. Stam AH, et al. Among authors: ferrari md. Curr Opin Neurol. 2008 Jun;21(3):288-93. doi: 10.1097/WCO.0b013e3282fd171a. Curr Opin Neurol. 2008. PMID: 18451712 Review.

2

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.

Ophoff RA, Terwindt GM, Vergouwe MN, van Eijk R, Oefner PJ, Hoffman SM, Lamerdin JE, Mohrenweiser HW, Bulman DE, Ferrari M, Haan J, Lindhout D, van Ommen GJ, Hofker MH, Ferrari MD, Frants RR. Ophoff RA, et al. Among authors: ferrari m, ferrari md. Cell. 1996 Nov 1;87(3):543-52. doi: 10.1016/s0092-8674(00)81373-2. Cell. 1996. PMID: 8898206 Free article.

3

Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine.

Terwindt G, Kors E, Haan J, Vermeulen F, Van den Maagdenberg A, Frants R, Ferrari M. Terwindt G, et al. Arch Neurol. 2002 Jun;59(6):1016-8. doi: 10.1001/archneur.59.6.1016. Arch Neurol. 2002. PMID: 12056940 Review.

4

Migraine genetics.

Kors E, Haan J, Ferrari M. Kors E, et al. Curr Pain Headache Rep. 2003 Jun;7(3):212-7. doi: 10.1007/s11916-003-0075-4. Curr Pain Headache Rep. 2003. PMID: 12720601 Review.

5

Evaluation of diagnostic NOTCH3 immunostaining in CADASIL.

Lesnik Oberstein SA, van Duinen SG, van den Boom R, Maat-Schieman ML, van Buchem MA, van Houwelingen HC, Hegeman-Kleinn IM, Ferrari MD, Breuning MH, Haan J. Lesnik Oberstein SA, et al. Among authors: ferrari md. Acta Neuropathol. 2003 Aug;106(2):107-11. doi: 10.1007/s00401-003-0701-6. Epub 2003 May 17. Acta Neuropathol. 2003. PMID: 12756589

6

Cerebral hemodynamics and white matter hyperintensities in CADASIL.

van den Boom R, Lesnik Oberstein SA, Spilt A, Behloul F, Ferrari MD, Haan J, Westendorp RG, van Buchem MA. van den Boom R, et al. Among authors: ferrari md. J Cereb Blood Flow Metab. 2003 May;23(5):599-604. doi: 10.1097/01.WCB.0000062341.61367.D3. J Cereb Blood Flow Metab. 2003. PMID: 12771575

7

Myocardial infarction in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Lesnik Oberstein SA, Jukema JW, Van Duinen SG, Macfarlane PW, van Houwelingen HC, Breuning MH, Ferrari MD, Haan J. Lesnik Oberstein SA, et al. Among authors: ferrari md. Medicine (Baltimore). 2003 Jul;82(4):251-6. doi: 10.1097/01.md.0000085054.63483.40. Medicine (Baltimore). 2003. PMID: 12861102 Free article.

8

Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions.

Vanmolkot KR, Kors EE, Hottenga JJ, Terwindt GM, Haan J, Hoefnagels WA, Black DF, Sandkuijl LA, Frants RR, Ferrari MD, van den Maagdenberg AM. Vanmolkot KR, et al. Among authors: ferrari md. Ann Neurol. 2003 Sep;54(3):360-6. doi: 10.1002/ana.10674. Ann Neurol. 2003. PMID: 12953268

9

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: MR imaging findings at different ages--3rd-6th decades.

van den Boom R, Lesnik Oberstein SA, Ferrari MD, Haan J, van Buchem MA. van den Boom R, et al. Among authors: ferrari md. Radiology. 2003 Dec;229(3):683-90. doi: 10.1148/radiol.2293021354. Epub 2003 Oct 30. Radiology. 2003. PMID: 14593195

10

New discoveries about the second gene for familial hemiplegic migraine, ATP1A2.

Vanmolkot KR, van den Maagdenberg AM, Haan J, Ferrari MD. Vanmolkot KR, et al. Among authors: ferrari md. Lancet Neurol. 2003 Dec;2(12):721. doi: 10.1016/s1474-4422(03)00591-x. Lancet Neurol. 2003. PMID: 14636773 No abstract available.

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