Ferrari MD - Search Results

1

Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation.

Vanmolkot KR, Stroink H, Koenderink JB, Kors EE, van den Heuvel JJ, van den Boogerd EH, Stam AH, Haan J, De Vries BB, Terwindt GM, Frants RR, Ferrari MD, van den Maagdenberg AM. Vanmolkot KR, et al. Among authors: ferrari md. Ann Neurol. 2006 Feb;59(2):310-4. doi: 10.1002/ana.20760. Ann Neurol. 2006. PMID: 16437583

2

The quest for migraine genes.

Terwindt GM, Haan J, Ophoff RA, Frants RR, Ferrari MD. Terwindt GM, et al. Among authors: ferrari md. Curr Opin Neurol. 1997 Jun;10(3):221-5. doi: 10.1097/00019052-199706000-00009. Curr Opin Neurol. 1997. PMID: 9229129 Review.

3

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. Terwindt GM, et al. Among authors: ferrari md. Neurology. 1998 Apr;50(4):1105-10. doi: 10.1212/wnl.50.4.1105. Neurology. 1998. PMID: 9566402

4

Genetics of primary headaches.

Kors EE, Haan J, Ferrari MD. Kors EE, et al. Among authors: ferrari md. Curr Opin Neurol. 1999 Jun;12(3):249-54. doi: 10.1097/00019052-199906000-00002. Curr Opin Neurol. 1999. PMID: 10499169 Review.

5

Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura.

Terwindt GM, Ophoff RA, van Eijk R, Vergouwe MN, Haan J, Frants RR, Sandkuijl LA, Ferrari MD; Dutch Migraine Genetics Research Group. Terwindt GM, et al. Among authors: ferrari md. Neurology. 2001 Apr 24;56(8):1028-32. doi: 10.1212/wnl.56.8.1028. Neurology. 2001. PMID: 11320173

6

Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine.

Kors EE, Terwindt GM, Vermeulen FL, Fitzsimons RB, Jardine PE, Heywood P, Love S, van den Maagdenberg AM, Haan J, Frants RR, Ferrari MD. Kors EE, et al. Among authors: ferrari md. Ann Neurol. 2001 Jun;49(6):753-60. doi: 10.1002/ana.1031. Ann Neurol. 2001. PMID: 11409427

7

Episodic ataxia type 2. Three novel truncating mutations and one novel missense mutation in the CACNA1A gene.

van den Maagdenberg AM, Kors EE, Brunt ER, van Paesschen W, Pascual J, Ravine D, Keeling S, Vanmolkot KR, Vermeulen FL, Terwindt GM, Haan J, Frants RR, Ferrari MD. van den Maagdenberg AM, et al. Among authors: ferrari md. J Neurol. 2002 Nov;249(11):1515-9. doi: 10.1007/s00415-002-0860-8. J Neurol. 2002. PMID: 12420090

8

Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine.

Kors EE, Haan J, Giffin NJ, Pazdera L, Schnittger C, Lennox GG, Terwindt GM, Vermeulen FL, Van den Maagdenberg AM, Frants RR, Ferrari MD. Kors EE, et al. Among authors: ferrari md. Arch Neurol. 2003 May;60(5):684-8. doi: 10.1001/archneur.60.5.684. Arch Neurol. 2003. PMID: 12756131

9

Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation.

Kors EE, Melberg A, Vanmolkot KR, Kumlien E, Haan J, Raininko R, Flink R, Ginjaar HB, Frants RR, Ferrari MD, van den Maagdenberg AM. Kors EE, et al. Among authors: ferrari md. Neurology. 2004 Sep 28;63(6):1136-7. doi: 10.1212/01.wnl.0000138571.48593.fc. Neurology. 2004. PMID: 15452324 No abstract available.

10

[From gene to disease; familial hemiplegic migraine as a result of mutations in a sodium-potassium pump gene].

Kors EE, Vanmolkot KR, Haan J, van den Maagdenberg AM, Frants RR, Ferrari MD. Kors EE, et al. Among authors: ferrari md. Ned Tijdschr Geneeskd. 2004 Sep 25;148(39):1919-20. Ned Tijdschr Geneeskd. 2004. PMID: 15495990 Review. Dutch.

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