Lindhout D - Search Results

1

Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndrome.

Terwindt GM, Ophoff RA, Lindhout D, Haan J, Halley DJ, Sandkuijl LA, Brouwer OF, Frants RR, Ferrari MD. Terwindt GM, et al. Among authors: lindhout d. Epilepsia. 1997 Aug;38(8):915-21. doi: 10.1111/j.1528-1157.1997.tb01257.x. Epilepsia. 1997. PMID: 9579893 Free article.

2

Is familial hemiplegic migraine a hereditary form of basilar migraine?

Haan J, Terwindt GM, Ophoff RA, Bos PL, Frants RR, Ferrari MD, Krommenhoek T, Lindhout DL, Sandkuyl LA, Van Eyk R. Haan J, et al. Among authors: lindhout dl. Cephalalgia. 1995 Dec;15(6):477-81. doi: 10.1046/j.1468-2982.1995.1506477.x. Cephalalgia. 1995. PMID: 8706110 Clinical Trial.

3

Familial partial epilepsy with variable foci in a Dutch family: clinical characteristics and confirmation of linkage to chromosome 22q.

Callenbach PM, van den Maagdenberg AM, Hottenga JJ, van den Boogerd EH, de Coo RF, Lindhout D, Frants RR, Sandkuijl LA, Brouwer OF. Callenbach PM, et al. Among authors: lindhout d. Epilepsia. 2003 Oct;44(10):1298-305. doi: 10.1046/j.1528-1157.2003.62302.x. Epilepsia. 2003. PMID: 14510823 Free article.

4

Genetic heterogeneity of familial hemiplegic migraine.

Ophoff RA, van Eijk R, Sandkuijl LA, Terwindt GM, Grubben CP, Haan J, Lindhout D, Ferrari MD, Frants RR. Ophoff RA, et al. Among authors: lindhout d. Genomics. 1994 Jul 1;22(1):21-6. doi: 10.1006/geno.1994.1340. Genomics. 1994. PMID: 7959770

5

Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura.

May A, Ophoff RA, Terwindt GM, Urban C, van Eijk R, Haan J, Diener HC, Lindhout D, Frants RR, Sandkuijl LA, et al. May A, et al. Among authors: lindhout d. Hum Genet. 1995 Nov;96(5):604-8. doi: 10.1007/BF00197420. Hum Genet. 1995. PMID: 8530012

6

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: lindhout d. Cell. 1996 Nov 1;87(3):543-52. doi: 10.1016/s0092-8674(00)81373-2. Cell. 1996. PMID: 8898206 Free article.

7

Evidence for linkage between juvenile myoclonic epilepsy-related idiopathic generalized epilepsy and 6p11-12 in Dutch families.

Pinto D, de Haan GJ, Janssen GA, Boezeman EH, van Erp MG, Westland B, Witte J, Bader A, Halley DJ, Kasteleijn-Nolst Trenité DG, Lindhout D, Koeleman BP. Pinto D, et al. Among authors: lindhout d. Epilepsia. 2004 Mar;45(3):211-7. doi: 10.1111/j.0013-9580.2004.36003.x. Epilepsia. 2004. PMID: 15009221 Free article.

8

A novel splicing mutation in KCNQ2 in a multigenerational family with BFNC followed for 25 years.

de Haan GJ, Pinto D, Carton D, Bader A, Witte J, Peters E, van Erp G, Vandereyken W, Boezeman E, Wapenaar MC, Boon P, Halley D, Koeleman BP, Lindhout D. de Haan GJ, et al. Among authors: lindhout d. Epilepsia. 2006 May;47(5):851-9. doi: 10.1111/j.1528-1167.2006.00552.x. Epilepsia. 2006. PMID: 16686649 Free article.

9

Benign familial infantile convulsions: a clinical study of seven Dutch families.

Callenbach PM, de Coo RF, Vein AA, Arts WF, Oosterwijk J, Hageman G, ten Houten R, Terwindt GM, Lindhout D, Frants RR, Brouwer OF. Callenbach PM, et al. Among authors: lindhout d. Eur J Paediatr Neurol. 2002;6(5):269-83. doi: 10.1053/ejpn.2002.0609. Eur J Paediatr Neurol. 2002. PMID: 12374579 Free article.

10

The gene for triphalangeal thumb maps to the subtelomeric region of chromosome 7q.

Heutink P, Zguricas J, van Oosterhout L, Breedveld GJ, Testers L, Sandkuijl LA, Snijders PJ, Weissenbach J, Lindhout D, Hovius SE, et al. Heutink P, et al. Among authors: lindhout d. Nat Genet. 1994 Mar;6(3):287-92. doi: 10.1038/ng0394-287. Nat Genet. 1994. PMID: 8012392

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