Lindhout DL - Search Results

1

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.

2

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. Epilepsia. 1997 Aug;38(8):915-21. doi: 10.1111/j.1528-1157.1997.tb01257.x. Epilepsia. 1997. PMID: 9579893 Free article.

3

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. Genomics. 1994 Jul 1;22(1):21-6. doi: 10.1006/geno.1994.1340. Genomics. 1994. PMID: 7959770

4

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. Hum Genet. 1995 Nov;96(5):604-8. doi: 10.1007/BF00197420. Hum Genet. 1995. PMID: 8530012

5

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

6

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. Eur J Paediatr Neurol. 2002;6(5):269-83. doi: 10.1053/ejpn.2002.0609. Eur J Paediatr Neurol. 2002. PMID: 12374579 Free article.

7

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. Epilepsia. 2003 Oct;44(10):1298-305. doi: 10.1046/j.1528-1157.2003.62302.x. Epilepsia. 2003. PMID: 14510823 Free article.

8

A leucine-to-proline mutation in the insulin receptor in a family with insulin resistance.

Klinkhamer MP, Groen NA, van der Zon GC, Lindhout D, Sandkuyl LA, Krans HM, Möller W, Maassen JA. Klinkhamer MP, et al. EMBO J. 1989 Sep;8(9):2503-7. doi: 10.1002/j.1460-2075.1989.tb08387.x. EMBO J. 1989. PMID: 2479553 Free PMC article.

9

A comparative study on genetic heterogeneity in tuberous sclerosis: evidence for one gene on 9q34 and a second gene on 11q22-23.

Janssen LA, Povey S, Attwood J, Sandkuyl LA, Lindhout D, Flodman P, Smith M, Sampson JR, Haines JL, Merkens EC, et al. Janssen LA, et al. Ann N Y Acad Sci. 1991;615:306-15. doi: 10.1111/j.1749-6632.1991.tb37772.x. Ann N Y Acad Sci. 1991. PMID: 2039153 No abstract available.

10

A case of ALS-FTD in a large FALS pedigree with a K17I ANG mutation.

van Es MA, Diekstra FP, Veldink JH, Baas F, Bourque PR, Schelhaas HJ, Strengman E, Hennekam EA, Lindhout D, Ophoff RA, van den Berg LH. van Es MA, et al. Neurology. 2009 Jan 20;72(3):287-8. doi: 10.1212/01.wnl.0000339487.84908.00. Neurology. 2009. PMID: 19153377 Free article. No abstract available.

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