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

2

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

3

Genetics of seven Dutch familial atypical multiple mole-melanoma syndrome families: a review of linkage results including chromosomes 1 and 9.

Bergman W, Gruis NA, Sandkuijl LA, Frants RR. Bergman W, et al. Among authors: sandkuijl la. J Invest Dermatol. 1994 Nov;103(5 Suppl):122S-125S. doi: 10.1111/1523-1747.ep12399430. J Invest Dermatol. 1994. PMID: 7963673 Free article.

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

5

Migraine, ataxia and epilepsy: a challenging spectrum of genetically determined calcium channelopathies. Dutch Migraine Genetics Research Group.

Terwindt GM, Ophoff RA, Haan J, Sandkuijl LA, Frants RR, Ferrari MD. Terwindt GM, et al. Among authors: sandkuijl la. Eur J Hum Genet. 1998 Jul-Aug;6(4):297-307. doi: 10.1038/sj.ejhg.5200206. Eur J Hum Genet. 1998. PMID: 9781035 Review.

6

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: sandkuijl la. Neurology. 2001 Apr 24;56(8):1028-32. doi: 10.1212/wnl.56.8.1028. Neurology. 2001. PMID: 11320173

7

Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3.

Ophoff RA, DeYoung J, Service SK, Joosse M, Caffo NA, Sandkuijl LA, Terwindt GM, Haan J, van den Maagdenberg AM, Jen J, Baloh RW, Barilla-LaBarca ML, Saccone NL, Atkinson JP, Ferrari MD, Freimer NB, Frants RR. Ophoff RA, et al. Among authors: sandkuijl la. Am J Hum Genet. 2001 Aug;69(2):447-53. doi: 10.1086/321975. Epub 2001 Jun 28. Am J Hum Genet. 2001. PMID: 11438888 Free PMC article.

8

Linkage analysis under locus heterogeneity: behaviour of the A-test in complex analyses.

Janssen B, Halley D, Sandkuijl L. Janssen B, et al. Hum Hered. 1997 Jul-Aug;47(4):223-33. doi: 10.1159/000154416. Hum Hered. 1997. PMID: 9239509

9

Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds.

Gruis NA, van der Velden PA, Sandkuijl LA, Prins DE, Weaver-Feldhaus J, Kamb A, Bergman W, Frants RR. Gruis NA, et al. Among authors: sandkuijl la. Nat Genet. 1995 Jul;10(3):351-3. doi: 10.1038/ng0795-351. Nat Genet. 1995. PMID: 7670475

10

Facioscapulohumeral muscular dystrophy in the Dutch population.

Padberg GW, Frants RR, Brouwer OF, Wijmenga C, Bakker E, Sandkuijl LA. Padberg GW, et al. Among authors: sandkuijl la. Muscle Nerve Suppl. 1995;2:S81-4. Muscle Nerve Suppl. 1995. PMID: 7739631 Free article.

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