Laan L - Search Results

1

Course and outcome of childhood epilepsy: a 15-year follow-up of the Dutch Study of Epilepsy in Childhood.

Geerts A, Arts WF, Stroink H, Peeters E, Brouwer O, Peters B, Laan L, van Donselaar C. Geerts A, et al. Among authors: laan l. Epilepsia. 2010 Jul;51(7):1189-97. doi: 10.1111/j.1528-1167.2010.02546.x. Epub 2010 Jun 14. Epilepsia. 2010. PMID: 20557350 Free article.

2

Evolution of epilepsy and EEG findings in Angelman syndrome.

Laan LA, Renier WO, Arts WF, Buntinx IM, vd Burgt IJ, Stroink H, Beuten J, Zwinderman KH, van Dijk JG, Brouwer OF. Laan LA, et al. Epilepsia. 1997 Feb;38(2):195-9. doi: 10.1111/j.1528-1157.1997.tb01097.x. Epilepsia. 1997. PMID: 9048672 Free article.

3

Angelman syndrome: a review of clinical and genetic aspects.

Laan LA, v Haeringen A, Brouwer OF. Laan LA, et al. Clin Neurol Neurosurg. 1999 Sep;101(3):161-70. doi: 10.1016/s0303-8467(99)00030-x. Clin Neurol Neurosurg. 1999. PMID: 10536901 Review.

4

Angelman syndrome in adulthood.

Laan LA, den Boer AT, Hennekam RC, Renier WO, Brouwer OF. Laan LA, et al. Am J Med Genet. 1996 Dec 18;66(3):356-60. doi: 10.1002/(SICI)1096-8628(19961218)66:3<356::AID-AJMG21>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 9072912

5

The diagnostic value of the EEG in Angelman and Rett syndrome at a young age.

Laan LA, Brouwer OF, Begeer CH, Zwinderman AH, van Dijk JG. Laan LA, et al. Electroencephalogr Clin Neurophysiol. 1998 May;106(5):404-8. doi: 10.1016/s0013-4694(98)00007-8. Electroencephalogr Clin Neurophysiol. 1998. PMID: 9680152

6

Adenylosuccinase deficiency presenting with epilepsy in early infancy.

Maaswinkel-Mooij PD, Laan LA, Onkenhout W, Brouwer OF, Jaeken J, Poorthuis BJ. Maaswinkel-Mooij PD, et al. Among authors: laan la. J Inherit Metab Dis. 1997 Aug;20(4):606-7. doi: 10.1023/a:1005323512982. J Inherit Metab Dis. 1997. PMID: 9266401 No abstract available.

7

Angelman syndrome without detectable chromosome 15q11-13 anomaly: clinical study of familial and isolated cases.

Laan LA, Halley DJ, den Boer AT, Hennekam RC, Renier WO, Brouwer OF. Laan LA, et al. Am J Med Genet. 1998 Mar 19;76(3):262-8. Am J Med Genet. 1998. PMID: 9508247 Review.

8

Alternating hemiplegia of childhood: no mutations in the second familial hemiplegic migraine gene ATP1A2.

Kors EE, Vanmolkot KR, Haan J, Kheradmand Kia S, Stroink H, Laan LA, Gill DS, Pascual J, van den Maagdenberg AM, Frants RR, Ferrari MD. Kors EE, et al. Among authors: laan la. Neuropediatrics. 2004 Oct;35(5):293-6. doi: 10.1055/s-2004-821082. Neuropediatrics. 2004. PMID: 15534763

9

A Rett patient with a typical Angelman EEG.

Laan LA, Vein AA. Laan LA, et al. Epilepsia. 2002 Dec;43(12):1590-2. doi: 10.1046/j.1528-1157.2002.30802.x. Epilepsia. 2002. PMID: 12460263 Free article.

10

Alternating hemiplegia of childhood: no mutations in the glutamate transporter EAAT1.

de Vries B, Haan J, Stam AH, Vanmolkot KR, Stroink H, Laan LA, Gill DS, Pascual J, Frants RR, van den Maagdenberg AM, Ferrari MD. de Vries B, et al. Among authors: laan la. Neuropediatrics. 2006 Oct;37(5):302-4. doi: 10.1055/s-2006-924609. Neuropediatrics. 2006. PMID: 17236110

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