Callenbach PM - Search Results

1

Familial cortical myoclonic tremor with epilepsy: a single syndromic classification for a group of pedigrees bearing common features.

van Rootselaar AF, van Schaik IN, van den Maagdenberg AM, Koelman JH, Callenbach PM, Tijssen MA. van Rootselaar AF, et al. Among authors: callenbach pm. Mov Disord. 2005 Jun;20(6):665-73. doi: 10.1002/mds.20413. Mov Disord. 2005. PMID: 15747356 Review.

2

δ-Catenin (CTNND2) missense mutation in familial cortical myoclonic tremor and epilepsy.

van Rootselaar AF, Groffen AJ, de Vries B, Callenbach PMC, Santen GWE, Koelewijn S, Vijfhuizen LS, Buijink A, Tijssen MAJ, van den Maagdenberg AMJM. van Rootselaar AF, et al. Neurology. 2017 Dec 5;89(23):2341-2350. doi: 10.1212/WNL.0000000000004709. Epub 2017 Nov 10. Neurology. 2017. PMID: 29127138

3

A Dutch family with 'familial cortical tremor with epilepsy'. Clinical characteristics and exclusion of linkage to chromosome 8q23.3-q24.1.

van Rootselaar F, Callenbach PM, Hottenga JJ, Vermeulen FL, Speelman HD, Brouwer OF, Tijssen MA. van Rootselaar F, et al. Among authors: callenbach pm. J Neurol. 2002 Jul;249(7):829-34. doi: 10.1007/s00415-002-0729-x. J Neurol. 2002. PMID: 12140665

4

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.

5

Clinical and genetic aspects of idiopathic epilepsies in childhood.

Callenbach PM, van den Maagdenberg AM, Frants RR, Brouwer OF. Callenbach PM, et al. Eur J Paediatr Neurol. 2005;9(2):91-103. doi: 10.1016/j.ejpn.2004.12.005. Eur J Paediatr Neurol. 2005. PMID: 15843076 Review.

6

PRRT2 mutation causes benign familial infantile convulsions.

de Vries B, Callenbach PM, Kamphorst JT, Weller CM, Koelewijn SC, ten Houten R, de Coo IF, Brouwer OF, van den Maagdenberg AM. de Vries B, et al. Among authors: callenbach pm. Neurology. 2012 Nov 20;79(21):2154-5. doi: 10.1212/WNL.0b013e3182752c30. Epub 2012 Oct 17. Neurology. 2012. PMID: 23077019

7

Mutations in DEPDC5 cause familial focal epilepsy with variable foci.

Dibbens LM, de Vries B, Donatello S, Heron SE, Hodgson BL, Chintawar S, Crompton DE, Hughes JN, Bellows ST, Klein KM, Callenbach PM, Corbett MA, Gardner AE, Kivity S, Iona X, Regan BM, Weller CM, Crimmins D, O'Brien TJ, Guerrero-López R, Mulley JC, Dubeau F, Licchetta L, Bisulli F, Cossette P, Thomas PQ, Gecz J, Serratosa J, Brouwer OF, Andermann F, Andermann E, van den Maagdenberg AM, Pandolfo M, Berkovic SF, Scheffer IE. Dibbens LM, et al. Among authors: callenbach pm. Nat Genet. 2013 May;45(5):546-51. doi: 10.1038/ng.2599. Epub 2013 Mar 31. Nat Genet. 2013. PMID: 23542697

8

Hereditary epilepsy syndromes.

Callenbach PM, Brouwer OF. Callenbach PM, et al. Clin Neurol Neurosurg. 1997 Aug;99(3):159-71. doi: 10.1016/s0303-8467(97)00019-x. Clin Neurol Neurosurg. 1997. PMID: 9350396 Review.

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. 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

Familial occurrence of epilepsy in children with newly diagnosed multiple seizures: Dutch Study of Epilepsy in Childhood.

Callenbach PM, Geerts AT, Arts WF, van Donselaar CA, Peters AC, Stroink H, Brouwer OF. Callenbach PM, et al. Epilepsia. 1998 Mar;39(3):331-6. doi: 10.1111/j.1528-1157.1998.tb01382.x. Epilepsia. 1998. PMID: 9578054 Free article.

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