المصدر: Epilepsia. 44(10):1298-1305

مصطلحات موضوعية: NORWEGIAN FAMILY, ELECTROCLINICAL PICTURE, FPEVF, CHRNA4 GENE, LATERAL TEMPORAL EPILEPSY, chromosome 22q, SUBUNIT, DOMINANT PARTIAL EPILEPSY, ADNFLE, genetics, AUDITORY FEATURES, LGI1, clinical characteristics, MUTATION, FRONTAL-LOBE EPILEPSY

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dris___00893::90003dfad2b2a4a78c98ba54412686c1
https://hdl.handle.net/11370/4256bf2c-dea6-4bb9-92a2-32c224e6bae9

المؤلفون: Klein, KM, O'Brien, TJ, Praveen, K, Heron, SE, Mulley, JC, Simon James Foote, Berkovic, SF, Scheffer, IE

مصطلحات موضوعية: Neurosciences not elsewhere classified, chromosome 22q12, FFEVF, FPEVF, focal epilepsy, genetic epilepsy

Relation: 102.100.100/580514; https://figshare.com/articles/journal_contribution/Familial_focal_epilepsy_with_variable_foci_mapped_to_chromosome_22q12_Expansion_of_the_phenotypic_spectrum/22896131

الاتاحة: https://figshare.com/articles/journal_contribution/Familial_focal_epilepsy_with_variable_foci_mapped_to_chromosome_22q12_Expansion_of_the_phenotypic_spectrum/22896131

المؤلفون: Klein, K., O'Brien, T., Praveen, K., Heron, S., Mulley, J., Foote, S., Berkovic, S., Scheffer, I.

المصدر: http://dx.doi.org/10.1111/j.1528-1167.2012.03585.x.

مصطلحات موضوعية: Chromosome 22q12, FFEVF, FPEVF, Focal epilepsy, Genetic epilepsy

Relation: Epilepsia, 2012; 53(8):151-155; http://hdl.handle.net/2440/73222; Heron, S. [0000-0001-8759-6748]

الاتاحة: http://hdl.handle.net/2440/73222
https://doi.org/10.1111/j.1528-1167.2012.03585.x

المساهمون: Klein, Karl Martin, O'Brien, Terence J, Praveen, Kavita, Heron, Sarah E, Mulley, John C, Foote, Simon, Berkovic, Samuel F, Scheffer, Ingrid E

مصطلحات موضوعية: focal epilepsy, chromosome 22q12, FFEVF, genetic epilepsy, FPEVF

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______1231::90e5397515519d00df0faa62d15eed78
https://hdl.handle.net/1959.8/128573

المؤلفون: Callenbach, PMC, van den Maagdenberg, AMJM, Hottenga, JJ, van den Boogerd, EH, de Coo, RFM, Lindhout, D, Frants, RR, Sandkuijl, LA, Brouwer, OF

المصدر: Callenbach , PMC , van den Maagdenberg , AMJM , Hottenga , JJ , van den Boogerd , EH , de Coo , RFM , Lindhout , D , Frants , RR , Sandkuijl , LA & Brouwer , OF 2003 , ' Familial partial epilepsy with variable foci in a Dutch family : Clinical characteristics and confirmation of linkage to chromosome 22q ' , Epilepsia , vol. 44 , no. 10 , pp. 1298-1305 .

مصطلحات موضوعية: FPEVF, ADNFLE, clinical characteristics, genetics, chromosome 22q, FRONTAL-LOBE EPILEPSY, DOMINANT PARTIAL EPILEPSY, LATERAL TEMPORAL EPILEPSY, AUDITORY FEATURES, ELECTROCLINICAL PICTURE, NORWEGIAN FAMILY, CHRNA4 GENE, MUTATION, LGI1, SUBUNIT

الاتاحة: https://hdl.handle.net/11370/4256bf2c-dea6-4bb9-92a2-32c224e6bae9
https://research.rug.nl/en/publications/4256bf2c-dea6-4bb9-92a2-32c224e6bae9

المؤلفون: Callenbach, PMC, van den Maagdenberg, AMJM, Hottenga, JJ, van den Boogerd, EH, de Coo, RFM, Lindhout, D, Frants, RR, Sandkuijl, LA, Brouwer, OF

المساهمون: Epidemiology, Neurology, Clinical Genetics

المصدر: Epilepsia, 44, 1298-1305. Wiley-Blackwell Publishing Ltd
Epilepsia, 44(10), 1298-1305. Wiley

مصطلحات موضوعية: NORWEGIAN FAMILY, ELECTROCLINICAL PICTURE, FPEVF, CHRNA4 GENE, LATERAL TEMPORAL EPILEPSY, chromosome 22q, SUBUNIT, DOMINANT PARTIAL EPILEPSY, ADNFLE, genetics, AUDITORY FEATURES, LGI1, clinical characteristics, MUTATION, FRONTAL-LOBE EPILEPSY

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a6fe7d51627a1a2aaa0cc0365f3cb623
https://pure.eur.nl/en/publications/23b29fff-5b0a-455e-b395-73cd2a54e8e1

المؤلفون: Klein, Karl, O'Brien, Terence J., Praveen, Kavita, Heron, Sarah, Mulley, John C., Foote, Simon, Berkovic, Sam F., Scheffer, Ingrid

المصدر: Epilepsia

مصطلحات الفهرس: Keywords: adolescent; adult; article; Australia; child; chromosome 22q; clinical article; controlled study; electroencephalography; familial disease; female; focal epilepsy; gene locus; gene mapping; genetic variability; genome analysis; human; infant; male; phenot Chromosome 22q12; FFEVF; Focal epilepsy; FPEVF; Genetic epilepsy, Journal article

URL: http://hdl.handle.net/1885/102818