Zobrazeno 1 - 10
of 80
pro vyhledávání: '"van den Boogerd, EH"'
Autor:
Callenbach, PMC, van den Boogerd, EH, Coo, IFM, ten Houten, R, Oosterwijk, JC, Hageman, G, Frants, RR, Brouwer, OF, Maagdenberg, AMJM
Publikováno v:
Clinical Genetics, 67(6), 517-525. Wiley
Clinical Genetics, 67(6), 517-525. Wiley-Blackwell Publishing Ltd
Clinical Genetics, 67(6), 517-525. Wiley-Blackwell Publishing Ltd
Benign familial infantile convulsions (BFIC) is an autosomal dominantly inherited partial epilepsy syndrome of early childhood with remission before the age of 3 years. The syndrome has been linked to loci on chromosomes 1q23, 2q24, 16p12-q12, and 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::65996f3e35953fb65b717ae888719089
https://research.rug.nl/en/publications/9c45d053-f89e-413d-83cf-dc3a134e329e
https://research.rug.nl/en/publications/9c45d053-f89e-413d-83cf-dc3a134e329e
Autor:
Callenbach, PMC, van den Maagdenberg, AMJM, Hottenga, JJ, van den Boogerd, EH, de Coo, RFM, Lindhout, D, Frants, RR, Sandkuijl, LA, Brouwer, OF
Publikováno v:
Epilepsia, 44, 1298-1305. Wiley-Blackwell Publishing Ltd
Epilepsia, 44(10), 1298-1305. Wiley
Epilepsia, 44(10), 1298-1305. Wiley
Purpose: Three forms of idiopathic partial epilepsy with autosomal dominant inheritance have been described: (a) autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE); (b) autosomal dominant lateral temporal epilepsy (ADLTE) or partial epilepsy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a6fe7d51627a1a2aaa0cc0365f3cb623
https://pure.eur.nl/en/publications/23b29fff-5b0a-455e-b395-73cd2a54e8e1
https://pure.eur.nl/en/publications/23b29fff-5b0a-455e-b395-73cd2a54e8e1
Akademický článek
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Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
de Vries B; Departments of Human Genetics, Leiden University Medical Centre, PO Box 9600, 2300 RC Leiden, The Netherlands., Freilinger T, Vanmolkot KR, Koenderink JB, Stam AH, Terwindt GM, Babini E, van den Boogerd EH, van den Heuvel JJ, Frants RR, Haan J, Pusch M, van den Maagdenberg AM, Ferrari MD, Dichgans M
Publikováno v:
Neurology [Neurology] 2007 Dec 04; Vol. 69 (23), pp. 2170-6.
Autor:
Vanmolkot KR; Department of Human Genetics, Leiden University Medical Centre, Leiden, The Netherlands., Stam AH, Raman A, Koenderink JB, de Vries B, van den Boogerd EH, van Vark J, van den Heuvel JJ, Bajaj N, Terwindt GM, Haan J, Frants RR, Ferrari MD, van den Maagdenberg AM
Publikováno v:
European journal of human genetics : EJHG [Eur J Hum Genet] 2007 Aug; Vol. 15 (8), pp. 884-8. Date of Electronic Publication: 2007 May 02.
Autor:
Callenbach PM; Department of Neurology, University Medical Center Groningen, Groningen, The Netherlands., van den Boogerd EH, de Coo RF, ten Houten R, Oosterwijk JC, Hageman G, Frants RR, Brouwer OF, van den Maagdenberg AM
Publikováno v:
Clinical genetics [Clin Genet] 2005 Jun; Vol. 67 (6), pp. 517-25.
Autor:
Callenbach PM; Deaprtment of Neurology, Leiden University Medical Center, Leiden, The Netherlands., van den Maagdenberg AM, Hottenga JJ, van den Boogerd EH, de Coo RF, Lindhout D, Frants RR, Sandkuijl LA, Brouwer OF
Publikováno v:
Epilepsia [Epilepsia] 2003 Oct; Vol. 44 (10), pp. 1298-305.
Autor:
Haj Mohammad Hassani B; Department of Medical Genetics, Faculty of Medicine, Hormozgan University of Medical Sciences, Bandar Abbas, Iran., Malekzadeh K; Department of Medical Genetics, Faculty of Medicine, Hormozgan University of Medical Sciences, Bandar Abbas, Iran. keyanoosh@gmail.com.; Molecular Medicine Research Center, Hormozgan Health Institute, Hormozgan University of Medical Sciences, Bandar Abbas, Iran. keyanoosh@gmail.com.
Publikováno v:
Neurogenetics [Neurogenetics] 2024 Oct; Vol. 25 (4), pp. 417-424. Date of Electronic Publication: 2024 Jul 24.
Autor:
Tian, Yang, Shi, Zhen, Cai, Jiahao, Hou, Chi, Wang, Xiuying, Zhu, Haixia, Peng, Binwei, Shi, Kaili, Li, Xiaojing, Gong, Sitang, Chen, Wen-Xiong
Publikováno v:
BMC Pediatrics; 10/25/2023, Vol. 23 Issue 1, p1-9, 9p