Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Eveline E O Hagebeuk"'
Autor:
R.H.C. Lazeron, Wendela de Lange, Roland D. Thijs, Eveline E O Hagebeuk, Marijke C. Kars, Anouk van Westrhenen
Publikováno v:
Epilepsy & Behavior, 124. ACADEMIC PRESS INC ELSEVIER SCIENCE
Introduction: Caring for a child with epilepsy has a significant impact on parental quality of life. Seizure unpredictability and complications, including sudden unexpected death in epilepsy (SUDEP), may cause high parental stress and increased anxie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6abddabceceea28fc6421b8d89c29c32
http://hdl.handle.net/1887/3251154
http://hdl.handle.net/1887/3251154
Autor:
Al W. de Weerd, Marieke Reuvekamp, Eveline E O Hagebeuk, Lydia van den Berg, Jaap van der Meere
Publikováno v:
Applied neuropsychology. Child. 10(2)
Thirty-two children with frontal lobe epilepsy (FLE) were assessed using different working memory measures. In addition, parents and teachers completed the working memory scale of the Behavioral Rating Inventory of Executive Functioning (BRIEF) to as
Autor:
Al W. de Weerd, Marieke Reuvekamp, Eveline E O Hagebeuk, Lydia van den Berg, Jaap van der Meere
Publikováno v:
Epilepsy & Behavior, 87, 117-122. ACADEMIC PRESS INC ELSEVIER SCIENCE
Objective: Epilepsy, as a chronic and neurological disease. is generally associated with an increased risk for social and emotional behavior problems in children. These findings are mostly derived from studies on children with different epilepsy type
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e222e91bee0df8e775dd5380dcd0e01
https://research.rug.nl/en/publications/231296d4-1f08-4dee-963a-10197a9df3d5
https://research.rug.nl/en/publications/231296d4-1f08-4dee-963a-10197a9df3d5
Autor:
Elly F. Ippel, Huibert H. Geesink, Bobby P. C. Koeleman, Jeanet M. Kemmeren, Oebele F. Brouwer, Anton de Louw, Paul B. Augustijn, W. Boudewijn Gunning, Eveline E. O. Hagebeuk, Patricia E. Vermeer-de Bondt, Nienke E. Verbeek, Floor E. Jansen, Kees P.J. Braun, Jolanda H. Schieving, Eva H. Brilstra, Nine V A M Knoers, Hans Stroink, Marjan J. A. van Kempen, Rinze F. Neuteboom, Nicoline A.T. van der Maas, Dick Lindhout, Anja C M Sonsma, R. Jeroen Vermeulen, Joost Nicolai, Carolien G.F. de Kovel
Publikováno v:
Neurology, 85(7), 596-603. LIPPINCOTT WILLIAMS & WILKINS
Verbeek, N E, van der Maas, N A T, Sonsma, A C M, Ippel, E, Bondt, P E V D, Hagebeuk, E, Jansen, F E, Geesink, H H, Braun, K P, de Louw, A, Augustijn, P B, Neuteboom, R F, Schieving, J H, Stroink, H, Vermeulen, R J, Nicolai, J, Brouwer, O F, van Kempen, M, de Kovel, C G F, Kemmeren, J M, Koeleman, B P C, Knoers, N V, Lindhout, D, Gunning, W B & Brilstra, E H 2015, ' Effect of vaccinations on seizure risk and disease course in Dravet syndrome ', Neurology, vol. 85, no. 7, pp. 596-603 . https://doi.org/10.1212/WNL.0000000000001855
Neurology, 85(7), 596-603. Lippincott Williams and Wilkins
Neurology, 85(7), 596-603. Lippincott Williams & Wilkins
Verbeek, N E, van der Maas, N A T, Sonsma, A C M, Ippel, E, Bondt, P E V D, Hagebeuk, E, Jansen, F E, Geesink, H H, Braun, K P, de Louw, A, Augustijn, P B, Neuteboom, R F, Schieving, J H, Stroink, H, Vermeulen, R J, Nicolai, J, Brouwer, O F, van Kempen, M, de Kovel, C G F, Kemmeren, J M, Koeleman, B P C, Knoers, N V, Lindhout, D, Gunning, W B & Brilstra, E H 2015, ' Effect of vaccinations on seizure risk and disease course in Dravet syndrome ', Neurology, vol. 85, no. 7, pp. 596-603 . https://doi.org/10.1212/WNL.0000000000001855
Neurology, 85(7), 596-603. Lippincott Williams and Wilkins
Neurology, 85(7), 596-603. Lippincott Williams & Wilkins
Objective:To study the effect of vaccination-associated seizure onset on disease course and estimate the risk of subsequent seizures after infant pertussis combination and measles, mumps, and rubella (MMR) vaccinations in Dravet syndrome (DS).Methods
Publikováno v:
Journal of inherited metabolic disease, 36(6), 967-972. Springer Netherlands
Rett syndrome is a neurodevelopmental disorder characterized by cognitive and locomotor regression and stereotypic hand movements. The disorder is caused by mutations in the X chromosomal MECP2 a gene encoding methyl CpG-binding protein. It has been
Publikováno v:
Developmental Medicine & Child Neurology. 55:480-484
Aim In female children with drug-resistant seizures and developmental delay from birth, atypical Rett syndrome caused by mutations in the CDKL5 gene should be considered. Several clinical features resemble classic Rett syndrome. Respiratory and sleep
Autor:
Johannes H. T. M. Koelman, Arno Vyth, Eveline E. O. Hagebeuk, N. G. G. M. Abeling, B. T. Poll-The, Marinus Duran
Publikováno v:
Journal of child neurology, 27(3), 304-309. SAGE Publications Inc.
Rett syndrome is a neurodevelopmental disorder in girls, related to mutations in MECP2 gene. It has been postulated that low 5-methyltetrahydrofolate (5-MTHF) levels are present in cerebrospinal fluid. Folinic acid demonstrated clinical improvement.
Autor:
Johannes H. van der Hoeven, Eveline E. O. Hagebeuk, Irenaeus F.M. de Coo, Bwee Tien Poll-The, Natasha M. Maurits, Levinus A. Bok, Laura K. Teune, Michèl A.A.P. Willemsen, Oebele F. Brouwer, Cornelis Jakobs, Mona C. Toet, Deborah A Sival
Publikováno v:
Epilepsia. 51:2406-2411
PURPOSE: Pyridoxine-dependent epilepsy (PDE) is characterized by therapy-resistant seizures (TRS) responding to intravenous (IV) pyridoxine. PDE can be identified by increased urinary alpha-aminoadipic semialdehyde (alpha-AASA) concentrations and mut
Publikováno v:
Journal of child neurology, 30(11), 1515-1519. SAGE Publications Inc.
Journal of Child Neurology, 30, 1515-9
Journal of Child Neurology, 30, 11, pp. 1515-9
Journal of Child Neurology, 30, 1515-9
Journal of Child Neurology, 30, 11, pp. 1515-9
Item does not contain fulltext This is the second report of a family with a recurrence of a CDKL5 mutation (c. 283-3_290del) in 2 sisters. Both parents tested negative for the mutation in all tissues, but germline mosaicism is likely. Clinically CDKL
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c106487c5965e3623f68acc844bf9578
https://pure.amc.nl/en/publications/two-siblings-with-a-cdkl5-mutation-genotype-and-phenotype-evaluation(b88ecea7-b05e-4c3e-afeb-8a06aaae3577).html
https://pure.amc.nl/en/publications/two-siblings-with-a-cdkl5-mutation-genotype-and-phenotype-evaluation(b88ecea7-b05e-4c3e-afeb-8a06aaae3577).html
Publikováno v:
Developmental medicine and child neurology. 55(5)
In female children with drug-resistant seizures and developmental delay from birth, atypical Rett syndrome caused by mutations in the CDKL5 gene should be considered. Several clinical features resemble classic Rett syndrome. Respiratory and sleep abn