Zobrazeno 1 - 10 of 57 pro vyhledávání: '"van Eeghen AM"'
1
Akademický článek
Everolimus for the treatment of refractory seizures associated with tuberous sclerosis complex (TSC): current perspectives
Autor: Overwater IE, Rietman AB, van Eeghen AM, de Wit MCY
Publikováno v: Therapeutics and Clinical Risk Management, Vol Volume 15, Pp 951-955 (2019)
Iris E Overwater,1 André B Rietman,2 Agnies M van Eeghen,3 Marie Claire Y de Wit11Department of Pediatric Neurology and ENCORE Expertise Center, Erasmus MC, Rotterdam, the Netherlands; 2Department of Child and Adolescent Psychiatry/Psychology and EN
Externí odkaz: https://doaj.org/article/fd8902b1515e4659b9774195ac1ebb71
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3
Integrale zorg voor kinderen met een verstandelijke beperking:samen met de AVG
Autor: van Eeghen, AM, Huisman, S.A.
Publikováno v: van Eeghen, AM & Huisman, S A 2019, ' Integrale zorg voor kinderen met een verstandelijke beperking : samen met de AVG ', Praktische Pediatrie .
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_____10172::2a7dd4ad0597e8f3c76002232b250fdd
https://research.vumc.nl/en/publications/227fc175-b442-4cd7-b30f-1eeaccb98663
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4
Somatische problemen bij mensen met een verstandelijke beperking in de psychiatrische praktijk
Autor: van Eeghen, AM, Sylvia, S.A., Boot, E.
Publikováno v: van Eeghen, AM, Sylvia, S A & Boot, E 2019, ' Somatische problemen bij mensen met een verstandelijke beperking in de psychiatrische praktijk ', Tijdschrift voor Psychiatrie .
Tijdschrift voor Psychiatrie. Uitgeverij Boom
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::de936f15066cd66e67236496f1c1ca31
https://research.vumc.nl/en/publications/280cab68-2ced-4265-bfc2-2b01b64be109
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5
Fragiele-X-syndroom: Nieuwe therapeutische strategieën
Autor: Zeidler, Shimriet, Dierckx, Bram, Lubbers, Kyra, van Eeghen, AM, Lincke, C.R., Kievit, J.A., Willemsen, Rob, Rietman, A.B.
Publikováno v: Tijdschrift voor Psychiatrie, 60(5), 338-342. Boom Uitgevers
Tijdschrift voor Psychiatrie, 338-442. Uitgeverij Boom
STARTPAGE=338;ENDPAGE=442;ISSN=0303-7339;TITLE=Tijdschrift voor Psychiatrie
background: Fragile X syndrome (fxs) is the most common hereditary cause of intellectual disability and autism spectrum disorders.Targeted treatment is currently lacking. In the past decades an enormous amount of knowledge has been obtained concernin
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::28fb031696a53a22529f11dd72a0c8aa
https://pure.eur.nl/en/publications/31d37658-4f19-49dd-9483-5dff5bba9a17
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6
Fragile X syndrome:New therapeutic strategies
Autor: Zeidler, Shimriet, Dierckx, Bram, Lubbers, Kyra, van Eeghen, AM, Lincke, C.R., Kievit, J.A., Willemsen, Rob, Rietman, A.B.
Publikováno v: Zeidler, S, Dierckx, B, Lubbers, K, van Eeghen, AM, Lincke, C R, Kievit, J A, Willemsen, R & Rietman, A B 2018, ' Fragiele-X-syndroom : Nieuwe therapeutische strategieën ', Tijdschrift voor Psychiatrie, pp. 338-442 . < http://www.tijdschriftvoorpsychiatrie.nl/issues/527/articles/11635 >
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_____10172::ee69e64b7ef245798469fc326416ae2c
https://research.vumc.nl/en/publications/b8de675e-535a-41fd-81cd-c266561b2a89
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7
Akademický článek
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8
Akademický článek
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9
Editorial & Opinion
Parkinsonism in people with intellectual disability.
Autor: Boot E; Advisium, 's Heeren Loo Zorggroep, Amersfoort, the Netherlands; Department of Psychiatry and Neuropsychology, MHeNs, Maastricht University, Maastricht, the Netherlands; The Dalglish Family 22q Clinic, University Health Network, Toronto, Ontario, Canada. Electronic address: erik.boot@maastrichtuniversity.nl., van Eeghen AM; Advisium, 's Heeren Loo Zorggroep, Amersfoort, the Netherlands; Emma Children's Hospital, University of Amsterdam, Amsterdam, the Netherlands., Bloem BR; Department of Neurology, Center of Expertise for Parkinson & Movement Disorders, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, the Netherlands., van de Warrenburg BP; Department of Neurology, Center of Expertise for Parkinson & Movement Disorders, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, the Netherlands., Cuypers M; Radboud University Medical Center, Department of Primary and Community Care, Nijmegen, the Netherlands; Academic Collaborative Intellectual Disability and Health - Sterker op Eigen Benen (SOEB), Nijmegen, the Netherlands.
Publikováno v: Parkinsonism & related disorders [Parkinsonism Relat Disord] 2024 Nov; Vol. 128, pp. 107079. Date of Electronic Publication: 2024 Jul 29.
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10
Akademický článek
PROs for RARE: protocol for development of a core patient reported outcome set for individuals with genetic intellectual disability.
Autor: van Silfhout NY; Department of Child and Adolescent Psychiatry & Psychosocial Care, Emma Children's Hospital, Amsterdam UMC location University of Amsterdam, Amsterdam, The Netherlands.; Department of Pediatrics, Amsterdam Gastroenterology Endocrinology Metabolism, Emma Children's Hospital, Amsterdam UMC location University of Amsterdam, Amsterdam, The Netherlands.; Emma Center for Personalized Medicine, Amsterdam UMC, Amsterdam, The Netherlands.; Amsterdam Public Health Research Institute, Mental health and Personalized Medicine, Amsterdam, The Netherlands.; Amsterdam Reproduction & Development Research Institute, Child Development, Amsterdam, The Netherlands., van Muilekom MM; Department of Child and Adolescent Psychiatry & Psychosocial Care, Emma Children's Hospital, Amsterdam UMC location University of Amsterdam, Amsterdam, The Netherlands.; Amsterdam Public Health Research Institute, Mental health and Personalized Medicine, Amsterdam, The Netherlands., van Karnebeek CD; Department of Pediatrics, Amsterdam Gastroenterology Endocrinology Metabolism, Emma Children's Hospital, Amsterdam UMC location University of Amsterdam, Amsterdam, The Netherlands.; Emma Center for Personalized Medicine, Amsterdam UMC, Amsterdam, The Netherlands.; Amsterdam Reproduction & Development Research Institute, Child Development, Amsterdam, The Netherlands., Haverman L; Department of Child and Adolescent Psychiatry & Psychosocial Care, Emma Children's Hospital, Amsterdam UMC location University of Amsterdam, Amsterdam, The Netherlands.; Amsterdam Public Health Research Institute, Mental health and Digital Health, Amsterdam, The Netherlands., van Eeghen AM; Department of Pediatrics, Amsterdam Gastroenterology Endocrinology Metabolism, Emma Children's Hospital, Amsterdam UMC location University of Amsterdam, Amsterdam, The Netherlands. a.m.vaneeghen@amsterdamumc.nl.; Emma Center for Personalized Medicine, Amsterdam UMC, Amsterdam, The Netherlands. a.m.vaneeghen@amsterdamumc.nl.; Amsterdam Reproduction & Development Research Institute, Child Development, Amsterdam, The Netherlands. a.m.vaneeghen@amsterdamumc.nl.; Amsterdam Public Health Research Institute, Aging & Later life and Personalized Medicine, Amsterdam, The Netherlands. a.m.vaneeghen@amsterdamumc.nl.; Advisium's Heeren Loo, Amersfoort, The Netherlands. a.m.vaneeghen@amsterdamumc.nl.
Publikováno v: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2024 Sep 27; Vol. 19 (1), pp. 354. Date of Electronic Publication: 2024 Sep 27.
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