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Preferences for genetic interventions for SCA and Huntington's disease: results of a discrete choice experiment among patients.

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Title: Preferences for genetic interventions for SCA and Huntington's disease: results of a discrete choice experiment among patients.
Authors: van Os NJH; Department of Neurology, Radboud University Medical Center, Nijmegen, the Netherlands. nienke.vanos@radboudumc.nl., Oosterloo M; Department of Neurology, Maastricht University Medical Centre+, Maastricht, the Netherlands.; School of Mental Health and Neuroscience, Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, The Netherlands., Grutters JPC; Science Department IQ Health, Radboud University Medical Center, Nijmegen, the Netherlands., Essers BAB; Department of Clinical Epidemiology and Medical Technology Assessment, Maastricht University Medical Centre+, Maastricht, the Netherlands., van de Warrenburg BPC; Department of Neurology, Radboud University Medical Center, Nijmegen, the Netherlands.
Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2024 Oct 28; Vol. 19 (1), pp. 398. Date of Electronic Publication: 2024 Oct 28.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Preferences for genetic interventions for SCA and Huntington's disease: results of a discrete choice experiment among patients.
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  Data: <searchLink fieldCode="AU" term="%22van+Os+NJH%22">van Os NJH</searchLink>; Department of Neurology, Radboud University Medical Center, Nijmegen, the Netherlands. nienke.vanos@radboudumc.nl.<br /><searchLink fieldCode="AU" term="%22Oosterloo+M%22">Oosterloo M</searchLink>; Department of Neurology, Maastricht University Medical Centre+, Maastricht, the Netherlands.; School of Mental Health and Neuroscience, Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Grutters+JPC%22">Grutters JPC</searchLink>; Science Department IQ Health, Radboud University Medical Center, Nijmegen, the Netherlands.<br /><searchLink fieldCode="AU" term="%22Essers+BAB%22">Essers BAB</searchLink>; Department of Clinical Epidemiology and Medical Technology Assessment, Maastricht University Medical Centre+, Maastricht, the Netherlands.<br /><searchLink fieldCode="AU" term="%22van+de+Warrenburg+BPC%22">van de Warrenburg BPC</searchLink>; Department of Neurology, Radboud University Medical Center, Nijmegen, the Netherlands.
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  Data: <searchLink fieldCode="JN" term="%22101266602%22">Orphanet journal of rare diseases</searchLink> [Orphanet J Rare Dis] 2024 Oct 28; Vol. 19 (1), pp. 398. <i>Date of Electronic Publication: </i>2024 Oct 28.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22BioMed+Central%22">BioMed Central </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101266602 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1750-1172 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2217501172%22">17501172 </searchLink><i>NLM ISO Abbreviation: </i>Orphanet J Rare Dis <i>Subsets: </i>MEDLINE
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        Value: 10.1186/s13023-024-03408-2
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              Text: 2024 Oct 28
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