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High prevalence of symptomatic spinal stenosis in Norwegian adults with achondroplasia: a population-based study.

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Title: High prevalence of symptomatic spinal stenosis in Norwegian adults with achondroplasia: a population-based study.
Authors: Fredwall SO; Sunnaas Rehabilitation Hospital, TRS National Resource Centre for Rare Disorders, Nesodden, Norway. svfred@sunnaas.no.; Faculty of Medicine, Institute of Clinical Medicine, University of Oslo, Oslo, Norway. svfred@sunnaas.no., Steen U; Sunnaas Rehabilitation Hospital, TRS National Resource Centre for Rare Disorders, Nesodden, Norway., de Vries O; Sunnaas Rehabilitation Hospital, TRS National Resource Centre for Rare Disorders, Nesodden, Norway., Rustad CF; Oslo University Hospital, Department of Medical Genetics, Oslo, Norway., Eggesbø HB; Oslo University Hospital, Division of Radiology and Nuclear Medicine, Oslo, Norway., Weedon-Fekjær H; Oslo Centre for Biostatistics and Epidemiology, Research Support Service, Oslo University Hospital, Oslo, Norway., Lidal IB; Sunnaas Rehabilitation Hospital, TRS National Resource Centre for Rare Disorders, Nesodden, Norway., Savarirayan R; Murdoch Children's Research Institute and University of Melbourne, Parkville, Australia., Månum G; Faculty of Medicine, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.; Sunnaas Rehabilitation Hospital, Department of Research, Nesodden, Norway.
Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2020 May 25; Vol. 15 (1), pp. 123. Date of Electronic Publication: 2020 May 25.
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: High prevalence of symptomatic spinal stenosis in Norwegian adults with achondroplasia: a population-based study.
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  Data: <searchLink fieldCode="AU" term="%22Fredwall+SO%22">Fredwall SO</searchLink>; Sunnaas Rehabilitation Hospital, TRS National Resource Centre for Rare Disorders, Nesodden, Norway. svfred@sunnaas.no.; Faculty of Medicine, Institute of Clinical Medicine, University of Oslo, Oslo, Norway. svfred@sunnaas.no.<br /><searchLink fieldCode="AU" term="%22Steen+U%22">Steen U</searchLink>; Sunnaas Rehabilitation Hospital, TRS National Resource Centre for Rare Disorders, Nesodden, Norway.<br /><searchLink fieldCode="AU" term="%22de+Vries+O%22">de Vries O</searchLink>; Sunnaas Rehabilitation Hospital, TRS National Resource Centre for Rare Disorders, Nesodden, Norway.<br /><searchLink fieldCode="AU" term="%22Rustad+CF%22">Rustad CF</searchLink>; Oslo University Hospital, Department of Medical Genetics, Oslo, Norway.<br /><searchLink fieldCode="AU" term="%22Eggesbø+HB%22">Eggesbø HB</searchLink>; Oslo University Hospital, Division of Radiology and Nuclear Medicine, Oslo, Norway.<br /><searchLink fieldCode="AU" term="%22Weedon-Fekjær+H%22">Weedon-Fekjær H</searchLink>; Oslo Centre for Biostatistics and Epidemiology, Research Support Service, Oslo University Hospital, Oslo, Norway.<br /><searchLink fieldCode="AU" term="%22Lidal+IB%22">Lidal IB</searchLink>; Sunnaas Rehabilitation Hospital, TRS National Resource Centre for Rare Disorders, Nesodden, Norway.<br /><searchLink fieldCode="AU" term="%22Savarirayan+R%22">Savarirayan R</searchLink>; Murdoch Children's Research Institute and University of Melbourne, Parkville, Australia.<br /><searchLink fieldCode="AU" term="%22Månum+G%22">Månum G</searchLink>; Faculty of Medicine, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.; Sunnaas Rehabilitation Hospital, Department of Research, Nesodden, Norway.
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  Data: <searchLink fieldCode="JN" term="%22101266602%22">Orphanet journal of rare diseases</searchLink> [Orphanet J Rare Dis] 2020 May 25; Vol. 15 (1), pp. 123. <i>Date of Electronic Publication: </i>2020 May 25.
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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/s13023-020-01397-6
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