|
rdf:type |
|
|
lifeskim:mentions |
umls-concept:C0006104,
umls-concept:C0015219,
umls-concept:C0026705,
umls-concept:C0087111,
umls-concept:C0205296,
umls-concept:C0376249,
umls-concept:C0871261,
umls-concept:C1527072,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C2348519,
umls-concept:C2911692
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|
pubmed:issue |
3
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|
pubmed:dateCreated |
2011-6-7
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|
pubmed:abstractText |
BACKGROUD: Hunter disease is a rare X-linked mucopolysaccharidosis. Despite frequent neurological involvement, characterizing the severe phenotype, neuroimaging studies are scarce.
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pubmed:language |
eng
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pubmed:journal |
|
|
pubmed:citationSubset |
IM
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|
pubmed:status |
MEDLINE
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pubmed:month |
Jun
|
|
pubmed:issn |
1573-2665
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|
pubmed:author |
pubmed-author:AstaritaLucaL,
pubmed-author:BaroneRitaR,
pubmed-author:ConcolinoDanielaD,
pubmed-author:Di RoccoMajaM,
pubmed-author:DonatiMaria AliceMA,
pubmed-author:FecarottaSimonaS,
pubmed-author:FiccadentiAnnaA,
pubmed-author:FiumaraAgataA,
pubmed-author:FurlanFrancescaF,
pubmed-author:GiovanniniIreneI,
pubmed-author:GrimaldiMarcoM,
pubmed-author:LilliuFrancoF,
pubmed-author:ManaraRenzoR,
pubmed-author:MardariRodicaR,
pubmed-author:PariniRossellaR,
pubmed-author:PolonaraGabrieleG,
pubmed-author:PrianteElenaE,
pubmed-author:ProcopioElenaE,
pubmed-author:RampazzoAngelicaA,
pubmed-author:RossiAndreaA,
pubmed-author:SannaGraziolinaG,
pubmed-author:SantoroLuciaL,
pubmed-author:ScarpaMaurizioM
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pubmed:issnType |
Electronic
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pubmed:volume |
34
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
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pubmed:pagination |
763-80
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|
pubmed:meshHeading |
pubmed-meshheading:21465231-Adolescent,
pubmed-meshheading:21465231-Adult,
pubmed-meshheading:21465231-Bone Diseases, Developmental,
pubmed-meshheading:21465231-Brain,
pubmed-meshheading:21465231-Child,
pubmed-meshheading:21465231-Child, Preschool,
pubmed-meshheading:21465231-Disease Progression,
pubmed-meshheading:21465231-Female,
pubmed-meshheading:21465231-Humans,
pubmed-meshheading:21465231-Incidence,
pubmed-meshheading:21465231-Magnetic Resonance Imaging,
pubmed-meshheading:21465231-Male,
pubmed-meshheading:21465231-Mucopolysaccharidosis II,
pubmed-meshheading:21465231-Phenotype,
pubmed-meshheading:21465231-Spinal Canal,
pubmed-meshheading:21465231-Treatment Outcome,
pubmed-meshheading:21465231-Young Adult
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pubmed:year |
2011
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|
pubmed:articleTitle |
Brain and spine MRI features of Hunter disease: frequency, natural evolution and response to therapy.
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|
pubmed:affiliation |
Neuroradiologic Unit, University Hospital of Padua, via Giustiniani 2, 35128 Padova, Italy. renzo.manara@sanita.padova.it
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pubmed:publicationType |
Journal Article,
Evaluation Studies
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