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Article: Clinical manifestations of neurofibromatosis-1 in Chinese children

TitleClinical manifestations of neurofibromatosis-1 in Chinese children
Authors
Wong, VCN
Issue Date1994
PublisherElsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/pedneu
Citation
Pediatric Neurology, 1994, v. 11 n. 4, p. 301-307 How to Cite?
DOI: http://dx.doi.org/10.1016/0887-8994(94)90006-X
AbstractThe complications of 50 Chinese children with neurofibromatosis-1 were found to be different from other ethnic groups. There was a predominance of scoliosis, speech problems, and blood malignancies, but brain tumors were rare. The majority had good prognosis. Clinical manifestations depend on the age of ascertainment and, therefore, the prediction of associated complications should be made accordingly.
Persistent Identifierhttp://hdl.handle.net/10722/143595
ISSN
0887-8994
2023 Impact Factor: 3.2
2023 SCImago Journal Rankings: 0.916
ISI Accession Number ID
WOS:A1994PZ52800006

 

DC FieldValueLanguage
dc.contributor.authorWong, VCNen_HK
dc.date.accessioned2011-12-12T03:52:11Z-
dc.date.available2011-12-12T03:52:11Z-
dc.date.issued1994en_HK
dc.identifier.citationPediatric Neurology, 1994, v. 11 n. 4, p. 301-307en_HK
dc.identifier.issn0887-8994en_HK
dc.identifier.urihttp://hdl.handle.net/10722/143595-
dc.description.abstractThe complications of 50 Chinese children with neurofibromatosis-1 were found to be different from other ethnic groups. There was a predominance of scoliosis, speech problems, and blood malignancies, but brain tumors were rare. The majority had good prognosis. Clinical manifestations depend on the age of ascertainment and, therefore, the prediction of associated complications should be made accordingly.en_HK
dc.languageengen_US
dc.publisherElsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/pedneuen_HK
dc.relation.ispartofPediatric Neurologyen_HK
dc.subject.meshAdolescenten_US
dc.subject.meshChilden_US
dc.subject.meshChild, Preschoolen_US
dc.subject.mesh*Cross-Cultural Comparisonen_US
dc.subject.meshFemaleen_US
dc.subject.meshFollow-Up Studiesen_US
dc.subject.meshHong Kongen_US
dc.subject.meshHumansen_US
dc.subject.meshInfanten_US
dc.subject.meshMaleen_US
dc.subject.meshNeurofibromatosis 1/*diagnosis/ethnology/geneticsen_US
dc.subject.meshNeurologic Examinationen_US
dc.subject.meshPhenotypeen_US
dc.titleClinical manifestations of neurofibromatosis-1 in Chinese childrenen_HK
dc.typeArticleen_HK
dc.identifier.emailWong, VCN:vcnwong@hku.hken_HK
dc.identifier.authorityWong, VCN=rp00334en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/0887-8994(94)90006-Xen_HK
dc.identifier.pmid7702690-
dc.identifier.scopuseid_2-s2.0-0028658412en_HK
dc.identifier.volume11en_HK
dc.identifier.issue4en_HK
dc.identifier.spage301en_HK
dc.identifier.epage307en_HK
dc.identifier.isiWOS:A1994PZ52800006-
dc.publisher.placeUnited Statesen_HK
dc.identifier.scopusauthoridWong, VCN=7202525632en_HK
dc.identifier.issnl0887-8994-

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