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Article: Phaeochromocytoma in children

TitlePhaeochromocytoma in children
Authors
KeywordsHippel-Lindau disease
Multiple endocrine neoplasia type 2a
Pheochromocytoma
Issue Date2002
PublisherHong Kong Medical Association. The Journal's web site is located at http://www.hkmj.org/resources/supp.html
Citation
Hong Kong Medical Journal, 2002, v. 8 n. 6, p. 452-455 How to Cite?
AbstractPhaeochromocytoma is a rare disease in childhood with a subtle and wide range of clinical presentations. We report two confirmed cases and one potential case of phaeochromocytoma, each belonging to a different disease spectrum or syndromal disorder, namely sporadic phaeochromocytoma, von Hippel-Lindau disease, and multiple endocrine neoplasia type 2a. Knowledge of the molecular basis of the condition helps to make the diagnosis. Affected individuals and their family members should be screened for any associated syndromal disorders that can carry a substantial degree of morbidity and mortality.
Persistent Identifierhttp://hdl.handle.net/10722/45234
ISSN
2015 Impact Factor: 0.887
2015 SCImago Journal Rankings: 0.279
References

 

DC FieldValueLanguage
dc.contributor.authorYeung, LPKen_HK
dc.contributor.authorKwan, EYWen_HK
dc.contributor.authorCheung, PTen_HK
dc.contributor.authorLow, LCKen_HK
dc.date.accessioned2007-10-30T06:20:28Z-
dc.date.available2007-10-30T06:20:28Z-
dc.date.issued2002en_HK
dc.identifier.citationHong Kong Medical Journal, 2002, v. 8 n. 6, p. 452-455en_HK
dc.identifier.issn1024-2708en_HK
dc.identifier.urihttp://hdl.handle.net/10722/45234-
dc.description.abstractPhaeochromocytoma is a rare disease in childhood with a subtle and wide range of clinical presentations. We report two confirmed cases and one potential case of phaeochromocytoma, each belonging to a different disease spectrum or syndromal disorder, namely sporadic phaeochromocytoma, von Hippel-Lindau disease, and multiple endocrine neoplasia type 2a. Knowledge of the molecular basis of the condition helps to make the diagnosis. Affected individuals and their family members should be screened for any associated syndromal disorders that can carry a substantial degree of morbidity and mortality.en_HK
dc.format.extent228676 bytes-
dc.format.extent1732 bytes-
dc.format.extent2234 bytes-
dc.format.mimetypeapplication/pdf-
dc.format.mimetypetext/plain-
dc.format.mimetypetext/plain-
dc.languageengen_HK
dc.publisherHong Kong Medical Association. The Journal's web site is located at http://www.hkmj.org/resources/supp.htmlen_HK
dc.relation.ispartofHong Kong Medical Journalen_HK
dc.rightsCreative Commons: Attribution 3.0 Hong Kong License-
dc.subjectHippel-Lindau diseaseen_HK
dc.subjectMultiple endocrine neoplasia type 2aen_HK
dc.subjectPheochromocytomaen_HK
dc.subject.meshAdrenal Gland Neoplasms - diagnosis - etiology - surgeryen_HK
dc.subject.meshPheochromocytoma - diagnosis - etiology - surgeryen_HK
dc.subject.meshHippel-Lindau Disease - complicationsen_HK
dc.subject.meshMultiple Endocrine Neoplasia Type 2a - complicationsen_HK
dc.subject.meshGenetic Predisposition to Diseaseen_HK
dc.titlePhaeochromocytoma in childrenen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1024-2708&volume=8&issue=6&spage=452&epage=455&date=2002&atitle=Phaeochromocytoma+in+childrenen_HK
dc.identifier.emailCheung, PT: ptcheung@hku.hken_HK
dc.identifier.emailLow, LCK: lcklow@hkucc.hku.hken_HK
dc.identifier.authorityCheung, PT=rp00351en_HK
dc.identifier.authorityLow, LCK=rp00337en_HK
dc.description.naturepublished_or_final_versionen_HK
dc.identifier.pmid12459603-
dc.identifier.scopuseid_2-s2.0-0036899172en_HK
dc.identifier.hkuros75565-
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0036899172&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume8en_HK
dc.identifier.issue6en_HK
dc.identifier.spage452en_HK
dc.identifier.epage455en_HK
dc.publisher.placeHong Kongen_HK
dc.identifier.scopusauthoridYeung, LPK=36762762700en_HK
dc.identifier.scopusauthoridKwan, EYW=7006484387en_HK
dc.identifier.scopusauthoridCheung, PT=7202595465en_HK
dc.identifier.scopusauthoridLow, LCK=7007049461en_HK

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