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dc.contributor.authorUysalol, Metin
dc.contributor.authorPasli, Ezgi
dc.contributor.authorEker, Nursah
dc.contributor.authorIncioglu, Ahmet
dc.date.accessioned2021-12-10T11:53:13Z
dc.date.available2021-12-10T11:53:13Z
dc.date.issued2007
dc.identifier.citationUysalol M., Eker N., Incioglu A., Pasli E., "Ataxia-telengiectasia: A case report", MEDICAL JOURNAL OF BAKIRKOY, cilt.3, sa.2, ss.73-77, 2007
dc.identifier.otherav_9b22aadb-a32a-4e15-add4-d0eed6372d75
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/172831
dc.description.abstractAtaxia-telengiectasia (AT) is a rare multisystemic autosomal-recessive disease characterized with oculocutaneous telengiectasies, recurrent sinopulmonary infections associated with humoral and cellular immune deficiencies, increased sensitivity to ionizing radiation and susceptibility to malignancies. Prevalence of the disease is known to be 1-3/40000- 100.000.
dc.language.isoeng
dc.subjectInternal Medicine
dc.subjectHealth Sciences
dc.subjectGeneral Medicine
dc.subjectMedicine (miscellaneous)
dc.subjectPathophysiology
dc.subjectAssessment and Diagnosis
dc.subjectTIP, GENEL & İÇECEK
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectFamily Practice
dc.subjectFundamentals and Skills
dc.subjectGeneral Health Professions
dc.titleAtaxia-telengiectasia: A case report
dc.typeMakale
dc.relation.journalMEDICAL JOURNAL OF BAKIRKOY
dc.contributor.departmentUysalol Sisil Etfal EAH , ,
dc.identifier.volume3
dc.identifier.issue2
dc.identifier.startpage73
dc.identifier.endpage77
dc.contributor.firstauthorID2756775


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