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Clinical management, psychosocial characteristics, and quality of life in patients with homozygous familial hypercholesterolemia undergoing LDL-apheresis in Turkey: Results of a nationwide survey (A-HIT1 registry)

dc.contributor.authorÖZCEBE, OSMAN İLHAMİ
dc.contributor.authorKayikcioglu, Meral
dc.contributor.authorKuman-Tuncel, Oztem
dc.contributor.authorPirildar, Sebnem
dc.contributor.authorYILMAZ, MEHMET
dc.contributor.authorKAYNAR, LEYLAGÜL
dc.contributor.authorGokce, Cumali
dc.contributor.authorTemizhan, Ahmet
dc.contributor.authorKARAAĞAÇ AKYOL, TÜLAY
dc.contributor.authorOkutan, Harika
dc.contributor.authorSag, Saim
dc.contributor.authorGul, Ozen Oz
dc.contributor.authorSalcioglu, Zafer
dc.contributor.authorYenercag, Mustafa
dc.contributor.authorAltunkeser, Bulet Behlul
dc.contributor.authorKUKU, İRFAN
dc.contributor.authorYasar, Hamiyet Yilmaz
dc.contributor.authorKurtoglu, Erdal
dc.contributor.authorDemir, Melis
dc.contributor.authorDemircioglu, Sinan
dc.contributor.authorPEKKOLAY, ZAFER
dc.contributor.authorİLHAN, OSMAN
dc.contributor.authorTokgozoglu, Lale
dc.contributor.authorDurms, Rana Berru
dc.contributor.authorAktan, Melih
dc.date.accessioned2021-03-04T19:04:36Z
dc.date.available2021-03-04T19:04:36Z
dc.date.issued2019
dc.identifier.citationKayikcioglu M., Kuman-Tuncel O., Pirildar S., YILMAZ M., KAYNAR L., Aktan M., Durms R. B. , Gokce C., Temizhan A., ÖZCEBE O. İ. , et al., "Clinical management, psychosocial characteristics, and quality of life in patients with homozygous familial hypercholesterolemia undergoing LDL-apheresis in Turkey: Results of a nationwide survey (A-HIT1 registry)", JOURNAL OF CLINICAL LIPIDOLOGY, cilt.13, ss.455-467, 2019
dc.identifier.issn1933-2874
dc.identifier.othervv_1032021
dc.identifier.otherav_8df8fd10-d0d0-4b19-955c-681e99076f58
dc.identifier.urihttp://hdl.handle.net/20.500.12627/95952
dc.identifier.urihttps://doi.org/10.1016/j.jacl.2019.02.001
dc.description.abstractBACKGROUND: Homozygous familial hypercholesterolemia (HoFH) is a rare, life-threatening inherited disease leading to early-onset atherosclerosis and associated morbidity. Because of its rarity, longitudinal data on the management of HoFH in the real world are lacking, particularly on the impact the condition has on quality of life (QoL), including the impact of the extracorporeal lipid removal procedure apheresis (LA).
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectSağlık Bilimleri
dc.subjectEczacılık
dc.subjectFARMAKOLOJİ VE ECZACILIK
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectTemel Eczacılık Bilimleri
dc.subjectYaşam Bilimleri
dc.titleClinical management, psychosocial characteristics, and quality of life in patients with homozygous familial hypercholesterolemia undergoing LDL-apheresis in Turkey: Results of a nationwide survey (A-HIT1 registry)
dc.typeMakale
dc.relation.journalJOURNAL OF CLINICAL LIPIDOLOGY
dc.contributor.departmentEge Üniversitesi , ,
dc.identifier.volume13
dc.identifier.issue3
dc.identifier.startpage455
dc.identifier.endpage467
dc.contributor.firstauthorID265210


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