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dc.contributor.authorFerreira, Carlos
dc.contributor.authorGokcay, Gulden
dc.contributor.authorKapoor, Seema
dc.contributor.authorDiRocco, Maja
dc.contributor.authorSolyom, Alexander
dc.contributor.authorSundberg, Erik
dc.contributor.authorMitchell, John
dc.contributor.authorGrant, Christina
dc.contributor.authorHarmatz, Paul
dc.contributor.authorMungan, Neslihan
dc.contributor.authorBulut, Fatma
dc.contributor.authorLampe, Christina
dc.contributor.authorHahn, Andreas
dc.contributor.authorGuelbert, Norberto
dc.contributor.authorARSLAN, NUR
dc.contributor.authorMAKAY, BALAHAN
dc.contributor.authorPuri, Ratna
dc.contributor.authorBijarnia-Mahay, Sunita
dc.contributor.authorSelim, Laila
dc.contributor.authorel Din, Iman Gamal
dc.contributor.authorÖZEN, SEZA
dc.contributor.authorBatu, Ezgi
dc.contributor.authorTorcoletti, Marta
dc.contributor.authorKimura, Alan
dc.contributor.authorMagnusson, Bo
dc.date.accessioned2021-03-03T13:32:53Z
dc.date.available2021-03-03T13:32:53Z
dc.identifier.citationSolyom A., Sundberg E., Mitchell J., Grant C., Ferreira C., Harmatz P., Mungan N., Bulut F., Lampe C., Hahn A., et al., "Farber Disease (Acid Ceramidase Deficiency): The First Natural History Study of This Rare Disease Involving Symptoms Which Can Mimic JIA", ARTHRITIS & RHEUMATOLOGY, cilt.71, 2019
dc.identifier.issn2326-5191
dc.identifier.othervv_1032021
dc.identifier.otherav_34aeaee3-367e-42bf-8604-317705a950ce
dc.identifier.urihttp://hdl.handle.net/20.500.12627/39609
dc.language.isoeng
dc.subjectKlinik Tıp (MED)
dc.subjectROMATOLOJİ
dc.subjectKlinik Tıp
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectİmmünoloji ve Romatoloji
dc.titleFarber Disease (Acid Ceramidase Deficiency): The First Natural History Study of This Rare Disease Involving Symptoms Which Can Mimic JIA
dc.typeMakale
dc.relation.journalARTHRITIS & RHEUMATOLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume71
dc.contributor.firstauthorID269447


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