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The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency

dc.contributor.authorUnal, Ekrem
dc.contributor.authorCANT, Andrew J.
dc.contributor.authorJones, Alison
dc.contributor.authorGaspar, Bobby H.
dc.contributor.authorARKWRIGHT, Peter D.
dc.contributor.authorPIETROGRANDE, Maria C.
dc.contributor.authorBAZ, Zeina
dc.contributor.authorAL-TAMEMI, Salem
dc.contributor.authorLOUGARIS, Vassilios
dc.contributor.authorGLOCKER, Cristina
dc.contributor.authorSAGHAFI, Shiva
dc.contributor.authorPOURPAK, Zahra
dc.contributor.authorCEJA, Ruben
dc.contributor.authorSASSI, Atfa
dc.contributor.authorGraham, Laura E.
dc.contributor.authorMassaad, Michel J.
dc.contributor.authorMELLOULI, Fethi
dc.contributor.authorBEN-MUSTAPHA, Imen
dc.contributor.authorKHEMIRI, Monia
dc.contributor.authorKilic, Sara Sebnem
dc.contributor.authorETZIONI, Amos
dc.contributor.authorLEFRANC, Gerard
dc.contributor.authorMEGARBANE, Andre
dc.contributor.authorBOUTROS, Jeannette
dc.contributor.authorGALAL, Nermeen
dc.contributor.authorBEJAOUI, Mohamed
dc.contributor.authorBARBOUCHE, Mohamed-Ridha
dc.contributor.authorGeha, Raif S.
dc.contributor.authorCHATILA, Talal A.
dc.contributor.authorGrimbacher, Bodo
dc.contributor.authorCamcioglu, Yildiz
dc.contributor.authorSomer, Ayper
dc.contributor.authorEngelhardt, Karin R.
dc.contributor.authorGERTZ, Michael E.
dc.contributor.authorKELES, Sevgi
dc.contributor.authorSCHAEFFER, Alejandro A.
dc.contributor.authorSIGMUND, Elena C.
dc.contributor.authorFREEMAN, Alexandra F.
dc.contributor.authorTHIEL, Jens
dc.contributor.authorSCHULZE, Ilka
dc.contributor.authorAl-Herz, Waleed
dc.contributor.authorMETIN, Ayse
dc.contributor.authorSanal, Oezden
dc.contributor.authorTezcan, Ilhan
dc.contributor.authorYEGANEH, Mehdi
dc.contributor.authorNIEHUES, Tim
dc.contributor.authorDUECKERS, Gregor
dc.contributor.authorWEINSPACH, Sebastian
dc.contributor.authorPatiroglu, Turkan
dc.contributor.authorDasouki, Majed
dc.contributor.authorYilmaz, Mustafa
dc.contributor.authorGENEL, Ferah
dc.contributor.authorAYTEKIN, Caner
dc.contributor.authorKutukculer, Necil
dc.contributor.authorKilic, Mehmet
dc.contributor.authorReisli, Ismail
dc.contributor.authorGENNERY, Andrew R.
dc.date.accessioned2021-03-02T22:16:31Z
dc.date.available2021-03-02T22:16:31Z
dc.date.issued2015
dc.identifier.citationEngelhardt K. R. , GERTZ M. E. , KELES S., SCHAEFFER A. A. , SIGMUND E. C. , GLOCKER C., SAGHAFI S., POURPAK Z., CEJA R., SASSI A., et al., "The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency", JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, cilt.136, sa.2, ss.402-412, 2015
dc.identifier.issn0091-6749
dc.identifier.otherav_0bb9581d-9f41-4ca5-b9ae-d41fb9dd0a0f
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/13551
dc.identifier.urihttps://doi.org/10.1016/j.jaci.2014.12.1945
dc.description.abstractBackground: Mutations in dedicator of cytokinesis 8 (DOCK8) cause a combined immunodeficiency (CID) also classified as autosomal recessive (AR) hyper-IgE syndrome (HIES). Recognizing patients with CID/HIES is of clinical importance because of the difference in prognosis and management.
dc.language.isoeng
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectALERJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectİmmünoloji
dc.subjectYaşam Bilimleri (LIFE)
dc.titleThe extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency
dc.typeMakale
dc.relation.journalJOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
dc.contributor.departmentUniversity Of London , ,
dc.identifier.volume136
dc.identifier.issue2
dc.identifier.startpage402
dc.identifier.endpage412
dc.contributor.firstauthorID38856


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