Clinical Features and HSCT Outcome for SCID in Turkey
Clinical Features and HSCT Outcome for SCID in Turkey
About this item
Full title
Author / Creator
on behalf of Turkish Pediatric Bone Marrow Transplantation Sub Group (TPBMT-SG) , Turkish Pediatric Bone Marrow Transplantation Sub Group (TPBMT-SG) , Ikinciogullari, Aydan , Cagdas, Deniz , Dogu, Figen , Tugrul, Tuba , Karasu, Gulsum , Haskologlu, Sule , Aksoylar, Serap , Uygun, Vedat , Kupesiz, Alphan , Yildiran, Alisan , Gursel, Orhan , Ates, Can , Elhan, Atilla , Kansoy, Savas , Yesilipek, Akif and Tezcan, Ilhan
Publisher
New York: Springer US
Journal title
Language
English
Formats
Publication information
Publisher
New York: Springer US
Subjects
More information
Scope and Contents
Contents
Severe combined immunodeficiency (SCID) is the most serious PID, characterized by T cell lymphopenia and lack of antigen-specific T cell and B cell immune responses, inevitably leading to death within the first year of life if hematopoietic stem cell transplantation (HSCT) is not performed.
Purpose and Methods
Since SCID is a common type of P...
Alternative Titles
Full title
Clinical Features and HSCT Outcome for SCID in Turkey
Authors, Artists and Contributors
Author / Creator
Turkish Pediatric Bone Marrow Transplantation Sub Group (TPBMT-SG)
Ikinciogullari, Aydan
Cagdas, Deniz
Dogu, Figen
Tugrul, Tuba
Karasu, Gulsum
Haskologlu, Sule
Aksoylar, Serap
Uygun, Vedat
Kupesiz, Alphan
Yildiran, Alisan
Gursel, Orhan
Ates, Can
Elhan, Atilla
Kansoy, Savas
Yesilipek, Akif
Tezcan, Ilhan
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_2200767190
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2200767190
Other Identifiers
ISSN
0271-9142
E-ISSN
1573-2592
DOI
10.1007/s10875-019-00610-x
