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Journal of Clinical Immunology
|
September 21, 2014
A novel mutation in leukocyte adhesion deficiency type II/CDGIIc
Deniz Cagdas, Mustafa Yilmaz, Nurgün Kandemir, et al.
The Turkish Journal of Pediatrics
|
December 23, 2015
Polymorphisms in FAS and CASP8 genes may contribute to the development of ALPS phenotype: a study in 25 patients with probable ALPS
Çağman Tan, Rıza Köksal Özgül, Deniz Çağdaş Ayvaz, et al.
The Turkish Journal of Pediatrics
|
March 10, 2017
Clinical and genetic features of IL12Rb1 deficiency: Single center experience of 18 patients
Çağman Tan, Deniz Çağdaş-Ayvaz, Ayşe Metin, et al.
Journal of Clinical Immunology
|
September 22, 2012
A novel mutation in the complement component 3 gene in a patient with selective IgA deficiency
Elisangela Santos-Valente, Ismail Reisli, Hasibe Artaç, et al.
Bone Marrow Transplantation
|
December 23, 2017
Successful hematopoietic stem cell transplantation after myeloablative conditioning in three patients with dedicator of cytokinesis 8 deficiency (DOCK8) related Hyper IgE syndrome
Barış Kuşkonmaz, Deniz Ayvaz, İlhan Tezcan, et al.
The Turkish Journal of Pediatrics
|
May 11, 2018
Defective pneumococcal antibody response in patients with recurrent respiratory tract infections
Baran Erman, Duygu Demirtaş, Hacer Neslihan Bildik, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
October 7, 2014
Griscelli syndrome type 3-like phenotype with MYO-5A exon-F deletion
Mustafa Yılmaz, Deniz Çağdaş, Virginie Grandin, et al.
Scandinavian Journal of Immunology
|
August 29, 2018
B lymphocyte subsets and outcomes in patients with an initial diagnosis of transient hypogammaglobulinemia of infancy
Fehime K Eroglu, Fatima Aerts Kaya, Deniz Cagdas, et al.
Scandinavian Journal of Immunology
|
February 22, 2023
A single-center study points to diverse features and outcome in patients with Hyperimmunoglobulin M Syndrome and Class- Switch Recombination defects
Ayşegül Akarsu, Sevil Halaçlı, Çağman Tan, et al.
Journal of Clinical Immunology
|
December 1, 2016
Low T Cell Numbers Resembling T-B+ SCID in a Patient with Wiskott-Aldrich Syndrome and the Outcome of Two Hematopoietic Stem Cell Transplantations
Deniz Cagdas, Selin Aytac, Barış Kuskonmaz, et al.
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Search research articles
Search
Showing results (1-10 of 22) with videos related to
Sort By:
Page
of 3
Journal of Clinical Immunology
|
September 21, 2014
A novel mutation in leukocyte adhesion deficiency type II/CDGIIc
Deniz Cagdas, Mustafa Yilmaz, Nurgün Kandemir, et al.
The Turkish Journal of Pediatrics
|
December 23, 2015
Polymorphisms in FAS and CASP8 genes may contribute to the development of ALPS phenotype: a study in 25 patients with probable ALPS
Çağman Tan, Rıza Köksal Özgül, Deniz Çağdaş Ayvaz, et al.
The Turkish Journal of Pediatrics
|
March 10, 2017
Clinical and genetic features of IL12Rb1 deficiency: Single center experience of 18 patients
Çağman Tan, Deniz Çağdaş-Ayvaz, Ayşe Metin, et al.
Journal of Clinical Immunology
|
September 22, 2012
A novel mutation in the complement component 3 gene in a patient with selective IgA deficiency
Elisangela Santos-Valente, Ismail Reisli, Hasibe Artaç, et al.
Bone Marrow Transplantation
|
December 23, 2017
Successful hematopoietic stem cell transplantation after myeloablative conditioning in three patients with dedicator of cytokinesis 8 deficiency (DOCK8) related Hyper IgE syndrome
Barış Kuşkonmaz, Deniz Ayvaz, İlhan Tezcan, et al.
The Turkish Journal of Pediatrics
|
May 11, 2018
Defective pneumococcal antibody response in patients with recurrent respiratory tract infections
Baran Erman, Duygu Demirtaş, Hacer Neslihan Bildik, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology
|
October 7, 2014
Griscelli syndrome type 3-like phenotype with MYO-5A exon-F deletion
Mustafa Yılmaz, Deniz Çağdaş, Virginie Grandin, et al.
Scandinavian Journal of Immunology
|
August 29, 2018
B lymphocyte subsets and outcomes in patients with an initial diagnosis of transient hypogammaglobulinemia of infancy
Fehime K Eroglu, Fatima Aerts Kaya, Deniz Cagdas, et al.
Scandinavian Journal of Immunology
|
February 22, 2023
A single-center study points to diverse features and outcome in patients with Hyperimmunoglobulin M Syndrome and Class- Switch Recombination defects
Ayşegül Akarsu, Sevil Halaçlı, Çağman Tan, et al.
Journal of Clinical Immunology
|
December 1, 2016
Low T Cell Numbers Resembling T-B+ SCID in a Patient with Wiskott-Aldrich Syndrome and the Outcome of Two Hematopoietic Stem Cell Transplantations
Deniz Cagdas, Selin Aytac, Barış Kuskonmaz, et al.
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of 3