Asena Pınar Sefer

发表

Low Density Granulocytes and Dysregulated Neutrophils Driving Autoinflammatory Manifestations in NEMO Deficiency

M. Haimel, L. Cinel, I. Gursel, 2022, Journal of Clinical Immunology.

Expanding the Clinical and Immunological Phenotypes and Natural History of MALT1 Deficiency

T. Chatila, D. Krappmann, N. Rezaei, 2022, Journal of Clinical Immunology.

A Patient with Novel ICOS Mutation Presented with Progressive Loss of B Cells

S. Barış, L. Charbonnier, E. Karakoc‐Aydiner, 2020, Journal of clinical immunology.

Lymphopenia with Low T and NK Cells in a Patient with USB1 Mutation, Rare Findings in Clericuzio-Type Poikiloderma with Neutropenia

S. Barış, E. Karakoc‐Aydiner, A. Ozen, 2021, Journal of Clinical Immunology.

Evolution and long‐term outcomes of combined immunodeficiency due to CARMIL2 deficiency

T. Chatila, H. Su, G. Baysoy, 2021, Allergy.

Clinical and Laboratory Factors Affecting the Prognosis of Severe Combined Immunodeficiency

S. Barış, E. Nain, E. Karakoc‐Aydiner, 2022, Journal of Clinical Immunology.

Congenital iRHOM2 deficiency causes ADAM17 dysfunction and environmentally directed immunodysregulatory disease

Andrew J. Oler, I. Vujkovic-Cvijin, Y. Belkaid, 2021, Nature Immunology.

Consensus Middle East and North Africa Registry on Inborn Errors of Immunity

R. Geha, A. Bousfiha, W. Al-Herz, 2021, Journal of Clinical Immunology.

A Patient with Novel ICOS Mutation Presented with Progressive Loss of B Cells

S. Barış, L. Charbonnier, E. Karakoc‐Aydiner, 2020, Journal of Clinical Immunology.

Adverse COVID‐19 outcomes in immune deficiencies: Inequality exists between subclasses

S. Barış, H. Artaç, F. Orhan, 2021, Allergy.

Severe Allergic Dysregulation Due to A Gain of Function Mutation in the Transcription Factor STAT6.

T. Chatila, M. Massaad, Mehdi Benamar, 2023, The Journal of allergy and clinical immunology.

Activated Phosphoinositide 3-Kinase δ Syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity.

A. Schulz, V. Lougaris, A. Plebani, 2023, Journal of Allergy and Clinical Immunology.

Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients.

L. Notarangelo, A. Worth, M. Bosticardo, 2023, Clinical immunology.

Evaluation of Clinical and Immunological Alterations Associated with ICF Syndrome.

S. Barış, E. Karakoc‐Aydiner, A. Kıykım, 2023, Journal of clinical immunology.

Genetic Evaluation of the Patients with Clinically Diagnosed Inborn Errors of Immunity by Whole Exome Sequencing: Results from a Specialized Research Center for Immunodeficiency in Türkiye

I. Tezcan, S. Barış, A. Ikinciogullari, 2024, Journal of clinical immunology.

Evaluating the efficacy and safety of pozelimab in patients with CD55 deficiency with hyperactivation of complement, angiopathic thrombosis, and protein-losing enteropathy disease: an open-label phase 2 and 3 study

P. Chatchatee, K. Suphapeetiporn, J. Jalbert, 2024, The Lancet.