Yasemin Kendir Demirkol

发表

COVID-19 PCR test performance on samples stored at ambient temperature

Betsi Kose, J. Yıldız, L. Doğanay, 2021, Journal of Virological Methods.

Parents of ataxia‐telangiectasia patients display a distinct cellular immune phenotype mimicking ATM‐mutated patients

A. Somer, S. Barış, M. Muftuoglu, 2020, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

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

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

Comparing the levels of CTLA‐4‐dependent biological defects in patients with LRBA deficiency and CTLA‐4 insufficiency

İ. Reisli, A. Yildiran, S. Barış, 2022, Allergy.

Familial early-onset obesity in Turkish children: variants and polymorphisms in the melanocortin-4 receptor (MC4R) gene

F. Dursun, H. Kırmızıbekmez, Yasemin Kendir Demirkol, 2022, Journal of pediatric endocrinology & metabolism : JPEM.

Catch-up growth and discontinuation of fludrocortisone treatment in aldosterone synthase deficiency.

A. Çayır, Elvan Bayramoğlu, M. Ozbek, 2021, The Journal of clinical endocrinology and metabolism.

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

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

ADA2 Deficiency: Case Series of Five Patients with Varying Phenotypes

H. E. Sönmez, M. Çakan, Ş. Karadağ, 2019, Journal of Clinical Immunology.

A boy with a novel homozygous ZAP70 mutation presenting with a dermatological phenotype and postnatal decrease in CD8+ T cells

S. Barış, E. Karakoc‐Aydiner, V. Zimmermann, 2022, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

ADA2 Deficiency: Case Series of Five Patients with Varying Phenotypes

H. E. Sönmez, M. Çakan, Ş. Karadağ, 2019, Journal of Clinical Immunology.

Inflammatory Bowel Disease and Guillain Barre Syndrome in FCHO1 Deficiency

G. Baysoy, S. Barış, A. Islek, 2021, Journal of Clinical Immunology.

Johanson–Blizzard's Syndrome with a Novel UBR1 Mutation

N. Gerenli, Yasemin Kendir Demirkol, Ezgi Aktaş Karabay, 2020, Journal of Pediatric Genetics.

Immune Reconstitution Inflammatory Syndrome After Hematopoietic Stem Cell Transplantation in a FOXN1-deficient Patient

A. Kıykım, Pinar Onal, S. Nepesov, 2023, Journal of pediatric hematology/oncology.

Evaluation of Clinical and Immunological Alterations Associated with ICF Syndrome.

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

Artemis deficiency: A large cohort including a novel variant with increased radiosensitivity

S. Barış, E. Karakoc‐Aydiner, A. Kıykım, 2024, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.