Nurhan Kasap

6PUBLICATIONS
41CO-AUTHORS
Genetic immunologyNeonatologyRespiratory diseasesGene and molecular therapyPredictive and prognostic markers
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (6)

|May 30, 2023
Biallelic NFATC1 mutations cause an inborn error of immunity with impaired CD8+ T-cell function and perturbed glycolysis.

Sevgi Kostel Bal, Sarah Giuliani, Jana Block

|Apr 21, 2022
A case of chronic kidney disease with pulmonary hypertension, hyperuricemia, immunodeficiency and other extrarenal findings: Answers.

Nilüfer Göknar, Emre Keleşoğlu, Nurhan Kasap

|Apr 21, 2022
A case of chronic kidney disease with pulmonary hypertension, hyperuricemia, immunodeficiency and other extrarenal findings: Questions.

Nilüfer Göknar, Emre Keleşoğlu, Nurhan Kasap

|Apr 15, 2022
A novel gain-of-function mutation in STAT5B is associated with treatment-resistant severe atopic dermatitis.

Nurhan Kasap, Kubra Aslan, Leman Tuba Karakurt

|Nov 19, 2019
Malignancy and lymphoid proliferation in primary immune deficiencies; hard to define, hard to treat.

Ayca Kiykim, Nursah Eker, Ozlem Surekli

|Jul 20, 2019
Immune system defects in DiGeorge syndrome and association with clinical course.

Ercan Nain, Ayca Kiykim, Ismail Ogulur

Pageof 1

Frequent Collaborators

3 joint publications

Ahmet Ozen

3 joint publications

Safa Baris

2 joint publications

Ercan Nain

2 joint publications

Ayca Kiykim