Suchergebnisse - "Abolhassani, Hassan"

PubPharm (59)

1

From variant of uncertain significance to likely pathogenic in two siblings with atypical RAG2 Deficiency : a case report and review of the literature

enthalten in: BMC pediatrics | 2024

von Taghizadeh, N. | Mohammadi, S. | Abolhassani, H. | +4

2

Cellular mechanisms and clinical applications for phenocopies of inborn errors of immunity : infectious susceptibility due to cytokine autoantibodies

enthalten in: Expert review of clinical immunology | 2023

von Sun, R. | Wang, Y. | Abolhassani, H.

3

JAGN1 mutation with distinct clinical features; two case reports and literature review

enthalten in: BMC pediatrics | 2023

von Hojabri, M. | Farsi, Y. | Jamee, M. | +6

4

Organ-based clues for diagnosis of inborn errors of immunity : A practical guide for clinicians

enthalten in: Immunity, inflammation and disease | 2023

von Mohammadi, F. | Yadegar, A. | Mardani, M. | +3

5

How do nuclear factor kappa B (NF-κB)1 and NF-κB2 defects lead to the incidence of clinical and immunological manifestations of inborn errors of immunity?

enthalten in: Expert review of clinical immunology | 2023

von Fathi, N. | Mojtahedi, H. | Nasiri, M. | +6

6

The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity

enthalten in: The journal of allergy and clinical immunology. In practice | 2023

von Baris, S. | Abolhassani, H. | Massaad, M. | +50

7

Updates of cancer hallmarks in patients with inborn errors of immunity

enthalten in: Current opinion in allergy and clinical immunology | 2022

von Wang, Y. | Abolhassani, H.

8

SARS-CoV-2 infection in patients with inborn errors of immunity due to DNA repair defects

enthalten in: Acta biochimica et biophysica Sinica | 2022

von Wang, Y. | Abolhassani, H. | Hammarström, L. | +1

9

Role of rare immune cells in common variable immunodeficiency

enthalten in: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology | 2022

von Soltani, M. | Rezaei, M. | Fekrvand, S. | +3

10

Protein Kinase C-Delta Defect in Autoimmune Lymphoproliferative Syndrome-Like Disease : First Case from the National Iranian Registry and Review of the Literature

enthalten in: Immunological investigations | 2022

von Sharifinejad, N. | Azizi, G. | Behniafard, N. | +5

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