Radwa S. Alkady

Cairo, C, Egypt

Last Updated: 09/26/2026

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Found 15 publications

Clinical and immunological features of four patients with activation-induced cytidine deaminase deficiency: Renal amyloidosis and other presentations.

Clinical and immunological features of four patients with activation-induced cytidine deaminase deficiency: Renal amyloidosis and other presentations.

Journal: Annals of human genetics

Published: May 31, 2024

A novel MALT1 variant in an Egyptian patient presenting with exfoliative dermatitis: a case-based review.

A novel MALT1 variant in an Egyptian patient presenting with exfoliative dermatitis: a case-based review.

Journal: Immunologic research

Published: May 02, 2024

Analysis of Clinical, Immunological and Molecular Features of Leukocyte Adhesion Deficiency Type I in Egyptian Children.

Analysis of Clinical, Immunological and Molecular Features of Leukocyte Adhesion Deficiency Type I in Egyptian Children.

Journal: Journal of clinical immunology

Published: November 29, 2023

Cernunnos deficiency: Further delineation in 5 Egyptian patients.

Cernunnos deficiency: Further delineation in 5 Egyptian patients.

Journal: European journal of medical genetics

Published: May 11, 2023

Chronic Granulomatous Disease: a Cohort of 173 Patients-10-Years Single Center Experience from Egypt.

Chronic Granulomatous Disease: a Cohort of 173 Patients-10-Years Single Center Experience from Egypt.

Journal: Journal of clinical immunology

Published: February 21, 2023

Flow cytometry optimizing the diagnostic approach in inborn errors of immunity: experience from Egypt.

Flow cytometry optimizing the diagnostic approach in inborn errors of immunity: experience from Egypt.

Journal: Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology

Published: February 10, 2022

Genetic Testing in Egyptian Patients with Inborn Errors of Immunity: a Single-Center Experience.

Genetic Testing in Egyptian Patients with Inborn Errors of Immunity: a Single-Center Experience.

Journal: Journal of clinical immunology

Published: January 03, 2022

Phenotypical heterogeneity in RAG-deficient patients from a highly consanguineous population.

Phenotypical heterogeneity in RAG-deficient patients from a highly consanguineous population.

Journal: Clinical and experimental immunology

Published: October 03, 2018

MHC-II Deficiency Among Egyptians: Novel Mutations and Unique Phenotypes.

MHC-II Deficiency Among Egyptians: Novel Mutations and Unique Phenotypes.

Journal: The journal of allergy and clinical immunology. In practice

Published: June 07, 2018

Genetic Counseling in Primary Immunodeficiency Disorders: An Emerging Experience in Egypt.

Genetic Counseling in Primary Immunodeficiency Disorders: An Emerging Experience in Egypt.

Journal: Molecular diagnosis & therapy

Published: September 14, 2017

Patterns of Primary Immunodeficiency Disorders Among a Highly Consanguineous Population: Cairo University Pediatric Hospital's 5-Year Experience.

Patterns of Primary Immunodeficiency Disorders Among a Highly Consanguineous Population: Cairo University Pediatric Hospital's 5-Year Experience.

Journal: Journal of clinical immunology

Published: January 16, 2016

Role of Flow Cytometry in the Diagnosis of Chronic Granulomatous Disease: the Egyptian Experience.

Role of Flow Cytometry in the Diagnosis of Chronic Granulomatous Disease: the Egyptian Experience.

Journal: Journal of clinical immunology

Published: July 31, 2015

Showing 1-12 of 15

Last Updated: 09/26/2026