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

Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification

(2020) Aziz Bousfiha et al.   JOURNAL OF CLINICAL IMMUNOLOGY

ALPS-Like Phenotype Caused by ADA2 Deficiency Rescued by Allogeneic Hematopoietic Stem Cell Transplantation

(2019) Federica Barzaghi et al.   Frontiers in Immunology

The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity

(2019) Markus G. Seidel et al.   Journal of Allergy and Clinical Immunology-In Practice

A Spectrum of Clinical Findings from ALPS to CVID: Several Novel LRBA Defects

(2019) Deniz Cagdas et al.   JOURNAL OF CLINICAL IMMUNOLOGY

Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis

(2018) Hassan Abolhassani et al.   JOURNAL OF CLINICAL IMMUNOLOGY

EBV Negative Lymphoma and Autoimmune Lymphoproliferative Syndrome Like Phenotype Extend the Clinical Spectrum of Primary Immunodeficiency Caused by STK4 Deficiency

(2018) Cyrill Schipp et al.   Frontiers in Immunology

CTLA-4 haploinsufficiency in a patient with an autoimmune lymphoproliferative disorder

(2017) Zeynep Yesim Kucuk et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Haploinsufficiency of TNFAIP3 ( A20 ) by germline mutation is involved in autoimmune lymphoproliferative syndrome

(2017) Masatoshi Takagi et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

RASGRP1 mutation in autoimmune lymphoproliferative syndrome-like disease

(2017) Huawei Mao et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Next Generation Sequencing Data Analysis in Primary Immunodeficiency Disorders – Future Directions

(2016) Mingyan Fang et al.   JOURNAL OF CLINICAL IMMUNOLOGY

Autoimmune lymphoproliferative syndrome-like disease in patients with LRBA mutation

(2015) Shoshana Revel-Vilk et al.   CLINICAL IMMUNOLOGY

Potentially Beneficial Effect of Hydroxychloroquine in a Patient with a Novel Mutation in Protein Kinase Cδ Deficiency

(2015) Ayca Kiykim et al.   JOURNAL OF CLINICAL IMMUNOLOGY

Spectrum of Phenotypes Associated with Mutations in LRBA

(2015) Omar K. Alkhairy et al.   JOURNAL OF CLINICAL IMMUNOLOGY

Protein Kinase Cδ Deficiency Causes Mendelian Systemic Lupus Erythematosus With B Cell-Defective Apoptosis and Hyperproliferation

(2013) Alexandre Belot et al.   ARTHRITIS AND RHEUMATISM

B-cell deficiency and severe autoimmunity caused by deficiency of protein kinase C  

(2013) E. Salzer et al.   BLOOD

Loss-of-function of the protein kinase C   (PKC ) causes a B-cell lymphoproliferative syndrome in humans

(2013) H. S. Kuehn et al.   BLOOD

The expanding spectrum of the autoimmune lymphoproliferative syndromes

(2013) João Bosco Oliveira   CURRENT OPINION IN PEDIATRICS

STIM1, PKC-δ and RasGRP set a threshold for proapoptotic Erk signaling during B cell development

(2011) Andre Limnander et al.   NATURE IMMUNOLOGY

Autoimmune lymphoproliferative syndrome-like disease with somatic KRAS mutation

(2010) M. Takagi et al.   BLOOD

Revised diagnostic criteria and classification for the autoimmune lymphoproliferative syndrome (ALPS): report from the 2009 NIH International Workshop

(2010) J. B. Oliveira et al.   BLOOD

Somatic KRAS mutations associated with a human nonmalignant syndrome of autoimmunity and abnormal leukocyte homeostasis

(2010) J. E. Niemela et al.   BLOOD

Autoimmune lymphoproliferative syndrome in a patient with a new minimal deletion in the death domain of the FAS gene

(2007) Gabriela Gualco et al.   HUMAN PATHOLOGY