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JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropeniaA syndrome with congenital neutropenia and mutations in G6PC3A homozygous CARD9 mutation in a family with susceptibility to fungal infectionsBacillus Calmette-Guérin (BCG) complications associated with primary immunodeficiency diseasesCytokine gene polymorphisms are associated with irritable bowel syndrome: a systematic review and meta-analysisDeleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunityRetinol binding protein 4 in relation to diet, inflammation, immunity, and cardiovascular diseasesHAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)TNF-receptor-associated periodic syndrome (TRAPS): an autosomal dominant multisystem disorderOptic neuritis, multiple sclerosis and human leukocyte antigen: results of a 4-year follow-up studyEffect of regular intravenous immunoglobulin therapy on prevention of pneumonia in patients with common variable immunodeficiencyXXIV World Allergy Congress 2015Y chromosome diversity among the Iranian religious groups: A reservoir of genetic variationAutoimmunity in common variable immunodeficiency: epidemiology, pathophysiology and management.Autoimmunity in primary T-cell immunodeficiencies.A hypomorphic recombination-activating gene 1 (RAG1) mutation resulting in a phenotype resembling common variable immunodeficiency.Potential role of immunoglobulin replacement therapy on MRI measures in multiple sclerosis: a systematic review.Congenital neutropenia and primary immunodeficiency disorders: a survey of 26 Iranian patients.Clinical and laboratory findings in Iranian children with cyclic neutropenia.Autosomal recessive chronic granulomatous disease, IgA deficiency and refractory autoimmune thrombocytopenia responding to Anti-CD20 monoclonal antibody.Novel WASP mutation in a patient with Wiskott-Aldrich syndrome: Case report and review of the literature.LPS-Responsive Beige-Like Anchor Gene Mutation Associated With Possible Bronchiolitis Obliterans Organizing Pneumonia Associated With Hypogammaglobulinemia and Normal IgM Phenotype and Low Number of B Cells.Alpha 1 antitrypsin deficiency in infants with neonatal cholestasisCosts of Hospital Admission on Primary Immunodeficiency Diseases.Systematic review and meta-analysis shows a specific micronutrient profile in people with Down Syndrome: Lower blood calcium, selenium and zinc, higher red blood cell copper and zinc, and higher salivary calcium and sodium.BCG vaccination in patients with severe combined immunodeficiency: complications, risks, and vaccination policiesSerum bactericidal antibody response 1 year after meningococcal polysaccharide vaccination of patients with common variable immunodeficiencyClinical and immunological features of 65 Iranian patients with common variable immunodeficiencyExtended spectrum of human glucose-6-phosphatase catalytic subunit 3 deficiency: novel genotypes and phenotypic variability in severe congenital neutropenia.Novel mutation of the activation-induced cytidine deaminase gene in a Tajik family: special review on hyper-immunoglobulin M syndrome.Mutations in tetratricopeptide repeat domain 7A result in a severe form of very early onset inflammatory bowel disease.Host-microbiota interaction and intestinal stem cells in chronic inflammation and colorectal cancer.Evaluation of physicians' awareness of pediatric diseases in iran.Cow's Milk Allergy among Children with Gastroesophageal Reflux Disease.Herpes simplex encephalitis in children with autosomal recessive and dominant TRIF deficiencyRAC2 loss-of-function mutation in 2 siblings with characteristics of common variable immunodeficiency.The phenotype of human STK4 deficiency.Evaluation of Educational Environment for Medical Students of a Tertiary Pediatric Hospital in Tehran, Using DREEM Questionnaire.mtDNA Deletion in an Iranian Infant with Pearson Marrow Syndrome.History of primary immunodeficiency diseases in iran
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2017-01-01T00:00:00Z
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