Asghar Aghamohammadi
Aghamohammadi, Asghar
VIAF ID: 307198847 (Personal)
Permalink: http://viaf.org/viaf/307198847
Preferred Forms
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- 100 0 _ ‡a Asghar Aghamohammadi
4xx's: Alternate Name Forms (2)
Works
Title | Sources |
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IgA deficiency and the MHC: assessment of relative risk and microheterogeneity within the HLA A1 B8, DR3 (8.1) haplotype. | |
IgA deficiency: correlation between clinical and immunological phenotypes. | |
Immunoglobulin class switch recombination deficiency type 1 or CD40 ligand deficiency: from bedside to bench and back again | |
Immunologic evaluation of patients with recurrent ear, nose, and throat infections | |
Immunomodulatory effect of G2013 (a-L-Guluronic acid) on theTLR2 and TLR4 in human mononuclear cells. | |
Impact of IgE-mediated Food Allergy on Parental Quality of Life in Iranian Patients | |
Indications and safety of intravenous and subcutaneous immunoglobulin therapy | |
Individual Radiosensitivity Assessment of the Families of Patients by G2-Checkpoint Abrogation | |
Inflammation, a significant player of Ataxia-Telangiectasia pathogenesis? | |
Interleukin-4 and Transforming Growth Factor-Beta Single Nucleotide Genes Polymorphisms Confer Susceptibility To Atopic Dermatitis | |
Investigation of underlying primary immunodeficiencies in patients with severe atopic dermatitis | |
Long-term follow-up of ninety eight Iranian patients with primary immune deficiency in a single tertiary centre | |
Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score | |
Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation | |
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 | |
Lymphocytic Interstitial Pneumonitis: An Unusual Presentation of X-Linked Hyper Ig M Syndrome. | |
Major histocompatibility complex class I and II antigens frequencies in Baloch ethnic group living in the southeast region of Iran | |
Managing patients with side effects and adverse events to immunoglobulin therapy | |
Mannose-binding lectin protein deficiency among patients with primary immunodeficiency disease receiving IVIG therapy. | |
Mortality and morbidity in patients with X-linked agammaglobulinaemia | |
Neutropenia associated with X-linked Agammaglobulinemia in an Iranian referral center. | |
New insights into physiopathology of immunodeficiency-associated vaccine-derived poliovirus infection; systematic review of over 5 decades of data. | |
New therapeutic approach by sirolimus for enteropathy treatment in patients with LRBA deficiency. | |
A novel CD40 ligand mutation in a patient with pneumonia, neutropenia, and hyperimmunoglobulin M phenotype | |
Novel mutation of the activation-induced cytidine deaminase gene in a Tajik family: special review on hyper-immunoglobulin M syndrome. | |
Novel mutations in TNFRSF7/CD27: Clinical, immunologic, and genetic characterization of human CD27 deficiency | |
A Novel TTC7A Deficiency Presenting With Combined Immunodeficiency and Chronic Gastrointestinal Problems | |
Oral and dental health status in patients with primary antibody deficiencies | |
Oral manifestations in selective IgA deficiency | |
Otological findings in pediatric patients with hypogammaglobulinemia. | |
Outcomes and Treatment Strategies for Autoimmunity and Hyperinflammation in Patients with RAG Deficiency | |
Patients with Primary Immunodeficiencies Are a Reservoir of Poliovirus and a Risk to Polio Eradication | |
Physicians awareness on primary immunodeficiency disorders in Iran | |
PIK3R1 Mutation Associated with Hyper IgM (APDS2 Syndrome): A Case Report and Review of the Literature | |
Polyautoimmunity in Patients with LPS-Responsive Beige-Like Anchor (LRBA) Deficiency. | |
Polymorphisms Of Genes Encoding Interleukin-4 and Its Receptor Are Associated With Chronic Idiopathic Urticaria | |
Preference of Genetic Diagnosis of CXCR4 Mutation Compared with Clinical Diagnosis of WHIM Syndrome | |
Prevalence of asthma related to BMI in adolescents in Tehran, Iran, 2004-2005 | |
Primary Antibody Deficiency in a Tertiary Referral Hospital: A 30-Year Experiment | |
Primary ciliary dyskinesia in six patients with bronchiectasis | |
Primary immunodeficiencies: a decade of shifting paradigms, the current status and the emergence of cutting-edge therapies and diagnostics | |
Primary Immunodeficiency Diseases and Bacillus Calmette-Guérin (BCG)-Vaccine-Derived Complications: A Systematic Review | |
Primary immunodeficiency diseases associated with neurologic manifestations | |
Primary immunodeficiency in Iran: first report of the National Registry of PID in Children and Adults | |
Protein Kinase C-Delta Defect in Autoimmune Lymphoproliferative Syndrome-Like Disease: First Case from the National Iranian Registry and Review of the Literature | |
Psychiatric aspects of primary immunodeficiency diseases: the parental study. | |
Recurrent Gallbladder Hydrops and Sclerosing Cholangitis in 11-Year-Old Male with Hyper IgM Syndrome | |
Recurrent infections and bilateral uveitis in a patient with CD8 deficiency. | |
Renal amyloidosis in common variable immunodeficiency | |
Report on the First Survey of Iranian Patients with Hereditary Angioedema. |