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Association of Interleukin-1 Gene Cluster and Interleukin-1 Receptor Polymorphisms With Febrile Seizures.
- Published in:
- Journal of Child Neurology, 2016, v. 31, n. 6, p. 673, doi. 10.1177/0883073815610429
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- Publication type:
- Article
Association of IL4 Single-Nucleotide Polymorphisms With Febrile Seizures.
- Published in:
- Journal of Child Neurology, 2015, v. 30, n. 4, p. 423, doi. 10.1177/0883073814551389
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- Publication type:
- Article
ASCIA-P69: A NOVEL AICDA MUTATION IN A CASE OF AUTOSOMAL RECESSIVE HYPER-IGM SYNDROME, GROWTH HORMONE DEFICIENCY AND AUTOIMMUNITY.
- Published in:
- Internal Medicine Journal, 2016, v. 46, p. 26, doi. 10.1111/imj.69_13197
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- Publication type:
- Article
APRIL gene polymorphism and serum sAPRIL levels in children with systemic lupus erythematosus.
- Published in:
- Clinical Rheumatology, 2017, v. 36, n. 4, p. 831, doi. 10.1007/s10067-016-3466-8
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- Publication type:
- Article
Association of interleukin-6 single nucleotide polymorphisms with juvenile idiopathic arthritis.
- Published in:
- Clinical Rheumatology, 2017, v. 36, n. 1, p. 77, doi. 10.1007/s10067-016-3407-6
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- Publication type:
- Article
Polymorphisms of genes encoding interleukin-4 and its receptor in Iranian patients with juvenile idiopathic arthritis.
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- Clinical Rheumatology, 2016, v. 35, n. 8, p. 1943, doi. 10.1007/s10067-016-3224-y
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- Publication type:
- Article
A novel X-linked mutation in IL2RG associated with early-onset inflammatory bowel disease: a case report of twin brothers.
- Published in:
- 2023
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- Publication type:
- Case Study
Germline biallelic mutation affecting the transcription factor Helios causes pleiotropic defects of immunity.
- Published in:
- Science Immunology, 2021, v. 6, n. 65, p. 1, doi. 10.1126/sciimmunol.abe3981
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- Publication type:
- Article
The cytoskeletal regulator HEM1 governs B cell development and prevents autoimmunity.
- Published in:
- Science Immunology, 2020, v. 5, n. 49, p. 1, doi. 10.1126/sciimmunol.abc3979
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- Publication type:
- Article
A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity.
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- Science Immunology, 2018, v. 3, n. 24, p. 1, doi. 10.1126/sciimmunol.aat4956
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- Publication type:
- Article
A Novel Recessive Mutation of Interferon-γ Receptor 1 in a Patient with Mycobacterium tuberculosis in Bone Marrow Aspirate.
- Published in:
- 2019
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- Publication type:
- Letter
Preference of Genetic Diagnosis of CXCR4 Mutation Compared with Clinical Diagnosis of WHIM Syndrome.
- Published in:
- 2017
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- Publication type:
- Letter
Hypomorphic DOCK8 deletion causes hypereosinophilic syndrome.
- Published in:
- 2020
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- Publication type:
- Case Study
A novel homozygous RAG1 mutation is associated with severe combined immunodeficiency and neurological presentations.
- Published in:
- Allergologia & Immunopathologia, 2021, v. 49, n. 4, p. 91, doi. 10.15586/aei.v49i4.194
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- Publication type:
- Article
Novel BTK mutation in X-linked agammaglobulinemia: Report of a 17-year-old male.
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- Allergologia & Immunopathologia, 2021, v. 49, n. 2, p. 80, doi. 10.15586/aei.v49i2.62
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- Publication type:
- Article
A gain-of-function mutation of STAT1: A novel genetic factor contributing to chronic mucocutaneous candidiasis.
- Published in:
- Acta Microbiologica et Immunologica Hungarica, 2017, v. 64, n. 2, p. 191, doi. 10.1556/030.64.2017.014
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- Publication type:
- Article
Efficiency of Nested-PCR in Detecting Asymptomatic Cases toward Malaria Elimination Program in an Endemic Area of Iran.
- Published in:
- Iranian Journal of Parasitology, 2015, v. 10, n. 1, p. 39
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- Publication type:
- Article
Whole Exome Sequencing Could Help to Distinguish Between Pediatric Systemic Lupus Erythematosus and Primary Immunodeficiency Disease.
- Published in:
- Acta Medica Iranica, 2018, v. 56, n. 9, p. 557
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- Publication type:
- Article
Non-Pathogenic Heterozygous Polymorphism in RAB27A Gene in a Case Suspicious to Griscelli Syndrome, Type II.
- Published in:
- Acta Medica Iranica, 2018, v. 56, n. 8, p. 494
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- Publication type:
- Article
Association of the Single Nucleotide Polymorphisms of the Genes Encoding IL-2 and IFN-γ with Febrile Seizure.
- Published in:
- Acta Medica Iranica, 2017, v. 55, n. 6, p. 354
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- Publication type:
- Article
Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype of a patient.
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- Allergy, Asthma & Clinical Immunology, 2023, v. 19, n. 1, p. 1, doi. 10.1186/s13223-023-00804-4
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- Article
Survey for asymptomatic malaria cases in low transmission settings of Iran under elimination programme.
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- Malaria Journal, 2012, v. 11, n. 1, p. 126, doi. 10.1186/1475-2875-11-126
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- Publication type:
- Article
Non-variant specific antibody responses to theC-terminal region of merozoite surface protein-1of Plasmodium falciparum (PfMSP-1<sub>19</sub>) in Iraniansexposed to unstable malaria transmission.
- Published in:
- Malaria Journal, 2010, v. 9, p. 257, doi. 10.1186/1475-2875-9-257
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- Publication type:
- Article