Connection

Nima Rezaei to Adult

This is a "connection" page, showing publications Nima Rezaei has written about Adult.
Connection Strength

0.269
  1. A systematic review of pregnant women with COVID-19 and their neonates. Arch Gynecol Obstet. 2021 07; 304(1):5-38.
    View in: PubMed
    Score: 0.015
  2. Cutaneous lesions and COVID-19: Cystic painful lesion in a case with positive SARS-CoV-2. Dermatol Ther. 2020 Nov; 33(6):e14266.
    View in: PubMed
    Score: 0.015
  3. Genetic predisposition models to COVID-19 infection. Med Hypotheses. 2020 09; 142:109818.
    View in: PubMed
    Score: 0.015
  4. COVID-19 affects healthy pediatricians more than pediatric patients. Infect Control Hosp Epidemiol. 2020 Sep; 41(9):1106-1107.
    View in: PubMed
    Score: 0.014
  5. Toll-like receptors pathway in common variable immune deficiency (CVID) and X-linked agammaglobulinemia (XLA). Eur Cytokine Netw. 2018 Nov 01; 29(4):153-158.
    View in: PubMed
    Score: 0.013
  6. Association of T Helper 1 Cytokine Gene Single Nucleotide Polymorphisms with Ulcerative Colitis and Crohn's Disease. Dig Dis. 2019; 37(1):21-32.
    View in: PubMed
    Score: 0.013
  7. Association of IL10 and TGFB single nucleotide polymorphisms with intervertebral disc degeneration in Iranian population: a case control study. BMC Med Genet. 2018 04 10; 19(1):59.
    View in: PubMed
    Score: 0.013
  8. Evaluation of regulatory T lymphocytes and IL2Ra and FOXP3 gene expression in peripheral mononuclear cells from patients with amyotrophic lateral sclerosis. Ir J Med Sci. 2018 Nov; 187(4):1065-1071.
    View in: PubMed
    Score: 0.013
  9. sICAM-1, sVCAM-1 and sE-Selectin Levels in Type 1 Diabetes. Fetal Pediatr Pathol. 2018 Feb; 37(1):69-73.
    View in: PubMed
    Score: 0.012
  10. Association of Transforming Growth Factor-Beta Gene Polymorphisms in Recurrent Aphthous Stomatitis. Acta Med Iran. 2017 Nov; 55(11):672-675.
    View in: PubMed
    Score: 0.012
  11. Interleukin-4 and Interleukin-10 Gene Polymorphisms in Patients with Inflammatory Bowel Disease. Immunol Invest. 2017 Oct; 46(7):714-729.
    View in: PubMed
    Score: 0.012
  12. 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. PLoS One. 2017; 12(4):e0175437.
    View in: PubMed
    Score: 0.012
  13. Association analysis of RAC1 single nucleotide polymorphisms with ulcerative colitis. Clin Res Hepatol Gastroenterol. 2017 09; 41(4):487-489.
    View in: PubMed
    Score: 0.012
  14. Evaluating Awareness of Pediatricians and General Practitioners on Transformation of the Health System in Iran. Acta Med Iran. 2017 Jan; 55(1):49-52.
    View in: PubMed
    Score: 0.012
  15. STAT4 single nucleotide gene polymorphisms and susceptibility to endometriosis-related infertility. Eur J Obstet Gynecol Reprod Biol. 2016 Aug; 203:20-4.
    View in: PubMed
    Score: 0.011
  16. Neurological manifestations as the predictors of severity and mortality in hospitalized individuals with COVID-19: a multicenter prospective clinical study. BMC Neurol. 2021 Mar 16; 21(1):116.
    View in: PubMed
    Score: 0.004
  17. Acute Cardiac Injury in COVID-19: A Systematic Review and Meta-analysis. Arch Iran Med. 2020 11 01; 23(11):801-812.
    View in: PubMed
    Score: 0.004
  18. Clinical Manifestations, Immunological Characteristics and Genetic Analysis of Patients with Hyper-Immunoglobulin M Syndrome in Iran. Int Arch Allergy Immunol. 2019; 180(1):52-63.
    View in: PubMed
    Score: 0.003
  19. Individual Radiosensitivity Assessment of the Families of Ataxia-Telangiectasia Patients by G2-Checkpoint Abrogation. Sultan Qaboos Univ Med J. 2018 Nov; 18(4):e440-e446.
    View in: PubMed
    Score: 0.003
  20. Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis. J Clin Immunol. 2018 10; 38(7):816-832.
    View in: PubMed
    Score: 0.003
  21. Association of nod-like receptor protein-3 single nucleotide gene polymorphisms and expression with the susceptibility to relapsing-remitting multiple sclerosis. Int J Immunogenet. 2018 Dec; 45(6):329-336.
    View in: PubMed
    Score: 0.003
  22. Clinical implications of systematic phenotyping and exome sequencing in patients with primary antibody deficiency. Genet Med. 2019 01; 21(1):243-251.
    View in: PubMed
    Score: 0.003
  23. A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity. Sci Immunol. 2018 06 15; 3(24).
    View in: PubMed
    Score: 0.003
  24. The imbalance of circulating T helper subsets and regulatory T cells in patients with LRBA deficiency: Correlation with disease severity. J Cell Physiol. 2018 11; 233(11):8767-8777.
    View in: PubMed
    Score: 0.003
  25. Evaluation of the TLR negative regulatory network in CVID patients. Genes Immun. 2019 03; 20(3):198-206.
    View in: PubMed
    Score: 0.003
  26. The Profile of Toll-like Receptor 2 (TLR2), TLR4 and Their Cytosolic Downstream Signaling Pathway in Common Variable Immunodeficiency (CVID) Patients. Iran J Allergy Asthma Immunol. 2018 Apr; 17(2):188-200.
    View in: PubMed
    Score: 0.003
  27. Polyautoimmunity in Patients with LPS-Responsive Beige-Like Anchor (LRBA) Deficiency. Immunol Invest. 2018 Jul; 47(5):457-467.
    View in: PubMed
    Score: 0.003
  28. Minimal residual disease (MRD) detection using rearrangement of immunoglobulin/T cell receptor genes in adult patients with acute lymphoblastic leukemia (ALL). Ann Hematol. 2018 Apr; 97(4):585-595.
    View in: PubMed
    Score: 0.003
  29. Immunomodulatory Effect of G2013 (a-L-Guluronic Acid) on the TLR2 and TLR4 in Human Mononuclear Cells. Curr Drug Discov Technol. 2018; 15(2):123-131.
    View in: PubMed
    Score: 0.003
  30. Role of Apoptosis in the Pathogenesis of Common Variable Immunodeficiency (CVID). Endocr Metab Immune Disord Drug Targets. 2017 Nov 16; 17(4):332-340.
    View in: PubMed
    Score: 0.003
  31. The potent suppressive effect of ß-d-mannuronic acid (M2000) on molecular expression of the TLR/NF-kB Signaling Pathway in ankylosing spondylitis patients. Int Immunopharmacol. 2017 Nov; 52:191-196.
    View in: PubMed
    Score: 0.003
  32. Expanding the mutational spectrum in Johanson-Blizzard syndrome: identification of whole exon deletions and duplications in the UBR1 gene by multiplex ligation-dependent probe amplification analysis. Mol Genet Genomic Med. 2017 11; 5(6):774-780.
    View in: PubMed
    Score: 0.003
  33. Increase Concentration of Transforming Growth Factor Beta (TGF-ß) in Breast Milk of Mothers With Psychological Disorders. Acta Med Iran. 2017 Jul; 55(7):429-436.
    View in: PubMed
    Score: 0.003
  34. Clinical, immunologic, molecular analyses and outcomes of iranian patients with LRBA deficiency: A longitudinal study. Pediatr Allergy Immunol. 2017 08; 28(5):478-484.
    View in: PubMed
    Score: 0.003
  35. A gain-of-function mutation of STAT1: A novel genetic factor contributing to chronic mucocutaneous candidiasis. Acta Microbiol Immunol Hung. 2017 Jun 01; 64(2):191-201.
    View in: PubMed
    Score: 0.003
  36. Measurement of Health-Related Quality of Life in Primary Antibody-Deficient Patients. Immunol Invest. 2017 May; 46(4):329-340.
    View in: PubMed
    Score: 0.003
  37. Vitamin D status, aeroallergen sensitization, and allergic rhinitis: A systematic review and meta-analysis. Int Rev Immunol. 2017 01 02; 36(1):41-53.
    View in: PubMed
    Score: 0.003
  38. Combined immunodeficiency and Epstein-Barr virus-induced B cell malignancy in humans with inherited CD70 deficiency. J Exp Med. 2017 01; 214(1):91-106.
    View in: PubMed
    Score: 0.003
  39. Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations. Blood. 2008 May 15; 111(10):4954-7.
    View in: PubMed
    Score: 0.002
  40. HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease). Nat Genet. 2007 Jan; 39(1):86-92.
    View in: PubMed
    Score: 0.001
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.