Items where Division is "Research Institute for Primordial Prevention of Non-communicable Disease > Pediatric Inherited Diseases Research Center" and Year is 2018

Article

(2018) A novel missense mutation in GIPC3 causes sensorineural hearing loss in an Iranian family revealed by targeted next-generation sequencing. International Journal of Pediatric Otorhinolaryngology. pp. 8-11. ISSN 0165-5876

(2018) Effect of Vitamin E in Prevention of Intraventricular Hemorrhage in Preterm Neonates. International Journal of Preventive Medicine. ISSN 2008-7802

(2018) Induction of Apoptosis in Toxoplasma gondii Infected Hela Cells by Cisplatin and Sodium Azide and Isolation of Apoptotic Bodies and Potential Use for Vaccination against Toxoplasma gondii. Iranian Journal of Parasitology. pp. 406-415. ISSN 1735-7020

(2018) Analysis of the expression of mir-34a, mir-199a, mir-30c and mir-19a in peripheral blood CD4+T lymphocytes of relapsing-remitting multiple sclerosis patients. Gene. pp. 109-117. ISSN 0378-1119

(2018) Allgrove Syndrome in Iranian Patients and Report on a Novel Mutation in AAAS Gene. Iranian Journal of Pediatrics. ISSN 2008-2142

(2018) Association between (GT)n Repeats in Heme Oxygenase-1 Gene Promoter and 3-Year Survival of Patients with Acute Leukemia: a Controlled, Cross-Sectional Study. Int J Hematol Oncol Stem Cell Res. pp. 49-56. ISSN 2008-3009 (Print) 2008-2207 (Linking)

(2018) GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants. International Journal of Pediatric Otorhinolaryngology. pp. 121-126. ISSN 0165-5876

(2018) Meta-Analysis of the Association between GABA Receptor Polymorphisms and Autism Spectrum Disorder (ASD). Journal of Molecular Neuroscience. pp. 1-9. ISSN 0895-8696

(2018) In silico analysis of SLC3A1 and SLC7A9 mutations in Iranian patients with Cystinuria. Molecular Biology Reports. pp. 1165-1173. ISSN 0301-4851

(2018) Association of Polymorphism in Fatty Acid Desaturase Gene with the Risk of Type 2 Diabetes in Iranian Population. Adv Biomed Res. p. 98. ISSN 2277-9175 (Print) 2277-9175 (Linking)

(2018) Is Vitamin D Supplementation Effective in Prevention of Recurrent Urinary Tract Infections in the Pediatrics? A Randomized Triple-Masked Controlled Trial. Adv Biomed Res. p. 150. ISSN 2277-9175 (Print) 2277-9175 (Linking)

(2018) Evaluation of the effects of AlkylPhenolic compounds on kinetic parameters in a moving bed biofilm reactor. Canadian Journal of Chemical Engineering. pp. 1762-1769. ISSN 0008-4034

(2018) Metal-Free and Ultrasound-Assisted C-C and O-Si (O-Protected) Bond Formation in Cyanosilylation of Aldehydes with TMSCN Catalyzed by Functionalized Graphene Oxide Derivatives. Chemistryselect. pp. 12131-12138. ISSN 2365-6549

(2018) Survey on the Prevalence of Allergic Rhinitis in Junior High School Students in Isfahan, Iran. International Journal of Pediatrics-Mashhad. pp. 8253-8260. ISSN 2345-5047

(2018) Novel Variants and Copy Number Variation in CDH1 Gene in Iranian Patients with Sporadic Diffuse Gastric Cancer. J Gastrointest Cancer. ISSN 1941-6636 (Electronic)

(2018) Applying Two Different Bioinformatic Approaches to Discover Novel Genes Associated with Hereditary Hearing Loss via Whole-Exome Sequencing: ENDEAVOUR and HomozygosityMapper. Adv Biomed Res. p. 141. ISSN 2277-9175 (Print) 2277-9175 (Linking)

(2018) Lack of Evidence of the Role of APOA5 3'UTR Polymorphisms in Iranian Children and Adolescents with Metabolic Syndrome. Diabetes & Metabolism Journal. pp. 74-81. ISSN 2233-6079

(2018) Immune Thrombocytopenia (ITP) in a Patient with Relapsing-Remitting Multiple Sclerosis (RRMS) Associated with b-Interferon-1 alpha Treatment. Indian Journal of Pharmaceutical Education and Research. pp. 540-542. ISSN 0019-5464

(2018) The efficacy of PLISSIT as adjuvant therapy with bupropion on sexual dysfunction and marital satisfaction among men patients on methadone maintenance therapy. Journal of Isfahan Medical School. pp. 814-822. ISSN 10277595 (ISSN)

(2018) Genetic study of the BRAF gene reveals new variants and high frequency of the V600E mutation among Iranian ameloblastoma patients. Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology. pp. 86-90. ISSN 1600-0714 (Electronic) 0904-2512 (Linking)

(2018) A Novel Pathologic Variant in OTOF in an Iranian Family Segregating Hereditary Hearing Loss. Otolaryngology-Head and Neck Surgery. pp. 1084-1092. ISSN 0194-5998

(2018) A novel pathogenic variant in the MARVELD2 gene causes autosomal recessive non-syndromic hearing loss in an Iranian family. Genomics. ISSN 1089-8646 (Electronic) 0888-7543 (Linking)