CFTR gene mutation spectrum among 735 Iranian patients with cystic fibrosis: A comprehensive systematic review.
Sign Up to like & getrecommendations! Published in 2021 at "Pediatric pulmonology"
DOI: 10.1002/ppul.25647
Abstract: In this study, the spectrum and frequency of cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations previously reported among Iranian cystic fibrosis (CF) patients have been reviewed and discussed. Using the keywords of Cystic Fibrosis,… read more here.
Keywords: cystic fibrosis; iranian patients; cftr gene; spectrum ... See more keywords
Rhodopsin gene mutation analysis in Iranian patients with autosomal dominant retinitis pigmentosa
Sign Up to like & getrecommendations! Published in 2019 at "International Ophthalmology"
DOI: 10.1007/s10792-019-01099-4
Abstract: PurposeRetinitis pigmentosa (RP) is the most common hereditary retinal degeneration and an important cause of visual disability worldwide. Rhodopsin gene is one of the most important genes implicated in autosomal dominant RP (ADRP). In this… read more here.
Keywords: pigmentosa; iranian patients; autosomal dominant; rhodopsin gene ... See more keywords
Isoenzyme profiles and phylogenetic analysis of Giardia duodenalis isolates from Iranian patients
Sign Up to like & getrecommendations! Published in 2020 at "Environmental Science and Pollution Research"
DOI: 10.1007/s11356-020-10062-1
Abstract: The main objective of this study was to characterize the Giardia duodenalis isolates from Iranian patients in Fars Province, south of Iran by biochemical and molecular methods. Fifteen mass cultivated of G. duodenalis isolates in… read more here.
Keywords: isolates iranian; duodenalis; iranian patients; giardia duodenalis ... See more keywords
Novel Variants and Copy Number Variation in CDH1 Gene in Iranian Patients with Sporadic Diffuse Gastric Cancer
Sign Up to like & getrecommendations! Published in 2018 at "Journal of Gastrointestinal Cancer"
DOI: 10.1007/s12029-018-0082-7
Abstract: IntroductionThe aim of this study was to survey the nucleotide changes and copy number variations (CNV) in the CDH1 gene in Iranian patients with sporadic diffuse gastric cancer (SDGC).Materials and MethodsIn this study, 28 patients… read more here.
Keywords: cdh1 gene; gene iranian; gastric cancer; iranian patients ... See more keywords
Clinical outcome and determinants of amputation in a large cohort of Iranian patients with diabetic foot ulcers.
Sign Up to like & getrecommendations! Published in 2020 at "Foot"
DOI: 10.1016/j.foot.2020.101688
Abstract: OBJECTIVE Determining the predictive factors of diabetes foot ulcer (DFU) development and lower extremity amputations (LEA) in patients with diabetes mellitus (DM) is of great importance to compose risk stratification models. The aim of this… read more here.
Keywords: outcome; dfu; cohort; iranian patients ... See more keywords
Genetic screening in Iranian patients with retinoblastoma
Sign Up to like & getrecommendations! Published in 2017 at "Eye"
DOI: 10.1038/eye.2016.289
Abstract: PurposeThe most common intraocular tumor in childhood, retinoblastoma, is largely associated with mutations in the RB1 gene. In the most comprehensive RB1 screening in Iran, we evaluated the RB1 mutations in 106 patients with retinoblastoma,… read more here.
Keywords: genetic screening; retinoblastoma; iranian patients; patients retinoblastoma ... See more keywords
Genetic screening of TGFBI in Iranian patients with TGFBI-associated corneal dystrophies and a meta-analysis of global variation frequencies
Sign Up to like & getrecommendations! Published in 2022 at "Ophthalmic Genetics"
DOI: 10.1080/13816810.2022.2068040
Abstract: ABSTRACT Purpose Transforming growth factor beta-induced (TGFBI)-associated corneal dystrophies (CDs) are a clinically heterogeneous group of CDs caused by mutations in the TGFBI gene. Nucleotide sequences encoding two arginine residues at positions 124 and 555… read more here.
Keywords: iranian patients; meta analysis; tgfbi associated; associated corneal ... See more keywords
In Vitro Antifungal Susceptibility of Candida Species Isolated from Iranian Patients with Denture Stomatitis
Sign Up to like & getrecommendations! Published in 2018 at "BioMed Research International"
DOI: 10.1155/2018/3086586
Abstract: Background Candida-associated denture stomatitis (CADS) is a common fungal infection in people who wear dentures. The main objective of this study was to make molecular identification of causative agents of CADS and in vitro antifungal… read more here.
Keywords: candida; vitro antifungal; iranian patients; denture stomatitis ... See more keywords
A Study on the CLCN5 Gene in Iranian Patients: A Report of Novel and Recurrent Mutations.
Sign Up to like & getrecommendations! Published in 2023 at "Nephron"
DOI: 10.1159/000528344
Abstract: INTRODUCTION Dent's disease is an X-linked inherited renal tubular disorder characterized by proteinuria, hypercalciuria, nephrocalcinosis, nephrolithiasis, rickets, and end-stage renal disease. Almost 60% of patients have causative mutations in the CLCN5 gene (Dent 1), and… read more here.
Keywords: gene iranian; dent disease; clcn5 gene; iranian patients ... See more keywords
Spiritual Health in Iranian Patients With Cardiovascular Diseases: A Systematic Review and Meta-analysis.
Sign Up to like & getrecommendations! Published in 2022 at "Omega"
DOI: 10.1177/00302228221108293
Abstract: This systematic review and meta-analysis aimed to evaluate the spiritual health status of Iranian patients with cardiovascular diseases. A literature search was conducted in national (MagIran and Scientific Information Database) and international (Scopus, PubMed, and… read more here.
Keywords: patients cardiovascular; spiritual health; cardiovascular diseases; iranian patients ... See more keywords
Comparison of the clinical phenotype of systemic sclerosis patients in Iran and France in two university centers
Sign Up to like & getrecommendations! Published in 2018 at "Journal of Scleroderma and Related Disorders"
DOI: 10.1177/2397198318809224
Abstract: Objectives: Systemic sclerosis is a severe and rare chronic auto-immune multisystem disorder characterized by vasculopathy and skin stiffness. Ethnic and geographical origin can influence the outcomes. In this study, we compared the phenotypic characteristics of… read more here.
Keywords: sclerosis; patients value; value 001; systemic sclerosis ... See more keywords