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Safety and Efficacy of Combined Intramuscular/Intranasal RAZI-COV PARS Vaccine Candidate Against SARS-CoV-2: A Preclinical Study in Several Animal Models

Frontiers in immunology, 2022-05, Vol.13, p.836745

2022

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Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient

Clinical case reports, 2019-06, Vol.7 (6), p.1149-1153

2019

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Cardiovascular, lactate and appetite response to light and spicy music tempo after an endurance swimming protocol in young girls

Pedagogy of physical culture and sports, 2020-08, Vol.24 (4), p.195-202

2020

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A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome

Frontiers in pediatrics, 2017-08, Vol.5, p.169

2017

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Genetics of intellectual disability in consanguineous families

Molecular psychiatry, 2019-07, Vol.24 (7), p.1027-1039

2019

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Reporting one very rare pathogenic variation c.1106G>A in POMT2 gene

Intractable & Rare Diseases Research, 2020/05/31, Vol.9(2), pp.104-108

2020

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Phase II, Safety and Immunogenicity of RAZI Cov Pars (RCP) SARS Cov-2 Vaccine in Adults Aged 18–70 Years; A Randomized, Double-Blind Clinical Trial

Journal of pharmaceutical sciences, 2023-12, Vol.112 (12), p.3012-3021

2023

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Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran

Journal of medical genetics, 2015-12, Vol.52 (12), p.823-829

2015

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The novel mutation in the COL7A1 gene in the patient with dystrophic forms of epidermolysis bullosa

Gene reports, 2020-12, Vol.21, p.100862, Article 100862

2020

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Advanced molecular approaches pave the road to a clear-cut diagnosis of hereditary retinal dystrophies

Molecular vision, 2018-10, Vol.24, p.679-689

2018

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Two Novel Mutations in LAMC2 Gene in Iranian Families Affected by Junctional Epidermolysis Bullosa

Reports of biochemistry and molecular biology, 2022-01, Vol.10 (4), p.597-601

2022

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Identification of a novel deletion within ALDH3A2 gene in an Iranian Family with Sjögren–Larsson Syndrome

Clinical case reports, 2018-01, Vol.6 (1), p.32-36

2018

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Safety and efficacy of RCP recombinant spike protein covid-19 vaccine compared to Sinopharm BBIBP: A phase III, non-inferiority trial

Heliyon, 2024-03, Vol.10 (5), p.e27370-e27370, Article e27370

2024

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The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss—A twelve year study

International journal of pediatric otorhinolaryngology, 2012-08, Vol.76 (8), p.1164-1174

2012

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Finding mutation within non-coding region of GJB2 reveals its importance in genetic testing of Hearing Loss in Iranian population

International journal of pediatric otorhinolaryngology, 2015-02, Vol.79 (2), p.136-138

2015

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Concomitant Increase of OX40 and FOXP3 transcripts in peripheral blood of patients with breast cancer

Iranian journal of immunology, 2013-03, Vol.10 (1), p.22-30

2013

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Identification of SLC26A4 gene mutations in Iranian families with hereditary hearing impairment

European journal of pediatrics, 2009-06, Vol.168 (6), p.651-653

2009

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Reporting one very rare pathogenic variation c.1106G>A in POMT2 gene

Intractable & Rare Diseases Research, 2020, pp.2020.03013

2020

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Identification of a novel deletion within ALDH3A2 gene in an Iranian Family with Sjögren-Larsson Syndrome

Clinical case reports, 2018, Vol.6 (1), p.32-36

2018

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Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient

Clinical case reports, 2019, Vol.7 (6), p.1149-1153

2019

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A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome

Frontiers in pediatrics, 2017, Vol.5, p.169-169

2017

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Control of cellular adhesiveness in hyaluronic acid‐based hydrogel through varying degrees of phenol moiety cross‐linking

Journal of biomedical materials research. Part A, 2021-05, Vol.109 (5), p.649-658

2021

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Safety and Efficacy of Combined Intramuscular/Intranasal RAZI-COV PARS Vaccine Candidate Against SARS-CoV-2: A Preclinical Study in Several Animal Models

Immunogenicity and safety of RAZI recombinant spike protein vaccine (RCP) as a booster dose after priming with BBIBP-CorV: a parallel two groups, randomized, double blind trial

Immunogenicity and Safety of a Combined Intramuscular/Intranasal Recombinant Spike Protein COVID-19 Vaccine (RCP) in Healthy Adults Aged 18 to 55 Years Old: A Randomized, Double-Blind, Placebo-Controlled, Phase I Trial

Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient

Cardiovascular, lactate and appetite response to light and spicy music tempo after an endurance swimming protocol in young girls

A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome

Genetics of intellectual disability in consanguineous families

Reporting one very rare pathogenic variation c.1106G>A in POMT2 gene

Phase II, Safety and Immunogenicity of RAZI Cov Pars (RCP) SARS Cov-2 Vaccine in Adults Aged 18–70 Years; A Randomized, Double-Blind Clinical Trial

Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran

The novel mutation in the COL7A1 gene in the patient with dystrophic forms of epidermolysis bullosa

Immunogenicity and safety of RAZI recombinant spike protein vaccine

Advanced molecular approaches pave the road to a clear-cut diagnosis of hereditary retinal dystrophies

Two Novel Mutations in LAMC2 Gene in Iranian Families Affected by Junctional Epidermolysis Bullosa

Identification of a novel deletion within ALDH3A2 gene in an Iranian Family with Sjögren–Larsson Syndrome

Safety and efficacy of RCP recombinant spike protein covid-19 vaccine compared to Sinopharm BBIBP: A phase III, non-inferiority trial

The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss—A twelve year study

Finding mutation within non-coding region of GJB2 reveals its importance in genetic testing of Hearing Loss in Iranian population

Concomitant Increase of OX40 and FOXP3 transcripts in peripheral blood of patients with breast cancer

Identification of SLC26A4 gene mutations in Iranian families with hereditary hearing impairment

Reporting one very rare pathogenic variation c.1106G>A in POMT2 gene

Identification of a novel deletion within ALDH3A2 gene in an Iranian Family with Sjögren-Larsson Syndrome

Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient

A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome

Control of cellular adhesiveness in hyaluronic acid‐based hydrogel through varying degrees of phenol moiety cross‐linking

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