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A novel c.973G>T mutation in the ε-subunit of the acetylcholine receptor causing congenital myasthenic syndrome in an iranian family

Balkan journal of medical genetics, 2019-08, Vol.22 (1), p.95-98

2019

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The rs2910164 variant is associated with reduced miR-146a expression but not cytokine levels in patients with type 2 diabetes

Journal of endocrinological investigation, 2018-05, Vol.41 (5), p.557-566

2018

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Association of SRD5A2 gene mutations with risk of hypospadias in the Iranian population

Journal of endocrinological investigation, 2017-04, Vol.40 (4), p.391-396

2017

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The pre-mir-27a variant rs895819 may contribute to type 2 diabetes mellitus susceptibility in an Iranian cohort

Journal of endocrinological investigation, 2016-10, Vol.39 (10), p.1187-1193

2016

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A bioinformatics approach for identification of miR-100 targets implicated in breast cancer

Cellular and Molecular Biology, 2017-10, Vol.63 (10), p.99-105

2017

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17-β-Hydroxysteroid Dehydrogenase Type 3 Deficiency in Three Adult Iranian Siblings

Sexual development, 2011-01, Vol.5 (6), p.273-276

2011

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Evaluating the association of common UBE2Z variants with coronary artery disease in an Iranian population

Cellular and molecular biology (Noisy-le-Grand, France), 2015-11, Vol.61 (7), p.50

2015

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Mutational screening of the NR5A1 in azoospermia

Andrologia, 2015-05, Vol.47 (4), p.395-401

2015

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An Iranian family with azoospermia and premature ovarian insufficiency segregating NR5A1 mutation

Climacteric : the journal of the International Menopause Society, 2014-06, Vol.17 (3), p.301-303

2014

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Expression analysis of protein inhibitor of activated STAT ( PIAS ) genes in IFNβ-treated multiple sclerosis patients [Corrigendum]

Journal of inflammation research, 2019-01, Vol.12, p.23-24

2019

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P38.01: Prenatal diagnosis of benign familial fetal macrocephaly

Ultrasound in obstetrics & gynecology, 2007-10, Vol.30 (4), p.593-593

2007

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Assessment of functional variants and expression of long noncoding RNAs in vitamin D receptor signaling in breast cancer

Cancer management and research, 2018-01, Vol.10, p.3451-3462

2018

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Autologous Hematopoietic Stem Cell Transplantation (AHSCT): An Evolving Treatment Avenue in Multiple Sclerosis

Biologics, 2021-01, Vol.15, p.53-59

2021

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Is Posterior Cruciate Ligament Needle Pie-Crusting Safe and Effective in Balancing Cruciate-Retained Total Knee Arthroplasty? A comparative study

Arthroplasty today, 2023-12, Vol.24, p.101277-101277, Article 101277

2023

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Ultrasensitive Electrochemical Detection of Cancer Cell Using Modified Graphene Nanostructures

Oriental journal of chemistry, 2017-01, Vol.33 (3), p.1200-1206

2017

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A Modified Technique for Artificial Fusion in Unreconstructable Revision Total Knee Arthroplasty

Arthroplasty today, 2021-08, Vol.10, p.128-132

2021

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Treatment of Iron-deficiency Anemia in Patients with Subclinical Hypothyroidism

The American journal of medicine, 2013-05, Vol.126 (5), p.420-424

2013

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Association of HLA alleles with autism

Neuropsychiatric disease and treatment, 2018-01, Vol.14, p.3259-3265

2018

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Expression analysis of protein inhibitor of activated STAT ( PIAS ) genes in IFNβ-treated multiple sclerosis patients

Journal of inflammation research, 2018-01, Vol.11, p.457-463

2018

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Two new mathematical models for prediction of early mortality risk in coronary artery bypass graft surgery

The Journal of thoracic and cardiovascular surgery, 2014-10, Vol.148 (4), p.1291-1298.e1

2014

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Laboratories Performance after Outsourcing in the Hospitals of Shahid Beheshti University of Medical Sciences

Medical laboratory journal, 2013-07, Vol.7 (2), p.42-48

2013

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Obstruction of a Percutaneous Pulmonary Valve by an Aspergillus Mycotic Thrombus Mimicking Massive Pulmonary Embolus

The Annals of thoracic surgery, 2012-07, Vol.94 (1), p.e5-e6

2012

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Recessively Inherited Severe Aortic Aneurysm Caused by Mutated EFEMP2

The American journal of cardiology, 2012-06, Vol.109 (11), p.1677-1680

2012

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The Rastelli Procedure for Transposition of the Great Arteries: Resection of the Infundibular Septum Diminishes Recurrent Left Ventricular Outflow Tract Obstruction Risk

The Annals of thoracic surgery, 2009-07, Vol.88 (1), p.137-143

2009

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Absence of motilin gene mutations in infantile hypertrophic pyloric stenosis

Journal of pediatric surgery, 2008-03, Vol.43 (3), p.443-446

2008

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A novel c.973G>T mutation in the ε-subunit of the acetylcholine receptor causing congenital myasthenic syndrome in an iranian family

The rs2910164 variant is associated with reduced miR-146a expression but not cytokine levels in patients with type 2 diabetes

Association of SRD5A2 gene mutations with risk of hypospadias in the Iranian population

The pre-mir-27a variant rs895819 may contribute to type 2 diabetes mellitus susceptibility in an Iranian cohort

A bioinformatics approach for identification of miR-100 targets implicated in breast cancer

17-β-Hydroxysteroid Dehydrogenase Type 3 Deficiency in Three Adult Iranian Siblings

Evaluating the association of common UBE2Z variants with coronary artery disease in an Iranian population

Mutational screening of the NR5A1 in azoospermia

An Iranian family with azoospermia and premature ovarian insufficiency segregating NR5A1 mutation

Expression analysis of protein inhibitor of activated STAT ( PIAS ) genes in IFNβ-treated multiple sclerosis patients [Corrigendum]

P38.01: Prenatal diagnosis of benign familial fetal macrocephaly

Assessment of functional variants and expression of long noncoding RNAs in vitamin D receptor signaling in breast cancer

Autologous Hematopoietic Stem Cell Transplantation (AHSCT): An Evolving Treatment Avenue in Multiple Sclerosis

Is Posterior Cruciate Ligament Needle Pie-Crusting Safe and Effective in Balancing Cruciate-Retained Total Knee Arthroplasty? A comparative study

Ultrasensitive Electrochemical Detection of Cancer Cell Using Modified Graphene Nanostructures

A Modified Technique for Artificial Fusion in Unreconstructable Revision Total Knee Arthroplasty

Treatment of Iron-deficiency Anemia in Patients with Subclinical Hypothyroidism

Association of HLA alleles with autism

Expression analysis of protein inhibitor of activated STAT ( PIAS ) genes in IFNβ-treated multiple sclerosis patients

Two new mathematical models for prediction of early mortality risk in coronary artery bypass graft surgery

Laboratories Performance after Outsourcing in the Hospitals of Shahid Beheshti University of Medical Sciences

Obstruction of a Percutaneous Pulmonary Valve by an Aspergillus Mycotic Thrombus Mimicking Massive Pulmonary Embolus

Recessively Inherited Severe Aortic Aneurysm Caused by Mutated EFEMP2

The Rastelli Procedure for Transposition of the Great Arteries: Resection of the Infundibular Septum Diminishes Recurrent Left Ventricular Outflow Tract Obstruction Risk

Absence of motilin gene mutations in infantile hypertrophic pyloric stenosis

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