Chromosome Duplication (14q) and The Genotype Phenotype Correlation

by Ariane Sadr-Nabavi, Morteza Saeidi
Published 2014-04-01

A Novel c.4822>T Mutation on SPG11 in an Iranian Patient Marked by Hereditary Spastic Paraparesis and Skeletal Deformity: An Incidental Finding or a True Association

by Karim Nikkhah, Ali Ghabeli-Juibary, Ariane Sadr-Nabavi
Published 2016-09-01

Evaluation of COVID-19 trend in Iran; Population response to the recent pandemic overtime

by Reza Jafarzadeh Esfehani, Mohammad Shariati, Ariane Sadr-Nabavi, Hamid Reza Bidkhori
Published 2022-01-01

Complications in Diagnosis of Susceptible Cases of Fragile X Syndrome

by Reza JAFARZADEH ESFEHANI, Mahtab DASTPAK, Mohammad Reza MIRINEZHAD, Ariane SADR-NABAVI
Published 2018-07-01

Cardiac Tamponade: A Rare Manifestation of Familial Mediterranean Fever

by Abdolreza Malek, Tina Zeraati, Ariane Sadr-Nabavi, Niloofar Vakili, Mohammad Reza Abbaszadegan
Published 2022-01-01

Spinal Muscular Atrophy: A Short Review Article

by Farah Ashrafzadeh, Ariane Sadr-Nabavi, Nazanin Asadian, Javad Akhondian, Mehran Beiraghi Toosi
Published 2014-07-01

A review of Genetic Etiology and Emerging Molecular Therapies for FSHD in Preclinical Studies

by Mohammad Reza Seyyed taghia, Reza Jafarzadeh Esfehani, Reza Boostani, Mohammad Shariati, Ariane Sadr Nabavi
Published 2021-03-01

Evaluation of bax, bcl-2, p21 and p53 genes expression variations on cerebellum of BALB/c mice before and after birth under mobile phone radiation exposure

by Najmeh Ghatei, Ariane Sadr Nabavi, Mohammad Hossein Bahreyni Toosi, Hosein Azimian, Mansour Homayoun, Reza Ghasemnezhad Targhi, Hossein Haghir
Published 2017-08-01

Non-collagenous extracellular matrix protein dermatopontin may play a role as another component of transforming growth factor-β signaling pathway in colon carcinogenesis

by Ariane Sadr-Nabavi, Samaneh Bouromand-Noughabi, Naser Tayebi-Meybodi, Kimia Dadkhah, Nafiseh Amini, Alfons Meindl, Mohammad Reza Abbaszadegan
Published 2021-04-01

Analysis of MTHFR Gene C.677C>T and C.1298A>C Polymorphisms in Iranian Patients with Non-Syndromic Cleft Lip and Palate.

by Arezoo Jahanbin, Nadia Hasanzadeh, Faraneh Abdolhoseinpour, Ariane Sadr-Nabavi, Mohammad-Ali Raisolsadat, Khosro Shamsian, Farnaz Mohajertehran, Hamidreza Kianifar
Published 2014-06-01

The effect of platelet-rich plasma on human mesenchymal stem cell-induced bone regeneration of canine alveolar defects with calcium phosphate-based scaffolds

by Reihaneh Shafieian, Maryam Moghaddam Matin, Amin Rahpeyma, Alireza Fazel, Hamideh Salari Sedigh, Ariane Sadr-Nabavi, Halimeh Hassanzadeh, Alireza Ebrahimzadeh-Bideskan
Published 2017-10-01

Renin-Angiotensin A1166C Polymorphism and the Rrisk of Stroke

by Peyman Zargari, Mohammad R. Ghasemi, Maryam Pirhoushiaran, Veda Vakili, Javad Hami, Mohammad Taghi Farzadfard, Payam Sasan-Nezhad, Mahmood R. Azarpazhooh, Ariane Sadr-Nabavi
Published 2015-07-01

PREVALENCE OF ß-THALASSEMIA MUTATIONS AMONG NORTHEASTERN IRANIAN POPULATION AND THEIR IMPACTS ON HEMATOLOGICAL INDICES AND APPLICATION OF PRENATAL DIAGNOSIS, A SEVEN-YEARS STUDY

by Mohammad Ehsan Jaripour, Kourosh Hayatigolkhatmi, Vahid Iranmanesh, Farhad Khadivi Zand, Zahra Badiei, Hamid Farhangi, Ali Ghasemi, Abdollah Banihashem, Reza Jafarzadeh Esfehani, Ariane Sadr-Nabavi
Published 2018-07-01

Copy number analysis from whole-exome sequencing data revealed a novel homozygous deletion in PARK7 leads to severe early-onset Parkinson's disease

by Mohammad Reza Seyedtaghia, Mohammad Soudyab, Mohammad Shariati, Reza Jafarzadeh Esfehani, Shabnam Vafadar, Neda Shalaei, Vahid Nouri, Michael Zech, Julianne Winkelmann, Ali shoeibi, Ariane Sadr-Nabavi
Published 2023-04-01