Fabrication of an Electrically-Resistive, Varistor-Polymer Composite

por Ahmad, Mansor Bin, Fatehi, Asma, Zakaria, Azmi, Mahmud, Shahrom, Mohammadi, Sanaz A.
Publicado 2012

VSX1 and SOD1 Mutation Screening in Patients with Keratoconus in the South of Iran

por Nejabat, Mahmood, Naghash, Payam, Dastsooz, Hassan, Mohammadi, Sanaz, Alipour, Mohsen, Fardaei, Majid
Publicado 2017

Does the c.-273T>C variant in the upstream region of the HBB gene cause a thalassemia phenotype?

por Dastsooz, Hassan, Alipour, Mohsen, Mohammadi, Sanaz, Dehghanian, Fatemeh, Kamgarpour, Fatemeh, Fardaei, Majid
Publicado 2017

Author's Reply

por Nejabat, Mahmood, Naghash, Payam, Dastsooz, Hassan, Mohammadi, Sanaz, Alipour, Mohsen, Fardaei, Majid
Publicado 2018

Identification of mutations in HEXA and HEXB in Sandhoff and Tay-Sachs diseases: a new large deletion caused by Alu elements in HEXA

por Dastsooz, Hassan, Alipour, Mohsen, Mohammadi, Sanaz, Kamgarpour, Fatemeh, Dehghanian, Fatemeh, Fardaei, Majid
Publicado 2018

Association of Serum 25-Hydroxyvitamin D and Chronic Periodontitis in Postmenopausal Women after Non-Surgical Periodontal Therapy

por Shirmohammadi, Adileh, Mohammadi, Sanaz, Faramarzi, Masoumeh, Babaloo, Amir Reza, Sadighi, Mehrnoosh, Maleki Dizaj, Solmaz
Publicado 2023

A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome

por Taghdiri, Maryam, Dastsooz, Hassan, Fardaei, Majid, Mohammadi, Sanaz, Farazi Fard, Mohammad Ali, Faghihi, Mohammad Ali
Publicado 2017

A novel PTRH2 missense mutation causing IMNEPD: a case report

por Khamirani, Hossein Jafari, Zoghi, Sina, Dianatpour, Mehdi, Jankhah, Aria, Tabei, Seyed Sajjad, Mohammadi, Sanaz, Dastgheib, Seyed Alireza
Publicado 2021

Signature pattern of gene expression and signaling pathway in premature diabetic patients uncover their correlation to early age coronary heart disease

por Ahmadloo, Salma, Ling, King-Hwa, Fazli, Ahmad, Larijani, Ghazaleh, Ghodsian, Nooshin, Mohammadi, Sanaz, Amini, Naser, Hosseinpour Sarmadi, Vahid, Ismail, Patimah
Publicado 2022

A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): A case report

por Manoochehri, Jamal, Dastgheib, Seyed Alireza, Khamirani, Hossein Jafari, Mollaie, Maryam, Sharifi, Zahra, Zoghi, Sina, Tabei, Seyed Mohammad Bagher, Mohammadi, Sanaz, Dehghanian, Fatemeh, Farbod, Zahra, Dianatpour, Mehdi
Publicado 2021

Correction: A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): a case report

por Manoochehri, Jamal, Dastgheib, Seyed Alireza, Khamirani, Hossein Jafari, Mollaie, Maryam, Sharifi, Zahra, Zoghi, Sina, Tabei, Seyed Mohammad Bagher, Mohammadi, Sanaz, Dehghanian, Fatemeh, Farbod, Zahra, Dianatpour, Mehdi
Publicado 2021