A Case of MPAN with “Eye of the Tiger Sign,” Mimicking PKAN
Dehghan Manshadi, Masoumeh, Rohani, Mohammd, Rezaei, Ali, Aryani, Omid
Published in Movement disorders clinical practice (Hoboken, N.J.) (01.07.2022)
Published in Movement disorders clinical practice (Hoboken, N.J.) (01.07.2022)
Get full text
Journal Article
Evaluation of DNA repair capacity in parents of pediatric patients diagnosed with autism spectrum disorder using the comet assay procedure
Akouchekian, Mansoureh, Alizadeh, Rasoul, Beiranvandi, Fatemeh, Dehghan Manshadi, Masoumeh, Taherizadeh, Fatemeh, Hakim Shooshtari, Mitra
Published in IBRO neuroscience reports (01.12.2023)
Published in IBRO neuroscience reports (01.12.2023)
Get full text
Journal Article
Four novel ARSA gene mutations with pathogenic impacts on metachromatic leukodystrophy: a bioinformatics approach to predict pathogenic mutations
Dehghan Manshadi, Masoumeh, Kamalidehghan, Behnam, Aryani, Omid, Khalili, Elham, Dadgar, Sepideh, Tondar, Mahdi, Ahmadipour, Fatemeh, Yong Meng, Goh, Houshmand, Massoud
Published in Therapeutics and clinical risk management (01.01.2017)
Published in Therapeutics and clinical risk management (01.01.2017)
Get full text
Journal Article
Immunomodulatory-based therapy as a potential promising treatment strategy against severe COVID-19 patients: A systematic review
Razmi, Mahdieh, Hashemi, Farideh, Gheytanchi, Elmira, Dehghan Manshadi, Masoumeh, Ghods, Roya, Madjd, Zahra
Published in International immunopharmacology (01.11.2020)
Published in International immunopharmacology (01.11.2020)
Get full text
Journal Article
Clinical significance of CD166 and HER-2 in different types of gastric cancer
Moradi, Leila, Tajik, Fatemeh, Saeednejad Zanjani, Leili, Panahi, Mahshid, Gheytanchi, Elmira, Biabanaki, Zahra Sadat, Kazemi-Sefat, Golnaz Ensieh, Hashemi, Farideh, Dehghan Manshadi, Masoumeh, Madjd, Zahra
Published in Clinical & translational oncology (01.03.2024)
Published in Clinical & translational oncology (01.03.2024)
Get full text
Journal Article
Four novel p.N385K, p.V36A, c.1033-1034insT and c.1417-1418delCT mutations in the sphingomyelin Phosphodiesterase 1 (SMPD1) gene in patients with types A and B Niemann-Pick disease (NPD)
Manshadi, Masoumeh Dehghan, Kamalidehghan, Behnam, Keshavarzi, Fatemeh, Aryani, Omid, Dadgar, Sepideh, Arastehkani, Ahoora, Tondar, Mahdi, Ahmadipour, Fatemeh, Meng, Goh Yong, Houshmand, Massoud
Published in International journal of molecular sciences (24.03.2015)
Published in International journal of molecular sciences (24.03.2015)
Get full text
Journal Article
Efficacy of Whole Cancer Stem Cell-Based Vaccines: A Systematic Review of Preclinical and Clinical Studies
Hashemi, Farideh, Razmi, Mahdieh, Tajik, Fatemeh, Zöller, Margot, Dehghan Manshadi, Masoumeh, Mahdavinezhad, Forough, Tiyuri, Amir, Ghods, Roya, Madjd, Zahra
Published in Stem cells (Dayton, Ohio) (17.03.2023)
Published in Stem cells (Dayton, Ohio) (17.03.2023)
Get full text
Journal Article
Clinical Significance of Talin-1 and HER-2 Status in Different Types of Gastric Carcinoma
Hashemi, Farideh, Tajik, Fatemeh, Saeednejad Zanjani, Leili, Dehghan Manshadi, Masoumeh, Safaei, Sadegh, Babaheidarian, Pegah, Fattahi, Fahimeh, Ghods, Roya, Madjd, Zahra
Published in Biomarkers (11.11.2024)
Published in Biomarkers (11.11.2024)
Get more information
Journal Article
A newly identified c.1824_1828dupATACG mutation in exon 13 of the GAA gene in infantile-onset glycogen storage disease type II (Pompe disease)
Aryani, Omid, Manshadi, Masoumeh Dehghan, Tondar, Mahdi, Khalili, Elham, Kamalidehghan, Behnam, Ahmadipour, Fatemeh, Fani, Somayeh, Houshmand, Massoud
Published in Molecular biology reports (01.09.2014)
Published in Molecular biology reports (01.09.2014)
Get full text
Journal Article
Huntington's disease and mitochondrial DNA deletions: event or regular mechanism for mutant huntingtin protein and CAG repeats expansion?
Banoei, Mohammad Mehdi, Houshmand, Massoud, Panahi, Mehdi Shafa Shariat, Shariati, Parvin, Rostami, Maryam, Manshadi, Masoumeh Dehghan, Majidizadeh, Tayebeh
Published in Cellular and molecular neurobiology (01.11.2007)
Published in Cellular and molecular neurobiology (01.11.2007)
Get full text
Journal Article
Four novel ARSA gene mutations with pathogenic impacts on metachromatic leukodystrophy: a bioinformatics approach to predict pathogenic mutations
Manshadi, Masoumeh Dehghan, Kamalidehghan, Behnam, Aryani, Omid, Khalili, Elham, Dadgar, Sepideh, Tondar, Mahdi, Ahmadipour, Fatemeh, Meng, Goh Yong, Houshmand, Massoud
Published in Therapeutics and clinical risk management (01.01.2017)
Published in Therapeutics and clinical risk management (01.01.2017)
Get full text
Journal Article