Emotional intelligence of medical students of Shiraz University of Medical Sciences cross sectional study

por Vasefi, Ali, Dehghani, Mohammadreza, Mirzaaghapoor, Mahmood
Publicado 2018

Introduction to clinical pathology: A brief course of laboratory medicine in the field for medical students

por Omidifar, Navid, Keshtkari, Ali, Dehghani, Mohammadreza, Shokripour, Mansoureh
Publicado 2017

Impact of clinical supervision on field training of nursing students at Urmia University of Medical Sciences

por DEHGHANI, MOHAMMADREZA, GHANAVATI, SHIRIN, SOLTANi, BEHROUZ, AGHAKHANI, NADER, HAGHPANAH, SEZANEH
Publicado 2016

Is there any relationship between mutation in CPS1 Gene and pregnancy loss?

por Talebi, Mehrdad, Yahya Vahidi Mehrjardi, Mohammad, Kalhor, Kambiz, Dehghani, Mohammadreza
Publicado 2019

Association study of ESR1 rs9340799, rs2234693, and MMP2 rs243865 variants in Iranian women with premature ovarian insufficiency: A case-control study

por Sadat Eshaghi, Farzaneh, Dehghan Tezerjani, Masoud, Ghasemi, Nasrin, Dehghani, Mohammadreza
Publicado 2022

Investigating the impacts of socio-economic vulnerability indicators on COVID-19: A case study of Yazd, Iran

por Fatemi, Farin, Fallah-Aliabadi, Saeed, Sarsangi, Alireza, Dehghani, Mohammadreza, Heydari, Ahad
Publicado 2023

A Novel Missense Mutation in the ALDH13 Gene Causes Anophthalmia in Two Unrelated Iranian Consanguineous Families

por Dehghani, Mohammadreza, Dehghan Tezerjani, Masoud, Metanat, Zahra, Vahidi Mehrjardi, Mohammad Yahya
Publicado 2017

A newborn with ambiguous genitalia and a complex X;Y rearrangement

por Dehghani, Mohammadreza, Rossi, Elena, Vetro, Annalisa, Russo, Gianni, Hashemian, Zahra, Zuffardi, Orsetta
Publicado 2014

The effect of regular resistance exercise, vitamin D, and calcium supplements on the gastrocnemius muscle in rats in the post-menopausal period: An experimental study

por Sisi, Seyedeh Zahra Hosseini, Azarbayjani, Mohammad Ali, Vafaeenasab, Mohammadreza, Peeri, Maghsoud, Dehghani, Mohammadreza
Publicado 2021

Multiple Arrhythmogenic Substrate for Tachycardia in a Patient with Frequent Palpitations

por Haghjoo, Majid, Arya, Arash, Dehghani, Mohammadreza, Emkanjoo, Zahra, Fazelifar, Amirfarjam, Sadr-Ameli, MohammadAli
Publicado 2005

Newborn with Supernumerary Marker Chromosome Derived from Chromosomes 11 And 22- A Case Report

por VAHIDI MEHRJARDI, Mohammad Yahya, DEHGHAN TEZERJANI, Masoud, NORI-SHADKAM, Mahmoud, KALANTAR, Seyed Mehdi, DEHGHANI, Mohammadreza
Publicado 2016

Coexistence of Atrioventricular Nodal Reentrant Tachycardia and Idiopathic Left Ventricular Outflow-Tract Tachycardia

por Haghjoo, Majid, Arya, Arash, Dehghani, Mohammadreza, Emkanjoo, Zahra, Fazelifar, Amirfarjam, Heidari, Alireza, Sadr-Ameli, MohammadAli
Publicado 2005

Novel variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability in Iranian consanguineous families

por Moudi, Mahdiyeh, Vahidi Mehrjardi, Mohammad Yahya, Hozhabri, Hossein, Metanat, Zahra, Kalantar, Seyed Mehdi, Taheri, Mohsen, Ghasemi, Nasrin, Dehghani, Mohammadreza
Publicado 2022

Evaluation of Teaching Methods in Mass CPCR Training in Different Groups of the Society, an Observational Study

por Hasani, Hamed, Bahrami, Mojtaba, Malekpour, Abdorrasoul, Dehghani, Mohammadreza, Allahyary, Elaheh, Amini, Mitra, Abdorahimi, Mehdi, khani, Sara, Kalantari Meibodi, Mohammad, Kojuri, Javad
Publicado 2015

A Novel Mutation in the OFD1 Gene in a Family with Oral-Facial-Digital Syndrome Type 1: A Case Report

por DEHGHAN TEZERJANI, Masoud, MAROOFIAN, Reza, VAHIDI MEHRJARDI, Mohammad Yahya, CHIOZA, Barry A., ZAMANINEJAD, Shiva, KALANTAR, Seyed Mehdi, NORI-SHADKAM, Mahmoud, GHADIMI, Hamidreza, BAPLE, Emma L., CROSBY, Andrew H., DEHGHANI, Mohammadreza
Publicado 2016

Pontocerebellar hypoplasia due to bi-allelic variants in MINPP1

por Appelhof, Bart, Wagner, Matias, Hoefele, Julia, Heinze, Anja, Roser, Timo, Koch-Hogrebe, Margarete, Roosendaal, Stefan D., Dehghani, Mohammadreza, Mehrjardi, Mohammad Yahya Vahidi, Torti, Erin, Houlden, Henry, Maroofian, Reza, Rajabi, Farrah, Sticht, Heinrich, Baas, Frank, Wieczorek, Dagmar, Jamra, Rami Abou
Publicado 2020

Defective phosphatidylethanolamine biosynthesis leads to a broad ataxia-spasticity spectrum

por Kaiyrzhanov, Rauan, Wortmann, Saskia, Reid, Taryn, Dehghani, Mohammadreza, Vahidi Mehrjardi, Mohammad Yahya, Alhaddad, Bader, Wagner, Matias, Deschauer, Marcus, Cordts, Isabell, Fernandez-Murray, J Pedro, Treffer, Veronika, Metanat, Zahra, Pittman, Alan, Houlden, Henry, Meitinger, Thomas, Carroll, Christopher, McMaster, Christopher R, Maroofian, Reza
Publicado 2021

Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy

por McMillan, Hugh J., Telegrafi, Aida, Singleton, Amanda, Cho, Megan T., Lelli, Daniel, Lynn, Francis C., Griffin, Julie, Asamoah, Alexander, Rinne, Tuula, Erasmus, Corrie E., Koolen, David A., Haaxma, Charlotte A., Keren, Boris, Doummar, Diane, Mignot, Cyril, Thompson, Islay, Velsher, Lea, Dehghani, Mohammadreza, Vahidi Mehrjardi, Mohammad Yahya, Maroofian, Reza, Tchan, Michel, Simons, Cas, Christodoulou, John, Martín-Hernández, Elena, Guillen Sacoto, Maria J., Henderson, Lindsay B., McLaughlin, Heather, Molday, Laurie L., Molday, Robert S., Yoon, Grace
Publicado 2018

Bi-allelic loss-of-function variants in BCAS3 cause a syndromic neurodevelopmental disorder

por Hengel, Holger, Hannan, Shabab B., Dyack, Sarah, MacKay, Sara B., Schatz, Ulrich, Fleger, Martin, Kurringer, Andreas, Balousha, Ghassan, Ghanim, Zaid, Alkuraya, Fowzan S., Alzaidan, Hamad, Alsaif, Hessa S., Mitani, Tadahiro, Bozdogan, Sevcan, Pehlivan, Davut, Lupski, James R., Gleeson, Joseph J., Dehghani, Mohammadreza, Mehrjardi, Mohammad Y.V., Sherr, Elliott H., Parks, Kendall C., Argilli, Emanuela, Begtrup, Amber, Galehdari, Hamid, Balousha, Osama, Shariati, Gholamreza, Mazaheri, Neda, Malamiri, Reza A., Pagnamenta, Alistair T., Kingston, Helen, Banka, Siddharth, Jackson, Adam, Osmond, Mathew, Rieß, Angelika, Haack, Tobias B., Nägele, Thomas, Schuster, Stefanie, Hauser, Stefan, Admard, Jakob, Casadei, Nicolas, Velic, Ana, Macek, Boris, Ossowski, Stephan, Houlden, Henry, Maroofian, Reza, Schöls, Ludger
Publicado 2021

Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder

por Dias, Caroline M., Punetha, Jaya, Zheng, Céline, Mazaheri, Neda, Rad, Abolfazl, Efthymiou, Stephanie, Petersen, Andrea, Dehghani, Mohammadreza, Pehlivan, Davut, Partlow, Jennifer N., Posey, Jennifer E., Salpietro, Vincenzo, Gezdirici, Alper, Malamiri, Reza Azizi, Al Menabawy, Nihal M., Selim, Laila A., Vahidi Mehrjardi, Mohammad Yahya, Banu, Selina, Polla, Daniel L., Yang, Edward, Rezazadeh Varaghchi, Jamileh, Mitani, Tadahiro, van Beusekom, Ellen, Najafi, Maryam, Sedaghat, Alireza, Keller-Ramey, Jennifer, Durham, Leslie, Coban-Akdemir, Zeynep, Karaca, Ender, Orlova, Valeria, Schaeken, Lieke L.M., Sherafat, Amir, Jhangiani, Shalini N., Stanley, Valentina, Shariati, Gholamreza, Galehdari, Hamid, Gleeson, Joseph G., Walsh, Christopher A., Lupski, James R., Seiradake, Elena, Houlden, Henry, van Bokhoven, Hans, Maroofian, Reza
Publicado 2019