Mothers’ lived experience of caring for children with inborn errors of amino acid metabolism

por Shirdelzade, Sara, Ramezani, Monir, Eshraghi, Peyman, Heydari, Abbas
Publicado 2023

Correction: Mothers’ lived experience of caring for children with inborn errors of amino acid metabolism

por Shirdelzade, Sara, Ramezani, Monir, Eshraghi, Peyman, Heydari, Abbas
Publicado 2023

Noonan syndrome – a new survey

por Tafazoli, Alireza, Eshraghi, Peyman, Koleti, Zahra Kamel, Abbaszadegan, Mohammadreza
Publicado 2016

The Report of Three Rare Cases of the Niemann-pick Disease in Birjand, South Khorasan, Eastern Iran

por NOROOZI ASL, Samaneh, VAKILI, Rahim, GHAEMI, Nosrat, ESHRAGHI, Peyman
Publicado 2017

Non-thyroidal illness syndrome and cardiopulmonary bypass in children with congenital heart disease

por Babazadeh, Kazem, Tabib, Avisa, Eshraghi, Peyman, Bakhshandeh, Hooman, Zamani, Hassan
Publicado 2014

Genetic evaluation of hyperphenylalaninemia patients with tetrahydrobiopterin deficiency in Iranian population: Identification of four novel disease‐causing variants

por Sadat Fatemi, Seyedeh Helia, Eshraghi, Peyman, Ghanei, Mahmoud, Hamzehloei, Tayebeh
Publicado 2022

Genotyping of ABCC8, KCNJ11, and HADH in Iranian Infants with Congenital Hyperinsulinism

por Hashemian, Somayyeh, Esfehani, Reza Jafarzadeh, Karimdadi, Siroos, Ghaemi, Nosrat, Eshraghi, Peyman, Gonabadi, Najmeh Malekzadeh, Sahebkar, Amirhossein, Vakili, Rahim, Abbaszadegan, Mohammad Reza
Publicado 2021

Investigating Genetic Mutations in a Large Cohort of Iranian Patients with Congenital Hyperinsulinism

por Razzaghy-Azar, Maryam, Saeedi, Saeedeh, Dayani, Sepideh Borhan, Enayati, Samaneh, Abbasi, Farzaneh, Hashemian, Somayyeh, Eshraghi, Peyman, Karimdadi, Siroos, Tajdini, Parisa, Vakili, Rahim, Amoli, Mahsa M., Yaghootkar, Hanieh
Publicado 2022

Impact of Intravenous Trehalose Administration in Patients with Niemann–Pick Disease Types A and B

por Mobini, Moein, Radbakhsh, Shabnam, Kubaski, Francyne, Eshraghi, Peyman, Vakili, Saba, Vakili, Rahim, Khalili, Manijeh, Varesvazirian, Majid, Jamialahmadi, Tannaz, Alamdaran, Seyed Ali, Sayedi, Seyed Javad, Rajabi, Omid, Emami, Seyed Ahmad, Reiner, Željko, Sebkar, Amirhossein
Publicado 2022

Recommendations for Infantile-Onset and Late-Onset Pompe Disease: An Iranian Consensus

por Fatehi, Farzad, Ashrafi, Mahmoud Reza, Babaee, Marzieh, Ansari, Behnaz, Beiraghi Toosi, Mehran, Boostani, Reza, Eshraghi, Peyman, Fakharian, Atefeh, Hadipour, Zahra, Haghi Ashtiani, Bahram, Moravej, Hossein, Nilipour, Yalda, Sarraf, Payam, Sayadpour Zanjani, Keyhan, Nafissi, Shahriar
Publicado 2021

Niemann-Pick Diseases: The Largest Iranian Cohort with Genetic Analysis

por Hashemian, Somayyeh, Eshraghi, Peyman, Dilaver, Nafi, Galehdari, Hamid, Shalbafan, Bita, Vakili, Rahim, Ghaemi, Nosrat, Ahangari, Najmeh, Rezazadeh Varaghchi, Jamileh, Zeighami, Jawaher, Sedaghat, Alireza, Aminzadeh, Majid, Hamid, Mohammad, Saberi, Alihossein, Ashtari, Fereshteh, Ghayoor Karimiani, Ehsan, Shariati, Gholamreza
Publicado 2019