Assessment of Anthropometric Indices in Patients with Phenylketonuria

por SHAKIBA, Marjan, Alaei, Mohammadreza, SANEIFARD, Hedyeh, MOSALLANEJAD, Asieh
Publicado 2020

3‐Hydroxyisobutyryl‐CoA hydrolase deficiency in an infant with developmental delay and high anion gap acidosis

por Saneifard, Hedyeh, Mosallanejad, Asieh, Fallahzadeh, Aida, Sheikhy, Ali
Publicado 2021

Non-progressive Nonimmune Hydrops Fetalis Caused by a Novel Mutation in GUSB Gene

por MOSALLANEJAD, Asieh, ALAEI, Mohammadreza, GHAFFARI, Saeed Reza, RAFATI, Maryam, SANEIFARD, Hedyeh
Publicado 2020

Dysgerminoma in a 15 years old phenotypically female Swyer syndrome with 46, XY pure gonadal dysgenesis: A case report

por Ashraf Ganjooei, Tahereh, Pirastehfar, Zanbagh, Mosallanejad, Asieh, Raoufi, Masoomeh, Afshar Moghaddam, Noushin, Hashemieh, Mozhgan
Publicado 2022

Assessment of Sexual Maturation Among Girls With Special Needs in Tehran, Iran

por Shabani Mirzaee, Hosein, Mosallanejad, Asieh, Rabbani, Ali, Setoodeh, Aria, Abbasi, Farzaneh, Sayarifard, Fatemeh, Memari, Amir Hosein
Publicado 2016

Clinical and Paraclinical Characteristics of Non-Classic Phenylketonuria

por SHAKIBA, Marjan, SANEIFARD, Hedyeh, ALAEI, Mohammad Reza, MOSALLANEJAD, Asieh, LOTFI, Mojtaba, YASAEI, Mehrdad, ALIZADE NADERI, Elahe
Publicado 2021

Utility of Seizure Pattern and Related Clinical Features in the Diagnosis of Neurometabolic Disorders

por JAFARI, Narjes, MOSALLANEJAD, Asieh, GHOBADIFAR, Asieh, KARIMZADEH, Parvaneh, GHASSEMABADI, Robabeh Ghodssi, NASEHI, Mohammadmehdi, SHAKIBA, Marjan, TABATABAEE, Shahrzad
Publicado 2020