Genetics and genomic medicine in Iran

por Behnam, Babak, Zakeri, Maryam
Publicado 2019

Mitochondrial Metabolism: A New Dimension of Personalized Oncology

por Behnam, Babak, Taghizadeh-Hesary, Farzad
Publicado 2023

Roberts-SC Phocomelia Syndrome (Pseudothalidomide Syndrome): A Case Report

por Keypour, Farideh, Naghi, Ilana, Behnam, Babak
Publicado 2013

A rare case of Sjogren-Larsson syndrome with recurrent pneumonia and asthma

por Tavasoli, Azita, Sayyahfar, Shirin, Behnam, Babak
Publicado 2016

TSGA10 is Specifically Expressed in Astrocyte and Over-expressed in Brain Tumors

por Behnam, Babak, Chahlavi, Ali, Pattisapu, Jogi, Wolfe, Jonathan
Publicado 2009

Visceral Leishmaniasis without Fever in an 11-Month-Old Infant: a Rare Clinical Feature of Kala-azar

por Sayyahfar, Shirin, Ansari, Shahla, Mohebali, Mehdi, Behnam, Babak
Publicado 2014

Recurrent Hepatitis in Two Iranian Children: A Novel (Q166R) Mutation in EIF2AK3 Leading to Wolcott-Rallison Syndrome

por Behnam, Babak, Shakiba, Marjan, Ahani, Ali, Razzaghy Azar, Maryam
Publicado 2013

Targeted Anti-Mitochondrial Therapy: The Future of Oncology

por Taghizadeh-Hesary, Farzad, Akbari, Hassan, Bahadori, Moslem, Behnam, Babak
Publicado 2022

First Report of Familial Juvenile Hyperuricemic Nephropathy (FJHN) in Iran Caused By a Novel De Novo Mutation (E197X) in UMOD

por Malakoutian, Tahereh, Amouzegar, Atefeh, Vali, Farzaneh, Asgari, Mojgan, Behnam, Babak
Publicado 2016

Clinical, laboratory data and outcomes of 17 Iranian citrullinemia type 1 patients: Identification of five novel ASS1 gene mutations

por Moarefian, Shirin, Zamani, Mahdi, Rahmanifar, Ali, Behnam, Babak, Zaman, Talieh
Publicado 2022

Evidence for reduced lymphatic CSF absorption in the H-Tx rat hydrocephalus model

por Rammling, Matthias, Madan, Meenu, Paul, Leena, Behnam, Babak, Pattisapu, Jogi V
Publicado 2008

First report of inherited thyroxine-binding globulin deficiency in Iran caused by a known de novo mutation in SERPINA7

por Soheilipour, Fahimeh, Fazilaty, Hassan, Jesmi, Fatemeh, Gahl, William A., Behnam, Babak
Publicado 2016

A rare case of mixed gonadal dysgenesis with mosaicism 45, X/46, X, +mar

por Soheilipour, Fahimeh, Abed, Ommolbanin, Behnam, Babak, Abdolhosseini, Mohammadreza, Alibeigi, Peyman, Pazouki, Abdolreza
Publicado 2014

An ABCD1 Mutation (c.253dupC) Caused Diverse Phenotypes of Adrenoleukodystrophy in an Iranian Consanguineous Pedigree

por Mehrpour, Masoud, Gohari, Faeze, Dizaji, Majid Zaki, Ahani, Ali, Malicdan, May Christine V., Behnam, Babak
Publicado 2016

Adenosine kinase deficiency with neurodevelopemental delay and recurrent hepatic dysfunction: A case report

por Shakiba, Marjan, Mahjoub, Fatemeh, Fazilaty, Hassan, Rezagholizadeh, Fereshteh, Shakiba, Arghavan, Ziadlou, Maryam, Gahl, William A., Behnam, Babak
Publicado 2016

Elimination of mouse tumor cells from neonate spermatogonial cells utilizing cisplatin-entrapped folic acid-conjugated poly(lactic-co-glycolic acid) nanoparticles in vitro

por Shabani, Ronak, Ashjari, Mohsen, Ashtari, Khadijeh, Izadyar, Fariborz, Behnam, Babak, Khoei, Samideh, Asghari-Jafarabadi, Mohamad, Koruji, Morteza
Publicado 2018

An optimized isolation protocol yields high‐quality RNA from cassava tissues (Manihot esculenta Crantz)

por Behnam, Babak, Bohorquez‐Chaux, Adriana, Castaneda‐Mendez, Oscar Fernando, Tsuji, Hiroyuki, Ishitani, Manabu, Becerra Lopez‐Lavalle, Luis Augusto
Publicado 2019

Characterization of the Promoter Region of an Arabidopsis Gene for 9-cis-Epoxycarotenoid Dioxygenase Involved in Dehydration-Inducible Transcription

por Behnam, Babak, Iuchi, Satoshi, Fujita, Miki, Fujita, Yasunari, Takasaki, Hironori, Osakabe, Yuriko, Yamaguchi-Shinozaki, Kazuko, Kobayashi, Masatomo, Shinozaki, Kazuo
Publicado 2013

The effect of intrathecal delivery of bone marrow stromal cells on hippocampal neurons in rat model of Alzheimer’s disease

por Eftekharzadeh, Mina, Nobakht, Maliheh, Alizadeh, Akram, Soleimani, Mansooreh, Hajghasem, Mahmood, Kordestani Shargh, Bahareh, Karkuki Osguei, Nushin, Behnam, Babak, Samadikuchaksaraei, Ali
Publicado 2015

Screening for large rearrangements of the RB1 gene in Iranian patients with retinoblastoma using multiplex ligation-dependent probe amplification

por Ahani, Ali, Akbari, Mohammad Taghi, Saliminejad, Kioomars, Behnam, Babak, Akhondi, Mohammad Mehdi, Vosoogh, Parvaneh, Ghassemi, Farriba, Naseripour, Masood, Bahoush, Gholamreza, Khorshid, Hamid Reza Khorram
Publicado 2013