Extensive cerebral Sinovenous Thrombosis in a 5 Year Old Girl, Following Mild Dehydration. (Case Report and Review of Literature)

por Ashrafzadeh, Farah, Akhondian, Javad, Beiraghi Toosi, Mehran, Hashemi, Nargess
Publicado 2013

Epstein-Barr Virus Encephalitis: A Case Report

por HASHEMIAN, Somayh, ASHRAFZADEH, Farah, AKHONDIAN, Javad, BEIRAGHI TOOSI, Mehran
Publicado 2015

Homocystinuria: A Rare Disorder Presenting as Cerebral Sinovenous Thrombosis

por ESLAMIYEH, Hossein, ASHRAFZADEH, Farah, AKHONDIAN, Javad, BEIRAGHI TOOSI, Mehran
Publicado 2015

The Gross, Fine, and Oral Motor Functions in a Patient with Megalencephalic Leukoencephalopathy with Subcortical Cyst: A Case Report

por SABERMOGHADAM, Reihane, MALEKI SHAHMAHMOOD, Toktam, SARVGHADI, Pooria, BEIRAGHI TOOSI, Mehran
Publicado 2023

Hypoparathyroidism as the First Manifestation of Kearns-Sayre Syndrome: A Case Report

por ASHRAFZADEH, Farah, GHAEMI, Nosrat, AKHONDIAN, Javad, BEIRAGHI TOOSI, Mehran, ELMI, Saghi
Publicado 2013

Psychological Signs as the Only Presentation of Wilson’s Disease in an 11-Year-Old Boy

por BEIRAGHI TOOSI, Mehran, AKHONDIAN, Javad, ASHRAF ZADEH, Farah, DONYADIDEH, Nahid, JAVID, Asma
Publicado 2018

Joubert Syndrome in Three Children in A Family: A Case Series

por Akhondian, Javad, Ashrafzadeh, Farah, Beiraghi Toosi, Mehran, Moazen, Nasrin, Mohammadpoor, Toktam, Karami, Reza
Publicado 2013

Angelman Syndrome: A Case Report

por Ashrafzadeh, Farah, Sadrnabavi, Arianeh, Akhondian, Javad, Beiraghi Toosi, Mehran, Mohammadi, Mohammadhassan, Hassanpour, Kazem
Publicado 2016

The Results of Whole Exome Sequencing Performed On Previously Undiagnosed Pediatric Neurology Patients

por AHMADNIA, Negin, BEIRAGHI TOOSI, Mehran, GHAYOUR KARIMIANI, Ehsan, ASHRAFZADEH, Farah, FARAJI RAD, Mohammad
Publicado 2021

Comparison of new biomarkers in the diagnosis of perinatal asphyxia

por BOSKABADI, Hassan, ZAKERIHAMIDI, Maryam, GHAYOUR MOBARHAN, Majid, BAGHERI, Fatemeh, MORADI, Ali, BEIRAGHI TOOSI, Mehran
Publicado 2023

Effect of Curcumin on Pediatric Intractable Epilepsy

por ERFANI, Mina, ASHRAFZADEH, Farah, RAHIMI, Hamid Reza, EBRAHIMI, Seyed Ali, KALALI, Keivan, BEIRAGHI TOOSI, Mehran, FARAJI RAD, Elnaz
Publicado 2022

Bilateral horizontal gaze palsy in an 8‐year‐old girl: A rare case with NDUFS4 gene mutation

por Vafaee‐Shahi, Mohammad, Ghasemi, Saeide, Beiraghi Toosi, Mehran, Ashrafi, Mahmoud Reza, Badv, Reza Shervin, Tavasoli, Ali Reza, Tahernia, Leila
Publicado 2021

A case report of Posterior reversible encephalopathy syndrome with spinal cord involvement (PRES-SCI) as an atypical presentation of PRES in children: A case report and review of t...

por AKHONDIAN, Javad, ASHRAFZADEH, Farah, SEILANIAN TOOSI, Farrokh, BEHNAM, Mahdi, BEIRAGHI TOOSI, Mehran, IMANNEZHAD, Shima, AKHOUNDIAN, Mohammad Reza, HASHEMI, Narges
Publicado 2022

Griscelli Syndrome: A Case Report

por MANSOURI NEJAD, Seyed Ebrahim, YAZDAN PANAH, Mohammad Javad, TAYYEBI MEIBODI, Naser, ASHRAF ZADEH, Farah, AKHONDIAN, Javad, BEIRAGHI TOOSI, Mehran, ESLAMIEH, Hossein
Publicado 2014

PLA2G6 gene mutation and infantile neuroaxonal degeneration; report of three cases from Iran

por Jafarzadeh Esfehani, Reza, Eslahi, Atieh, Beiraghi Toosi, Mehran, Sadr-Nabavi, Ariane, Kerachian, Mohammad Amin, Asl Mohajeri, Mahsa Sadat, Farjami, Mahsa, Alizade, Farzaneh, Mojarrad, Majid
Publicado 2021

Childhood‐Onset Choreo‐Dystonia Due to a Recurrent Novel Homozygous Nonsense HPCA Variant: Case Series and Literature Review

por Magrinelli, Francesca, Bhatia, Kailash P., Beiraghi Toosi, Mehran, Arab, Fatemeh, Karimiani, Ehsan Ghayoor, Sedighzadeh, Sahar, Ansari, Behnaz, Neshatdoust, Maedeh, Rocca, Clarissa, Houlden, Henry, Maroofian, Reza
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

TTC5 syndrome: Clinical and molecular spectrum of a severe and recognizable condition

por Musante, Luciana, Faletra, Flavio, Meier, Kolja, Tomoum, Hoda, Najarzadeh Torbati, Paria, Blair, Edward, North, Sally, Gärtner, Jutta, Diegmann, Susann, Beiraghi Toosi, Mehran, Ashrafzadeh, Farah, Ghayoor Karimiani, Ehsan, Murphy, David, Murru, Flora Maria, Zanus, Caterina, Magnolato, Andrea, La Bianca, Martina, Feresin, Agnese, Girotto, Giorgia, Gasparini, Paolo, Costa, Paola, Carrozzi, Marco
Publicado 2022