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Expanding the mutational landscape and clinical phenotype of the YIF1B related brain disorder.
Published in:
2021
By:
- Salsench, Eva Medico;
- Maroofian, Reza;
- Deng, Ruizhi;
- Lanko, Kristina;
- Nikoncuk, Anita;
- Pérez, Belén;
- Sánchez-Lijarcio, Obdulia;
- Ibáñez-Mico, Salvador;
- Wojcik, Antonina;
- Vargas, Marcelo;
- Al-Sannaa, Nouriya Abbas;
- Girgis, Marian Y;
- Silveira, Tainá Regina Damaceno;
- Bauer, Peter;
- Schroeder, Audrey;
- Fong, Chin-To;
- Begtrup, Amber;
- Babaei, Meisam;
- Toosi, Mehran Beiraghi;
- Ashrafzadeh, Farah
Publication type:
journal article
A novel missense variant in EIF2B5 identified in a consanguineous Iranian family with vanishing white matter disease and a brief review of the literature.
Published in:
Journal of Genetics, 2023, v. 102, n. 2, p. 1, doi. 10.1007/s12041-023-01436-8
By:
- Nourmohammadi, Parisa;
- Asadollahi, Mostafa;
- Karamzade, Arezou;
- Eshaghkhani, Yeganeh;
- Babaei, Meisam;
- Golchehre, Zahra;
- Taheri, Seyedeh Roksana;
- Hasani, Sepideh;
- Taghizadeh, Mahdieh;
- Keramatipour, Mohammad
Publication type:
Article
Symptomatic care of late-onset Alexander disease presenting with area postrema-like syndrome with prednisolone; a case report.
Published in:
2022
By:
- Zardadi, Safoura;
- Razmara, Ehsan;
- Rasoulinezhad, Maryam;
- Babaei, Meisam;
- Ashrafi, Mohammad Reza;
- Pak, Neda;
- Garshasbi, Masoud;
- Tavasoli, Ali Reza
Publication type:
journal article
The First Report of Iranian Registry of Patients with Spinal Muscular Atrophy.
Published in:
Journal of Neuromuscular Diseases, 2023, v. 10, n. 2, p. 211, doi. 10.3233/JND-221614
By:
- Mansouri, Vahid;
- Heidari, Morteza;
- Bemanalizadeh, Maryam;
- Azizimalamiri, Reza;
- Nafissi, Shahriar;
- Akbari, Masood Ghahvechi;
- Barzegar, Mohammad;
- Moayedi, Ali Reza;
- Badv, Reza Shervin;
- Mohamadi, Mahmood;
- Tavasoli, Ali Reza;
- Amirsalari, Susan;
- Khajeh, Ali;
- Inaloo, Soroor;
- Fatehi, Farzad;
- Hosseinpour, Sareh;
- Babaei, Meisam;
- Hosseini, Seyed Ahmad;
- Mahdi Hosseiny, Seyyed Mohammad;
- Fayyazi, Afshin
Publication type:
Article
Identification of a Novel ASAH1 Gene Mutation in Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy.
Published in:
Iranian Journal of Child Neurology, 2024, v. 18, n. 3, p. 131, doi. 10.22037/ijcn.v18i3.44081
By:
- Ahangari, Najmeh;
- Arab, Fatemeh;
- Babaei, Meisam
Publication type:
Article
The Effect of Melatonin on Sleep Disorders in Children with Cerebral Palsy A Randomized Clinical Trial.
Published in:
Iranian Journal of Child Neurology, 2024, v. 18, n. 1, p. 51, doi. 10.22037/ijcn.v18i1.41949
By:
- GOLDOUZI, Hamid Reza;
- AKHONDIAN, Javad;
- BEIRAGHI TOOSI, Mehran;
- MEHRAD MAJD, Hassan;
- SHEKARI, Shima;
- Babaei, Meisam
Publication type:
Article
Infantile Spasms, Clinical Manifestations of a Rare Brain Tumor: A Case Report and Literature Review.
Published in:
Iranian Journal of Child Neurology, 2022, v. 16, n. 2, p. 161, doi. 10.22037/ijcn.v16i4.34911
By:
- HOSSEINZADEH, Rezvan;
- TAVALLAII, Amin;
- KEYKHOSRAVI, Ehsan;
- BEHNAMFAR, Morteza;
- BANAEI, Mahnaz;
- BABAEI, Meisam
Publication type:
Article
Acute Necrotizing Encephalopathy Following Presumed COVID-19 Infection: The First Iranian Report in Children.
Published in:
2022
By:
- Babaei, Meisam;
- Hosseini, Susan;
- Tavakoli, Maryam;
- Banaei, Mahnaz;
- Bagheri, Maryam
Publication type:
Case Study
Identification of a novel truncating variant in AHI1 gene and a brief review on mutations spectrum.
Published in:
Molecular Biology Reports, 2021, v. 48, n. 6, p. 5339, doi. 10.1007/s11033-021-06508-5
By:
- Karamzade, Arezou;
- Babaei, Meisam;
- Saberi, Mohammad;
- Golchin, Neda;
- Khalil Nejad Sani Banaei, Aysun;
- Eshaghkhani, Yeganeh;
- Golchehre, Zahra;
- Keramatipour, Mohammad
Publication type:
Article

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