Search Results - BEIRAGHI TOOSI, Mehran
- Showing 1 - 14 results of 14
-
1
-
2
-
3
-
4
-
5
-
6
-
7
-
8
Bilateral horizontal gaze palsy in an 8‐year‐old girl: A rare case with NDUFS4 gene mutation by Vafaee‐Shahi, Mohammad, Ghasemi, Saeide, Beiraghi Toosi, Mehran, Ashrafi, Mahmoud Reza, Badv, Reza Shervin, Tavasoli, Ali Reza, Tahernia, Leila
Published 2021Text -
9
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... by AKHONDIAN, Javad, ASHRAFZADEH, Farah, SEILANIAN TOOSI, Farrokh, BEHNAM, Mahdi, BEIRAGHI TOOSI, Mehran, IMANNEZHAD, Shima, AKHOUNDIAN, Mohammad Reza, HASHEMI, Narges
Published 2022Text -
10
-
11
PLA2G6 gene mutation and infantile neuroaxonal degeneration; report of three cases from Iran by Jafarzadeh Esfehani, Reza, Eslahi, Atieh, Beiraghi Toosi, Mehran, Sadr-Nabavi, Ariane, Kerachian, Mohammad Amin, Asl Mohajeri, Mahsa Sadat, Farjami, Mahsa, Alizade, Farzaneh, Mojarrad, Majid
Published 2021Text -
12
Recommendations for Infantile-Onset and Late-Onset Pompe Disease: An Iranian Consensus by 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
Published 2021Text -
13
Bi-allelic Loss of Human APC2, Encoding Adenomatous Polyposis Coli Protein 2, Leads to Lissencephaly, Subcortical Heterotopia, and Global Developmental Delay by Lee, Sangmoon, Chen, Dillon Y., Zaki, Maha S., Maroofian, Reza, Houlden, Henry, Di Donato, Nataliya, Abdin, Dalia, Morsy, Heba, Mirzaa, Ghayda M., Dobyns, William B., McEvoy-Venneri, Jennifer, Stanley, Valentina, James, Kiely N., Mancini, Grazia M.S., Schot, Rachel, Kalayci, Tugba, Altunoglu, Umut, Karimiani, Ehsan Ghayoor, Brick, Lauren, Kozenko, Mariya, Jamshidi, Yalda, Manzini, M. Chiara, Beiraghi Toosi, Mehran, Gleeson, Joseph G.
Published 2019Text -
14
A form of muscular dystrophy associated with pathogenic variants in JAG2 by Coppens, Sandra, Barnard, Alison M., Puusepp, Sanna, Pajusalu, Sander, Õunap, Katrin, Vargas-Franco, Dorianmarie, Bruels, Christine C., Donkervoort, Sandra, Pais, Lynn, Chao, Katherine R., Goodrich, Julia K., England, Eleina M., Weisburd, Ben, Ganesh, Vijay S., Gudmundsson, Sanna, O’Donnell-Luria, Anne, Nigul, Mait, Ilves, Pilvi, Mohassel, Payam, Siddique, Teepu, Milone, Margherita, Nicolau, Stefan, Maroofian, Reza, Houlden, Henry, Hanna, Michael G., Quinlivan, Ros, Beiraghi Toosi, Mehran, Ghayoor Karimiani, Ehsan, Costagliola, Sabine, Deconinck, Nicolas, Kadhim, Hazim, Macke, Erica, Lanpher, Brendan C., Klee, Eric W., Łusakowska, Anna, Kostera-Pruszczyk, Anna, Hahn, Andreas, Schrank, Bertold, Nishino, Ichizo, Ogasawara, Masashi, El Sherif, Rasha, Stojkovic, Tanya, Nelson, Isabelle, Bonne, Gisèle, Cohen, Enzo, Boland-Augé, Anne, Deleuze, Jean-François, Meng, Yao, Töpf, Ana, Vilain, Catheline, Pacak, Christina A., Rivera-Zengotita, Marie L., Bönnemann, Carsten G., Straub, Volker, Handford, Penny A., Draper, Isabelle, Walter, Glenn A., Kang, Peter B.
Published 2021Text