Výsledky vyhledávání - BEIRAGHI TOOSI, Mehran
- Zobrazuji výsledky 1 - 14 z 14
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Bilateral horizontal gaze palsy in an 8‐year‐old girl: A rare case with NDUFS4 gene mutation Autor Vafaee‐Shahi, Mohammad, Ghasemi, Saeide, Beiraghi Toosi, Mehran, Ashrafi, Mahmoud Reza, Badv, Reza Shervin, Tavasoli, Ali Reza, Tahernia, Leila
Vydáno 2021Text -
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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... Autor AKHONDIAN, Javad, ASHRAFZADEH, Farah, SEILANIAN TOOSI, Farrokh, BEHNAM, Mahdi, BEIRAGHI TOOSI, Mehran, IMANNEZHAD, Shima, AKHOUNDIAN, Mohammad Reza, HASHEMI, Narges
Vydáno 2022Text -
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PLA2G6 gene mutation and infantile neuroaxonal degeneration; report of three cases from Iran Autor Jafarzadeh Esfehani, Reza, Eslahi, Atieh, Beiraghi Toosi, Mehran, Sadr-Nabavi, Ariane, Kerachian, Mohammad Amin, Asl Mohajeri, Mahsa Sadat, Farjami, Mahsa, Alizade, Farzaneh, Mojarrad, Majid
Vydáno 2021Text -
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Recommendations for Infantile-Onset and Late-Onset Pompe Disease: An Iranian Consensus Autor 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
Vydáno 2021Text -
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Bi-allelic Loss of Human APC2, Encoding Adenomatous Polyposis Coli Protein 2, Leads to Lissencephaly, Subcortical Heterotopia, and Global Developmental Delay Autor 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.
Vydáno 2019Text -
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A form of muscular dystrophy associated with pathogenic variants in JAG2 Autor 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.
Vydáno 2021Text