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1مؤتمر
المؤلفون: Farzad Fatehi (4392418), Kamyar Moradi (11334840), Ali Asghar Okhovat (11334843), Ghazaleh Shojatalab (11334846), Behnaz Sedighi (11334849), Reza Boostani (5956715), Payam Sarraf (8945408), Bahram Haghi Ashtiani (11334852), Majid Ghasemi (11334855), Soussan Moussavi (11334858), Nassim Anjidani (9850450), Shahriar Nafissi (547379)
مصطلحات موضوعية: Neurology and Neuromuscular Diseases, Neurogenetics, clinical response, myasthenia gravis, refractory, rituximab, zytux TM
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2مؤتمر
المؤلفون: Farzad Fatehi, Kamyar Moradi, Ali Asghar Okhovat, Ghazaleh Shojatalab, Behnaz Sedighi, Reza Boostani, Payam Sarraf, Bahram Haghi Ashtiani, Majid Ghasemi, Soussan Moussavi, Nassim Anjidani, Shahriar Nafissi
مصطلحات موضوعية: Neurology and Neuromuscular Diseases, Neurogenetics, clinical response, myasthenia gravis, refractory, rituximab, zytux TM
الإتاحة: https://doi.org/10.3389/fneur.2021.682622.s001Test
https://figshare.com/articles/presentation/Presentation_1_Zytux_in_Refractory_Myasthenia_Gravis_A_Multicenter_Open-Labeled_Clinical_Trial_Study_of_Effectiveness_and_Safety_of_a_Rituximab_Biosimilar_pdf/16443705Test -
3دورية أكاديمية
المؤلفون: Helia Mojtabavi (9607092), Shahriar Nafissi (547379), Behrooz Mahmoodi-Bakhtiari (8111114), Davood Fathi (10155694), Farzad Fatehi (4392418)
مصطلحات موضوعية: Medicine, Neuroscience, Ecology, Sociology, Hematology, Space Science, Biological Sciences not elsewhere classified, Amyotrophic lateral sclerosis, ALS, cognition, Edinburg Cognitive and Behavioral screen, ECAS, validation, Persian Version of ECAS
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4
المؤلفون: Mahdieh Pashaei (10485652), Atefeh Davarzani (10485655), Reza Hajati (10485658), Babak Zamani (9302810), Shahriar Nafissi (547379), Farzaneh Larti (10485661), Yalda Nilipour (6041981), Mohammad Rohani (9302807), Afagh Alavi (6041975)
مصطلحات موضوعية: Biochemistry, Medicine, Genetics, Neuroscience, Cancer, Computational Biology, Space Science, Biological Sciences not elsewhere classified, Hereditary spastic paraplegia (HSP), CYP7B1 (SPG5A), ENTPD1 (SPG64), ZFYVE26 (SPG15), Whole-exome sequencing (WES)