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pro vyhledávání: '"Soltani, Babak"'
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Publikováno v:
In Precision Engineering November 2019 60:394-404
Autor:
Soltani, Babak1 (AUTHOR) Babak.soltani2001@gmail.com, Hojati, Faramarz1 (AUTHOR), Daneshi, Amir1 (AUTHOR), Azarhoushang, Bahman1 (AUTHOR)
Publikováno v:
International Journal of Advanced Manufacturing Technology. Jun2021, Vol. 114 Issue 11/12, p3719-3738. 20p. 2 Color Photographs, 3 Black and White Photographs, 6 Diagrams, 2 Charts, 8 Graphs.
Publikováno v:
International Journal of Advanced Manufacturing Technology. Nov2017, Vol. 93 Issue 5-8, p2517-2529. 13p. 1 Diagram, 2 Charts, 2 Graphs.
Autor:
Rismantab-Sani, Sahar1, Soltani, Babak2, Soltani, Siamak3 siamaksoltani92@yahoo.com, Memarian, Azadeh3
Publikováno v:
Addiction & Health. 2017, Vol. 9 Issue 2, p96-102. 7p.
Autor:
Sharif, Mohammad Reza1, Soltani, Babak1 babak_soltani1969@yahoo.com, Moravveji, Alireza2, Erami, Mahzad3, Soltani, Nika4
Publikováno v:
Electronic Physician. Mar2016, Vol. 8 Issue 3, p2081-2087. 7p.
Publikováno v:
Iranian Journal of Child Neurology
Objective Headaches are common neurologic problems for children and adolescents. They are divided into two types: primary and secondary. Primary headaches include migraines and tension-type as well as comprise the majority of headaches. We detect the
Autor:
TALEBIAN, Ahmad, SOLTANI, Babak, SEHAT, Mojtaba, ZAHEDI, Abolfazl, NOORIAN, Akram, TALEBIAN, Motahhareh
Publikováno v:
Iranian Journal of Child Neurology
Objective Neural tube defects (NTDs) are the most common congenital defects of central nervous system due to neural tube closure deficit during the third and fourth weeks of gestational age. Our study was performed to detect the incidence and risk fa
Autor:
Soltani, Babak, Sahebfosooli, Azin, Gilasi, Hamid Reza, Barati, Hooman, Erami, Mahzad, Haddad Kashani, Hamed
Publikováno v:
Drugs & Therapy Perspectives; Jun2021, Vol. 37 Issue 6, p265-271, 7p
Publikováno v:
Iranian Journal of Child Neurology
Objective Guillain-Barre syndrome (GBS) is the most common cause of acute weakness in children. It has multiple variant forms with different presentations. A rare initial sign is ptosis. In this study, we present a 10-year-old girl with bilateral pto