Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Farzaneh Alizadeh"'
Publikováno v:
Boundary Value Problems, Vol 2024, Iss 1, Pp 1-25 (2024)
Abstract The current paper undertakes an in-depth exploration of the dynamics of nonlinear waves governed by a 3D-modified nonlinear wave equation, a significant model in the study of complex wave phenomena. To this end, the study employs both classi
Externí odkaz:
https://doaj.org/article/d8b2708f61b24e1cb703ed50fed013a8
Autor:
Shima Farrokhi, Atieh Eslahi, Farzaneh Alizadeh, Zahra Farshchian, Yasamin Yousefi, Majid Mojarrad
Publikováno v:
Heliyon, Vol 10, Iss 20, Pp e36560- (2024)
HLD17 (Hypomyelinating Leukodystrophy 17) is an inherited white matter disorder characterized by insufficient myelin production due to biallelic loss of function mutations in the aminoacyl-tRNA synthetase complex-interacting multifunctional protein 2
Externí odkaz:
https://doaj.org/article/42d765711c9a4821ba36c759692cd89b
Publikováno v:
Fractal and Fractional, Vol 8, Iss 7, p 425 (2024)
This article introduces a new numerical algorithm dedicated to solving the most general form of variable-order fractional partial differential models. Both the time and spatial order of derivatives are considered as non-constant values. A combination
Externí odkaz:
https://doaj.org/article/f6e545bccf1e43b289ca7215303920f1
Autor:
Farzaneh Alizadeh, Ahmad Mansouri
Publikováno v:
Taḥqīqāt-i ̒Ulūm-i Raftārī, Vol 21, Iss 1, Pp 11-21 (2023)
Aim and Background: The Coronavirus disease pandemic has caused high stress, anxiety and distress for the healthcare workers. Although the relationship between emotion regulation strategies and spiritual coping with psychological distress has been co
Externí odkaz:
https://doaj.org/article/e672cbdd40cd48169fdc26c47a626bab
Autor:
Reza Jafarzadeh Esfehani, Atieh Eslahi, Mehran Beiraghi Toosi, Ariane Sadrnabavi, Mohammad Amin Kerachian, Mahsa Sadat Mohajeri Asl, Mahsa Farjami, Farzaneh Alizadeh, Majid Mojarad
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 24, Iss 9, Pp 1190-1195 (2021)
Objective(s): Infantile neuroaxonal degeneration (INAD) is a rare subgroup of neurodegeneration with brain iron accumulation (NBIA) disorders. This progressive disorder may develop during the early years of life. Affected individuals mostly manifest
Externí odkaz:
https://doaj.org/article/1fc333edf17f421fae6747ceeffc028f
Autor:
Mahsa Sadat Asl Mohajeri, Atieh Eslahi, Zeinab Khazaii, Mohammad Reza Moradi, Reza Pazhoomand, Shima Farrokhi, Masoumeh Heidari Feizabadi, Farzaneh Alizadeh, Majid Mojarrad
Publikováno v:
Human Genomics, Vol 15, Iss 1, Pp 1-5 (2021)
Abstract Introduction Skeletal dysplasia is a common, clinically and genetically heterogeneous disorder in the human population. An increasing number of different genes are being identified causing this disorder. We used whole exome sequencing (WES)
Externí odkaz:
https://doaj.org/article/03640e4a71da4719828ec0c68e92c6c9
Publikováno v:
ARKIVOC, Vol 2019, Iss 6, Pp 228-238 (2019)
Externí odkaz:
https://doaj.org/article/17b5c582eae64e60aaab92f93eb0fc6a
Publikováno v:
ARKIVOC, Vol 2019, Iss 6, Pp 55-63 (2019)
Externí odkaz:
https://doaj.org/article/7f01ca6c4b08471991b10493b8a3907b
Publikováno v:
Polycyclic Aromatic Compounds. :1-12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0aa5628f30770597a7db27489331984
https://doi.org/10.1080/10406638.2022.2150654
https://doi.org/10.1080/10406638.2022.2150654
Publikováno v:
Arkivoc. 2022:90-99
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1c96202a34c20a0e7d7e440fac37b63
https://doi.org/10.24820/ark.5550190.p011.859
https://doi.org/10.24820/ark.5550190.p011.859