Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Hamidreza Moazzen"'
Publikováno v:
Shiraz E-Medical Journal. 23
Background: For patients with end-stage renal disease (ESRD) who undergo peritoneal dialysis (PD) at home or in non-clinical centers, it is crucial to design and implement a hands-on self-care clinical decision aid system (CDAS). To this end, this de
Publikováno v:
Electronics Letters. 56:155-157
A new model for the power consumption of RF power amplifiers (PAs) in terms of the input power based on Lambert W-function is presented. In the derivation of the model, the knee voltage effect of the field effect transistors is taken into account. Ac
Publikováno v:
IEEE Transactions on Communications. 67:6753-6765
In this paper, we investigate the effect of power amplifier (PA) nonlinearity on a multi user multiple-input multiple-output orthogonal frequency division multiplexing (MU-MIMO-OFDM) system where the base station (BS) uses linear precoding to transmi
Publikováno v:
International Journal of RF and Microwave Computer-Aided Engineering. 31
Publikováno v:
Analog Integrated Circuits and Signal Processing. 90:361-372
In this paper, a simple and efficient architecture for implementation of multilevel outphasing systems is presented. The architecture consists of a six-port modulator and a Doherty power amplifier in each outphasing branch. Pin diodes are used as var
Autor:
Marzieh Khani, Hosein Shamshiri, Shahriar Nafissi, Najmeh Salehi, Hamidreza Moazzeni, Hanieh Taheri, Elahe Elahi
Publikováno v:
Clinical Case Reports, Vol 12, Iss 1, Pp n/a-n/a (2024)
Key Clinical Message Fazio‐Londe disease and Brown‐Vialetto‐Van Laere syndrome are rare related neurological disorders. Although SLC52A3 and SLC52A2 that encode riboflavin transporters are their only known causative genes, many patients without
Externí odkaz:
https://doaj.org/article/2726eafbefe64b43acbff02336e65555
Autor:
Marzieh Khani, Hosein Shamshiri, Farzad Fatehi, Mohammad Rohani, Bahram Haghi Ashtiani, Fahimeh Haji Akhoundi, Afagh Alavi, Hamidreza Moazzeni, Hanieh Taheri, Mina Tolou Ghani, Leila Javanparast, Seyyed Saleh Hashemi, Ramona Haji‐Seyed‐Javadi, Matineh Heidari, Shahriar Nafissi, Elahe Elahi
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 7, Pp n/a-n/a (2020)
Abstract Background SPG11 mutations can cause autosomal recessive hereditary spastic paraplegia (ARHSP) and juvenile amyotrophic lateral sclerosis (JALS). Because these diseases share some clinical presentations and both can be caused by SPG11 mutati
Externí odkaz:
https://doaj.org/article/17893aa063484e249714d0aee191d73f
Publikováno v:
Journal of Ophthalmic & Vision Research, Vol 12, Iss 4, Pp 407-412 (2017)
Purpose: We aimed to assess whether the transcription factor PAX6 affects transcription of FMNL2. PAX6 is a transcription factor with significant roles in development of the eye and eye-related functions. FMNL2 encodes a member of the formin family o
Externí odkaz:
https://doaj.org/article/230acddc14514dfe934f3e00bcb3d45b
Autor:
Amir Banaei-Esfahani, Hamidreza Moazzeni, Pooya Naseri Nosar, Sadaf Amin, Ehsan Arefian, Masoud Soleimani, Shahin Yazdani, Elahe Elahi
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 18, Iss 2, Pp 108-114 (2015)
Objective(s):An earlier meta-analysis on gene expression data derived from four microarray, two cDNA library, and one SAGE experiment had identified RGS5 as one of only ten non-housekeeping genes that were reported to be expressed in human trabecular
Externí odkaz:
https://doaj.org/article/f3b578fe65914f2db863abb17baf4a99