Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Mahsa Hojabri"'
Autor:
Masoomeh Raoufi, Mahsa Hojabri, Danial Samiei Nasr, Hanieh Najafiarab, Aryan Salahi-Niri, Nastaran Ebrahimi, Shideh Ariana, Hamidreza Khodabandeh, Sara Salarian, Mehdi Azizmohammad Looha, Mohamad Amin Pourhoseingholi, Seyed Amir Ahmad Safavi-Naini
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-13 (2024)
Abstract This study aimed to assess the severity and outcomes of COVID-19 in pregnant women, focusing on laboratory and radiological discrepancies between pregnant women and matched nonpregnant women. In this retrospective cross-sectional analysis, w
Externí odkaz:
https://doaj.org/article/56c76f24396e4b94a54a71e13baa5af8
Autor:
Mahsa Hojabri, Yeganeh Farsi, Mahnaz Jamee, Hassan Abolhassani, Hedieh Haji Khodaverdi Khani, Abdollah Karimi, Mehrnaz Mesdaghi, Zahra Chavoshzadeh, Samin Sharafian
Publikováno v:
BMC Pediatrics, Vol 23, Iss 1, Pp 1-7 (2023)
Abstract Jagunal homolog 1 (JAGN1) has been recognized as an essential protein in neutrophil function. The mutated JAGN1 is responsible for immunodeficiency related to innate and humoral defense mechanisms. This deficiency impairs neutrophil developm
Externí odkaz:
https://doaj.org/article/4657443782c44d6194d1852aacdd3447
Publikováno v:
Clinical Medicine Insights: Case Reports, Vol 16 (2023)
Background: Primary deficiency of coenzyme Q 10 deficiency-4 (CoQ 10 D4) is a heterogeneous disorder affecting different age groups. The main clinical manifestation consists of cerebellar ataxia, exercise intolerance, and dystonia. Case report: We pr
Externí odkaz:
https://doaj.org/article/2b7deb6f8810464393f7bcaab78936fa
Autor:
Mahsa Hojabri, Tahereh Tayebi, Mohammadreza Kasravi, Amirhossein Aghdaee, Armin Ahmadi, Radman Mazloomnejad, Roghayeh Tarasi, Alireza Shaabani, Soheyl Bahrami, Hassan Niknejad
Publikováno v:
International Journal of Biological Macromolecules. 240:124492
Autor:
Yeganeh Farsi, Mahsa Hojabri, Golnaz Eslamian, Bibi Shahin Shamsian, Roxana Mansour Ghanaie, Mohammad Keramatipour, Zahra Chavoshzadeh, Shabnam Eskandarzadeh
Cernunnos deficiency is a rare radiosensitive form of severe combined immunodeficiency (SCID). Herein, we report a patient with recurrent infections, birdlike face, microcephaly, Failure to thrive (FTT), and hypogammaglobinemia accompanied by conside
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3c46462ba6c2675106b6a3a82b1053d
https://doi.org/10.21203/rs.3.rs-1398608/v1
https://doi.org/10.21203/rs.3.rs-1398608/v1
Autor:
Yeganeh Farsi, Mahsa Hojabri, Golnaz Eslamian, Bibi Shahin Shamsian, Roxana Mansour Ghanaie, Mohammad Keramatipour, Zahra Chavoshzadeh, Shabnam Eskandarzadeh
Publikováno v:
SSRN Electronic Journal.