Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Nazanin Khodayari Namin"'
Autor:
Zhaleh Fazel-Sarjoui, Amirali Khodayari Namin, Maryam Kamali, Nazanin Khodayari Namin, Ali Tajik
Publikováno v:
Iranian Journal of Reproductive Medicine, Vol 14, Iss 4, Pp 275-278 (2016)
Background: Gestational diabetes mellitus (GDM) is a common obstetrical complication with both maternal and fetal side effects. Objective: This study was performed to determine the complications in neonates of mothers with GDM receiving insulin vs.
Externí odkaz:
https://doaj.org/article/70e1e237b512431b9c8a3bf1c4ef4450
Autor:
Amirali Khodayari Namin, Maryam Kamali, Ali Tajik, Zhaleh Fazel-Sarjoui, Nazanin Khodayari Namin
Publikováno v:
International Journal of Reproductive Biomedicine
Iranian Journal of Reproductive Medicine, Vol 14, Iss 4, Pp 275-278 (2016)
Iranian Journal of Reproductive Medicine, Vol 14, Iss 4, Pp 275-278 (2016)
Background: Gestational diabetes mellitus (GDM) is a common obstetrical complication with both maternal and fetal side effects. Objective: This study was performed to determine the complications in neonates of mothers with GDM receiving insulin vs. d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa4e5135ef6891dafd407d3ad2404092
https://doi.org/10.29252/ijrm.14.4.275
https://doi.org/10.29252/ijrm.14.4.275
Autor:
Seyedeh Zalfa Modarresi, Nastaran Sabetkish, Mohsen Badalzadeh, Shaghayegh Tajik, Behnaz Esmaeili, Mohammad Reza Fazlollahi, Massoud Houshmand, Jaber Gharehdaghi, Shirin Niroomanesh, Fatemeh Rahimi Sherbaf, Zahra Alizadeh, Nazanin Khodayari Namini, Marzieh Maddah, Zahra Pourpak, Mostafa Moin
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 19, Iss 5 (2020)
This study aims to investigate the role of prenatal diagnosis (PND) in Iranian couples with a previous history of primary immunodeficiency disorders (PIDD) in their family. All referred couples with a family history of PIDD and a tendency for PND wer
Externí odkaz:
https://doaj.org/article/7417154740e44c9e95d0ec71b2447598
Autor:
Maryam Vahidi, Mohsen Badalzadeh, Masoomeh Jannesar, Marzieh Mazinani, Mohammad Reza Fazlollahi, Nazanin Khodayari Namini, Massoud Houshmand, Amir Ali Hamidieh, Leila Moradi, Zahra Pourpak, Mostafa Moin
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 18, Iss 5 (2019)
Familial haemophagocytic lymphohistiocytosis (FHL) is a rare disorder of immune dysregulation. FHL inherited in an autosomal recessive pattern is classified into five subtypes based on underlying genetic defects. Mutations in four genes including PRF
Externí odkaz:
https://doaj.org/article/dfae81c8de3f4f6098e01614efbad261