Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Farida Djabi"'
Autor:
Imene Adouani, Tassaadit Bendaoud, Hadjer Belaaliat, Wahiba Teniou, Faiza Keriou, Farida Djabi
Publikováno v:
Journal of Acute Disease, Vol 11, Iss 4, Pp 140-149 (2022)
Objective: To identify helpful laboratory paprameters for the diagnosis and prognosis of COVID-19. Methods: An observational retrospective study was conducted to analyze the biological profile of COVID-19 patients hospitalized in the Unit of Pulmonol
Externí odkaz:
https://doaj.org/article/92225897c1a84553b6ba74f1fbe14cbb
Publikováno v:
Journal of Drug Delivery and Therapeutics. 10:320-325
This prospective study aims to measure and compare the level of umbilical cord blood and venous blood procalcitonin (PCT) for a better and more rapid prediction of maternofetal infections in Algerian newborns. The study was conducted at the hospital
Publikováno v:
Journal of Biological Research - Bollettino della Società Italiana di Biologia Sperimentale. 93
Preeclampsia (PE) is a multisystem pregnancy disease inflecting maternal and fetal mortality and morbidity. This case-control study aims to determine the biochemical changes in lipid profile, hepatic and renal functions among sixty late-onset preecla
Autor:
Kamel Mokhnache, Ahlem Karbab, Soraya Ouhida, Noureddine Charef, Farida Djabi, Lekhmici Arrar, Mohammad S. Mubarak
Publikováno v:
Journal of Ethnopharmacology. 258:112936
Ethnopharmacological relevance Pituranthos scoparius is a medicinal plant that is used in traditional medicine in Algeria and other North African nations to treat several diseases such as asthma, rheumatism, measles, dermatoses, jaundice, and digesti
Autor:
Bakhouche Houcher, Nejat Akar, Ayşenur Öztürk, Abderezak Touabti, Farida Djabi, Zahira Houcher, Yonca Egin, Samia Begag
Publikováno v:
Pteridines, Vol 21, Iss 1, Pp 103-109 (2010)
The aim of the present study was to explore the influence of age and gender, on the association between the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and plasma total homocysteine (tHcy) concentrations in patients with cardiovasc
Publikováno v:
Pediatric Neurosurgery. 45:472-477
Background: Neural tube defects (NTD) are severe congenital malformations due to a failure in neural tube formation at the beginning of pregnancy. The etiology of NTD is multifactorial, with environmental and genetic determinants. We suggest a study
Autor:
Karam Moon, Nabil Sherif Mahmood, Soo Han Yoon, Farideh Nejat, Thomas J. Gruber, Manish K. Kasliwal, Ash Singhal, Mostafa El Khashab, Sang Won Lee, Erkan Yilmaz, Gerlant van Berlaer, Zuhal Erdem, Dong Ha Park, Hadihally Byregowda Suresh, Kwan-Sung Lee, Christopher G. Filippi, Yong-Kil Hong, Izabela Tarasiewicz, Cumhur Aydemir, Andreas Filis, Nilufer Eldes, Sin-Soo Jeun, Curtis J. Rozzelle, Bakhouche Houcher, N. Baradaran, Viola Van Gorp, Woo Young Jang, Shreedhara Avabratha, Alan R. Cohen, Bektas Acikgoz, Romyla Bourouba, Ebru Kolsal, Farida Djabi, Trevor Andrews, Sara Riemer, Katrijn Van Rompaey, Byung Chul Son, Bhawani Shankar Sharma, Carole Brathwaite, Marc K. Rosenblum, Kaivon Pakzad-Vaezi, Karen K. Anderson, Doug Cochrane, Nima Baradaran, Burak Bahadir, J K C Emejulu, Sanser Gul, Michael Söderman, Sajan Joy Andrews, Yonca Egin, Derek Covington, Said Hachimi-Idrissi, Michael B. Salmela, Gonca Ustundag, Murat Kalayci, Seung-Ho Yang, Jaiho Chung, Paul M. Arnold, Keith A. Cauley, Nejat Akar, Sushant Govindan, Frederic Dricot, Michael A. Sargent, Gumballi Krishnamurthy Swethadri, Jay V. Gonyea, Timothy M. George, David I. Sandberg, Jideofor Okechukwu Ugwu
Publikováno v:
Pediatric Neurosurgery. 45:I-VI
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis. 15:529-534
The polymorphic mutation 677 C-T in the methylenetetrahydrofolate reductase (MTHFR) gene presents a heterogeneous worldwide distribution and is associated with different disorders such as cardiovascular disease. Its frequency shows great ethnic and g
Publikováno v:
Pteridines, Vol 19, Iss 1, Pp 12-18 (2008)
Neural tube defects (NTDs) including spina bifida, anencephaly and encephalocele are among the most common birth defects, with high associated mortality and morbidity. There are no data concerning the incidence, associated anomalies, treatment and ou
Autor:
Karam Moon, Farideh Nejat, Jay V. Gonyea, Yonca Egin, Zuhal Erdem, Sushant Govindan, Shreedhara Avabratha, Burak Bahadir, Katrijn Van Rompaey, Kaivon Pakzad-Vaezi, Bakhouche Houcher, N. Baradaran, Carole Brathwaite, Michael B. Salmela, Cumhur Aydemir, Michael A. Sargent, Andreas Filis, Woo Young Jang, Derek Covington, Kwan-Sung Lee, Nima Baradaran, Doug Cochrane, Christopher G. Filippi, Ebru Kolsal, Trevor Andrews, Sin-Soo Jeun, Nilufer Eldes, David I. Sandberg, Izabela Tarasiewicz, Gerlant van Berlaer, Said Hachimi-Idrissi, Sajan Joy Andrews, Curtis J. Rozzelle, Timothy M. George, Manish K. Kasliwal, Sanser Gul, Seung-Ho Yang, Byung Chul Son, Yong-Kil Hong, Hadihally Byregowda Suresh, Keith A. Cauley, Michael Söderman, Viola Van Gorp, Gonca Ustundag, Jaiho Chung, Paul M. Arnold, Nejat Akar, Dong Ha Park, Marc K. Rosenblum, J K C Emejulu, Bektas Acikgoz, Murat Kalayci, Frederic Dricot, Romyla Bourouba, Alan R. Cohen, Gumballi Krishnamurthy Swethadri, Bhawani Shankar Sharma, Farida Djabi, Sara Riemer, Karen K. Anderson, Jideofor Okechukwu Ugwu, Nabil Sherif Mahmood, Soo Han Yoon, Thomas J. Gruber, Ash Singhal, Mostafa El Khashab, Sang Won Lee, Erkan Yilmaz
Publikováno v:
Pediatric Neurosurgery. 45:487-488