Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mahsa Fallahi"'
Publikováno v:
Advanced Biomedical Research, Vol 13, Iss 1, Pp 20-20 (2024)
Klippel Trenaunay Syndrome (KTS) is an uncommon inherited syndrome identified by venous varicosities and capillary abnormalities. von Willebrand Disease is the most common inherited hemorrhage disturbance in humans, leading to insufficiency in von Wi
Externí odkaz:
https://doaj.org/article/ef319f3793f94465aab61bfa510fc66a
Publikováno v:
Journal of Preventive Epidemiology, Vol 4, Iss 1, Pp e03-e03 (2019)
Introduction: Ocular toxicity is a serious side effect following chelation therapy in patients suffering from major beta-thalassemia. Objectives: We aimed to assess ocular toxicity (lens opacity) of the Iranian brand of deferasirox named "Osveral" ma
Externí odkaz:
https://doaj.org/article/723cc14bd6f24c8d8e12ad9614c417c0
Autor:
Maryam Daneshpazhooh, Shahriar Haddady Abianeh, Amir Teimourpour, Zahra Hallaji, Soheil Tavakolpour, Hamidreza Mahmoudi, Ali Nili, Mahsa Fallahi, Javad Rahmati, Ali Salehi Farid, Somayeh Niknam
Publikováno v:
Journal of cosmetic dermatologyREFERENCES. 20(8)
Introduction Port Wine Stain (PWS) is a congenital capillary malformation. Although multiple treatments are required, the gold standard treatment for PWS is Pulsed Dye Laser (PDL). Given its anti-angiogenic effects, sirolimus can be considered as an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c1792af0cd4a865705937b912c2d081
https://pubmed.ncbi.nlm.nih.gov/33251650
https://pubmed.ncbi.nlm.nih.gov/33251650
Autor:
i Rafsanjani, Khadijeh Arjm, Mahsa Fallahi, Vahid Falahati, Azadeh Kiumarsi, Shabnam Moghaddam
Publikováno v:
Journal of Neoplasm.
Background: Red cell distribution width (RDW) is one of the standard parameters with blood cell counts. Studies have revealed that RDW could be used as a predictor of mortality in different contexts. However, data about the relation of RDW with hemat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0db504520361ee1cb1ef1f1272eb1f3e
https://doi.org/10.21767/2576-3903.100011
https://doi.org/10.21767/2576-3903.100011
Publikováno v:
Molecular biology reports. 36(8)
It has been suggested that the allele frequency of thrombophilic mutations is affected by glucose-6-phosphate dehydrogenase (G6PD) deficiency. The prevalence of thrombophilic mutations were studied in sixty G6PD deficient individuals including 57 mal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::588bb88db69346f9fe3d2fcabafb2744
https://pubmed.ncbi.nlm.nih.gov/19219640
https://pubmed.ncbi.nlm.nih.gov/19219640
Autor:
Fallahi, Mahsa1,2 (AUTHOR), Hallaji, Zahra1 (AUTHOR), Tavakolpour, Soheil1,3 (AUTHOR), Niknam, Somayeh4 (AUTHOR), Salehi Farid, Ali1 (AUTHOR), Nili, Ali1 (AUTHOR), Teimourpour, Amir5 (AUTHOR), Daneshpazhooh, Maryam1 (AUTHOR), Rahmati, Javad6 (AUTHOR), Haddady Abianeh, Shahriar6 (AUTHOR), Mahmoudi, Hamidreza1 (AUTHOR) hr_mahmoody@yahoo.com
Publikováno v:
Journal of Cosmetic Dermatology. Aug2021, Vol. 20 Issue 8, p2498-2506. 9p.
Autor:
Mansour Ghanaiee, Roxana, Fallah, Tina, Karimi, Abdollah, Sedighi, Iraj, Tariverdi, Marjan, Nazari, Tayebe, Nahanmoghaddam, Negin, Sedighi, Parinaz, Nateghian, Alireza, Amirali, Arezu, Monavari, Seyed Hamidreza, Fallahi, Mahsa, Zahraei, Seyed Mohsen, Mahmoudi, Sussan, Elikaei, Ameneh, Alebouyeh, Masoud
Publikováno v:
Pediatric Infectious Disease Journal; Apr2024, Vol. 43 Issue 4, p320-327, 8p
Publikováno v:
Advanced Biomedical Research; Feb2024, Vol. 13, p1-5, 5p