Výsledky vyhledávání - "Mahsa Fallahi"

Akademický článek

A Rare Case of Klippel Trenaunay Syndrome with Von Willebrand Factor Deficiency and Multiple Accessory Spleens: A Case Report and Brief Literature Review

Autor: Vahid Falahati, Mahsa Fallahi, Mona Shahriarpour, Ali Ghasemi, Kazem Ghaffari

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

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Akademický článek

Lens opacity as a serious side effect following chelation therapy in beta thalassemia: A comparison between deferoxamine and deferasirox; randomized double-blinded clinical trial

Autor: Mohammad Reza Golpayegani, Vahid Falahati, Sam Habibollahi Habibollahi, Mahsa Fallahi

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

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Evaluating the efficacy and safety of topical sirolimus 0.2% cream as adjuvant therapy with pulsed dye laser for the treatment of port wine stain: A randomized, double-blind, placebo-controlled trial

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

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The Association between Red Cell Distribution Width and Mortality in Pediatric Acute Lymphoblastic Leukemia

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

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The prevalence of factor V Leiden, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T among G6PD deficient individuals from Western Iran

Autor: Azadeh Heidarpour, Mahsa Fallahi, Hadi Mozafari, Adraiana Muniz, Zohreh Rahimi

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

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