Zobrazeno 1 - 10
of 295
pro vyhledávání: '"Ashraf, T Soliman"'
Autor:
SALVATORE DI MAIO, VINCENZO DE SANCTIS, PIERLUIGI MARZUILLO, CHRISTOS KATTAMIS, SHAHINA DAAR, MEHERAN KARIMI, SAKI FOROUGH, ATANAS BANKEV, VALERIA KALEVA, SOTEROULA CHRISTOU, CARMELO FORTUGNO, POLYXENI DELAPORTA, ASHRAF T SOLIMAN, PLOUTARCHOS TZOULIS
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 15, Iss 1 (2023)
Abstract. Objective: To evaluate the age at menarche and menstrual characteristics in patients with transfusion-dependent thalassemia (TDT) who started early chelation therapy (≤ 3 years) with a variety of chelating agents. Design: A retrospective
Externí odkaz:
https://doaj.org/article/f91a52e79be64c3eb1b707a4bfbeb961
Autor:
Eihab A. Subahi, Fateen Ata, Hassan Choudry, Phool Iqbal, Mousa A. AlHiyari, Ashraf T. Soliman, Vincenzo De Sanctis, Mohamed A. Yassin
Publikováno v:
Annals of Medicine, Vol 54, Iss 1, Pp 764-774 (2022)
Introduction Around 5% of the world’s population is expected to have some degree and type of thalassaemia. Beta thalassaemia (BT) occurs due to a deficient production of the beta-globin chain of haemoglobin. Extramedullary haematopoiesis (EMH) is o
Externí odkaz:
https://doaj.org/article/cd46d120574043f596ee08f44e61ee94
Publikováno v:
Bulletin of the Iraq Natural History Museum, Vol 16, Iss 4, Pp 429-467 (2021)
he taxonomy of FicusL., 1753 species is confusing because of the intense morphological variability and the ambiguity of the taxa. This study handled 36 macro-morphological characteristics to clarify the taxonomic identity of the taxa. The study revea
Externí odkaz:
https://doaj.org/article/1eb5a8063ac24c2092f5b62a24b04b9d
Autor:
Ibrahim Khamees, Fateen Ata, Hassan Choudry, Ashraf T. Soliman, Vincenzo De Sanctis, Mohamed A. Yassin
Publikováno v:
Journal of Translational Medicine, Vol 19, Iss 1, Pp 1-10 (2021)
Abstract Background Sickle cell disease (SCD) is commonly encountered in Africa and Middle Eastern countries. The causative mutation in the gene encoding the hemoglobin subunit β (HBB) leads to various genotypic variants of the disease. This results
Externí odkaz:
https://doaj.org/article/6c4b269f05cf48509a03434fc009e776
Autor:
Mohamed A. Yassin, MBBS, MSc, Ashraf T. Soliman, MD, PhD, Abdulqadir J. Nashwan, MSc, Ans A. Alamami, MD, Mohammad A. J. Abdulla, MD, Saloua M. Hmissi, MD, Mahmood B. Aldapt, MD, Prem Chandra, PhD, Aasir M. Suliman, MD, MRCP (UK), Ezzeddin A. Ibrahim, MD, Khadra S. Yassin, MSc, Niloofar Allahverdi, MSc, Shehab F. Mohamed, MD
Publikováno v:
Medicine, Vol 101, Iss 24, p e29271 (2022)
Abstract. Hematologic reference intervals vary with gender, age, ethnicity, and geographic area. Therefore, local or national laboratory reference ranges are essential to enhance the accuracy when diagnosing health conditions. Still, no comprehensive
Externí odkaz:
https://doaj.org/article/a3965226495a4dd59fd14bcfad2dad92
Autor:
Adnan Al Shaikh, Yasser AlGhanmi, Saniah Awidah, Abdullah Bahha, Mohamed E Ahmed, Ashraf T Soliman
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 23, Iss 3, Pp 298-306 (2019)
Objective: An important goal in treating children with congenital adrenal hyperplasia (CAH) is to achieve a normal final adult height (FH). The aim of this study was to describe the clinical presentations and evaluate linear growth and possible facto
Externí odkaz:
https://doaj.org/article/9c8c57a48d614263b6f1049ebf46d69c
Publikováno v:
World Journal of Advanced Research and Reviews. 15:157-167
Primary (acute and chronic) malnutrition is still prevalent in developing countries because of inadequate nutrition and poor sanitation caused by social, economic, and environmental factors. In addition, acute malnutrition can occur secondary to an u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0f131d258250ccd95d07c810709519d
https://doi.org/10.30574/wjarr.2022.15.1.0673
https://doi.org/10.30574/wjarr.2022.15.1.0673
Autor:
Vincenzo De Sanctis, Heba Elsedfy, Ashraf T Soliman, Ihab Zaki Elhakim, Nada A Soliman, Rania Elalaily, Christos Kattamis
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 20, Iss 4, Pp 451-459 (2016)
Aim: Chronic iron overload resulting from frequent transfusions, poor compliance to efficient chelation therapy and chronic liver disease is basically responsible for the most severe complications of thalassemia major (TM). Before conventional treatm
Externí odkaz:
https://doaj.org/article/8e2c350827d94275bde723c58c8666b9
Autor:
Mohamed A. Yassin, Abdulqadir J. Nashwan, Ashraf T Soliman, Anil Yousif, Afra Moustafa, Afaf AlBattah, Shehab F. Mohamed, Deena S. Mudawi, Sarah Elkourashy, Deena-Raiza Asaari, Hope-Love G. Gutierrez, Mohamed Almusharaf, Radwa M. Hussein, Abbas H. Moustafa, Hatim El Derhoubi, Sarra Boukhris, Samah Kohla, Nader AlDewik
Publikováno v:
Clinical Medicine Insights: Case Reports, Vol 2015, Iss 8, Pp 77-81 (2015)
Externí odkaz:
https://doaj.org/article/2aad6ec85e3c4e31ab2b7f22f2efcdce
Autor:
Mohamed A. Yassin, Abbas H. Moustafa, Abdulqadir J. Nashwan, Ashraf T. Soliman, Hatim El Derhoubi, Shehab F. Mohamed, Deena S. Mudawi, Sarah ELkourashy, Deena-Raiza Asaari, Hope-Love G. Gutierrez, Radwa M. Hussein, Mohamed Al Musharraf, Samah Kohla, Ahmed Elsayed, Nader Al-Dewik
Publikováno v:
Clinical Medicine Insights: Blood Disorders, Vol 2015, Iss 8, Pp 19-23 (2015)
Externí odkaz:
https://doaj.org/article/43c94870f0cd4951ae387161824ef5c9