Zobrazeno 1 - 10
of 277
pro vyhledávání: '"VINCENZO DE SANCTIS"'
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 16, Iss 1 (2024)
Background: Prediabetes and diabetes mellitus (DM) are complications in adult patients with transfusion dependent β-thalassemia (β-TDT), with their incidence increasing with age. Objective: This retrospective observational study describes the glyce
Externí odkaz:
https://doaj.org/article/31dbadb931f44007ac73d23c71b43faf
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
Autor:
Vincenzo De Sanctis, Ashraf Soliman, Shahina Daar, Ploutarchos Tzoulis, Salvatore Di Maio, Christos Kattamis
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 15, Iss 1 (2023)
Aims: The primary aim of this study was to evaluate retrospectively the glucose homeostasis and surrogate indexes of insulin sensitivity and resistance, during a 3-hour oral glucose tolerance test (OGTT), in β- thalassemia major patients (β-TM) wit
Externí odkaz:
https://doaj.org/article/ca59a1179800480eb888255906814db8
Autor:
Dimitrios Farmakis, John Porter, Ali Taher, Maria Domenica Cappellini, Michael Angastiniotis, Androulla Eleftheriou, for the 2021 TIF Guidelines Taskforce, Ali Alassaf, Emanuele Angelucci, Yesim Aydinok, Rayan Bou-Fakhredin Rayan, Loris Brunetta, George Constantinou, Shahina Daar, Vincenzo De Sanctis, Geoffrey Dusheiko, Riyad Elbard, Perla Eleftheriou, Panos Englezos, Dru Haines, Faiez N Hattab, George Kaltsounis, Antonios Kattamis, John Koskinas, Navdeep Kumar, Andreas Kulozik, Andreas Kyriakou, Aurelio Maggio, Roanna Maharai, Lauren Mednick, Eleni Michalaki, Wendy Murphy, Lena Oevermann, Raffaella Origa, Penelope-Georgia Papayanni, Constantina Politis, Farukh Shah, Anton Skafi, Nikos Skordis, Pietro Sodani, Ashraf Soliman, Seni Subair, Maria Tampaki, Sara Trompeter, Shobha Tuli, Malcolm Walker, Robert Yamashita, Evangelia Yannaki, Anne Yardumian
Publikováno v:
HemaSphere, Vol 6, Iss 8, p e732 (2022)
Beta-thalassemia and particularly its transfusion-dependent form (TDT) is a demanding clinical condition, requiring life-long care and follow-up, ideally in specialized centers and by multidisciplinary teams of experts. Despite the significant progre
Externí odkaz:
https://doaj.org/article/e09c27ab622646e18fe28c7d0ec0779e
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:
Mehran Karimi, Tahereh Zarei, Sezaneh Haghpanah, Azita Azarkeiva, Maryam Naderi, Sara Matin, Asghar Bazrafshan, Zohreh Zahedi, Afshan Shirkavand, Parisa pishdad, Vincenzo De Sanctis
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 14, Iss 1 (2022)
Background: The ongoing COVID-19 pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has led to high morbidity and mortality worldwide. Vaccination against SARS-CoV-2 is a leading strategy to change the course of the COV
Externí odkaz:
https://doaj.org/article/27a235fa01644c5d9f65e57b780cf449
Autor:
Amr Shier, Mohamed Abdelrazek, Ashraf Soliman, Vincenzo De Sanctis, Ahmed Elsayed, Mohamed Abdulla, Shehab Mohamed, Khadra Yassin, Ilham Bilal, Mohamed Yassin
Publikováno v:
Case Reports in Oncology, Vol 13, Iss 1, Pp 365-372 (2020)
Background: Musculoskeletal manifestations are common in sickle cell disease (SCD). Vaso-occlusive crisis can manifest acutely as joint and bone pain, osteomyelitis and/or arthritis. It can also lead to chronic bone aches, bone deformities, degenerat
Externí odkaz:
https://doaj.org/article/6562c1c7831a4a1797868d9d8c12bdbe
Autor:
Eihab Subahi, Fateen Ata, Phool Iqbal, Mousa AlHiyari, Mohamed Yassin, Hassan Choudry, Ashraf Soliman, Vincenzo De Sanctis
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S50-S51 (2021)
Objective: Thalassemia is one of the most common hemoglobinopathies, with around 5% of the world's population expected to have some degree and type of thalassemia. Beta thalassemia (BT) occurs due to a deficient production of the beta-globin chain of
Externí odkaz:
https://doaj.org/article/57437c422e69460d84aa52c0d02b6516
Autor:
Vincenzo De Sanctis, Ashraf Soliman, Ploutarchos Tzoulis, Shahina Daar, Salvatore Di Maio, Bernadette Fiscina, Christos Kattamis
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 13, Iss 1 (2021)
Background: Glucose dysregulation (GD), including prediabetes and diabetes mellitus (DM), is a common complication of transfusion dependent β-thalassemia (TDT) patients. The prevalence increases with age and magnitude of iron overload, affecting a s
Externí odkaz:
https://doaj.org/article/632d4a80fc794665bab7b8669634e758