Zobrazeno 1 - 10
of 1 369
pro vyhledávání: '"Thalassemia Intermedia"'
Publikováno v:
Middle East Current Psychiatry, Vol 31, Iss 1, Pp 1-13 (2024)
Abstract Introduction Beta-thalassemia is a prevalent autosomal recessive haemolytic disorder, particularly in the Middle East. Patients with beta-thalassemia major (βTM) require iron chelation therapy and regular blood transfusions, while those wit
Externí odkaz:
https://doaj.org/article/26001208a58d4bb2bf0a9bdaf490ff05
Publikováno v:
Journal of Applied Hematology, Vol 15, Iss 2, Pp 121-129 (2024)
BACKGROUND: Alloantibodies against donor red blood cells (RBCs) are developed by patients with transfusion-dependent thalassemia (TDT), which causes the donor RBCs to hemolyze. This decreases the transfusion’s efficacy and increases the risk of adv
Externí odkaz:
https://doaj.org/article/70ca61b9c53347c3a7338924465bdc60
Autor:
Chng Chiaw Ling
Publikováno v:
Journal of the ASEAN Federation of Endocrine Societies, Vol 26, Iss 1 (2024)
These are the magnetic resonance images (MRI) of the pituitary gland of a 37-year old male with β-thalassemia intermedia diagnosed at age 17, who was referred to the Endocrine clinic by his hematologist for evaluation of hypogonadism. He was on mont
Externí odkaz:
https://doaj.org/article/f63b2df9c59943949855199fd8205aae
Autor:
Atefeh Ghareghani, Sedighe Pirdadi, Marzieh Nikparvar, Shideh Rafati, Hanie Bagheri, Mohammad Hamed Ersi
Publikováno v:
Disease and Diagnosis, Vol 13, Iss 1, Pp 13-17 (2024)
Background: Pulmonary hypertension (PH) is associated with an increased risk of cardiac failure among asymptomatic patients with beta-thalassemia. This study aimed to determine the prevalence of PH and associated risk factors in patients with beta-th
Externí odkaz:
https://doaj.org/article/27ea1cc5898b43bdb999100ef564d526
Autor:
Coralea Stephanou, Miranda Petrou, Petros Kountouris, Christiana Makariou, Soteroula Christou, Michael Hadjigavriel, Marina Kleanthous, Thessalia Papasavva
Publikováno v:
Biomedicines, Vol 12, Iss 2, p 296 (2024)
The +33 C>G variant [NM_000518.5(HBB):c.-18C>G] in the 5′ untranslated region (UTR) of the β-globin gene is described in the literature as both mild and silent, while it causes a phenotype of thalassemia intermedia in the presence of a severe β-t
Externí odkaz:
https://doaj.org/article/602ef8c19edc49abad13e789fc66f16f
Akademický článek
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Publikováno v:
Caspian Journal of Internal Medicine, Vol 13, Iss 4, Pp 765-771 (2022)
Background: Due to anemia in thalassemia major (TM) and thalassemia intermedia (TI) patients, bone changes occur, especially in the broad bones like jaw and skull, which are the main sites of hematopoiesis. Therefore, the dentist should be aware of t
Externí odkaz:
https://doaj.org/article/9b85a066e1634c58acbd8b5d3b97c74f
Autor:
Veroniki Komninaka, Pagona Flevari, Georgios Karkaletsis, Theodoros Androutsakos, Theofili Karkaletsi, Ioannis Ntanasis-Stathopoulos, Evaggelia-Eleni Ntelaki, Evangelos Terpos
Publikováno v:
Diseases, Vol 11, Iss 4, p 161 (2023)
We describe two cases of thalassemia intermedia (TI) patients with the presence of Gaucher-like cells in hematopoietic tissue biopsies, raising diagnostic dilemmas. The first is a 56-year-old female with bone lesions, splenomegaly, hypochromic microc
Externí odkaz:
https://doaj.org/article/c8b40d2b1ebb40b79322a7df21e844e0
Autor:
Seyyed Aboozar Fakhr-Moosavi, Arsalan Salari, Yasaman Borghei, Tolou Hasandokht, Afrooz Haghdoost, Seyed Mehdi Mousavi, Sajad Ramezani
Publikováno v:
Research in Cardiovascular Medicine, Vol 11, Iss 4, Pp 102-106 (2022)
Introduction: Pulmonary hypertension (PH) is quite common among patients with thalassemia, and it can lead to cardiac failure and even death in those patients. Methods: This current cross-sectional study was conducted with 155 patients with β-thalas
Externí odkaz:
https://doaj.org/article/d6e269dfacba4445b8c68927bb774d54
Autor:
Patrizia Caprari, Elisabetta Profumo, Sara Massimi, Brigitta Buttari, Rachele Riganò, Vincenza Regine, Marco Gabbianelli, Stefania Rossi, Roberta Risoluti, Stefano Materazzi, Giuseppina Gullifa, Laura Maffei, Francesco Sorrentino
Publikováno v:
Frontiers in Molecular Biosciences, Vol 9 (2023)
The rheological properties of blood play an important role in regulating blood flow in micro and macro circulation. In thalassemia syndromes red blood cells exhibit altered hemodynamic properties that facilitate microcirculatory diseases: increased a
Externí odkaz:
https://doaj.org/article/b0771f24bc184c2abd043af2793f94e3