Zobrazeno 1 - 10
of 875
pro vyhledávání: '"anemias"'
Publikováno v:
Journal of Epidemiology and Global Health, Vol 14, Iss 1, Pp 72-85 (2023)
Abstract Inherited anemia continues to pose a significant public health concern on a global scale, owing to its extensive geographical prevalence, substantial patient population, and profound ramifications. Here, we investigated detailed information
Externí odkaz:
https://doaj.org/article/6f2c4c87d3d74085970984fbba7db8c1
Autor:
Christos Savvidis, Dimitra Ragia, Sophia Delicou, Aikaterini Xydaki, Manfredi Rizzo, Ioannis Ilias
Publikováno v:
Medicina, Vol 60, Iss 10, p 1571 (2024)
Background and Objectives: Adrenal insufficiency (AI) can be a significant concern in patients with transfusion-dependent homozygous beta thalassemia (bThal) due to the chronic disease burden and frequent blood transfusions that these patients requir
Externí odkaz:
https://doaj.org/article/8823d9aafaa245298890ab84863d018b
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 8, p 4296 (2024)
Autoimmune hemolytic anemias (AIHAs) are conditions involving the production of antibodies against one’s own red blood cells (RBCs). These can be primary with unknown cause or secondary (by association with diseases or infections). There are severa
Externí odkaz:
https://doaj.org/article/28bb10da93514543bcd677bd967b8e88
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Clinical Case Reports, Vol 11, Iss 5, Pp n/a-n/a (2023)
Key Clinical Message We highlight a novel case of TAFRO syndrome with disseminated intravascular coagulation, neurologic changes, and non‐ischemic cardiomyopathy. Through this clinical vignette, we hope to raise awareness of TAFRO syndrome and enco
Externí odkaz:
https://doaj.org/article/45a467ee1ab648f1b3d7eb98729bf06f
Autor:
Yuanyuan Huang, Hongxia Ren
Publikováno v:
Frontiers in Surgery, Vol 10 (2023)
BackgroundHirschsprung-associated enterocolitis (HAEC) is a common and life-threatening complication of Hirschsprung's disease (HSCR), which can occur before and after surgery. The aim of this study was to identify the risk factors associated with th
Externí odkaz:
https://doaj.org/article/80cc42b51e974d12ac473e62d37e6693
Autor:
Bruno Fattizzo, Irene Motta
Publikováno v:
Frontiers in Medicine, Vol 9 (2023)
Therapeutic options for rare congenital (hemoglobinopathies, membrane and enzyme defects, congenital dyserythropoietic anemia) and acquired anemias [warm autoimmune hemolytic anemia (wAIHA), cold agglutinin disease CAD, paroxysmal nocturnal hemoglobi
Externí odkaz:
https://doaj.org/article/e769325d96754ef3af0b4054496f7b15
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-12 (2021)
Abstract Congenital hemolytic anemias (CHAs) comprise defects of the erythrocyte membrane proteins and of red blood cell enzymes metabolism, along with alterations of erythropoiesis. These rare and heterogeneous conditions may generate several diffic
Externí odkaz:
https://doaj.org/article/5ab92eba01744aee8d72c30447593e5e
Autor:
Melina Mara Musri, Veronica Venturi, Xènia Ferrer-Cortès, Lídia Romero-Cortadellas, Gonzalo Hernández, Pilar Leoz, María Pilar Ricard Andrés, Marta Morado, María del Carmen Fernández Valle, David Beneitez Pastor, Ana Ortuño Cabrero, Maite Moreno Gamiz, Leonor Senent Peris, Amanda Isabel Perez-Valencia, Santiago Pérez-Montero, Cristian Tornador, Mayka Sánchez
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 12, p 9935 (2023)
Congenital dyserythropoietic anemia type II (CDA II) is an inherited autosomal recessive blood disorder which belongs to the wide group of ineffective erythropoiesis conditions. It is characterized by mild to severe normocytic anemia, jaundice, and s
Externí odkaz:
https://doaj.org/article/f544ba52d5e34f1fadc2230634bf24b6
Autor:
Cristina Vercellati, Anna Paola Marcello, Bruno Fattizzo, Anna Zaninoni, Agostino Seresini, Wilma Barcellini, Paola Bianchi, Elisa Fermo
Publikováno v:
Frontiers in Physiology, Vol 13 (2022)
We investigated by targeted next generation sequencing the genetic bases of hereditary spherocytosis in 25 patients and compared the molecular results with the biochemical lesion of RBC membrane obtained by SDS-PAGE analysis. The HS diagnosis was bas
Externí odkaz:
https://doaj.org/article/21299625cbbe4185b034bf08490ad166