Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Sickle Beta Thalassemia"'
Autor:
Laura Pistoia, Antonella Meloni, Vincenzo Positano, Filomena Longo, Zelia Borsellino, Anna Spasiano, Riccardo Righi, Stefania Renne, Daniela Izzo, Ketty Savino, Sophie Mavrogeni, Emilio Quaia, Filippo Cademartiri, Alessia Pepe
Publikováno v:
Diagnostics, Vol 14, Iss 7, p 691 (2024)
Cardiac involvement in sickle beta thalassemia (Sβ-thal) patients has been poorly investigated. We aimed to evaluate cardiac function and myocardial iron overload by cardiovascular magnetic resonance (CMR) in patients with Sβ-thal. One-hundred and
Externí odkaz:
https://doaj.org/article/2a1758399a514700b4885173b9fc6ce1
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:
JK Science, Vol 23, Iss 3 (2021)
Sickle beta thalassemia represents the double heterozygous state of HbS and beta-thalassemia genes. Clinical manifestation varies from those indistinguishable from homozygous sickle cell anemia to completely asymptomatic ones. This disorder is diagno
Externí odkaz:
https://doaj.org/article/d79683869508453fbdcfbbab42989e33
Publikováno v:
Journal of Applied Hematology, Vol 12, Iss 1, Pp 46-47 (2021)
Sickle cell disease (SCD) is an autosomal recessive hemoglobinopathy. SCD patients commonly present with skin ulceration. This case is about a 22-year-old male whose initial presentation was reddish spots on both lower legs. Skin biopsy revealed feat
Externí odkaz:
https://doaj.org/article/53b3bea9d2624c6b80637c640c55ddc9
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
L. H. R. A. Premathilaka, M. S. Lakmini, L. G. Thamal Dharshana, S. B. Nawaratne, S. Mettananda, S. T. De Silva, A. P. Premawardhena
Publikováno v:
Sri Lanka Journal of Medicine, Vol 26, Iss 2, Pp 55-57 (2017)
Stroke in Sickle cell disease is a devastating complication. As Sickle cell disease is uncommon in Sri Lanka many clinicians may be unfamiliar with management of the disease and its complications. A 10-year-old boy presented with a transient ischaemi
Externí odkaz:
https://doaj.org/article/e2eaf169bc6842848a3c3a21e8a77ff8
Autor:
Raida Oudat, Hala A Alsoukhni, Rawan A Al-Hiari, Heba S Abualruz, Eman A Al-Mashaqba, Ma'mon Abu Hammad, Nazih Kh Abu Al-Shiek
Publikováno v:
Medical Archives
Introduction Sickle cell disorders are the most frequently encountered hemoglobin variants in Jordan. Both alpha and beta thalassemias are also prevalent in this population. However, studies on the interaction between these hemoglobin disorders are l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::304e2400d4f3e7538dc76cff7c5ce63d
http://europepmc.org/articles/PMC8116085
http://europepmc.org/articles/PMC8116085
Publikováno v:
Indian Journal of Pathology and Oncology. 8:283-286
Background: Hemolytic anaemia is caused due to the higher rate of destruction of red cells (membrane) than the rate of their generation. It can be inherited from or acquired. Membrane destruction is majorly caused due to the defects of membrane and e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6872130db482f13ab028471c7b0d1033
https://doi.org/10.18231/j.ijpo.2021.055
https://doi.org/10.18231/j.ijpo.2021.055
Publikováno v:
Zanco Journal of Medical Sciences, Vol 25, Iss 1, Pp 486-492 (2021)
Background and objective: One of the important health problems in Duhok city, Iraqi Kurdistan Region, is sickle cell disease. Blood transfusion remains a significant therapeutic intervention in patients with sickle cell disease that reduces complicat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a6c3e37f813db68e33aab450160a350
https://zjms.hmu.edu.krd/index.php/zjms/article/view/828
https://zjms.hmu.edu.krd/index.php/zjms/article/view/828
Autor:
MA Mujeeb Siddiqui, V Swetha
Publikováno v:
International Journal of Clinical and Diagnostic Pathology. 4:91-94
Introduction: The destruction of the red cell membrane causes hemolytic anemia, which can be affected by a variety of underlying pathologies. Membrane mutations, enzyme defects, hemoglobinopathies, immune destruction, and non-immune destruction are a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d9594dfcd79bcaae61ce51693beb839
https://doi.org/10.33545/pathol.2021.v4.i2b.365
https://doi.org/10.33545/pathol.2021.v4.i2b.365