Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Chronic haemolytic anaemia"'
Autor:
Gabriel O. Ogun, Adebola E. Orimadegun, Stephen Allen, Olusegun O. Akinyinka, A Akere, Babatunde O. Ogunbosi, O Bello, A A Adepoju, Adanze Onyenonachi Asinobi
Publikováno v:
Paediatrics and International Child Health. 42:29-35
Sickle cell anaemia (SCA) is a chronic haemolytic anaemia associated with vaso-occlusive painful crises which may affect several systems including the gastro-intestinal system, resulting in abdominal pain. The concurrence of inflammatory bowel diseas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3122cae3613c28ad1a6774b80f9701c8
https://doi.org/10.1080/20469047.2021.1936393
https://doi.org/10.1080/20469047.2021.1936393
Publikováno v:
International Blood Research & Reviews. :1-15
Major beta thalassemia is a severe form of thalassemia caused by the alteration of two beta globin genes resulting in a defective synthesis of hemoglobin. It is characterized by chronic severe anemia, ineffective erythropoiesis (IE) and iron overload
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b17cd07b915075ea3bb18944075c7254
https://doi.org/10.9734/ibrr/2019/v10i230118
https://doi.org/10.9734/ibrr/2019/v10i230118
Publikováno v:
Blood Reviews. 32:300-311
Beta-thalassaemia causes defective haemoglobin synthesis leading to ineffective erythropoiesis, chronic haemolytic anaemia, and subsequent clinical complications. Blood transfusion and iron chelation allow long-term disease control, and haematopoieti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a414cad6d1e184f0a251801ae90a88a
https://doi.org/10.1016/j.blre.2018.02.001
https://doi.org/10.1016/j.blre.2018.02.001
Publikováno v:
Education Thérapeutique du Patient - Therapeutic Patient Education. 5:147-153
Introduction: Sickle cell disease (SCD) is a genetic haemoglobin abnormality responsible for various complications including chronic haemolytic anaemia and vaso-occlusive crises. Hydroxyurea (HU) therapy is used in patients with severe symptoms to im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b57c3af0e8249400e10fadd04343d9b
https://doi.org/10.1051/tpe/2013024
https://doi.org/10.1051/tpe/2013024
Publikováno v:
Scandinavian Journal of Haematology. 15:339-346
A new case of congenital stomatocytosis associated with haemolytic anaemia, increased autohaemolysis, abnormalities in the erythrocyte metabolism, increased osmotic fragility and shortened erythrocyte survival is described. Intracellular cation conce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c87a01ef07d9055f7db25b6bb3af7e31
https://doi.org/10.1111/j.1600-0609.1975.tb01089.x
https://doi.org/10.1111/j.1600-0609.1975.tb01089.x
Autor:
M.-L. Couëc
Publikováno v:
Transfusion Clinique et Biologique. 19:142-144
Sickle cell disease is a genetic hemoglobinopathy characterised by vasoocclusive events and chronic haemolytic anaemia. Transfusion is a major therapeutic modality in this disease by decreasing the percentage of abnormal haemoglobin Hb S while increa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::458ddb6d8ce2923c37929b22f7704ad2
https://doi.org/10.1016/j.tracli.2012.07.018
https://doi.org/10.1016/j.tracli.2012.07.018
Autor:
Roberto Di Bartolomeo, Giorgio Arpesella, Luca Botta, Andrea Dell ' Amore, Sofia Martin-Suarez, Nicola Camurri, Carlo Savini
Publikováno v:
Heart, Lung and Circulation. 17:77-79
beta-Thalassaemia is an inherited haemoglobin (Hb) disorder resulting in chronic haemolytic anaemia. The most anaemic patients require regular red blood cell (RBC) transfusions for survival but iron accumulation leads to multisystem dysfunction. Hear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d6e58f4737f335f7b0b947d5b9f36c4
https://doi.org/10.1016/j.hlc.2006.09.010
https://doi.org/10.1016/j.hlc.2006.09.010
Publikováno v:
South African Journal of Child Health, Volume: 7, Issue: 2, Pages: 70-73, Published: MAY 2013
South African Journal of Child Health; Vol 7, No 2 (2013); 70-73
South African Journal of Child Health; Vol 7, No 2 (2013); 70-73
Haemoglobinopathies are a group of inherited disorders caused by structural variations of the haemoglobin molecule. We report the case of a 5-year-old girl suffering from chronic haemolytic anaemia. A diagnosis of compound heterozygous sickle cell di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2119cd3a716132c45a025421920fe43f
http://www.scielo.org.za/scielo.php?script=sci_arttext&pid=S1999-76712013000200009&lng=en&tlng=en
http://www.scielo.org.za/scielo.php?script=sci_arttext&pid=S1999-76712013000200009&lng=en&tlng=en
Publikováno v:
Blood Reviews. 9:165-175
The hereditary red cell enzymopathies are an uncommon but important cause of chronic haemolytic anaemia. Their clinical diversity is mirrored by increasingly evident heterogeneity at the molecular level. The structure, function, and expression of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::489a2908e36f2352e4078dd165057d14
https://doi.org/10.1016/0268-960x(95)90022-5
https://doi.org/10.1016/0268-960x(95)90022-5
Publikováno v:
International Journal of Medicine and Health Development; Vol 15, No 2 (2010); 82-85
Introduction: Autoimmune haemolytic anaemia is an important cause of acute or chronic anaemia. Its association with lymphoproliferative disorders such as non-Hodgkin lymphoma, and Hodgkin disease is well documented in the literature. Subjects and Met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7999eb1c16811b7ece12279c6ea706e
https://doi.org/10.4314/jcm.v15i2.11
https://doi.org/10.4314/jcm.v15i2.11