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pro vyhledávání: '"sickle cell beta-thalassemia"'
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Autor:
Rakesh B M, Sahithi Sharma
Publikováno v:
Cureus
Sickle beta-thalassemia is a rare variant of sickle cell disease (SCD) that manifests with milder symptoms. Musculoskeletal complications arising from this condition can mimic inflammatory arthritis and hence delay the diagnosis of rheumatoid arthrit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::780b6061658444f3dff6ad602d177341
https://doi.org/10.7759/cureus.17378
https://doi.org/10.7759/cureus.17378
Publikováno v:
Cureus
Parvovirus infection and thrombotic thrombocytopenic purpura (TTP) are rare manifestations in adults with sickle cell beta-thalassemia. Due to the lack of a clear demarcation between the complications related to sickle cell disease (SCD) and TTP, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69824c18dfaaa1eb2af1348c6d1a4062
http://europepmc.org/articles/PMC8331060
http://europepmc.org/articles/PMC8331060
Publikováno v:
QJM: An International Journal of Medicine. 114
Background Hematologic diseases are a group of prevalent and clinically diverse diseases that can affect any organ system. Hematologic disorders frequently involve bone and associated tissues causing significant alterations in the bone marrow and may
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc35677f9fab9174fbb60a038d089507
https://doi.org/10.1093/qjmed/hcab106.057
https://doi.org/10.1093/qjmed/hcab106.057
Publikováno v:
Bali Medical Journal, Vol 8, Iss 2, Pp 623-627 (2019)
Background: The prevalence of Hb S/β Thalassemia has not been widely reported, and until now, there is a lack of statistical data on the prevalence of the disease in Indonesia. In 1974, cases of β thalassemia with Hb S were found in one family in J
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01855adaa47cea2b56aac91d743ae8d4
https://balimedicaljournal.org/index.php/bmj/article/view/1417
https://balimedicaljournal.org/index.php/bmj/article/view/1417
Autor:
Evangelos Terpos, Konstantina Repa, Veroniki Komninaka, Ersi Voskaridou, Maria N. Dimopoulou, Ioannis Ntanasis-Stathopoulos, Dimitrios Christoulas, Athanasios Papatheodorou
Publikováno v:
Annals of Hematology. 98:1583-1592
Despite the advances in the management of hemoglobinopathies, further insight into disease pathophysiology is necessary to improve our therapeutic approach. Activin-A has emerged as a regulator of erythropoiesis and bone turnover in malignant disorde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5f3a59aa0779838d263659753af29e0
https://doi.org/10.1007/s00277-019-03695-x
https://doi.org/10.1007/s00277-019-03695-x
Autor:
Hayder Al-Momen
Publikováno v:
AL-Kindy College Medical Journal. 13:76-81
Background: Sickle cell-beta thalassemia (HbS/β-thal) is a good example of a mixture of two types of common hereditary anemias in the Middle East and Mediterranean area, and lately throughout the world (because of continuous people movement to diffe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e8c68ce8a7ece0891be46f9669445c9
https://doi.org/10.47723/kcmj.v13i1.130
https://doi.org/10.47723/kcmj.v13i1.130
Autor:
Aditya V. Maheshwari, David B. Frumberg, Robert Pivec, Samantha E. Epstein, Julio J. Jauregui
Publikováno v:
Journal of Clinical Orthopaedics and Trauma. 7:130-133
Periprosthetic infection following total hip arthroplasty is a devastating complication that has been reported to occur in up to 1.6% of all primary total hip arthroplasties. We report a previously unrecognized gram-negative bacillus as the infecting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::606f276c09bebd2451b66d6fca2eee01
https://doi.org/10.1016/j.jcot.2016.02.008
https://doi.org/10.1016/j.jcot.2016.02.008
Autor:
Paridhi Dayama, Vinit Warthe, Roshan B. Colah, Dipty Jain, Dilip Sarate, Pallavi Mehta, Graham R. Serjeant
Publikováno v:
The Indian Journal of Pediatrics. 83:1071-1076
To explore clinical, hematological and molecular features of homozygous sickle cell (SS) disease in central India.Focusing on the pediatric age group attending a clinic at the Akola Government Medical College, Akola, Maharashtra State, India, a cross
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0571943de34deb582c33d1dbf980165d
https://doi.org/10.1007/s12098-016-2081-7
https://doi.org/10.1007/s12098-016-2081-7
Publikováno v:
International Journal of Medical and Pharmaceutical Case Reports. 5:1-4
Sickle cell disease is a single gene disorder causing a debilitating systemic syndrome characterized by chronic anaemia, acute painful episodes, organ infarction and chronic organ damage and by a significant reduction in life expectancy. Combined sic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84056745ce767bbafcfdc2d511672076
https://doi.org/10.9734/ijmpcr/2015/20027
https://doi.org/10.9734/ijmpcr/2015/20027