Zobrazeno 1 - 10
of 228
pro vyhledávání: '"Thalassaemia intermedia"'
Publikováno v:
International Journal of Anatomy Radiology and Surgery, Vol 7, Iss 4, Pp SC01-SC05 (2018)
Extramedullary Haematopoesis (EMH) is a normal physiologic phenomenon in inadequately transfused patients of chronic severe anaemia due to haemoglobinopathies or myelodysplasia. Although mostly asymptomatic, these haematopoetic cells rests when prese
Externí odkaz:
https://doaj.org/article/21456e497c0c4699bbf8afb6935601e8
Autor:
John Chapin, Alan R. Cohen, Sean Trimble, Patricia J. Giardina, Jeanne Boudreaux, Elliott Vichinsky, Kristy Kenney, Ellis J. Neufeld, Alexis A. Thompson, Binh C. Le
Publikováno v:
British Journal of Haematology. 196:380-389
Thalassaemia is caused by genetic globin defects leading to anaemia, transfusion-dependence and comorbidities. Reduced survival and systemic organ disease affect transfusion-dependent thalassaemia major and thalassaemia intermedia. Recent improvement
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad063c045acb0074a3b8c04cd36c8f94
https://doi.org/10.1111/bjh.17920
https://doi.org/10.1111/bjh.17920
Autor:
Poh Shean Wong, Nor Afidah Binti Karim, Noor Lita Binti Adam, Ee Leng Gan, Lit Sin Yong, See Guan Toh
Publikováno v:
Journal of the ASEAN Federation of Endocrine Societies
Extramedullary hematopoiesis (EMH) is a rare cause of adrenal mass. We present a 44-year-old woman who has thalassaemia intermedia, referred to Endocrinology clinic for huge adrenal mass. Along with a paraspinal lesion discovered in this patient, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de0bdc4d8e62b627485f6f77129be8a6
http://europepmc.org/articles/PMC8214356
http://europepmc.org/articles/PMC8214356
Autor:
Beuy Joob, Viroj Wiwanitkit
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 7, p OL03 (2016)
Externí odkaz:
https://doaj.org/article/b00a38b27f444fa8b2135a489c61be08
Autor:
Vassilios Voudris, Apostolos Armaganidis, Anastasia Anthi, Panagiotis Karyofyllis, Dimitrios Tsiapras, Stylianos E. Orfanos
Publikováno v:
Pulmonary Circulation, Vol 11 (2021)
Pulmonary Circulation
Pulmonary Circulation
Pulmonary hypertension (PH) development remains a significant cardiovascular complication of haemoglobinopathies, severely affecting the morbidity and mortality of such patients. According to the 5th World Symposium on PH, PH related with chronic hae
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a6da88be304252c2c28d49a6b1dab28
https://doaj.org/article/6f5fb2a5236e43e78cdbc3d3abdae78b
https://doaj.org/article/6f5fb2a5236e43e78cdbc3d3abdae78b
Publikováno v:
European Heart Journal: Case Reports
Background Pulmonary hypertension (PH) is a haemodynamic condition, secondary to different causes. Thalassaemia may lead to PH of different origin and needs a comprehensive analysis to be correctly characterized and possibly treated. Case summary We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91fc1d41d756d0567dda1d6fd10b4a73
http://europepmc.org/articles/PMC8207166
http://europepmc.org/articles/PMC8207166
Publikováno v:
International Journal of Clinical and Diagnostic Pathology. 3:296-298
Haemoglobinopathies and thalassemias are inherited conditions, being diagnosed with increasing prevalence in India. An accurate diagnosis of β-thalassemia carriers, homozygous patients, double heterozygous patients and identification of different st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90229ccf3831057e0aff81e3bff19262
https://doi.org/10.33545/pathol.2020.v3.i1e.187
https://doi.org/10.33545/pathol.2020.v3.i1e.187
Autor:
M. Nirmali Wickramarathne, Dimitar G. Efremov, Chris Fisher, David C. Rees, Anuja Premawardhena, David J. Weatherall, Stephen Allen, S. Perera, Ishari Silva, Menaka Hapugoda, Indira Wijesiriwardena, Angela Allen
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-9 (2019)
Scientific Reports
Scientific Reports
β thalassaemia intermedia (βTI) are a heterogeneous group of disorders known to be extremely phenotypically diverse. This group is more complex to manage as no definitive treatment guidelines exist unlike for β thalassaemia major (βTM). There are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9e5cdf4682054463a28f2d6c2a15f95
https://doaj.org/article/6778d9b209994bc0ba59c70f57f95b78
https://doaj.org/article/6778d9b209994bc0ba59c70f57f95b78
Publikováno v:
Current Medical Imaging Formerly Current Medical Imaging Reviews. 17:1177-1178
Finding spurious thrombocytopenia is a common occurrence in clinical practice, whereas pseudothrombocytosis is a very uncommon event. Despite several technical advancements in automated haematology analysers, a careful peripheral smear examination re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4319affaf41709862e9c98066e3c0a68
https://doi.org/10.2174/1573405617666210311112717
https://doi.org/10.2174/1573405617666210311112717
Autor:
Mohammed Q. saadoon, Bushra H. Ali
Publikováno v:
Ibn AL-Haitham Journal For Pure and Applied Sciences. 31:70-78
β-thalassaemia consists of 3 chief forms: thalassaemia primary (other called "cooley's Anaemia" or "Mediterranean durability Anaemia"), thalassaemia intermedia or thalassaemia minor also frequent termed "β-thalassaemia carrier", "β-thalassae
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f75e51bb632ade542c5af42ab5270242
https://doi.org/10.30526/31.3.2013
https://doi.org/10.30526/31.3.2013