Zobrazeno 1 - 10
of 256
pro vyhledávání: '"thalassemia beta"'
Publikováno v:
Jurnal Kedokteran dan Kesehatan, Vol 8, Iss 2, Pp 111-120 (2021)
Berdasarkan data dari World Health Organization (WHO) tahun 2001, terdapat 7% populasi di seluruh dunia yang merupakan karier thalassemia atau penderita thalassemia minor. Di Indonesia, frekuensinya pun cukup tinggi yaitu 3-10%. Pada thalassemia beta
Externí odkaz:
https://doaj.org/article/e2f6b136b496453dbdfceabf0b8f4ba4
Publikováno v:
Clinical Case Reports, Vol 9, Iss 2, Pp 861-865 (2021)
Abstract To optimize care for patients with hemoglobinopathies, frequent screening for COVID‐19 is prudent as viral kinetics in asplenic patients are unknown and differentiating prolonged viral shedding versus reinfection remains a challenge.
Externí odkaz:
https://doaj.org/article/d2f4784900794d96847e94fcc0093ba6
Publikováno v:
Clinical Case Reports, Vol 8, Iss 12, Pp 2917-2921 (2020)
Abstract Although the possibility of asymptomatic course for COVID‐19 infection in splenectomized thalassemia beta major patients is present, screening them for COVID‐19 is important as the progression is still not clear.
Externí odkaz:
https://doaj.org/article/8c60ee9c64e04207bf6db2cb7cee6bd8
Autor:
Nelly Rosdiana, Christian Nasir
Publikováno v:
Sari Pediatri, Vol 21, Iss 1, Pp 31-6 (2019)
Latar belakang. Komplikasi dari thalassemia beta mayor disebabkan akumulasi zat besi yang diukur melalui pemeriksaan feritin. Penyandang thalassemia beta mayor juga mengalami gangguan profil lipid akibat kelebihan zat besi. Namun, penelitian mengenai
Externí odkaz:
https://doaj.org/article/d177d24722ee4633afcca67d9fc30f61
Pregnancy Outcomes in Women with Homozygous Beta Thalassaemia : A single-centre experience from Oman
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 14, Iss 3, Pp 337-341 (2014)
Objectives: Pregnancy in women with homozygous beta thalassaemia (HBT) carries a high risk to both the mother and fetus. The aim of this study was to investigate pregnancy outcomes among this group at a single tertiary centre. Methods: This retrospec
Externí odkaz:
https://doaj.org/article/44ce0b3f62c547f4801ddbd14276d04e
Publikováno v:
Clinical Case Reports, Vol 9, Iss 2, Pp 861-865 (2021)
Clinical Case Reports
Clinical Case Reports
To optimize care for patients with hemoglobinopathies, frequent screening for COVID‐19 is prudent as viral kinetics in asplenic patients are unknown and differentiating prolonged viral shedding versus reinfection remains a challenge.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::4927a27c68eebb8a025f00ecc5f737d8
https://doaj.org/article/d2f4784900794d96847e94fcc0093ba6
https://doaj.org/article/d2f4784900794d96847e94fcc0093ba6
Autor:
Ivan L. Angulo, Sandra B. R. Picado
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 31, Iss 6, Pp 408-412 (2009)
A hemoglobina C (Hb C) é originária do oeste da África e é detectada por migração lenta na eletroforese alcalina em acetato de celulose. Consiste na mutação do gene da globina beta no códon 6 (GAG-AAG), resultando na substituição do sexto
Externí odkaz:
https://doaj.org/article/c6e1f83b796e4746b1197cef500a69d0
Publikováno v:
Journal of Musculoskeletal & Neuronal Interactions
Avascular necrosis (AVNFH) of the femoral head is a relatively rare condition linked with numerous causes. If not treated promptly then arthritis may be inevitable, making hip replacement the only treatment option. In this case report we present a yo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c4a32885f24dd5e111e08a1cc1b99609
http://europepmc.org/articles/PMC6737561
http://europepmc.org/articles/PMC6737561
Autor:
Aldo Filosa, Paolo Ricchi
Publikováno v:
Clinical Case Reports
Although the possibility of asymptomatic course for COVID‐19 infection in splenectomized thalassemia beta major patients is present, screening them for COVID‐19 is important as the progression is still not clear.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a00d48f66cf198d9557b984d6aad39b
https://pubmed.ncbi.nlm.nih.gov/33363851
https://pubmed.ncbi.nlm.nih.gov/33363851
Publikováno v:
Hemoglobin, 44(3), 214-217. TAYLOR & FRANCIS LTD
A woman completely lacking Hb A(2)on the high performance liquid chromatography (HPLC) analysis, presented with a novel deletional (epsilon gamma)delta beta(0)-thal and a delta-globin gene variant. This combination causes a beta-thalassemia (beta-tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b5f92ab0afceb7a752a902ab3241c585
http://hdl.handle.net/1887/3184789
http://hdl.handle.net/1887/3184789
