Hereditary Spherocytosis due to an SPTA1 Nonsense Mutation Coinherited With α spectrin<sup>LELY</sup> in Trans. [PDF]
Am J HematolAmerican Journal of Hematology, Volume 100, Issue 12, Page 2355-2356, December 2025.
Molina-Arrebola MA, Bain BJ.
europepmc +2 more sources
Rare onset of congenital thrombotic thrombocytopenic purpura during pregnancy: A novel ADAMTS13 gene variant. [PDF]
TransfusionAbstract Background Congenital thrombotic thrombocytopenic purpura (cTTP) is a rare autosomal recessive thrombotic microangiopathy caused by biallelic mutations in ADAMTS13, leading to severe enzyme deficiency. The absence of ADAMTS13 prevents cleavage of ultra‐large von Willebrand factor multimers, resulting in platelet‐rich microthrombi formation ...
González-Resina R +6 more
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Revista Brasileira de Hematologia e Hemoterapia, 2007 Os riscos envolvidos na transfusão de sangue e hemoderivados podem ser conseqüentes de procedimentos inadequados, erros ou omissões dos profissionais responsáveis pela transfusão.
Oranice Ferreira +3 more
doaj +1 more source
Differential diagnosis of iron deficiency [PDF]
, 2010 Iron deficiency is considered to be the commonest hematological pathology in humans. Thus, the essential steps in an adequate approach of iron deficiency include: the proper identification of its causes and the differentiation between iron deficiency and
Figueiredo, Maria Stella, Vicari, Perla
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Hereditary Elliptocytosis Resulting From Heterozygosity for β Spectrin Tandil. [PDF]
Am J HematolAmerican Journal of Hematology, Volume 100, Issue 9, Page 1629-1630, September 2025.
Molina-Arrebola MA, Bain BJ.
europepmc +2 more sources
Not All Hereditary Iron Overload Is Hemochromatosis: A Case of Hereditary Xerocytosis Unmasked by Blood Smear Morphology. [PDF]
Am J HematolAmerican Journal of Hematology, Volume 100, Issue 11, Page 2091-2092, November 2025.
Molina-Arrebola MA, Bain BJ.
europepmc +2 more sources
Hemoterapia e febre Dengue [PDF]
Revista Brasileira de Hematologia e Hemoterapia, 2008 Dengue is an endemic/epidemic arboviral disease with a variable symptomatic benign course, but potentially fatal. Once in an inhabited area, the disease will exist forever, with the best achievement being to keep vectors suppressed and the disease under control.
openaire +3 more sources
Guidelines on the treatment of primary immune thrombocytopenia in children and adolescents: Associacao Brasileira de Hematologia, Hemoterapia e Terapia Celular Guidelines Project: Associacao Medica Brasileira - 2012 [PDF]
, 2013 Centro de Hematologia de São PauloUniversidade Federal de São Paulo (UNIFESP) Escola Paulista de MedicinaCentro Infantil BoldriniUniversidade de São Paulo Faculdade de MedicinaAssociacao Medica BrasileiraHospital Ana CostaCentro de Hematologia e ...
Bernardo, Wanderley Marques +5 more
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Análise do perfil de Rh e Kell em doadores de sangue em Porto Alegre, Rio Grande do Sul
Clinical and Biomedical Research, 2022 Introdução: A hemoterapia é uma prática terapêutica pelo meio de transfusão sanguínea. Devido ao baixo estoque de bolsas de sangue e o aumento de pacientes crônicos e emergenciais, se faz necessária a realização de testes imuno-hematológicos para ...
Vanessa D’Avila Siqueira Siqueira +2 more
doaj
Functional and molecular characterization of inherited platelet disorders in the Iberian Peninsula: results from a collaborative study [PDF]
, 2014 BACKGROUND: The diagnostic evaluation of inherited platelet disorders (IPDs) is complicated and time-consuming, resulting in a relevant number of undiagnosed and incorrectly classified patients.
Antón, AI +12 more
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