Results 61 to 70 of about 3,173 (204)

Utilizzo della tecnologia microchip per l'identificazione di geni candidati responsabili dell'aumento di HbF. [PDF]

open access: yes, 2007
Expression of fetal globin is silenced normally in adult life; however, determinants linked and/or unlinked to the globin-gene clusters could modify Hb F expression so it persists into adults.
Anni, Franco
core   +1 more source

Prefazione [PDF]

open access: yes, 2014
Le politiche sull’ambiente assumono un ruolo fondamentale e sempre più importante, perché possono riuscire a modificare quei comportamenti che, se accompagnati a politiche economiche di sostenibilità, possono permetterci di raggiungere un equilibrio tra ...
ANGELINI, Aurelio, Toro, P.
core  

Fetal hemoglobin inducing factors [PDF]

open access: yes, 2007
Sickle cell anemia is a heterogeneous disorder with variable severity. Initial observations showed that a high level of fetal hemoglobin (HbF) was associated with minor clinical manifestations, as HbF interferes with HbS polymerization.
Figueiredo, Maria Stella [UNIFESP]
core   +3 more sources

Deferiprone versus Deferoxamine in Sickle Cell Disease: Results from a 5-year long-term Italian multi-center randomized clinical trial. [PDF]

open access: yes, 2014
Blood transfusion and iron chelation currently represent a supportive therapy to manage anemia, vasculopathy and vaso-occlusion crises in Sickle-Cell-Disease.
Ballas, Samir K.   +10 more
core   +2 more sources

Por ocasião de um caso de anemia falciforme. [PDF]

open access: yes, 1978
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Tocoginecologia, Curso de Medicina, Florianópolis ...
D'acampora, Armando José
core  

Resultados do estudo do Doppler transcraniano em crianças e adolescentes portadores de doença falciforme e correlação entre a velocidade média máxima e características hematológicas: um estudo transversal analítico [PDF]

open access: yes, 2011
CONTEXT AND OBJECTIVE: Transcranial Doppler (TCD) detects stroke risk among children with sickle cell anemia (SCA). Our aim was to evaluate TCD findings in patients with different sickle cell disease (SCD) genotypes and correlate the time-averaged ...
Braga, Josefina Aparecida Pellegrini   +3 more
core   +2 more sources

Prevalência de hemoglobinopatias na população adulta brasileira: Pesquisa Nacional de Saúde 2014-2015

open access: yesRevista Brasileira de Epidemiologia
RESUMO: Objetivo: Descrever a prevalência das hemoglobinopatias da população adulta brasileira, segundo exames laboratoriais da Pesquisa Nacional de Saúde.
Luiz Gastão Rosenfeld   +7 more
doaj   +1 more source

Hubungan Kekerapan Transfusi Darah dengan Kejadian Kolelitiasis dan Biliary Sludge pada Pasien Talassemia Mayor Anak

open access: yesSari Pediatri, 2016
Latar belakang. Kolelitiasis (batu kandung empedu) merupakan penyakit kandung empedu yang dapat terjadi pada talassemia. Biliary sludge (pelumpuran kandung empedu) merupakan keadaan yang dapat menjadi kolelitiasis.
Dandy Utama Jaya   +2 more
doaj   +1 more source

Hyper-hemolytic transfusional reaction in sickle cell patients: two case reports [PDF]

open access: yes, 2002
The chronic character of sickle cell anemia associated with the greater capacity to liberate oxygen by the Hb S, results in patients exhibiting few symptoms in relation to the anemia and they do not require regular hemacias transfusions. Nevertheless, in
Bordin, Jose Orlando   +4 more
core   +4 more sources

Incidência de anemia ferripriva numa população pediátrica detectada na rotina pré-operatória [PDF]

open access: yes, 2006
O despiste de ferropenia pré operatório numa população pediátrica, pode constituir uma oportunidade para detectar e corrigir estadios deficitários de ferro, susceptíveis de provocar sequelas a médio/longo prazo.
Barbot, José   +5 more
core  

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