Results 101 to 110 of about 904,909 (193)
Alterazioni del metabolismo osseo nel bambino con ß-talassemia major
La ß-talassemia major è una anemia ereditaria trasfusione-dipendente, causata da mutazioni puntiformi del gene ß-globinico, che determinano una completa o quasi completa assenza della sintesi delle catene ß-globiniche.
Antonucci, Roberto, Vacca, Nadia
core
Phi Beta Kappa: The Key Reporter Winter 2012-2013
Announcement of the Beta of Nebraska chapter installation at Creighton University, p.
Phi Beta Kappa Society
core
Sickle cell disease is a generic term used to determine a group of genetic alterations characterized by a dominance of Hb S. The main genotypes which compose the sickle cell disease group are as follows: SS, SF (S/beta0 thalassemia and S/Hereditary ...
Souza, Patricia Caetano de +1 more
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Hemoglobinopathies are a heterogeneous group of genetic disorders which represent a public health problem, with significant morbidity, in countries where the prevalence is high.
Paula J. A. Zamaro +1 more
doaj
Effects of Sirolimus Treatment on Fetal Hemoglobin Production and Response to SARS-CoV-2 Vaccination: A Case Report Study. [PDF]
Gamberini MR +5 more
europepmc +1 more source
Phi Beta Kappa Minutes, December 5, 1776-January 6,1781 [PDF]
Ledger of the Phi Beta Kappa minutes of meetings from December 5, 1776-January 6, 1781. These are the earliest meetings of Phi Beta Kappa.
Phi Beta Kappa
core
Foi investigada a viabilidade da aplicação da técnica de fluorescência de raios X (XRF) como alternativa para acompanhamento dos níveis de ferro em pacientes portadores de talassemia maior (beta-thalassemia) e hemocromatose hereditária (HH).
Marcelo Estevam, Carlos R. Appoloni
doaj
Impact of the COVID-19 Pandemic on Iron Overload Assessment by MRI in Patients with Hemoglobinopathies: The E-MIOT Network Experience. [PDF]
Meloni A +19 more
europepmc +1 more source
Orthodontic and Craniofacial Skeletal Alterations in Individuals With Thalassemia: A Scoping Review. [PDF]
da Silva LC +8 more
europepmc +1 more source

