Results 111 to 120 of about 357 (169)

Talassemias

, 2017
Thalassemias are genetic disorders of hemoglobin production. Individuals with heterozygous state, known as carriers donot present health problems. However, some carriers may experience mild anemia.
Fabron Junior, Antonio
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International dissemination of Brazil's public health system and its technical cooperation initiatives for sickle cell disease, 2006-2010. [PDF]

Hist Cienc Saude Manguinhos
Cavalcanti JM.
europepmc   +1 more source

REAÇÃO ADVERSA NO TRATAMENTO DA TALASSEMIA MAJOR. [PDF]

Blucher Medical Proceedings, 2020
Roberto Kenji Nakamura Cuman, Ricardo Alexandre Spironello   +1 more
openaire   +1 more source

Position Statement on Multimodal Cardiac Imaging in Patients with Systemic Diseases - 2026. [PDF]

Arq Bras Cardiol
Hotta VT, Costa IBSDS, Felix RCM, Bosco MEO, Romano MMD, Santorio NC, Brandão SCS, Frota DDCR, Lianza AC, Santos SND, Melo MDT, Rodrigues ACT, Fialho GL, Sawamura KSS, Alves MSL, Mattoso AAA, Mesquita CT, Mancuso FJN, Garcia MI, Pena JLB, Beck ALS, Soares AM, Silva SME, Torreão JA, Schvartzman PR, Fernandes F, Rochitte CE, Barberato SH.   +27 more
europepmc   +1 more source

Differential diagnosis of microcytic and hypochromic anemia

, 2011
The microcytic and hypochromic anemia are the results of several pathologic conditions. They are the most prevalent forms of anemia in the Brazilian population , and frequently the clinical diagnosis depends on the laboratorial analysis. In many cases it
Naoum, Paulo Cesar [UNESP]
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Hemoglobinopatias e talassemias: as tecnologias de identificação devem ser ampliadas em neonatos? Hemoglobinopathies and thalassemia: should identification technology be amplified for neonates?

Revista Brasileira de Hematologia e Hemoterapia, 2008
Paulo Cesar Naoum
doaj   +1 more source

Cardiovascular Computed Tomography and Magnetic Resonance Imaging Guideline of the Brazilian Society of Cardiology and the Brazilian College of Radiology - 2024. [PDF]

Arq Bras Cardiol
Magalhães TA, Carneiro ACC, Moreira VM, Trad HS, Lopes MMU, Cerci RJ, Nacif MS, Schvartzman PR, Chagas ACP, Costa IBSDS, Schmidt A, Shiozaki AA, Montenegro ST, Piegas LS, Zapparoli M, Nicolau JC, Fernandes F, Hadlich MS, Ghorayeb N, Mesquita ET, Gonçalves LFG, Ramires FJA, Fernandes JL, Schwartzmann PV, Rassi S, Torreão JA, Mateos JCP, Beck-da-Silva L, Silva MC, Liberato G, Oliveira GMM, Feitosa Filho GS, Carvalho HDSM, Markman Filho B, Rocha RPS, Azevedo Filho CF, Taratsoutchi F, Coelho-Filho OR, Kalil Filho R, Hajjar LA, Ishikawa WY, Melo CA, Jatene IB, Albuquerque AS, Rimkus CM, Silva PSDD, Vieira TDR, Jatene FB, Azevedo GSAA, Santos RD, Monte GU, Ramires JAF, Bittencourt MS, Avezum A, Silva LSD, Abizaid A, Gottlieb I, Precoma DB, Szarf G, Sousa ACS, Pinto IMF, Medeiros FM, Caramelli B, Parga Filho JR, Santos TSGD, Prazeres CEED, Lopes MACQ, Avila LFR, Scanavacca MI, Gowdak LHW, Barberato SH, Nomura CH, Rochitte CE.   +72 more
europepmc   +1 more source

Programa preventivo de hemoglobinopatias em diferentes grupos populacionais de São José do Rio Preto-SP

, 2001
O programa de investigação populacional denominado "Você tem anemia hereditária?", iniciado em 1983, tem o objetivo de identificar variantes de hemoglobinas e talassemias em diferentes grupos populacionais de São José do Rio Preto, conscientizar os ...
Naoum, Paulo Cesar
core  

Estudo da membrana eritrocitaria em Beta Talassemia heterozigota

, 2018
Orientador: Nilce Correa MeirellesTese (doutorado) - Universidade Estadual de Campinas, Instituto de BiologiaResumo: 'beta¿ talassemia é uma desordem genética caracterizada pela redução ou ausência de produção da cadeia 'beta¿ da globina.
Stella, Mercia Breda
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