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PreviewIssue DateTitleAuthor(s)AdvisorType
2009International Society of Blood Transfusion Committee on Terminology for Red Blood Cell Surface Antigens: Macao reportDaniels, G; Castilho, L; Flegel, WA; Fletcher, A; Garratty, G; Levene, C; Lomas-Francis, C; Moulds, JM; Moulds, JJ; Olsson, ML; Overbeeke, M; Poole, J; Reid, ME; Rouger, P; van der Schoot, E; Scott, M; Sistonen, P; Smart, E; Storry, JR; Tani, Y; Yu, LC; Wendel, S; Westhoff, C; Yahalom, V; Zelinski, T-Artigo de periódico
2004Febrile seizures and mesial temporal sclerosisCendes, F-Artigo de periódico
2010Family-based association study for bipolar affective disorderSecolin, R; Banzato, CEM; Oliveira, MCM; Bittar, MFR; Santos, ML; Dalgalarrondo, P; Lopes-Cendes, I-Artigo de periódico
2008Family history of cancer in Brazil: is it being used?Viana, DV; Goes, JRN; Coy, CSR; Ayrizono, MDS; Lima, CSP; Lopes-Cendes, I-Artigo de periódico
2010Leber's hereditary optic neuropathy: Clinical and molecular profile of a Brazilian sampleMaciel-Guerra, AT; Zanchetta, LM; Fernandes, MSA; Andrade, PB; Miranda, PMDD; Sartorato, EL-Artigo de periódico
2013Refinement of chromosome 3p22.3 region and identification of a susceptibility gene for bipolar affective disorderSecolin, R; Banzato, CEM; Mella, LFB; Santos, ML; Dalgalarrondo, P; Lopes-Cendes, I-Artigo de periódico
2013A new beta(0)-thalassemia frameshift mutation [beta 48 (-T)] in a Uruguayan familyDa Luz, J; Lopez, P; Kimura, EM; Albuquerque, DM; Costa, FF; Sans, M; Sonati, MF-Artigo de periódico
1-Sep-2008Estudos genéticos e moleculares em um grande grupo de pacientes com malformações do córtex cerebralTorres, Fábio Rossi; Souza-Kols, Daniela Aguiar de; Tsuneda, Simone Sayuri; Secolin, Rodrigo; Almeida, Iara Leda Brandão de; Lopes, Camila Fernanda; Rodrigues, Maria do Carmo Sousa; Montenegro, Maria Augusta; Marques-de-Faria, Antonia Paula; Guerreiro, Marilisa Mantovani; Llerena Jr, Juan Clinton; Cendes, Fernando; Lopes-Cendes, Iscia-Artigo de periódico
1-Mar-2014Clinical features and management of hereditary spastic paraplegiaFaber, Ingrid; Servelhere, Katiane R.; Martinez, Alberto R. M.; D?Abreu, Anelyssa; Lopes-Cendes, Iscia; França Jr, Marcondes C.-Artigo de periódico
1-Mar-2007Linkage study of voltage-gated potassium channels in familial mesial temporal lobe epilepsyMaurer-Morelli, Cláudia Vianna; Marchesini, Rafael Breglio; Secolin, Rodrigo; Santos, Neide Ferreira; Kobayashi, Eliane; Cendes, Fernando; Lopes-Cendes, Iscia-Artigo de periódico
2000Angiotensin-converting enzyme and apolipoproteins genes polymorphism in coronary artery diseaseMansur, AP; Annicchino-Bizzacchi, J; Favarato, D; Avakian, SD; Cesar, LAM; Ramires, JAF-Artigo de periódico
1-Jan-2009Respostas ao adoecimento: mecanismos de defesa utilizados por mulheres com síndrome de Turner e variantesChvatal, Vera Lúcia Soares; Böttcher-Luiz, Fátima; Turato, Egberto Ribeiro-Artigo de periódico
1-Jan-2009Responses to falling lll: defense mechanisms used by women with Turner syndrome and variantsChvatal, Vera Lúcia Soares; Böttcher-Luiz, Fátima; Turato, Egberto Ribeiro-Artigo de periódico
2006THE SCN2A gene is not a likely candidate for familial mesial temporal lobe epilepsyMaurer-Morelli, CV; Secolin, R; Marchesini, RB; Santos, NF; Kobayashi, E; Cendes, F; Lopes-Cendes, I-Artigo de periódico
2009Responses to falling ill: defense mechanisms used by women with Turner syndrome and variantsChvatal, VLS; Bottcher-Luiz, F; Turato, ER-Artigo de periódico
1-Oct-2008Interação entre audiologia e genética no estudo de uma família: a complexidade do diagnóstico molecular e do aconselhamento genéticoHoffmann, Flavia Maria Rodrigues; Rodrigues, Patrícia Fernandes; Santos, Teresa Maria Momensohn dos; Sartorato, Edi Lucia; Maciel-Guerra, Andréa Trevas; Matas, Carla Gentile; de Moraes, Vanessa Cristine Sousa-Artigo de periódico
2012Hereditary Autoinflammatory Syndromes: A Brazilian Multicenter StudyJesus, Adriana A.; Fujihira, Erika; Watase, Mariana; Terreri, Maria T.; Hilario, Maria O.; Carneiro-Sampaio, Magda; Len, Claudio A.; Oliveira, Sheila K.; Rodrigues, Marta C.; Pereira, Rosa M.; Bica, Blanca; Silva, Nilzio A.; Cavalcanti, Andre; Marini, Roberto; Sztajnbok, Flavio; Quintero, Maria V.; Ferriani, Virginia P.; Moraes-Vasconcelos, Dewton; Silva, Clovis A.; Oliveira, Joao B.-Artigo de periódico
2009Glu298Asp eNOS gene polymorphism causes attenuation in nonexercising muscle vasodilatationDIAS, Rodrigo G.; ALVES, Maria-Janieire N. N.; PEREIRA, Alexandre C.; RONDON, Maria Urbana P. B.; SANTOS, Marcelo R. dos; KRIEGER, Jose E.; KRIEGER, Marta H.; NEGRAO, Carlos E.-Artigo de periódico
2006AtALMT1, which encodes a malate transporter, is identified as one of several genes critical for aluminum tolerance in ArabidopsisHoekenga, OA; Maron, LG; Pineros, MA; Cancado, GMA; Shaff, J; Kobayashi, Y; Ryan, PR; Dong, B; Delhaize, E; Sasaki, T; Matsumoto, H; Yamamoto, Y; Koyama, H; Kochian, LV-Artigo de periódico
1-Sep-2001The G209A mutation in the alpha-synuclein gene in Brazilian families with Parkinson's diseaseTeive, Hélio A.G.; Raskin, Salmo; Iwamoto, Fábio M.; Germiniani, Francisco M.B.; Baran, Maria H.H.; Werneck, Lineu C.; Allan, Nasser; Quagliato, Elizabeth; Leroy, Elisabeth; Ide, Susan E.; Polymeropoulos, Mihael H.-Artigo de periódico