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Results 1-10 of 45 (Search time: 0.023 seconds).
Issue DateTitleAuthor(s)
2019Associations between fetal testosterone and pro-social tendencies, anxiety and autistic symptoms in Williams syndrome: a preliminary studyOSORIO, Ana Alexandra Caldas; EGITO, Julia Horta Tabosa do; MARTINS, Gabriela Carneiro; KIM, Chong Ae; HONJO, Rachel Sayuri; SAMPAIO, Adriana da Conceicao Soares; MESQUITA, Ana Raquel Marcelino; MACEDO, Elizeu Coutinho; BOGGIO, Paulo Sergio; TEIXEIRA, Maria Cristina Triguero Veloz
2019Validation of PNPLA3 polymorphisms as risk factor for NAFLD and liver fibrosis in an admixed populationMAZO, Daniel F.; MALTA, Fernanda M.; STEFANO, Jose Tadeu; SALLES, Ana Paula M.; GOMES-GOUVEA, Michele S.; NASTRI, Ana Catharina S.; ALMEIDA, Jazon R.; PINHO, Joao Renato R.; CARRILHO, Flair J.; OLIVEIRA, Claudia P.
2019Genetic and virulence characterization of colistin-resistant and colistin-sensitive A. baumannii clinical isolatesLEITE, Gleice Cristina; STABLER, Richard A.; NEVES, Patricia; PERDIGAO NETO, Lauro V.; MARTINS, Roberta C. Ruedas; RIZEK, Camila; ROSSI, Flavia; LEVIN, Anna S.; COSTA, Silvia Figueiredo
2019Tuberculous pleural effusion: diagnosis & managementANTONANGELO, Leila; FARIA, Caroline S.; SALES, Roberta K.
2019Reply to ""Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0""MENDONCA, Rodrigo H.; ROCHA, Antonio J.; LOZANO-ARANGO, Andres; DIAZ, Astry B.; CASTIGLIONI, Claudia; SILVA, Andre M. S.; REED, Umbertina C.; KULIKOWSKI, Leslie; PARAMONOV, Ida; CUSCO, Ivon; TIZZANO, Eduardo F.; ZANOTELI, Edmar
2019Comprehensive genetic analysis of 57 families with clinically suspected Cornelia de Lange syndromeAOI, Hiromi; MIZUGUCHI, Takeshi; CERONI, Jose Ricard; KIM, Veronica Eun Hue; FURQUIM, Isabel; HONJO, Rachel S.; IWAKI, Takuma; SUZUKI, Toshifumi; SEKIGUCHI, Futoshi; UCHIYAMA, Yuri; AZUMA, Yoshiteru; HAMANAKA, Kohei; KOSHIMIZU, Eriko; MIYATAKE, Satoko; MITSUHASHI, Satomi; TAKATA, Atsushi; MIYAKE, Noriko; TAKEDA, Satoru; ITAKURA, Atsuo; BERTOLA, Debora R.; KIM, Chong Ae; MATSUMOTO, Naomichi
2019Autosomal-Recessive Mutations in MESD Cause Osteogenesis ImperfectaMOOSA, Shahida; YAMAMOTO, Guilherme L.; GARBES, Lutz; KEUPP, Katharina; BELEZA-MEIRELES, Ana; MORENO, Carolina Araujo; VALADARES, Eugenia Ribeiro; SOUSA, Sergio B. de; MAIA, Sofia; SARAIVA, Jorge; HONJO, Rachel S.; KIM, Chong Ae; MENEZES, Hamilton Cabral de; LAUSCH, Ekkehart; LORINI, Pablo Villavicencio; LAMOUNIER JR., Arsonval; CARNIERO, Tulio Canella Bezerra; GIUNTA, Cecilia; ROHRBACH, Marianne; JANNER, Marco; SEMLER, Oliver; BELEGGIA, Filippo; LI, Yun; YIGIT, Goekhan; REINTJES, Nadine; ALTMUELLER, Janine; NUERNBERG, Peter; CAVALCANTI, Denise P.; ZABEL, Bernhard; WARMAN, Matthew L.; BERTOLA, Debora R.; WOLLNIK, Bernd; NETZER, Christian
2019Prevalence and genotyping of hepatitis B virus: a cross-sectional study conducted with female sex workers in the Marajo Archipelago, BrazilFRADE, Paula C. R.; RAIOL, Nairis C.; COSTA, Luana M. da; PINHEIRO, Luiz M. L.; SILVA-OLIVEIRA, Glaucia C.; PINHO, Joao R. R.; LEMOS, Jose A. R.; MARTINS, Luisa C.; OLIVEIRA-FILHO, Aldemir B.
2019Impact of Growth Hormone Therapy on Adult Height in Patients with PTPN11 Mutations Related to Noonan SyndromeMALAQUIAS, Alexsandra C.; NORONHA, Renata M.; SOUZA, Thaiana T. O.; HOMMA, Thais K.; FUNARI, Mariana F. A.; YAMAMOTO, Guilherme L.; SILVA, Fernanda Viana; MORAES, Michelle B.; HONJO, Rachel S.; KIM, Chong A.; NESI-FRANCA, Suzana; CARVALHO, Julienne A. R.; QUEDAS, Elisangela P. S.; BERTOLA, Debora R.; JORGE, Alexander A. L.
2019Estimating HIV-1 Genetic Diversity in Brazil Through Next-Generation SequencingALVES, Brunna M.; SIQUEIRA, Juliana D.; PRELLWITZ, Isabel M.; BOTELHO, Ornella M.; HORA, Vanusa P. Da; SANABANI, Sabri; RECORDON-PINSON, Patricia; FLEURY, Herve; SOARES, Esmeralda A.; SOARES, Marcelo A.