Browsing "Comunicações em Eventos - FM/MPE" by Title
Showing results 49 to 68 of 250
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| Issue Date | Title | Author(s) |
|---|---|---|
| 2014 | Complete Transcriptional Network Driven-View of Thymic Hypofunction in Down Syndrome | MOREIRA-FILHO, Carlos Alberto; BANDO, Silvia Yumi; BERTONHA, Fernanda Bernardi; FEREIRA, Leandro Rodrigues; SILVA, Filipi Nascimento; COSTA, Luciano da Fontoura; GRASSI, Marcilia Sierro; CARNEIRO-SAMPAIO, Magda |
| 2019 | Conditions of Vulnerability to Inadequate Treatment of Bronchiolitis | NAVES, Kattia; VIEIRA, Sandra |
| 2022 | Congenital hypothyroidism associated with IPEX Congenital hypothyroidism associated with IPEX Congenital hypothyroidism associated with IPEX Congenital hypothyroidism and IPEX | LIMA, Susana; NUNCIO, Fabio De; BARROS-CAMPOS, Nathalia; MOREIRA-FILHO, Carlos; CARNEIRO-SAMPAIO, Magda |
| 2014 | Cumulative Long-Term Safety, Efficacy and Patient-Reported Outcomes in Children With Juvenile Idiopathic Arthritis Treated With Intravenous Abatacept: Up to 7 Years of Treatment | LOVELL, Daniel J.; RUPERTO, Nicolino; MOUY, Richard; PAZ, Eliana; RUBIO-PEREZ, Nadina; SILVA, Clovis A.; ABUD-MENDOZA, Carlos; BURGOS-VARGAS, Ruben; GERLONI, Valeria; MELO-GOMES, Jose A., et al |
| 2013 | Cytogenomic Diagnosis of Congenital Heart Diseases | KULIKOWSKI, Leslie; ZANARDO, Evelin; DUTRA, Roberta; PIAZZON, Flavia; DIAS, Alexandre; MONTENEGRO, Marilia; NOVO-FILHO, Gil; BASSO, Mariana; COSTA, Thais; NASCIMENTO, Amom, et al |
| 2015 | Cytogenomic investigation in patients with Oculoauriculovertebral Spectrum (OAVS) and candidate loci relevant to phenotype | COLOVATI, Mileny Esbravatti Stephano; BRAGAGNOLO, Silvia; GUILHERME, Roberta Santos; DANTAS, Anelisa Gollo; SOARES, Maria de Fatima; KIM, Chong Ae; PEREZ, Ana Beatriz Alvarez; MELARAGNO, Maria Isabel |
| 2012 | Cytokine profile of healthy preterm and term cord blood and peripheral blood of septic newborns | QUINELLO, C.; SILVEIRA-LESSA, A. L.; CIANCIARULLO, M. A.; REDONDO, A. C. C.; CECCON, M. E. J. R.; CARNEIRO-SAMPAIO, M.; PALMEIRA, P. |
| 2012 | Dendritic-tumor cell hybrids in therapeutic vaccination against advanced neuroblastoma | BERGAMI-SANTOS, P. C.; CRISTOFANI, L.; ODONE-FILHO, V.; BARBUTO, J. A. |
| 2013 | Detection of 22q11.2 Deletion in Infants with Congenital Heart Disease (Preliminary Data) | CARNEIRO-SAMPAIO, M.; GRASSI, M. Sierro; KULIKOWSKI, L. Domenici; JACOB, C. Miuki Abe; DUTRA, R. Lelis; MIURA, N.; CECCON, M. E. Jurfest Rivero; KREBS, V. L. Jornada; CARVALHO, W. Brunow; JATENE, M. |
| 2019 | Development and Initial Validation of the MS Score for Diagnosis of Macrophage Activation Syndrome in Systemic Juvenile Idiopathic Arthritis | MINOIA, Francesca; BOVIS, Francesca; DAVI, Sergio; HORNE, AnnaCarin; FISCHBACH, Michel; FROSCH, Michael; HUBER, Adam; JELUSIC, Marija; SAWHNEY, Sujata; MCCURDY, Deborah, et al |
| 2022 | Diagnostic Power and Clinical Impact of Exome Sequencing in a Cohort of 500 Patients with Rare Diseases | QUAIO, Caio Robledo D. A. C.; MOREIRA, Caroline Monaco; NOVO FILHO, Gil Monteiro; SACRAMENTO-BOBOTIS, Patricia Rossi; PERAZZIO, Sandro Felix; DUTRA, Aurelio Pimenta; PENNA, Michele Groenner; SILVA, Rafael Alves de; RAMALHO, Rodrigo Fernandes; SOUSA, Rafaela Rogerio Floriano de, et al |
| 2021 | Diagnostic power and clinical impact of exome sequencing in a cohort of 500 patients with rare diseases | QUAIO, Caio Robledo; MOREIRA, Caroline Monaco; NOVO FILHO, Gil Monteiro; SACRAMENTO-BOBO, Patricia Rossi; PERAZZIO, Sandro Felix; DUTRA, Aurelio Pimenta; PENNA, Michele Groenner; SILVA, Rafael Alves da; RAMALHO, Rodrigo Fernandes; SOUSA, Rafaela Rogerio Floriano de, et al |
| 2018 | Differential cytogenomic diagnosis in five patients with 8p23.1 deletion suggesting 22q11.2 deletion syndrome | ZANARDO, E. A.; MONTENEGRO, M. M.; SOARES, D. C. Q.; GRASSI, M. S.; NOVO-FILHO, G. M.; MADIA, F. A. R.; NASCIMENTO, A. M.; CHEHIMI, S. N.; DAMASCENO, J. G.; HONJO, R. S., et al |
| 2014 | Difficulties in confirming the diagnosis of mucolipidosis II/III: case reports | LUDWIG, Fernanda S.; CURY, Gabriela K.; VELHO, Renata V.; ALEGRA, Taciane; KIM, Chong A.; MEEL, Eline van; KORNFELD, Stuart; SCHWARTZ, Ida V. D. |
| 2017 | DIFFUSE ALVEOLAR HEMORRHAGE: A MULTICENTER STUDY IN 847 CHILDHOOD-ONSET SYSTEMIC LUPUS ERYTHEMATOSUS PATIENTS | SILVA, C. A.; BLAY, G.; RODRIGUES, J. C.; LEAL, G. N.; FERREIRA, J. C.; NOVAK, G.; PEREIRA, R. M. R.; TERRERI, M. T.; MAGALHAES, C. S.; MOLINARI, B. C., et al |
| 2020 | DIFFUSE LEPTOMENINGEAL DISSEMINATED GLIONEURONAL TUMOR: CASE-SERIES | SANDERS, Felipe Hada; MATUSHITA, Hamilton; AZAMBUJA, Alessandra; FRASSETO, Fernando; ROSEMBERG, Sergio; ODONE, Vicente; TEIXEIRA, Manoel Jacobsen |
| 2015 | Digital vasculitis survey in 852 childhood-onset systemic lupus erythematosus patients: a multicenter cohort study | SAKAMOTO, A. P.; SILVA, C. A.; SILVA, M. F. C.; LOPES, A. S.; FRAGA, M. M.; BONFA, E.; MAGALHAES, C. S.; PEREIRA, R. M. R.; LEN, C. A.; TERRERI, M. T. |
| 2021 | Discovering Resources Beyond the Standard of Care - Impact of an integrative care program for children with cancer in Brazil | MARC, Troendle; WIEBKE, Stritter; VICENTE, Odone; KARINA, Peron; RICARDO, Ghelman; GEORG, Seifert |
| 2021 | Discovering Resources Beyond the Standard of Care - Impact of an integrative care program for children with cancer in Brazil | MARC, Troendle; WIEBKE, Stritter; VICENTE, Odone; KARINA, Peron; RICARDO, Ghelman; GEORG, Seifert |
| 2019 | DISEASE PRESENTATION OF 1,312 CHILDHOOD-ONSET SYSTEMIC LUPUS ERYTHEMATOSUS: INFLUENCE OF ETHNICITY | CAMPOS, Lucia; FIOROT, Fernanda; ISLABAO, Aline G.; PEREIRA, Rosa M.; TERERRI, Maria T.; SAAD-MAGALHAES, Claudia; NOVAK, Glaucia V.; MOLINARI, Beatriz; SAKAMOTO, Ana Paula; AIKAWA, Nadia, et al |