Browsing "Artigos e Materiais de Revistas Científicas - FM/MPE" by Title

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Showing results 861 to 880 of 1092 < previous   next >
Issue DateTitleAuthor(s)
2012Radiologia pediátrica: quando o diagnóstico deve ser ""amigo"" da criançaVALENTE, Marcelo; OLIVEIRA, Luiz Antonio Nunes de; CARNEIRO-SAMPAIO, Magda
2016Randomized controlled trial comparing nasal intermittent positive pressure ventilation and nasal continuous positive airway pressure in premature infants after tracheal extubationKOMATSU, Daniela Franco Rizzo; DINIZ, Edna Maria De Albuquerque; FERRARO, Alexandre Archanjo; CECCON, Maria Esther Jurvest Rivero; VAZ, Flavio Adolfo Costa
2021A randomized controlled trial testing the efficacy of a Nurse Home Visiting Program for Pregnant AdolescentsFATORI, Daniel; ZUCCOLO, Pedro Fonseca; SHEPHARD, Elizabeth; BRENTANI, Helena; MATIJASEVICH, Alicia; FERRARO, Alexandre Archanjo; FRACOLLI, Lislaine Aparecida; CHIESA, Anna Maria; LECKMAN, James; MIGUEL, Euripedes Constantino, et al
2015Randomized, Double-Blind, Dose-Escalation Trial of Triptorelin for Ovary Protection in Childhood-Onset Systemic Lupus ErythematosusBRUNNER, Hermine I.; SILVA, Clovis A.; REIFF, Andreas; HIGGINS, Gloria C.; IMUNDO, Lisa; WILLIAMS, Calvin B.; WALLACE, Carol A.; AIKAWA, Nadia E.; NELSON, Shannen; KLEIN-GITELMAN, Marisa S., et al
2017Rapid antigen detection test for respiratory syncytial virus diagnosis as a diagnostic toolMESQUITA, Flavio da Silva; OLIVEIRA, Danielle Bruna Leal de; CREMA, Daniela; PINEZ, Celia Miranda Nunes; COLMANETTI, Thais Cristina; THOMAZELLI, Luciano Matsumia; GILIO, Alfredo Elias; VIEIRA, Sandra Elisabeth; MARTINEZ, Marina Baquerizo; BOTOSSO, Viviane Fongaro, et al
2022A rare association between factor H deficiency and lupus: Case report and experimental treatment with curcuminMACEDO, Ana Catarina Lunz; LORES, Lazara Elena Santisteban; ALBUQUERQUE, Jose Antonio Tavares; DUARTE, Nilo Jose Coelho; ROMANO, Paschoalina; EBNER, Persio Almeida Rezende; REZENDE, Vinicius Marcondes; SILVA, Clovis A. A.; ANDRADE, Luis Eduardo Coelho; VASCONCELOS, Dewton Moraes, et al
2023A rare case of hepatoblastoma in a syndromic child with a de novo germline JAG1 mutationDANGONI, Gustavo Dib; TEIXEIRA, Anne Caroline Barbosa; AGUIAR, Talita Ferreira; SUGAYAMA, Sofia Mizuho Miura; FILHO, Vicente Odone; BERTOLA, Debora Romeo; KREPISCHI, Ana Cristina Victorino
2015Rare Genomic Rearrangement in a Boy with Williams-Beuren Syndrome Associated to XYY Syndrome and Intriguing BehaviorDUTRA, Roberta L.; PIAZZON, Flavia B.; ZANARDO, Evelin A.; COSTA, Thais Virginia Moura Machado; MONTENEGRO, Marilia M.; NOVO-FILHO, Gil M.; DIAS, Alexandre T.; NASCIMENTO, Amom M.; KIM, Chong Ae; KULIKOWSKI, Leslie D.
2015Rare variants in SOS2 and LZTR1 are associated with Noonan syndromeYAMAMOTO, Guilherme Lopes; AGUENA, Meire; GOS, Monika; HUNG, Christina; PILCH, Jacek; FAHIMINIYA, Somayyeh; ABRAMOWICZ, Anna; CRISTIAN, Ingrid; BUSCARILLI, Michelle; NASLAVSKY, Michel Satya, et al
2017Rastreamento da infecção latente por tuberculose em pacientes com artrite idiopática juvenil previamente à terapia anti-TNF em um país de alto risco para tuberculoseBRUNELLI, Juliana Barbosa; BONFIGLIOLI, Karina Rossi; SILVA, Clovis A.; KOZU, Katia Tomie; GOLDENSTEIN-SCHAINBERG, Claudia; BONFA, Eloisa; AIKAWA, Nadia Emi
2024Reassessing the role of milrinone in the treatment of heart failure and pulmonary hypertension in neonates and children: a systematic review and meta-analysisMATSUSHITA, Felipe Yu; KREBS, Vera Lucia Jornada; CAMPOS, Carolina Vieira de; GAIOLLA, Paula Vieira de Vincenzi; CARVALHO, Werther Brunow de
2019Recommendations for Assessment and Management of Health-Related Quality of Life in Patients with Mucopolysaccharidoses in Latin AmericaGIUGLIANI, Roberto; FAINBOIM, Alejandro; KIM, Chong Ae; HOROVITZ, Dafne Dain Gandelman; SAKATA, Edna Tiemi; DAMIANO, Ana Paula; MAGALHÃES, Tatiana Sá Pacheco Carneiro; VILLAREAL, Martha Solano
2015Recurrence of Frontometaphyseal Dysplasia in Two Sisters With a Mutation in FLNA and an Atypical Paternal Phenotype: Insights Into Genotype-Phenotype CorrelationBERTOLA, Debora; PASSOS-BUENO, Maria Rita; PEREIRA, Alexandre; KIM, Chong; MORGAN, Tim; ROBERTSON, Stephen P.
2018Recurrent Copy Number Variants Associated with Syndromic Short Stature of Unknown CauseHOMMA, Thais K.; KREPISCHI, Ana C. V.; FURUYA, Tatiane K.; HONJO, Rachel S.; MALAQUIAS, Alexsandra C.; BERTOLA, Debora R.; COSTA, Silvia S.; CANTON, Ana P.; ROELA, Rosimeire A.; FREIRE, Bruna L., et al
2022The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestryALI, Taccyanna M.; LINNENKAMP, Bianca D. W.; YAMAMOTO, Guilherme L.; HONJO, Rachel S.; MENEZES FILHO, Hamilton Cabral de; KIM, Chong Ae; BERTOLA, Debora R.
2016Reduced Aerobic Capacity and Quality of Life in Physically Inactive Patients With Systemic Lupus Erythematosus With Mild or Inactive DiseasePINTO, Ana J.; MIYAKE, Cintia N. H.; BENATTI, Fabiana B.; SILVA, Clovis A.; SALLUM, Adriana M. E.; BORBA, Eduardo; SA-PINTO, Ana L. de; BONFA, Eloisa; GUALANO, Bruno
2015Reduced ovarian reserve in patients with adult polymyositisSOUZA, Fernando Henrique Carlos de; SILVA, Clovis Artur da; YAMAKAMI, Lucas Yugo Shiguehara; VIANA, Vilma dos Santos Trindade; BONFA, Eloisa; SHINJO, Samuel Katsuyuki
2014Reduced Ovarian Reserve in Patients with Takayasu ArteritisMONT'ALVERNE, Andrea Rocha S.; PEREIRA, Rosa Maria R.; YAMAKAMI, Lucas Yugo S.; VIANA, Vilma Santos T.; BARACAT, Edmund Chada; BONFA, Eloisa; SILVA, Clovis Artur
2015Reducing Unplanned Extubations in the Pediatric ICU: Are We Seeing the Whole Picture?SILVA, Paulo Sergio Lucas da; CARVALHO, Werther Brunow de; FONSECA, Marcelo Cunio Machado
2015Reduction of ovarian reserve in adult patients with dermatomyositisSOUZA, F. H. C. de; SHINJO, S. K.; YAMAKAMI, L. Y. S.; VIANA, V. S. T.; BARACAT, E. C.; BONFA, E.; SILVA, C. A.