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Issue DateTitleAuthor(s)
2017Baked milk tolerant patient: Is there any special feature?BARBOSA, C. P. G.; CASTRO, A. P. M.; YONAMINE, G. H.; GUSHKEN, A. K. F.; BECK, C. M. L.; MACEDO, P. R. C.; DORNA, M. B.; SANTOS, C. J. N.; PASTORINO, A. C.; JACOB, C. M. A.
2016Bartonella henselae AS A PUTATIVE CAUSE OF CONGENITAL CHOLESTASISVELHO, Paulo Eduardo Neves Ferreira; BELLOMO-BRANDAO, Maria Angela; DRUMMOND, Marina Rovani; MAGALHAES, Renata Ferreira; HESSEL, Gabriel; BARJAS-CASTRO, Maria de Lourdes; ESCANHOELA, Cecilia Amelia Fazzio; NEGRO, Gilda Maria Barbaro Del; OKAY, Thelma Suely
2023Bartter Syndrome-Related Variants Distribution: Brazilian Data and Its Comparison with Worldwide CohortsVAISBICH, Maria Helena; MESSA, Ana Carola Hebbia Lobo; RANGEL-SANTOS, Andreia Cristiane; FERREIRA, Juliana Caires de Oliveira Achili; NUNES, Fernanda Andrade Macaferri da Fonseca; WATANABE, Andreia
2014Bedside Echocardiography for Pediatric Hemodynamic Monitoring: What Is the Impact in the Outcome?GASPAR, Heloisa Amaral; TUMA, Patricia Leao; CARVALHO, Werther Brunow; DELGADO, Artur Figueredo
2021Beyond the Standard of Care: An Exploratory Qualitative Study of an Implemented Integrative Therapeutic Care Program in a Brazilian Pediatric Oncology UnitTROENDLE, Marc; STRITTER, Wiebke; ODONE, Vicente; PERON, Karina; GHELMAN, Ricardo; SEIFERT, Georg
2020Beyond ventilatory support: challenges in general practice and in the treatment of critically Ill children and adolescents with SARS-CoV-2 infectionFERRANTI, Juliana Ferreira; RODRIGUEZ, Isadora Souza; MOTT, Emiliana; JOHNSTON, Cintia; CARVALHO, Werther Brunow de B.; DELGADO, Artur Figueiredo
2019Bi-allelic CSF1R Mutations Cause Skeletal Dysplasia of Dysosteosclerosis-Pyle Disease Spectrum and Degenerative Encephalopathy with Brain MalformationGUO, Long; BERTOLA, Debora Romeo; TAKANOHASHI, Asako; SAITO, Asuka; SEGAWA, Yuko; YOKOTA, Takanori; ISHIBASHI, Satoru; NISHIDA, Yoichiro; YAMAMOTO, Guilherme Lopes; FRANCO, Jose Francisco da Silva, et al
2023Biallelic structural variations within FGF12 detected by long-read sequencing in epilepsyOHORI, Sachiko; MIYAUCHI, Akihiko; OSAKA, Hitoshi; LOURENCO, Charles Marques; ARAKAKI, Naohiro; SENGOKU, Toru; OGATA, Kazuhiro; HONJO, Rachel Sayuri; KIM, Chong Ae; MITSUHASHI, Satomi, et al
2023Biallelic variants in <i>DNA2</i> cause poikiloderma with congenital cataracts and severe growth failure reminiscent of Rothmund-Thomson syndromeLAZZARO FILHO, Ricardo Di; YAMAMOTO, Guilherme Lopes; SILVA, Tiago J.; ROCHA, Leticia A.; LINNENKAMP, Bianca D. W.; CASTRO, Matheus Augusto Araujo; BARTHOLDI, Deborah; SCHALLER, Andre; LEEB, Tosso; KELMANN, Samantha, et al
2019Biochemical profile in an infant with neonatal hemochromatosis shows evidence of impairment of mitochondrial long-chain fatty acid oxidationBASTOS, Karina Lucio de Medeiros; QUAIO, Caio Robledo; LIMA, Fabiana Roberto; ARAUJO, Iana Manuelle; ARAUJO, Candice Alves Tavares; PIAZZON, Flavia Balbo; SILVA, Ismael Dale Cotrim Guerreiro da; BENEVIDES, Gabriel Nuncio; TANNURI, Ana Cristina; TANNURI, Uenis, et al
2019Bioelectrical Impedance Phase Angle and Morbidity and Mortality in Critically Ill ChildrenZAMBERLAN, Patricia; FEFERBAUM, Rubens; DORIA FILHO, Ulysses; CARVALHO, Werther Brunow de; DELGADO, Artur Figueiredo
2020Bioelectrical impedance phase angle and morbidity and mortality in critically ill children (vol 34, pg 163, 2019)ZAMBERLAN, Patricia; FEFERBAUM, Rubens; DORIA FILHO, Ulysses; CARVALHO, Werther Brunow de; DELGADO, Artur Figueiredo
2021Birth by cesarean section and mood disorders among adolescents of a birth cohort study in northern BrazilCOELHO, S. J. D. C.; SIMOES, V. M. F.; BATISTA, R. F. L.; RIBEIRO, C. C. C.; LAMY, Z. C.; LAMY-FILHO, F.; CARVALHO, C. A.; VIOLA, P. C. A. F.; QUEIROZ, R. C. S.; FERRARO, A. A., et al
2021Birth weight associated with dual energy X-ray absorptiometry-determined muscle-bone unit in young healthy women from the Nutritionists' Health StudyVALENTE, Angelica Marques Martins; ALMEIDA-PITITTO, Bianca de; FERRARO, Alexandre Archanjo; FOLCHETTI, Luciana G. Dias; SILVA, Isis Tande; FERREIRA, Sandra Roberta G.
2016BLM germline and somatic PKMYT1 and AHCY mutations: Genetic variations beyond MYCN and prognosis in neuroblastomaNOVAK, E. M.; HALLEY, N. S.; GIMENEZ, T. M.; RANGEL-SANTOS, A.; AZAMBUJA, A. M. P.; BRUMATTI, M.; PEREIRA, P. L.; VINCE, C. S. C.; GIORGI, R. R.; BENDITE, I., et al
2023Blood leukocyte transcriptional modules and differentially expressed genes associated with disease severity and age in COVID-19 patientsBANDO, Silvia Y.; BERTONHA, Fernanda B.; VIEIRA, Sandra E.; OLIVEIRA, Danielle B. L. de; CHALUP, Vanessa N.; DURIGON, Edison L.; PALMEIRA, Patricia; CURI, Ana Cristina P.; FARIA, Caroline S.; ANTONANGELO, Leila, et al
2023Body Composition and Phase Angle: How to Improve Nutritional Evaluation in Juvenile Dermatomyositis PatientsPUGLIESE, Camila; DELGADO, Artur Figueiredo; KOZU, Katia Tomie; CAMPOS, Lucia Maria de Arruda; AIKAWA, Nadia Emi; SILVA, Clovis Artur; ELIAS, Adriana Maluf
2015Borderline tuberculoid leprosy in childhood onset systemic lupus erythematosus patientLOPES, V. A. P.; LOURENCO, D. M. R.; GUARIENTO, A.; TRINDADE, M. A.; AVANCINI, J.; SILVA, C. A.
2023Born into an isolating world: family-centred care for babies born to mothers with COVID-19DOWSE, G.; PERKINS, E. J.; STEIN, H. M.; CHIDINI, G.; DANHAIVE, O.; ELSAYE, Y. N.; CARVALHO, W. B.; ALNAQEEB, N.; ROOZE, S.; CETINKAYA, M., et al
2023Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individualsSAIDA, Ken; MAROOTAIN, Reza; SENGOKU, Toru; MITANI, Tadahiro; PAGNAMENTA, Alistair T.; MARAFI, Dana; ZAKI, Maha S.; O'BRIAN, Thomas J.; KARIMIANI, Ehsan Ghayoor; KAIYRZHANOV, Rauan, et al