Browsing "Artigos e Materiais de Revistas Científicas - FM/MPE" by Title
Showing results 693 to 712 of 1092
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Issue Date | Title | Author(s) |
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2021 | Mucopolysaccharidosis VII in Brazil: natural history and clinical findings | GIUGLIANI, Roberto; BARTH, Anneliese Lopes; DUMAS, Melissa Rossi Calvao; FRANCO, Jose Francisco da Silva; GIULIANI, Liane de Rosso; GRANGEIRO, Carlos Henrique Paiva; HOROVITZ, Dafne Dain Gandelman; KIM, Chong Ae; LEAO, Emilia Katiane Embirucu de Araujo; MEDEIROS, Paula Frassinetti Vasconcelos de, et al |
2014 | Multicentric Carpotarsal Osteolysis Is Caused by Mutations Clustering in the Amino-Terminal Transcriptional Activation Domain of MAFB (vol 90, pg 494, 2012) | ZANKL, Andreas; DUNCAN, Emma L.; LEO, Paul J.; CLARK, Graeme R.; GLAZOV, Evgeny A.; ADDOR, Marie-Claude; HERLIN, Troels; KIM, Chong Ae; LEHEUP, Bruno P.; MCGILL, Jim, et al |
2015 | Multicentric study on the diagnosis of Fabry's disease using angiokeratoma biopsy registries | KELMANN, Samantha Vernaschi; QUAIO, Caio Robledo D'Angioli Costa; HONJO, Rachel Sayuri; BERTOLA, Debora Romeo; ROSA NETO, Nilton Salles; LOURENCO, Charles Marques; D'ALMEIDA, Vania; LELLIS, Rute Facchini; RIVITTI-MACHADO, Maria Cecilia; ENOKIHARA, Milvia Maria Simoes e Silva, et al |
2018 | Multimodal image analysis of the retina in Hunter syndrome (mucopolysaccharidosis type II): Case report | SALVUCCI, Isadora Darriba Macedo; FINZI, Simone; OYAMADA, Maria Kiyoko; KIM, Chong Ae; PIMENTEL, Sergio Luis Gianotti |
2012 | Multiple, diffuse schwannomas in a RASopathy phenotype patient with germline KRAS mutation: a causal relationship? | BERTOLA, D. R.; PEREIRA, A. C.; BRASIL, A. S.; SUZUKI, L.; LEITE, C.; FALZONI, R.; TANNURI, U.; POPLAWSKI, A. B.; JANOWSKI, K. M.; KIM, C. A., et al |
2020 | Multisystem Inflammatory Syndrome Associated With COVID-19 With Neurologic Manifestations in a Child: A Brief Report | PAULIS, Milena De; OLIVEIRA, Danielle Bruna Leal; VIEIRA, Rodolfo P.; PINTO, Isabella Coutinho; MACHADO, Rafael Rahal Guaragna; CAVALCANTI, Mariana Pauferro; SOARES, Camila Pereira; ARAUJO, Ananda Medeiros Pereira de; ARAUJO, Danielle Bastos; BACHI, Andre Luis Lacerda, et al |
2019 | Munchausen by proxy syndrome mimicking childhood-onset systemic lupus erythematosus | KUHNE, A. C. A.; PITTA, A. C.; GALASSI, S. C.; GONCALVES, A. M. F.; CARDOSO, A. C. A.; PAZ, J. A.; CAMPOS, L. M. A.; SILVA, C. A. |
2014 | Musculoskeletal manifestations and autoantibodies in children and adolescents with leprosy | NEDER, Luciana; RONDON, Daniel A.; CURY, Silvana S.; SILVA, Clovis A. da |
2018 | Musculoskeletal pain and musculoskeletal syndromes in adolescents are related to electronic devices | QUEIROZ, Ligia Bruni; LOURENCO, Benito; SILVA, Luiz Eduardo Vargas; LOURENCO, Daniela Mencaroni Rodrigues; SILVA, Clovis Artur |
2021 | MUSIC INTERVENTIONS IN PEDIATRIC ONCOLOGY: Systematic review and meta-analysis | SANTA, Ivone Nunes da Silva; SCHVEITZER, Mariana Cabral; SANTOS, Maria Lucia Barbosa Maia dos; GHELMAN, Ricardo; ODONE FILHO, Vicente |
2016 | Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal Dysplasia | WADE, Emma M.; DANIEL, Philip B.; JENKINS, Zandra A.; MCINERNEY-LEO, Aideen; LEO, Paul; MORGAN, Tim; ADDOR, Marie Claude; ADES, Lesley C.; BERTOLA, Debora; BOHRING, Axel, et al |
2014 | Mutations in PCYT1A Cause Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy | YAMAMOTO, Guilherme L.; BARATELA, Wagner A. R.; ALMEIDA, Tatiana F.; LAZAR, Monize; AFONSO, Clara L.; OYAMADA, Maria K.; SUZUKI, Lisa; OLIVEIRA, Luiz A. N.; RAMOS, Ester S.; KIM, Chong A., et al |
2011 | Myocarditis in children and detection of viruses in myocardial tissue: Implications for immunosuppressive therapy | CAMARGO, Paulo Roberto; OKAY, Thelma Suely; YAMAMOTO, Lidia; NEGRO, Gilda Maria Barbaro Del; LOPES, Antonio Augusto |
2014 | N-acetyl-cysteine is associated to renal function improvement in patients with nephropathic cystinosis | GUIMARAES, Luciana Pache de Faria; SEGURO, Antonio Carlos; SHIMIZU, Maria Heloisa Mazzola; NERI, Leticia Aparecida Lopes; SUMITA, Nairo Massakasu; BRAGANCA, Ana Carolina de; VOLPINI, Rildo Aparecido; SANCHES, Talita Rojas Cunha; FONSECA, Fernanda Andrade Macaferri da; MOREIRA FILHO, Carlos Alberto, et al |
2014 | Nager syndrome: confirmation of SF3B4 haploinsufficiency as the major cause | PETIT, F.; ESCANDE, F.; JOURDAIN, A. S.; PORCHET, N.; AMIEL, J.; DORAY, B.; DELRUE, M. A.; FLORI, E.; KIM, C. A.; MARLIN, S., et al |
2013 | Nasojejunal Versus Nasogastric Nutritional Support: Ending a Debate | ZAMBERLAN, Patricia; CARVALHO, Werther Brunow de; DELGADO, Artur Figueiredo |
2021 | Nationwide questionnaire data of 229 Williams-Beuren syndrome patients using WhatsApp tool | PIRES, Lucas Vieira Lacerda; RIBEIRO, Rogerio Lemos; SOUSA, Adriana Modesto de; LINNENKAMP, Bianca Domit Werner; PONTES, Sue Ellen; TEIXEIRA, Maria Cristina Triguero Veloz; BEFI-LOPES, Debora Maria; HONJO, Rachel Sayuri; BERTOLA, Debora Romeo; KIM, Chong Ae |
2018 | Natural history of 39 patients with Achondroplasia | CERONI, Jose Ricardo Magliocco; SOARES, Diogo Cordeiro de Queiroz; TESTAI, Larissa de Cassia; KAWAHIRA, Rachel Sayuri Honjo; YAMAMOTO, Guilherme Lopes; SUGAYAMA, Sofia Mizuho Miura; OLIVEIRA, Luiz Antonio Nunes de; BERTOLA, Debora Romeo; KIM, Chong Ae |
2012 | Nebulized 0.5, 2.5 and 5 ml L-epinephrine for post-extubation stridor in children: a prospective, randomized, double-blind clinical trial | SILVA, Paulo Sergio Lucas da; FONSECA, Marcelo Cunio Machado; IGLESIAS, Simone Brasil Oliveira; LOPES JUNIOR, Emilio; AGUIAR, Vania Euzebio de; CARVALHO, Werther Brunow de |
2019 | Neonatal Hypotension: What Is the Efficacy of Each Anti-Hypotensive Intervention? A Systematic Review | MATSUSHITA, F.Y.; KREBS, V.L.J.; CARVALHO, W.B. de |