Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Marilia M. Montenegro"'
Autor:
Fernanda Martins, Fernanda T. Gonçalves, Marta Imamura, Daniela S. Barboza, Denise Matheus, Maria Fernanda B. Pereira, Heloisa H. S. Marques, Simone Correa-Silva, Marilia M. Montenegro, Thais T. Fink, Livia Lindoso, Vera Bain, Juliana C. O. A. Ferreira, Camilla Astley, Olivia M. Matsuo, Priscila Suguita, Vitor Trindade, Camila S. Y. Paula, Nadia Litvinov, Patricia Palmeira, Bruno Gualano, Artur F. Delgado, Magda Carneiro-Sampaio, Silvana Forsait, Vicente Odone-Filho, Leila Antonangelo, Linamara R. Battistella, Clovis A. Silva
Publikováno v:
Frontiers in Public Health, Vol 11 (2023)
ObjectivesTo prospectively assess health-related quality of life (HRQoL), global functionality, and disability in primary caregivers of surviving children and adolescents after COVID-19.MethodsA longitudinal observational study was carried out on pri
Externí odkaz:
https://doaj.org/article/55a9a98ec47541c6b3de41cd4d2fad63
Autor:
Marilia M. Montenegro, Caio R. Quaio, Patricia Palmeira, Yanca Gasparini, Andreia Rangel‐Santos, Julian Damasceno, Estela M. Novak, Thamires M. Gimenez, Guilherme L. Yamamoto, Rachel S. Ronjo, Gil M. Novo‐Filho, Samar N. Chehimi, Evelin A. Zanardo, Alexandre T. Dias, Amom M. Nascimento, Thais V. M. M. Costa, Alberto J. da S. Duarte, Luiz L. Coutinho, Chong A. Kim, Leslie D. Kulikowski
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 4, Pp n/a-n/a (2020)
Abstract Background Bloom syndrome (BS) is a rare autosomal recessive chromosome instability disorder. The main clinical manifestations are growth deficiency, telangiectasic facial erythema, immunodeficiency, and increased risk to develop neoplasias
Externí odkaz:
https://doaj.org/article/35c3a715a56746a0b7510a3254638fb4
Autor:
Vanessa Tavares Almeida, Samar N. Chehimi, Gleyson F. S. Carvalho, Yanca Gasparini, Amom M. Nascimento, Lucas L. Vieira, Beatriz M. Wolff, Marília M. Montenegro, Leslie D. Kulikowski
Publikováno v:
BMC Research Notes, Vol 17, Iss 1, Pp 1-10 (2024)
Abstract Cri Du Chat syndrome, or 5p− syndrome, is characterized by a terminal or interstitial deletion on the short arm of chromosome 5 that causes variable clinical manifestations, including high-pitched cry in newborns, delayed growth, and globa
Externí odkaz:
https://doaj.org/article/e822577d976446828a4009c567e4c7bf
Autor:
Samar N. Chehimi, Évelin A. Zanardo, José R. M. Ceroni, Amom M. Nascimento, Fabrícia A. R. Madia, Alexandre T. Dias, Gil M. N. Filho, Marília M. Montenegro, Jullian Damasceno, Thaís V. M. M. Costa, Yanca Gasparini, Chong A. Kim, Leslie D. Kulikowski
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 2, Pp n/a-n/a (2020)
Abstract Background Cri du chat syndrome (CdCS) is a rare syndrome caused by a partial or complete deletion of the short arm of chromosome 5 (5p‐). The main clinical features include a high‐pitched cry, facial asymmetry, microcephaly, round face
Externí odkaz:
https://doaj.org/article/efd42a79e0bf410cb0c3de2027bd665a
Autor:
Cangemi DJ; Division of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, Florida, USA., Montenegro M; Division of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, Florida, USA., Spiegel BMR; Division of Health Sciences Research, Department of Medicine, Cedars-Sinai Health System, Los Angeles, California, USA., Lacy ABE; Division of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, Florida, USA.
Publikováno v:
The American journal of gastroenterology [Am J Gastroenterol] 2024 Jan 01; Vol. 119 (1), pp. 210-213. Date of Electronic Publication: 2023 Sep 01.
Autor:
Soares DC; Department of Pediatrics, Faculdade de Medicina FMUSP, Universidade de São Paulo, São Paulo, SP, Brazil. Electronic address: dsoares@usp.br., Dantas AG; Genetics Division, Department of Morphology and Genetics, Universidade Federal de São Paulo (UNIFESP), São Paulo, SP, Brazil., Matta MC; Translational Research Laboratory, Instituto de Medicina Integral Prof. Fernando Figueira (IMIP), Recife, PE, Brazil., Pastorino AC; Department of Pediatrics, Faculdade de Medicina FMUSP, Universidade de São Paulo, São Paulo, SP, Brazil., Melaragno MI; Genetics Division, Department of Morphology and Genetics, Universidade Federal de São Paulo (UNIFESP), São Paulo, SP, Brazil., Kulikowski L; Department of Pathology, Faculdade de Medicina FMUSP, Universidade de São Paulo, São Paulo, SP, Brazil., Montenegro M; Department of Pediatrics, Faculdade de Medicina FMUSP, Universidade de São Paulo, São Paulo, SP, Brazil., Kim CA; Department of Pediatrics, Faculdade de Medicina FMUSP, Universidade de São Paulo, São Paulo, SP, Brazil., Carneiro-Sampaio M; Department of Pediatrics, Faculdade de Medicina FMUSP, Universidade de São Paulo, São Paulo, SP, Brazil., Torres LC; Translational Research Laboratory, Instituto de Medicina Integral Prof. Fernando Figueira (IMIP), Recife, PE, Brazil.
Publikováno v:
Clinical immunology (Orlando, Fla.) [Clin Immunol] 2020 Nov; Vol. 220, pp. 108590. Date of Electronic Publication: 2020 Sep 11.