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Akademický článek

Impact of prehabilitation during neoadjuvant chemotherapy and interval cytoreductive surgery on ovarian cancer patients: a pilot study

Autor: Ester Miralpeix, Josep-Maria Sole-Sedeno, Cristina Rodriguez-Cosmen, Alvaro Taus, Maria-Dolors Muns, Berta Fabregó, Gemma Mancebo

Publikováno v: World Journal of Surgical Oncology, Vol 20, Iss 1, Pp 1-10 (2022)

Abstract Background Cytoreductive surgery followed by systemic chemotherapy is the standard of treatment in advanced ovarian cancer where feasible. Neoadjuvant chemotherapy (NACT) followed by surgery is applicable where upfront cytoreductive surgery

Externí odkaz: https://doaj.org/article/d67362543553411e970d6d72522b96d8

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Akademický článek

Familial lecithin-cholesterol acyltransferase deficiency: If so rare, why so frequent in the state of Piauí, northeastern Brazil?

Autor: Rafael Melo Santos de Serpa Brandão, Fábio Barros Britto, José Tiburcio do Monte Neto, Marcelo Cunha Lima, Semiramis Jamil Hadad do Monte, Antonio Vanildo de Sousa Lima, Ester Miranda Pereira, Higo José Neri da Silva, Deylane Menezes Teles e Oliveira, Antonio Gilberto Borges Coelho, Adalberto Socorro da Silva

Publikováno v: Molecular Genetics and Metabolism Reports, Vol 30, Iss , Pp 100840- (2022)

Lecithin-cholesterol acyltransferase (LCAT), an enzyme that participates in lipoprotein metabolism, plays an important role in cholesterol homeostasis. Mutations in the LCAT gene can cause two rare genetic disorders: familial LCAT deficiency (FLD), w

Externí odkaz: https://doaj.org/article/694f8b74d4ff47ecbd3601e535daa857

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Akademický článek

Podocitúria na doença de Fabry

Autor: Ester Miranda Pereira, Adalberto Socorro da Silva, Anatália Labilloy, José Tiburcio do Monte Neto, Semiramis Jamil Hadad do Monte

Publikováno v: Brazilian Journal of Nephrology, Vol 38, Iss 1, Pp 49-53 (2016)

Resumo Introdução: A doença de Fabry (DF) é uma desordem lisossômica ligada ao cromossomo X ocasionada por mutações no gene que codifica a enzima lisossômica α-galactosidase A (α-GAL). A redução ou ausência da atividade dessa enzima leva

Externí odkaz: https://doaj.org/article/0055c93a40324fe1b530349ef3b65b43

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Akademický článek

CD77 levels over enzyme replacement treatment in Fabry Disease Family (V269M)

Autor: Ester Miranda Pereira, Adalberto Socorro da Silva, Raimundo Nonato da Silva, José Tiburcio Monte Neto, Fernando F. do Nascimento, Jackeline L. M. Sousa, Henrique César Saraiva de Arêa Leão Costa Filho, Herton Luiz Alves Sales Filho, Anatalia Labilloy, Semiramis Jamil Hadad do Monte

Publikováno v: Brazilian Journal of Nephrology, Iss 0 (2018)

ABSTRACT Introduction: Fabry disease (FD) is a disorder caused by mutations in the gene encoding for lysosomal enzyme α-galactosidase A (α-GAL). Reduced α-GAL activity leads to progressive accumulation of globotriaosylceramide (Gb3), also known as

Externí odkaz: https://doaj.org/article/1c4abbd8235d42e8ba5923c57c525428

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Akademický článek

Deslizamento funcional de marcadores discursivos e entoação em narrativas infantis

Autor: Ester Mirian Scarpa, Cláudia Andrea Rost Snichelotto Snichelotto, Flaviane Romani Fernandes-Svartman

Publikováno v: Cadernos de Estudos Lingüísticos, Vol 59, Iss 3 (2017)

Este trabalho objetiva estudar a coesão entoacional e o deslocamento funcional do marcador discursivo “então” na fala da criança. Baseia-se em duas hipóteses conexas: (i) as primeiras manifestações de coesão textual nas protonarrativas inf

Externí odkaz: https://doaj.org/article/211cf2287222426db052089cb80559bc

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