Accès ouvert
2026
article
OpenAlex
Bibiana Mello de Oliveira, Monique Sartori Broch, Carolina Peçaibes de Oliveira, Angélica Piovesana et autres
BACKGROUND: The diagnostic odyssey of individuals with rare diseases is prolonged and associated with clinical, emotional, and financial burden. In Brazil, data on diagnostic delays and their determinants remain scarce. OBJECTIVE: This study aims to characterize the diagnostic odyssey of individuals with …
br, pt, Mozambique
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2026
article
OpenAlex
Carolina Sánchez Aranda, Sandra Obikawa Kyosen, Ana Margarida Martins
Accès ouvert
2025
article
OpenAlex
LAURA CAROLINE ANDRADE REIS, Larissa Nascimento, Sandra Obikawa Kyosen
A Epidermólise Bolhosa hereditária (EB) é uma doença genética rara que causa fragilidade da pele e a formação de bolhas em resposta a traumas mínimos. A condição possui tipos fenotipicamente distintos, EB simples, juncional, distrófica e tipo Kindler, com uma clínica heterogênea, …
2025
book-chapter
OpenAlex
GIOVANNA RAJEVSKI ALVES, Nathalia Isabelle Alves da Silva, Sandra Obikawa Kyosen
2025
article
OpenAlex
Marco A. Curiati, Sandra Obikawa Kyosen, Ana María Martins
2025
article
OpenAlex
Ana Maria Martins, Sandra Obikawa Kyosen, Marco A. Curiati, Jessica Espolaor et autres
2025
article
OpenAlex
Ana María Martins, Marcelo Hideki Yamamoto, Camila Ferreira Azevedo, Débora Chagas Cardoso de Melo et autres
Accès ouvert
2025
article
OpenAlex
Zenia Brasil, Francisco Antônio Helfenstein Fonseca, Marco A. Curiati, Sandra Obikawa Kyosen et autres
Abstract Background Lysosomal acid lipase deficiency (LAL-D) is a rare autosomal recessive disease, with massive accumulation of cholesteryl esters and triglycerides in many organs, leading to hepatosplenomegaly, microvesicular steatosis, cirrhosis and premature death. Early recognition is crucial for timely enzyme replacement therapy. …
br
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Accès ouvert
2025
article
OpenAlex
Zenia Brasil, Francisco Antônio Helfenstein Fonseca, Marco A. Curiati, Sandra Obikawa Kyosen et autres
BACKGROUND: Lysosomal acid lipase deficiency (LAL-D) is a rare autosomal recessive disease, with massive accumulation of cholesteryl esters and triglycerides in many organs, leading to hepatosplenomegaly, microvesicular steatosis, cirrhosis and premature death. Early recognition is crucial for timely enzyme replacement therapy. OBJECTIVES: …
br
(code pays fourni par la source)
Accès ouvert
2024
article
OpenAlex
Tânia Barbosa Santos, Camila Apolinário Roberto, Diego Veneziani Zogaib, Isabela Granato Travalini et autres
Introdução: O avanço das mídias digitais se tornou algo marcante no cotidiano das crianças e adolescentes, mas o seu uso exagero tem se tornado preocupante para a saúde das crianças e seus consequentes impactos no desenvolvimento infantil. Objetivo: identificar se há correlação …
br
(code pays fourni par la source)
Accès ouvert
2024
article
OpenAlex
Fernanda Teresa de Lima, Maria Angélica de Faria Domingues de Lima, Patrícia Santana Correia, Rachel Sayuri Honjo et autres
br
(code pays fourni par la source)
2024
article
OpenAlex
Carolina Sánchez Aranda, Carmen Curiati, Marco A. Curiati, Sandra Obikawa Kyosen et autres