Publications by authors named "Filipa Espada"

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Phenotypic Heterogeneity of 16p11.2 Microdeletion Syndrome: 5 Case Reports.
Sílvia Duarte Costa, Catarina Fraga, Nádia Rodrigues, Cláudia Gonçalves, Sara Pires Silva, Filipa Espada

J Child Neurol· January 2026

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Height benefit of GnRH agonists after age 8 in a Portuguese cohort of central precocious puberty.
Carolina Castro, Filipa Espada, Ana Luísa Leite, Ana Antunes, Brígida Robalo

Clin Endocrinol (Oxf)· May 2023

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Hypothalamic hamartoma: a cause of precocious puberty.
Carolina Castro, Joana Machado Morais, Ana Luísa Correia, Filipa Espada

BMJ Case Rep· March 2023

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Do GnRH Agonists Really Increase Body Weight Gain? Evaluation of a Multicentric Portuguese Cohort of Patients With Central Precocious Puberty.
Ana Luísa Leite, Elisa Galo, Ana Antunes, Brígida Robalo, Daniela Amaral, Filipa Espada

Front Pediatr· March 2022

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Wolfram syndrome: Phenotypic heterogeneity and novel genetic variants in the WFS1 gene.
Joana Lima Ferreira, Vanessa Carvalho, Filipa Espada, João Massano, Ana Paula Marques

Endocrinol Diabetes Nutr (Engl Ed)· February 2022

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CYP21A2 Gene Pathogenic Variants: A Multicenter Study on Genotype-Phenotype Correlation from a Portuguese Pediatric Cohort.
Rita Santos-Silva, Rita Cardoso, Lurdes Lopes, Marcelo Fonseca, Filipa Espada

Horm Res Paediatr· November 2019

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Rib osteomyelitis in a pediatric patient case report and literature review.
Marta Nascimento, Eliana Oliveira, Sérgia Soares, Rui Almeida, Filipa Espada

Pediatr Infect Dis J· November 2012

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Adrenoleukodystrophy: a forgotten diagnosis in children with primary Addison's disease.
Marta Nascimento, Nádia Rodrigues, Filipa Espada, Marcelo Fonseca

BMJ Case Rep· August 2012

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Bloody nipple discharge in infancy--report of two cases.
Marta Nascimento, Alexandrina Portela, Filipa Espada, Marcelo Fonseca

BMJ Case Rep· July 2012

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[Spondylodiscitis].
Filipa V Espada, Pedro M Costa, A Leite Da Cunha, António Sarmento, J Mesquita Montes

Acta Med Port· May 2012

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