Publications by authors named "Filipa Briosa"

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Meningocele: when facial dysmorphism holds the diagnostic key.
Cristel Gonçalves, Filipa Briosa, Ana Rita Azevedo, Samuel Lemos

BMJ Case Rep· August 2025

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Hypogonadotropic hypogonadism due to compound heterozygous mutations TACR3 in siblings.
Rita Valsassina, Filipa Briosa, Joana Soares, Marta Amorim, Catarina Limbert

Clin Case Rep· December 2020

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Zinner and Mayer-Rokitansky-Küster-Hauser syndromes: when unilateral renal agenesis meets genital anomalies.
Filipa Briosa, Rita Valsassina, Catarina Mira, Ana Zagalo

BMJ Case Rep· May 2019

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Stickler syndrome: a possible presentation of Pierre Robin sequence.
Filipa Briosa, Sara Oliveira, Rodrigo Sousa, Paulo Oom

BMJ Case Rep· January 2019

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