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Filipa Dias Costa

Showing results (1-10 of 7) with videos related to

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BMJ Case Reports|July 16, 2017
Complement factor B mutation-associated aHUS and myocardial infarctionNatália Noronha, Filipa Dias Costa, Andrea Dias, et al.
BMJ Case Reports|January 22, 2017
Child with multiple fractures: a rare presentation of a common diseaseFilipa Dias Costa, Carla Maia, Susana Almeida, et al.
BMJ Case Reports|June 12, 2015
Group B streptococcal neonatal parotitisFilipa Dias Costa, Daniel Ramos Andrade, Filipa Inês Cunha, et al.
BMJ Case Reports|February 14, 2018
Teenage boy with high fever and rash: what could we be missing?Gracinda Nogueira Oliveira, Sofia Costa, Filipa Dias Costa, et al.
Sleep Science (Sao Paulo, Brazil)|October 21, 2015
Narcolepsy in pediatric age - Experience of a tertiary pediatric hospitalFilipa Dias Costa, Maria Inês Barreto, Vanda Clemente, et al.
Anales De Pediatria|April 16, 2017
[Acute liver failure related to inherited metabolic diseases in young children]Filipa Dias Costa, Rita Moinho, Sandra Ferreira, et al.
JIMD Reports|March 2, 2017
Galactose Epimerase Deficiency: Expanding the PhenotypeFilipa Dias Costa, Sacha Ferdinandusse, Carla Pinto, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
BMJ Case Reports|July 16, 2017
Complement factor B mutation-associated aHUS and myocardial infarctionNatália Noronha, Filipa Dias Costa, Andrea Dias, et al.
BMJ Case Reports|January 22, 2017
Child with multiple fractures: a rare presentation of a common diseaseFilipa Dias Costa, Carla Maia, Susana Almeida, et al.
BMJ Case Reports|June 12, 2015
Group B streptococcal neonatal parotitisFilipa Dias Costa, Daniel Ramos Andrade, Filipa Inês Cunha, et al.
BMJ Case Reports|February 14, 2018
Teenage boy with high fever and rash: what could we be missing?Gracinda Nogueira Oliveira, Sofia Costa, Filipa Dias Costa, et al.
Sleep Science (Sao Paulo, Brazil)|October 21, 2015
Narcolepsy in pediatric age - Experience of a tertiary pediatric hospitalFilipa Dias Costa, Maria Inês Barreto, Vanda Clemente, et al.
Anales De Pediatria|April 16, 2017
[Acute liver failure related to inherited metabolic diseases in young children]Filipa Dias Costa, Rita Moinho, Sandra Ferreira, et al.
JIMD Reports|March 2, 2017
Galactose Epimerase Deficiency: Expanding the PhenotypeFilipa Dias Costa, Sacha Ferdinandusse, Carla Pinto, et al.
Pageof 1