Doença invasiva por Streptococcus pyogenes num hospital pediátrico - 1996-2009. by Joana Serra Caetano, Paula Neto, Manuela Costa Alves, Fernanda Rodrigues

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Rare Coexistence of Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency and Turner Syndrome: A Case Report and Brief Literature Review by Isabel Inácio, Joana Serra-Caetano, Rita Cardoso, Isabel Dinis, Alice Mirante

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Autoimmune Primary Adrenal Insufficiency in Children by Nádia Mourinho Bala, Raquel S. Gonçalves, Joana Serra Caetano, Rita Cardoso, Isabel Dinis, Alice Mirante

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Neonates Born to Mothers with Graves’ Disease: 15 Year Experience of a Pediatric Endocrinology Department by Inês Romão Luz, João Rio Martins, Mónica Jerónimo, Joana Serra Caetano, Rita Cardoso, Isabel Dinis, Alice Mirante

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A variant in the CASR gene (c.368T>C) causing hypocalcemia refractory to standard medical therapy by Diana Festas Silva, Adriana De Sousa Lages, Joana Serra Caetano, Rita Cardoso, Isabel Dinis, Leonor Gomes, Isabel Paiva, Alice Mirante

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A serious and unusual presentation of congenital isolated ACTH deficiency due to TBX19 mutation, beyond the neonatal period by Inês Henriques Vieira, Nádia Mourinho Bala, Fabiana Ramos, Isabel Dinis, Rita Cardoso, Joana Serra Caetano, Dírcea Rodrigues, Isabel Paiva, Alice Mirante

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