Search Results - Mirante, Maria Alice

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  1. 1
    PREPUBERTAL GYNECOMASTIA: A RARE MANIFESTATION OF MYOTONIC DYSTROPHY TYPE 1

    PREPUBERTAL GYNECOMASTIA: A RARE MANIFESTATION OF MYOTONIC DYSTROPHY TYPE 1 by Miranda, Patrícia Sofia Ferreira, Pereira, Ester Preciosa Maio Nunes, Barreto, Joana Serra Caetano Baltazar, Henriques, Margarida Maria Videira, Mirante, Maria Alice Santos Cordeiro, Ramos, Lina Maria Jesus Ferreira Cardoso

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  2. 2
    Congenital adrenal hyperplasia in adolescence — a gynecological perspective

    Congenital adrenal hyperplasia in adolescence — a gynecological perspective by Oliveira, Joana Correia, Sousa, Filipa Costa, Campos, Sara Teixeira, Geraldes, Fernanda Bento, Belo, Joana Lopes, Leite, Maria Helena, Mirante, Maria Alice, Águas, Maria Fernanda

    Published in Ginekologia polska
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  3. 3
    Effect of ultra-rapid insulin aspart on glycemic control in children with type 1 diabetes: the experience of a Portuguese tertiary centre

    Effect of ultra-rapid insulin aspart on glycemic control in children with type 1 diabetes: the experience of a Portuguese tertiary centre by Costa, Cláudia, Linhares, Maria Inês, Bastos, Filipa, Cardoso, Rita, Dinis, Isabel, Santos, Ana Paula, Mirante, Alice, Serra-Caetano, Joana

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  4. 4
    A rare cause of neonatal persistent jaundice

    A rare cause of neonatal persistent jaundice by Oliveira, Gracinda Nogueira, Dinis, Isabel, Noruegas, Maria José, Mirante, Alice

    Published in BMJ case reports
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  5. 5
    Maturity-Onset Diabetes of the Young (MODY) in Portugal: Novel GCK , HNFA1 and HNFA4 Mutations

    Maturity-Onset Diabetes of the Young (MODY) in Portugal: Novel GCK , HNFA1 and HNFA4 Mutations by Alvelos, Maria I, Gonçalves, Catarina I, Coutinho, Eduarda, Almeida, Joana T, Bastos, Margarida, Sampaio, Maria L, Melo, Miguel, Martins, Sofia, Dinis, Isabel, Mirante, Alice, Gomes, Leonor, Saraiva, Joana, Pereira, Bernardo D, Gama-de-Sousa, Susana, Moreno, Carolina, Guelho, Daniela, Martins, Diana, Baptista, Carla, Barros, Luísa, Ventura, Mara, Gomes, Maria M, Lemos, Manuel C

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  6. 6
    CYP21A2 mutations in Portuguese patients with congenital adrenal hyperplasia: Identification of two novel mutations and characterization of four different partial gene conversions

    CYP21A2 mutations in Portuguese patients with congenital adrenal hyperplasia: Identification of two novel mutations and characterization of four different partial gene conversions by Friães, Ana, Rêgo, Ana Toste, Aragüés, José Maria, Moura, Luís Francisco, Mirante, Alice, Mascarenhas, Mário Rui, Kay, Teresa Taylor, Lopes, Lurdes Afonso, Rodrigues, José Cidade, Guerra, Sílvia, Dias, Teresa, Teles, Alberto Galvão, Gonçalves, João

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