Showing 1 - 10 results of 10 for search 'Albina Silva', query time: 0.09s Refine Results
  1. 1
    Picnocitosis, una forma rara de anemia hemolítica neonatal

    Picnocitosis, una forma rara de anemia hemolítica neonatal by Ana Fraga, Ana Raquel Conde, Beatriz Araújo, Albina Silva

    Published 2023
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  2. 2
    Pyknocytosis, a rare form of neonatal haemolytic anaemia

    Pyknocytosis, a rare form of neonatal haemolytic anaemia by Ana Fraga, Ana Raquel Conde, Beatriz Araújo, Albina Silva

    Published 2023
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  3. 3
    Síndrome Cri du Chat

    Síndrome Cri du Chat by Sandra Costa, Joana Dias, Albina Silva, Eduarda Abreu, Almerinda Pereira

    Published 2013
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  4. 4
    Split-Hand/Split Foot - a propósito de um caso clínico

    Split-Hand/Split Foot - a propósito de um caso clínico by Clara Machado, Maria João Magalhães, Albina Silva, Isabel Cunha, Almerinda Pereira

    Published 2013
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  5. 5
    Isotretinoin embryopathy: report of one case

    Isotretinoin embryopathy: report of one case by Cláudia Patraquim, Albina Silva, Ângela Pereira, Miguel Gonçalves-Rocha, João Fernandes, Almerinda Pereira

    Published 2015
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  6. 6
    A novel SRY nonsense mutation in a case of Swyer syndrome

    A novel SRY nonsense mutation in a case of Swyer syndrome by Clara Machado, Angela Pereira, José Matos Cruz, Alexandra Cadilhe, Albina Silva, Almerinda Pereira

    Published 2014
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  7. 7
    Late-preterm birth in a level III hospital: incidence and associated morbidity

    Late-preterm birth in a level III hospital: incidence and associated morbidity by Carla Garcez, Nicole Silva, Liliana Pinheiro, Miguel Costa, Carla Sá, Eduarda Abreu, Albina Silva, Almerinda Pereira

    Published 2016
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  8. 8
    Adams-Oliver syndrome, a successful conservative approach for a large scalp defect

    Adams-Oliver syndrome, a successful conservative approach for a large scalp defect by Vera Baptista, Albina Silva, Carla Sá, Joana Dias, Ana Raquel Silva, Angélica Osório, Carla Garcez, Almerinda Pereira

    Published 2015
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  9. 9
    Novel chromosomal translocation t(7;14)(q36.3;q11.2)dn in a female child with dysmorphic features

    Novel chromosomal translocation t(7;14)(q36.3;q11.2)dn in a female child with dysmorphic features by Jean-Pierre Antunes Gonçalves, Liliana Pinheiro, Maria João Magalhães, Arnaldo Cerqueira, Eduarda Abreu, Albina Silva, Carla Sá, Almerinda Pereira

    Published 2014
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  10. 10
    Prader-Willi Syndrome: an under-recognized cause of hypotonia?

    Prader-Willi Syndrome: an under-recognized cause of hypotonia? by Marlene Rodrigues, Miguel Costa, Joana Teixeira, Carla Sá, Liliana Pinheiro, Eduarda Abreu, Albina Silva, Nicole Silva, Matos Marques, Miguel Rocha, Almerinda Pereira

    Published 2017
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