Showing 1 - 2 results of 2 for search 'Raphael de Paula Doyle Maia', query time: 0.02s Refine Results
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    SYNE1 gene mutation: A recessive ataxic syndrome presenting with weakness and muscle atrophy. A case report

    SYNE1 gene mutation: A recessive ataxic syndrome presenting with weakness and muscle atrophy. A case report by Lucas Grobério Moulim de Moraes, Caroline Colnago Demoner, Giselle Alves de Oliveira, Raphael de Paula Doyle Maia, Paula Zago Melo Dias, Mariana Lacerda Reis Grenfell, Renann Nunes Pirola, Marcelo Ramos Muniz

    Published 2024-06-01
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  2. 2
    Variegate porphyria onset as neurovisceral manifestation and unusual sensory impairment distribution. Case report

    Variegate porphyria onset as neurovisceral manifestation and unusual sensory impairment distribution. Case report by Lucas Grobério Moulim de Moraes, Caroline Colnago Demoner, Amanda Ambrosini Cipriano, Giselle Alves de Oliveira, Raphael de Paula Doyle Maia, Paula Zago Melo Dias, Mariana Lacerda Reis Grenfell, Renann Nunes Pirola, Marcelo Ramos Muniz

    Published 2024-06-01
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    Article

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