Search Results - Pavanello, Rita de C.M.

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  1. 1
    Central core myopathy with autophagy

    Central core myopathy with autophagy by Cotta, Ana, Paim, Julia F., Pavanello, Rita De C. M., Nogueira, Leticia, Leão, Leonardo G., Xavier‐Neto, Rafael, Navarro, Monica M., Carvalho, Elmano, Valicek, Jaquelin, Silveira, Eni B., Takata, Reinaldo I., Vainzof, Mariz

    Published in Muscle & nerve
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  2. 2
    Premature ovarian failure (POF) in Brazilian fragile X carriers

    Premature ovarian failure (POF) in Brazilian fragile X carriers by Vianna-Morgante, Angela M., Costa, Silvia S., Pavanello, Rita de C.M., Otto, P.A., Mingroni-Netto, Regina C.

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    Genomic Screening for β-Sarcoglycan Gene Mutations: Missense Mutations May Cause Severe Limb-girdle Muscular Dystrophy Type 2E (LGMD 2E)

    Genomic Screening for β-Sarcoglycan Gene Mutations: Missense Mutations May Cause Severe Limb-girdle Muscular Dystrophy Type 2E (LGMD 2E) by Bönnemann, Carsten G., Passos-Bueno, M. Rita, McNally, Elizabeth M., Vainzof, Mariz, Moreira, Eloísa de Sá, Marie, Suely K., Pavanello, Rita C. M., Noguchi, Satoru, Ozawa, Eijiro, Zatz, Mayana, Kunkel, Louis M.

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  4. 4
    The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females

    The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females by Zatz, Mayana, Marie, Suely K., Cerqueira, Antonia, Vainzof, Mariz, Pavanello, Rita C.M., Passos-Bueno, Maria Rita

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