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
    Central core myopathy with autophagy: Central Core With Autophagy

    Central core myopathy with autophagy: Central Core 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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  3. 3
    Nemaline Myopathy in Brazilian Patients: Molecular and Clinical Characterization

    Nemaline Myopathy in Brazilian Patients: Molecular and Clinical Characterization by Gurgel-Giannetti, Juliana, Souza, Lucas Santos, Yamamoto, Guilherme L, Belisario, Marina, Lazar, Monize, Campos, Wilson, Pavanello, Rita de Cassia M, Zatz, Mayana, Reed, Umbertina, Zanoteli, Edmar, Oliveira, Acary Bulle, Lehtokari, Vilma-Lotta, Casella, Erasmo B, Machado-Costa, Marcela C, Wallgren-Pettersson, Carina, Laing, Nigel G, Nigro, Vincenzo, Vainzof, Mariz

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  4. 4
    Development of a comprehensive noninvasive prenatal test

    Development of a comprehensive noninvasive prenatal test by Malcher, Carolina, Yamamoto, Guilherme L, Burnham, Philip, Ezquina, Suzana A M, Lourenço, Naila C V, Balkassmi, Sahilla, Antonio, David S Marco, Hsia, Gabriella S P, Gollop, Thomaz, Pavanello, Rita C, Lopes, Marco Antonio, Bakker, Egbert, Zatz, Mayana, Bertola, Débora, Vlaminck, Iwijn De, Passos-Bueno, Maria Rita

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  5. 5
    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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  6. 6
    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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  7. 7
    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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