Showing 1 - 11 results of 11 for search 'Luísa Villa', query time: 0.04s
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The Breaking of the Square: Late Victorian Representations of Anglo-Sudanese Warfare by Luisa Villa
Published 2021-12-01
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First Family of MATR3-Related Distal Myopathy From Italy: The Role of Muscle Biopsy in the Diagnosis and Characterization of a Still Poorly Understood Disease by Michele Cavalli, Rosanna Cardani, Laura Valentina Renna, Mauro Toffetti, Luisa Villa, Giovanni Meola
Published 2021-10-01
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Papilomavírus humano associado a lesões de cérvice uterina by Vânia Noronha, Wyller Mello, Luísa Villa, Arival Brito, Roberto Macêdo, Fátima Bisi, Rosilda Mota, Kyio Sassamoto, Talita Monteiro, Alexandre Linhares
Published 1999-06-01
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Human herpesvirus-8 infection leads to expansion of the preimmune/natural effector B cell compartment. by Silvia Della Bella, Adriano Taddeo, Elena Colombo, Lucia Brambilla, Monica Bellinvia, Fabrizio Pregliasco, Monica Cappelletti, Maria Luisa Calabrò, Maria Luisa Villa
Published 2010-11-01
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Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect. A Case Report and a Review of the Literature by Delia Gagliardi, Irene Faravelli, Luisa Villa, Guglielmo Pero, Claudia Cinnante, Roberta Brusa, Eleonora Mauri, Laura Tresoldi, Francesca Magri, Alessandra Govoni, Nereo Bresolin, Giacomo P. Comi, Stefania Corti
Published 2018-08-01
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Typical CIDP, distal variant CIDP, and anti-MAG antibody neuropathy: An ultra-high frequency ultrasound comparison of nerve structure by Angela Puma, Nicolae Grecu, Raluca Ș. Badea, Adeline Morisot, Roxana Zugravu, Mihai B. Ioncea, Michele Cavalli, Oana Lăcătuș, Andra Ezaru, Chorfa Hacina, Luisa Villa, Charles Raffaelli, Nicolas Azulay, Sabrina Sacconi
Published 2024-02-01
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Síndrome de Cowden: relato de um caso Cowden's Syndrome: a new case report by Patrícia de Barros Guimarães, Adeíza de Alencar Branco, Elaine Carvalho, Francisco Eduardo Lima, José Roberto Almeida, Josemir Belo dos Santos, Luisa Villa, Sílvia Helena Rodrigues, Roberta Siqueira, Tatiana De Perreli
Published 2002-12-01
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Large genotype–phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis by Giulia Ricci, Fabiano Mele, Monica Govi, Lucia Ruggiero, Francesco Sera, Liliana Vercelli, Cinzia Bettio, Lucio Santoro, Tiziana Mongini, Luisa Villa, Maurizio Moggio, Massimiliano Filosto, Marina Scarlato, Stefano C. Previtali, Silvia Maria Tripodi, Elena Pegoraro, Roberta Telese, Antonio Di Muzio, Carmelo Rodolico, Elisabetta Bucci, Giovanni Antonini, Maria Grazia D’Angelo, Angela Berardinelli, Lorenzo Maggi, Rachele Piras, Maria Antonietta Maioli, Gabriele Siciliano, Giuliano Tomelleri, Corrado Angelini, Rossella Tupler
Published 2020-12-01
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Interpretation of the Epigenetic Signature of Facioscapulohumeral Muscular Dystrophy in Light of Genotype-Phenotype Studies by Ana Nikolic, Takako I Jones, Monica Govi, Fabiano Mele, Louise Maranda, Francesco Sera, Giulia Ricci, Lucia Ruggiero, Liliana Vercelli, Simona Portaro, Luisa Villa, Chiara Fiorillo, Lorenzo Maggi, Lucio Santoro, Giovanni Antonini, Massimiliano Filosto, Maurizio Moggio, Corrado Angelini, Elena Pegoraro, Angela Berardinelli, Maria Antonetta Maioli, Grazia D’Angelo, Antonino Di Muzio, Gabriele Siciliano, Giuliano Tomelleri, Maurizio D’Esposito, Floriana Della Ragione, Arianna Brancaccio, Rachele Piras, Carmelo Rodolico, Tiziana Mongini, Frederique Magdinier, Valentina Salsi, Peter L. Jones, Rossella Tupler
Published 2020-04-01
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