Search Results - Cirò Candiano, Innocenza C.

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  1. 1
    Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy

    Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy by De Marco, Elvira V., Annesi, Grazia, Tarantino, Patrizia, Rocca, Francesca E., Provenzano, Giovanni, Civitelli, Donatella, Cirò Candiano, Innocenza C., Annesi, Ferdinanda, Carrideo, Sara, Condino, Francesca, Nicoletti, Giuseppe, Messina, Demetrio, Novellino, Fabiana, Morelli, Maurizio, Quattrone, Aldo

    Published in Movement disorders
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  2. 2
    Two Novel SCN1A Missense Mutations in Generalized Epilepsy with Febrile Seizures Plus

    Two Novel SCN1A Missense Mutations in Generalized Epilepsy with Febrile Seizures Plus by Annesi, Grazia, Gambardella, Antonio, Carrideo, Sara, Incorpora, Gemma, Labate, Angelo, Pasqua, Angela Aurora, Civitelli, Donatella, Polizzi, Agata, Annesi, Ferdinanda, Spadafora, Patrizia, Tarantino, Patrizia, Cirò Candiano, Innocenza C., Romeo, Nelide, De Marco, Elvira Valeria, Ventura, Patrizia, LePiane, Emilio, Zappia, Mario, Aguglia, Umberto, Pavone, Lorenzo, Quattrone, Aldo

    Published in Epilepsia (Copenhagen)
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  3. 3
    Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern

    Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern by Valentino, Paola, Annesi, Grazia, Cirò Candiano, Innocenza C., Annesi, Ferdinanda, Civitelli, Donatella, Tarantino, Patrizia, Naso, Francesco, Spadafora, Patrizia, Carrideo, Sara, De Marco, Elvira V., Consoli, Domenico, Zappia, Mario, Gambardella, Antonio, Quattrone, Aldo

    Published in Movement disorders
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  4. 4
    A Novel Exon 1 Mutation in a Patient with Atypical Lafora Progressive Myoclonus Epilepsy Seen as Childhood‐onset Cognitive Deficit

    A Novel Exon 1 Mutation in a Patient with Atypical Lafora Progressive Myoclonus Epilepsy Seen as Childhood‐onset Cognitive Deficit by Annesi, Grazia, Sofia, Vito, Gambardella, Antonio, Candiano, Innocenza C. Cirò, Spadafora, Patrizia, Annesi, Ferdinanda, Cutuli, Nunzio, De Marco, Elvira V., Civitelli, Donatella, Carrideo, Sara, Tarantino, Patrizia, Barone, Rita, Zappia, Mario, Quattrone, Aldo

    Published in Epilepsia (Copenhagen)
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  5. 5
    Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy

    Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy by De Marco, Elvira V, Gambardella, Antonio, Annesi, Ferdinanda, Labate, Angelo, Carrideo, Sara, Forabosco, Paola, Civitelli, Donatella, Candiano, Innocenza C. Cirò, Tarantino, Patrizia, Annesi, Grazia, Quattrone, Aldo

    Published in Epilepsy research
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  6. 6
    A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit

    A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit by Annesi, Grazia, Sofia, Vito, Gambardella, Antonio, Candiano, Innocenza C Cirò, Spadafora, Patrizia, Annesi, Ferdinanda, Cutuli, Nunzio, De Marco, Elvira V, Civitelli, Donatella, Carrideo, Sara, Tarantino, Patrizia, Barone, Rita, Zappia, Mario, Quattrone, Aldo

    Published in Epilepsia
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  7. 7
    FRAXE intermediate alleles are associated with Parkinson’s disease

    FRAXE intermediate alleles are associated with Parkinson’s disease by Annesi, Grazia, Nicoletti, Giuseppe, Tarantino, Patrizia, Cutuli, Nunzio, Annesi, Ferdinanda, Marco, Elvira Valeria De, Zappia, Mario, Morgante, Letterio, Arabia, Gennarina, Pugliese, Pierfrancesco, Condino, Francesca, Carrideo, Sara, Civitelli, Donatella, Caracciolo, Manuela, Romeo, Nelide, Spadafora, Patrizia, Candiano, Innocenza Cirò, Quattrone, Aldo

    Published in Neuroscience letters
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