Antonio Gambardella - Dissemin

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Papers authored by Antonio Gambardella

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2007 Ida Manna, Angelo Labate, Antonio Gambardella

ORCID

, Paola Forabosco, Antonella La Russa, Emilio Le Piane, Umberto Aguglia, Aldo Quattrone

ORCID

Serotonin transporter gene (5-Htt): Association analysis with temporal lobe epilepsy

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Elvira V. De Marco, Antonio Gambardella

ORCID

, Ferdinanda Annesi, Angelo Labate, Sara Carrideo, Paola Forabosco, Donatella Civitelli, Innocenza C. Cirò Candiano, Patrizia Tarantino, Grazia Annesi, Aldo Quattrone

ORCID

Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy

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Mauro Giordano, Paolo Tirelli, Tiziana Ciarambino, Antonio Gambardella

ORCID

, Nicola Ferrara

ORCID

, Giuseppe Signoriello, Giuseppe Paolisso, Michele Varricchio

Screening of Depressive Symptoms in Young–Old Hemodialysis Patients: Relationship between Beck Depression Inventory and 15-Item Geriatric Depression Scale

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2006 Giuseppe Capovilla, Francesca Beccaria, Antonio Gambardella

ORCID

, Alessandra Montagnini, Paolo Avantaggiato, Stefano Seri

Photosensitive benign myoclonic epilepsy in infancy

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Angela Magariello, Maria Muglia, Alessandra Patitucci, Rosalucia Mazzei

ORCID

, Francesca Luisa Conforti, Anna Lia Gabriele, Teresa Sprovieri, Carmine Ungaro, Antonio Gambardella

ORCID

, Michelangelo Mancuso, Gabriele Siciliano, Damiano Branca, Umberto Aguglia, Maria Vittoria de Angelis, Katia Longo and 1 other authors

Novel spastin (SPG4) mutations in Italian patients with hereditary spastic paraplegia

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Angelo Labate, Eleonora Colosimo, Antonio Gambardella

ORCID

, Ugo Leggio, Roberta Ambrosio, Mario Loi, Aldo Quattrone

ORCID

Reflex periodic spasms induced by eating

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Angelo Labate, Eleonora Colosimo, Antonio Gambardella

ORCID

, Ugo Leggio, Roberta Ambrosio, Aldo Quattrone

ORCID

Levetiracetam in patients with generalised epilepsy and myoclonic seizures: An open label study

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Giuseppe Capovilla, Antonio Gambardella

ORCID

, Guido Rubboli, Francesca Beccaria, Alessandra Montagnini, Umberto Aguglia, Maria Paola Canevini, Susanna Casellato, Tiziana Granata, Francesco Paladin, Antonino Romeo, Giuseppe Stranci, Paolo Tinuper

ORCID

, Pierangelo Veggiotti, Giuliano Avanzini and 1 other authors

Suppressive Efficacy by a Commercially Available Blue Lens on PPR in 610 Photosensitive Epilepsy Patients

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Silvana Franceschetti, Antonio Gambardella

ORCID

, Laura Canafoglia

ORCID

, Pasquale Striano, Hannes Lohi, Elena Gennaro, Leonarda Ianzano, Pierangelo Veggiotti, Vito Sofia, Roberto Biondi, Salvatore Striano, Cinzia Gellera

ORCID

, Grazia Annesi, Francesca Madia, Donata Civitelli and 6 other authors

Clinical and Genetic Findings in 26 Italian Patients with Lafora Disease

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U. Leggio, A. Labate, I. Manna, E. Colosimo, R. Ambrosio, U. Aguglia, A. Gambardella

ORCID

The presence of M129V of PRNP gene influences mild temporal lobe epilepsy in women | La presenza del polimorfismo M129V del gene PRNP influenza l'insorgenza dell'epilessia del lobo temporale "mild" solo nelle donne

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M. L. Specchio, Luigi Maria Specchio, Nicola Specchio, Antonio Gambardella

ORCID

, Anna Teresa Giallonardo, Roberto Michelucci, Giovanni Boero, Angela La Neve

Open label, long-term, pragmatic study on levetiracetam in the treatment of juvenile myoclonic epilepsy

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Paola Valentino, Grazia Annesi, Innocenza C. Cirò Candiano, Cirò Candiano Ic, Ferdinanda Annesi, Donatella Civitelli, Patrizia Tarantino, Francesco Naso, Patrizia Spadafora, Sara Carrideo, Elvira V. De Marco, De Marco Ev, Domenico Consoli, Mario Zappia, Antonio Gambardella

ORCID

and 1 other authors

Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern

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Pasquale Striano, Lispi Ml, Maria Luisa Lispi, Francesca Madia, Boneschi Fm, Laura Bordo, A. Falace, Paolo Aridon, Emilia Gennaro, Marzia Traverso, Filippo Martinelli Boneschi, Baldassare Barone, B. Dalla Bernardina, Bernardo dalla Bernardina, Amedeo Bianchi and 19 other authors

Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families

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E. Colosimo, A. Gambardella

ORCID

, M. Mantegazza

ORCID

, A. Labate, R. Rusconi, E. Schiavon, F. Annesi, R. R. Cassulini, S. Carrideo, R. Chifari, Canevini, R. Canger, S. Franceschetti, G. Annesi, E. Wanke and 1 other authors

Electroclinical features of a family with SCN1A loss-of-function mutation associated with simple febrile seizures | Caratteristiche elettrocliniche di una famiglia con convulsioni febbrili semplici associata a mutazione con perdita della funzione di SCN1A

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A. Labate, P. Ventura, A. Gambardella

ORCID

, E. Le Piane, E. Colosimo, U. Leggio, R. Ambrosio, F. Condino, D. Messina, P. Lanza, U. Aguglia, A. Quattrone

ORCID

MRI evidence of mesial temporal sclerosis in sporadic " benign " temporal lobe epilepsy

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2005 Giuseppe Nicoletti, Gennarina Arabia, Pierfrancesco Pugliese, Giusi Torchia, Franco Pucci, Antonio Gambardella

ORCID

, Aldo Quattrone

ORCID

, Mario Zappia

Movement time and aging: A normative study in healthy subjects with the "Movement Time Analyzer®"

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P. Valentino, F. L. Conforti, D. Pirritano, R. Nisticò, R. Mazzei

ORCID

, A. Patitucci, T. Sprovieri, A. L. Gabriele, M. Muglia, A. Clodomiro, A. Gambardella

ORCID

, M. Zappia, A. Quattrone

ORCID

Brachial amyotrophic diplegia associated with a novel SOD1 mutation (L106P)

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

U. Leggio, A. Labate, E. Colosimo, R. Ambrosio, M. Loi, M. Sturniolo, E. Nero, F. Pucci, A. Gambardella

ORCID

Reflex periodic spasms induced by eating | Spasmi riflessi periodici scatenati dall'atto del mangiare

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A. J. Risti?, Aleksandar Ristic

ORCID

, S. Jankovi?, Slavko Jankovic, Grazzia Annesi, Sara Carrideo, Ferdinanda Annesi, Antonio Gambardella

ORCID

, G. Maksimovi?, Goran Maksimovic, B. Gnjatovi?, Nikola Vojvodic, Brankica Gnjatovic, I. Petrovi?, Igor Petrovic and 3 other authors

Generalized epilepsy with febrile seizures plus: Clinical and genetic analysis of three Serbian families

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