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2020

Acute flaccid paralysis due to Echovirus 30 in an immunosuppressed transplant recipient

Mauri, E., Mastrangelo, A., Testa, S., Pellegrinelli, L., Pariani, E., Binda, S., Triulzi, F., Barbieri, S., Bana, C., Montini, G. & Dilena, R., 2020, In : Journal of NeuroVirology. 26, 2, p. 284-288

Research output: Contribution to journalArticle

2019

Influence of etiology on treatment choices for neonatal seizures: A survey among pediatric neurologists

Dilena, R., De Liso, P., Di Capua, M., Consonni, D., Capovilla, G., Pisani, F., Suppiej, A., Vitaliti, G., Falsaperla, R. & Pruna, D., Apr 3 2019, In : Brain and Development.

Research output: Contribution to journalArticle

Influence of etiology on treatment choices for neonatal seizures: A survey among pediatric neurologists

Dilena, R., De Liso, P., Di Capua, M., Consonni, D., Capovilla, G., Pisani, F., Suppiej, A., Vitaliti, G., Falsaperla, R. & Pruna, D., Jan 1 2019, In : Brain and Development. 41, 7, p. 595-599

Research output: Contribution to journalArticle

Open Access

Therapeutic effect of Anakinra in the relapsing chronic phase of febrile infection–related epilepsy syndrome

Dilena, R., Mauri, E., Aronica, E., Bernasconi, P., Bana, C., Cappelletti, C., Carrabba, G., Ferrero, S., Giorda, R., Guez, S., Scalia Catenacci, S., Triulzi, F., Barbieri, S., Calderini, E. & Vezzani, A., Jun 1 2019, In : Epilepsia Open. 4, 2, p. 344-350 7 p.

Research output: Contribution to journalArticle

Open Access
2018

A de novo C19orf12 heterozygous mutation in a patient with MPAN

Monfrini, E., Melzi, V., Buongarzone, G., Franco, G., Ronchi, D., Dilena, R., Scola, E., Vizziello, P., Bordoni, A., Bresolin, N., Comi, G. P., Corti, S. & Di Fonzo, A., 2018, In : Parkinsonism and Related Disorders. 48, p. 109-111

Research output: Contribution to journalArticle

Early Treatment with Quinidine in 2 Patients with Epilepsy of Infancy with Migrating Focal Seizures (EIMFS) Due to Gain-of-Function KCNT1 Mutations: Functional Studies, Clinical Responses, and Critical Issues for Personalized Therapy

Dilena, R., DiFrancesco, J. C., Soldovieri, M. V., Giacobbe, A., Ambrosino, P., Mosca, I., Galli, M. A., Guez, S., Fumagalli, M., Miceli, F., Cattaneo, D., Darra, F., Gennaro, E., Zara, F., Striano, P., Castellotti, B., Gellera, C., Varesio, C., Veggiotti, P. & Taglialatela, M., 2018, In : Neurotherapeutics. 15, 4, p. 1112-1126

Research output: Contribution to journalArticle

Familial dominant epilepsy and mild pachygyria associated with a constitutional LIS1 mutation

De Vita, D., Mei, D., Rutigliano, D., Bartalucci, N., Cinnante, C. M., Parrini, E., Dilena, R. & Guerrini, R., 2018, In : American Journal of Medical Genetics, Part A. 176, 12, p. 2808-2812

Research output: Contribution to journalArticle

Subclinical Leber's hereditary optic neuropathy with pediatric acute spinal cord onset: More than meets the eye

Mauri, E., Dilena, R., Boccazzi, A., Ronchi, D., Piga, D., Triulzi, F., Gagliardi, D., Brusa, R., Faravelli, I., Bresolin, N., Magri, F., Corti, S. & Comi, G. P., Dec 27 2018, In : BMC Neurology. 18, 1, 220.

Research output: Contribution to journalArticle

2017

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

Wolff, M., Johannesen, K. M., Hedrich, U. B. S., Masnada, S., Rubboli, G., Gardella, E., Lesca, G., Ville, D., Milh, M., Villard, L., Afenjar, A., Chantot-Bastaraud, S., Mignot, C., Lardennois, C., Nava, C., Schwarz, N., Gérard, M., Perrin, L., Doummar, D., Auvin, S. & 30 others, Miranda, M. J., Hempel, M., Brilstra, E., Knoers, N., Verbeek, N., van Kempen, M., Braun, K. P., Mancini, G., Biskup, S., Hörtnagel, K., Döcker, M., Bast, T., Loddenkemper, T., Wong-Kisiel, L., Baumeister, F. M., Fazeli, W., Striano, P., Dilena, R., Fontana, E., Zara, F., Kurlemann, G., Klepper, J., Thoene, J. G., Arndt, D. H., Deconinck, N., Schmitt-Mechelke, T., Maier, O., Muhle, H., Trivisano, M. & Specchio, N., May 1 2017, In : Brain. 140, 5, p. 1316-1336 21 p.

Research output: Contribution to journalArticle

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

Wolff, M., Johannesen, K. M., Hedrich, U. B. S., Masnada, S., Rubboli, G., Gardella, E., Lesca, G., Ville, D., Milh, M., Villard, L., Afenjar, A., Chantot-Bastaraud, S., Mignot, C., Lardennois, C., Nava, C., Schwarz, N., Gérard, M., Perrin, L., Doummar, D., Auvin, S. & 65 others, Miranda, M. J., Hempel, M., Brilstra, E., Knoers, N., Verbeek, N., Van Kempen, M., Braun, K. P., Mancini, G., Biskup, S., Hörtnagel, K., Döcker, M., Bast, T., Loddenkemper, T., Wong-Kisiel, L., Baumeister, F. M., Fazeli, W., Striano, P., Dilena, R., Fontana, E., Zara, F., Kurlemann, G., Klepper, J., Thoene, J. G., Arndt, D. H., Deconinck, N., Schmitt-Mechelke, T., Maier, O., Muhle, H., Wical, B., Finetti, C., Brückner, R., Pietz, J., Golla, G., Jillella, D., Linnet, K. M., Charles, P., Moog, U., Õiglane-Shlik, E., Mantovani, J. F., Park, K., Deprez, M., Lederer, D., Mary, S., Scalais, E., Selim, L., Van Coster, R., Lagae, L., Nikanorova, M., Hjalgrim, H., Korenke, G. C., Trivisano, M., Specchio, N., Ceulemans, B., Dorn, T., Helbig, K. L., Hardies, K., Stamberger, H., De Jonghe, P., Weckhuysen, S., Lemke, J. R., Krägeloh-Mann, I., Helbig, I., Kluger, G., Lerche, H. & Møller, R. S., May 1 2017, In : Brain. 140, 5, p. 1316-1336 21 p.

Research output: Contribution to journalArticle

2016

Dramatic effect of levetiracetam in early-onset epileptic encephalopathy due to STXBP1 mutation

Dilena, R., Striano, P., Traverso, M., Viri, M., Cristofori, G., Tadini, L., Barbieri, S., Romeo, A. & Zara, F., 2016, In : Brain and Development. 38, 1, p. 128-131 4 p.

Research output: Contribution to journalArticle

Epilepsy surgery in a liver-transplanted girl with temporal lobe epilepsy and hippocampal sclerosis following PRES with status epilepticus

Dilena, R., Nebbia, G., Fiorica, L., Farallo, M., Degrassi, I., Gozzo, F., Pelliccia, V., Barbieri, S., Cossu, M. & Tassi, L., 2016, In : European Journal of Paediatric Neurology. 20, 4, p. 652-656 5 p.

Research output: Contribution to journalArticle

Locked-in-like fulminant infantile Guillain-Barré syndrome associated with herpes simplex virus 1 infection

Dilena, R., Strazzer, S., Esposito, S., Paglialonga, F., Tadini, L., Barbieri, S. & Giannini, A. M., Jan 1 2016, In : Muscle and Nerve. 53, 1, p. 140-143 4 p.

Research output: Contribution to journalArticle

Locked-in-like fulminant infantile Guillain-Barré syndrome associated with herpes simplex virus 1 infection

Dilena, R., Strazzer, S., Esposito, S., Paglialonga, F., Tadini, L., Barbieri, S. & Giannini, A., Jan 1 2016, In : Muscle and Nerve. 53, 1, p. 140-143 4 p.

Research output: Contribution to journalArticle

Posterior reversible encephalopathy syndrome after kidney transplantation in pediatric recipients: Two cases

Giussani, A., Ardissino, G., Belingheri, M., Dilena, R., Raiteri, M., Pasciucco, A., Colico, C. & Beretta, C., Feb 1 2016, In : Pediatric Transplantation. 20, 1, p. 68-71 4 p.

Research output: Contribution to journalArticle

STXBP1 encephalopathy

Stamberger, H., Nikanorova, M., Willemsen, M. H., Accorsi, P., Angriman, M., Baier, H., Benkel-Herrenbrueck, I., Benoit, V., Budetta, M., Caliebe, A., Cantalupo, G., Capovilla, G., Casara, G., Courage, C., Deprez, M., Destrée, A., Dilena, R., Erasmus, C. E., Fannemel, M., Fjær, R. & 37 others, Giordano, L., Helbig, K. L., Heyne, H. O., Klepper, J., Kluger, G. J., Lederer, D., Lodi, M., Maier, O., Merkenschlager, A., Michelberger, N., Minetti, C., Muhle, H., Phalin, J., Ramsey, K., Romeo, A., Schallner, J., Schanze, I., Shinawi, M., Sleegers, K., Sterbova, K., Syrbe, S., Traverso, M., Tzschach, A., Uldall, P., Van Coster, R., Verhelst, H., Viri, M., Winter, S., Wolff, M., Zenker, M., Zoccante, L., De Jonghe, P., Helbig, I., Striano, P., Lemke, J. R., Møller, R. S. & Weckhuysen, S., Mar 8 2016, In : Neurology. 86, 10, p. 954-962 9 p.

Research output: Contribution to journalArticle

2015

Paediatric anti-N-methyl-d-aspartate receptor encephalitis: The first Italian multicenter case series

Sartori, S., Nosadini, M., Cesaroni, E., Falsaperla, R., Capovilla, G., Beccaria, F., Mancardi, M. M., Santangelo, G., Giunta, L., Boniver, C., Cantalupo, G., Cappellari, A., Costa, P., Dalla Bernardina, B., Dilena, R., Natali Sora, M. G., Pelizza, M. F., Pruna, D., Serino, D., Vanadia, F. & 5 others, Vigevano, F., Zamponi, N., Zanus, C., Toldo, I. & Suppiej, A., Jul 1 2015, In : European Journal of Paediatric Neurology. 19, 4, p. 453-463 11 p.

Research output: Contribution to journalArticle

2014

Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis

Citterio, A., Arnoldi, A., Panzeri, E., D'Angelo, M. G., Filosto, M., Dilena, R., Arrigoni, F., Castelli, M., Maghini, C., Germiniasi, C., Menni, F., Martinuzzi, A., Bresolin, N. & Bassi, M. T., 2014, In : Journal of Neurology. 261, 2, p. 373-381 9 p.

Research output: Contribution to journalArticle

2013

Un caso di epilessia ad esordio precoce resistente ai farmaci antiepilettici di prima scelta, drammaticamente responsiva al levetiracetam: Significato di un profilo di risposta inusuale ai farmaci antiepilettici

Translated title of the contribution: A case of early onset epilepsy resistant to first line antiepileptic drugs dramatically responsive to levetiracetam: Significance of an unusual response to antiepileptic drugsDilena, R., Tadini, L., Cristofori, G., Cappellari, A., Nossa, A., Belli, M., Mosca, F., Barbieri, S. & Romeo, A., Apr 2013, In : Bollettino - Lega Italiana contro l'Epilessia. 145, p. 271-274 4 p.

Research output: Contribution to journalArticle

2011

Medulloblastoma presenting as dialysis disequilibrium syndrome

Dilena, R., Paglialonga, F., Barbieri, S. & Edefonti, A., Oct 2011, In : Hemodialysis International. 15, SUPPL. 1

Research output: Contribution to journalArticle

Spinal direct current stimulation modulates the activity of gracile nucleus and primary somatosensory cortex in anaesthetized rats

Aguilar, J., Pulecchi, F., Dilena, R., Oliviero, A., Priori, A. & Foffani, G., Oct 2011, In : Journal of Physiology. 589, 20, p. 4981-4996 16 p.

Research output: Contribution to journalArticle

2008

Transcranial direct current stimulation in two patients with Tourette syndrome

Mrakic-Sposta, S., Marceglia, S., Mameli, F., Dilena, R., Tadini, L. & Priori, A., Nov 15 2008, In : Movement Disorders. 23, 15, p. 2259-2261 3 p.

Research output: Contribution to journalArticle