1992 …2020

Research output per year

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Research Output

2020

Age and sex prevalence estimate of Joubert syndrome in Italy

Nuovo, S., Bacigalupo, I., Ginevrino, M., Battini, R., Bertini, E., Borgatti, R., Casella, A., Micalizzi, A., Nardella, M., Romaniello, R., Serpieri, V., Zanni, G., Valente, E. M., Vanacore, N. & Group, JS. I. S., 2020, In : Neurology. 94, 8, p. e797-e801

Research output: Contribution to journalArticle

A novel IRF2BPL truncating variant is associated with endolysosomal storage

Ginevrino, M., Battini, R., Nuovo, S., Simonati, A., Micalizzi, A., Contaldo, I., Serpieri, V. & Valente, E. M., 2020, In : Molecular Biology Reports. 47, 1, p. 711-714 4 p.

Research output: Contribution to journalArticle

Genetic and phenotypic spectrum associated with IFIH1 gain-of-function

Orcesi Simona, 2020, In : Human Mutation. 41, 4, p. 837-849 13 p.

Research output: Contribution to journalArticle

Loss of ap4s1 in zebrafish leads to neurodevelopmental defects resembling spastic paraplegia 52

D’Amore, A., Tessa, A., Naef, V., Bassi, M. T., Citterio, A., Romaniello, R., Fichi, G., Galatolo, D., Mero, S., Battini, R., Bertocci, G., Baldacci, J., Sicca, F., Gemignani, F., Ricca, I., Rubegni, A., Hirst, J., Marchese, M., Sahin, M., Ebrahimi-Fakhari, D. & 1 others, Santorelli, F. M., 2020, (Accepted/In press) In : Annals of Clinical and Translational Neurology.

Research output: Contribution to journalArticle

Open Access
2019

Age and sex prevalence estimate of Joubert syndrome in Italy

JS Italian Study Group, Sep 2 2019, In : Neurology.

Research output: Contribution to journalArticle

Age and sex prevalence estimate of Joubert syndrome in Italy

Group, JS. I. S., Nuovo, S., Bacigalupo, I., Ginevrino, M., Battini, R., Bertini, E., Borgatti, R., Casella, A., Micalizzi, A., Nardella, M., Romaniello, R., Serpieri, V., Zanni, G., Valente, E. M. & Vanacore, N., Sep 2 2019, In : Neurology.

Research output: Contribution to journalArticle

A novel compound heterozygous genotype associated with aromatic amino acid decarboxylase deficiency: Clinical aspects and biochemical studies

Montioli, R., Battini, R., Paiardini, A., Tolve, M., Bertoldi, M., Carducci, C., Leuzzi, V. & Borri Voltattorni, C., Jun 2019, In : Molecular Genetics and Metabolism. 127, 2, p. 132-137 6 p.

Research output: Contribution to journalArticle

A novel IRF2BPL truncating variant is associated with endolysosomal storage

Ginevrino, M., Battini, R., Nuovo, S., Simonati, A., Micalizzi, A., Contaldo, I., Serpieri, V. & Valente, E. M., Jan 1 2019, In : Molecular Biology Reports.

Research output: Contribution to journalArticle

A novel IRF2BPL truncating variant is associated with endolysosomal storage

Ginevrino, M., Battini, R., Nuovo, S., Simonati, A., Micalizzi, A., Contaldo, I., Serpieri, V. & Valente, E. M., Oct 3 2019, In : Molecular Biology Reports. 47, 1, p. 711-714 4 p.

Research output: Contribution to journalArticle

A novel IRF2BPL truncating variant is associated with endolysosomal storage

Ginevrino, M., Battini, R., Nuovo, S., Simonati, A., Micalizzi, A., Contaldo, I., Serpieri, V. & Valente, E. M., Jan 1 2019, (Accepted/In press) In : Molecular Biology Reports.

Research output: Contribution to journalArticle

Correction: Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53

on behalf on the International DMD group, Aug 1 2019, In : PLoS One. 14, 7, p. e0220714

Research output: Contribution to journalArticle

Early neurodevelopmental characterization in children with cobalamin C/defect

Ricci, D., Martinelli, D., Ferrantini, G., Lucibello, S., Gambardella, ML., Olivieri, G., Chieffo, D., Battaglia, D., Diodato, D., Iarossi, G., Donati, A. M., Dionisi-Vici, C. & Battini, R., Jan 1 2019, (Accepted/In press) In : Journal of Inherited Metabolic Disease.

Research output: Contribution to journalArticle

Early neurodevelopmental characterization in children with cobalamin C/defect

Ricci, D., Martinelli, D., Ferrantini, G., Lucibello, S., Gambardella, ML., Olivieri, G., Chieffo, D., Battaglia, D., Diodato, D., Iarossi, G., Donati, A. M., Dionisi-Vici, C. & Battini, R., Jan 1 2019, In : Journal of Inherited Metabolic Disease.

Research output: Contribution to journalArticle

Genetic and phenotypic spectrum associated with IFIH1 gain-of-function

Rice, G. I., Park, S., Gavazzi, F., Adang, L. A., Ayuk, L. A., Van Eyck, L., Seabra, L., Barrea, C., Battini, R., Belot, A., Berg, S., Billette de Villemeur, T., Bley, A. E., Blumkin, L., Boespflug-Tanguy, O., Briggs, T. A., Brimble, E., Dale, R. C., Darin, N., Debray, F. G. & 30 others, De Giorgis, V., Denecke, J., Doummar, D., Drake af Hagelsrum, G., Eleftheriou, D., Estienne, M., Fazzi, E., Feillet, F., Galli, J., Hartog, N., Harvengt, J., Heron, B., Heron, D., Kelly, D. A., Lev, D., Levrat, V., Livingston, J. H., Marti, I., Mignot, C., Mochel, F., Nougues, M. C., Oppermann, I., Pérez-Dueñas, B., Popp, B., Rodero, M. P., Rodriguez, D., Saletti, V., Sharpe, C., Tonduti, D. & Orcesi, S., Dec 30 2019, (Accepted/In press) In : Human Mutation.

Research output: Contribution to journalArticle

Open Access

Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53

Brogna, C., Coratti, G., Pane, M., Ricotti, V., Messina, S., D’Amico, A., Bruno, C., Vita, G., Berardinelli, A., Mazzone, E., Magri, F., Ricci, F., Mongini, T., Battini, R., Bello, L., Pegoraro, E., Baranello, G., Previtali, S. C., Politano, L., Comi, G. P. & 6 others, Sansone, V. A., Donati, A., Bertini, E., Muntoni, F., Goemans, N. & Mercuri, E., 2019, In : PLoS One. 14, 6

Research output: Contribution to journalArticle

Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53

on behalf on the International DMD group, 2019, In : PLoS One. 14, 6, p. e0218683

Research output: Contribution to journalArticle

Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53

group, O. B. O. T. I. DMD., Brogna, C., Coratti, G., Pane, M., Ricotti, V., Messina, S., D'Amico, A., Bruno, C., Vita, G., Berardinelli, A., Mazzone, E., Magri, F., Ricci, F., Mongini, T., Battini, R., Bello, L., Pegoraro, E., Baranello, G., Previtali, S. C., Politano, L. & 7 others, Comi, G. P., Sansone, V. A., Donati, A., Bertini, E., Muntoni, F., Goemans, N. & Mercuri, E., 2019, In : PLoS One. 14, 6, p. e0218683

Research output: Contribution to journalArticle

Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53

Brogna, C., Coratti, G., Pane, M., Ricotti, V., Messina, S., D’Amico, A., Bruno, C., Vita, G., Berardinelli, A., Mazzone, E., Magri, F., Ricci, F., Mongini, T., Battini, R., Bello, L., Pegoraro, E., Baranello, G., Previtali, S. C., Politano, L., Comi, G. P. & 6 others, Sansone, V. A., Donati, A., Bertini, E., Muntoni, F., Goemans, N. & Mercuri, E., 2019, In : PLoS One. 14, 6, e0218683.

Research output: Contribution to journalArticle

Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review

Garau, J., Cavallera, V., Valente, M., Tonduti, D., Sproviero, D., Zucca, S., Battaglia, D., Battini, R., Bertini, E., Cappanera, S., Chiapparini, L., Crasà, C., Crichiutti, G., Dalla Giustina, E., D'Arrigo, S., De Giorgis, V., De Simone, M., Galli, J., La Piana, R., Messana, T. & 19 others, Moroni, I., Nardocci, N., Panteghini, C., Parazzini, C., Pichiecchio, A., Pini, A., Ricci, F., Saletti, V., Salvatici, E., Santorelli, F. M., Sartori, S., Tinelli, F., Uggetti, C., Veneselli, E., Zorzi, G., Garavaglia, B., Fazzi, E., Orcesi, S. & Cereda, C., May 26 2019, In : Journal of Clinical Medicine. 8, 5

Research output: Contribution to journalArticle

Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review

Garau, J., Cavallera, V., Valente, M., Tonduti, D., Sproviero, D., Zucca, S., Battaglia, D., Battini, R., Bertini, E., Cappanera, S., Chiapparini, L., Crasà, C., Crichiutti, G., Dalla Giustina, E., D’Arrigo, S., De Giorgis, V., De Simone, M., Galli, J., La Piana, R., Messana, T. & 19 others, Moroni, I., Nardocci, N., Panteghini, C., Parazzini, C., Pichiecchio, A., Pini, A., Ricci, F., Saletti, V., Salvatici, E., Santorelli, F. M., Sartori, S., Tinelli, F., Uggetti, C., Veneselli, E., Zorzi, G., Garavaglia, B., Fazzi, E., Orcesi, S. & Cereda, C., 2019, In : Journal of Clinical Medicine. 8, 5

Research output: Contribution to journalArticle

Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review

Garau, J., Cavallera, V., Valente, M., Tonduti, D., Sproviero, D., Zucca, S., Battaglia, D., Battini, R., Bertini, E., Cappanera, S., Chiapparini, L., Crasà, C., Crichiutti, G., Dalla Giustina, E., D'Arrigo, S., De Giorgis, V., De Simone, M., Galli, J., La Piana, R., Messana, T. & 19 others, Moroni, I., Nardocci, N., Panteghini, C., Parazzini, C., Pichiecchio, A., Pini, A., Ricci, F., Saletti, V., Salvatici, E., Santorelli, F. M., Sartori, S., Tinelli, F., Uggetti, C., Veneselli, E., Zorzi, G., Garavaglia, B., Fazzi, E., Orcesi, S. & Cereda, C., May 26 2019, In : Journal of Clinical Medicine. 8, 5

Research output: Contribution to journalArticle

2018

Brain morphometry of preschool age children affected by autism spectrum disorder: Correlation with clinical findings

Lucibello, S., Verdolotti, T., Giordano, F. M., Lapenta, L., Infante, A., Piludu, F., Tartaglione, T., Chieffo, D., Colosimo, C., Mercuri, E. & Battini, R., Aug 16 2018, In : Clinical Anatomy. 32, 1, p. 143-150 8 p.

Research output: Contribution to journalArticle

Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study

Astrea, G., Romano, A., Angelini, C., Antozzi, C. G., Barresi, R., Battini, R., Battisti, C., Bertini, E., Bruno, C., Cassandrini, D., Fanin, M., Fattori, F., Fiorillo, C., Guerrini, R., Maggi, L., Mercuri, E., Morani, F., Mora, M., Moro, F., Pezzini, I. & 16 others, Picillo, E., Pinelli, M., Politano, L., Rubegni, A., Sanseverino, W., Savarese, M., Striano, P., Torella, A., Trevisan, C. P., Trovato, R., Zaraieva, I., Muntoni, F., Nigro, V., D'Amico, A., Santorelli, F. M. & Network, I. CMD., 2018, In : Orphanet Journal of Rare Diseases. 13, 1

Research output: Contribution to journalArticle

Four years follow up of ACY1 deficient patient and pedigree study

Alessandrì, M. G., Milone, R., Casalini, C., Nesti, C., Cioni, G. & Battini, R., Aug 1 2018, In : Brain and Development. 40, 7, p. 570-575 6 p.

Research output: Contribution to journalArticle

Functional levels and MRI patterns of muscle involvement in upper limbs in Duchenne muscular dystrophy

Brogna, C., Cristiano, L., Tartaglione, T., Verdolotti, T., Fanelli, L., Ficociello, L., Tasca, G., Battini, R., Coratti, G., Forcina, N., De Santis, R., Norcia, G., Carnicella, S., Colosimo, C., Carlier, P., Pane, M. & Mercuri, E., Jun 1 2018, In : PLoS One. 13, 6, e0199222.

Research output: Contribution to journalArticle

Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndrome

Nuovo, S., Fuiano, L., Micalizzi, A., Battini, R., Bertini, E., Borgatti, R., Caridi, G., D'Arrigo, S., Fazzi, E., Fischetto, R., Ghiggeri, G. M., Giordano, L., Leuzzi, V., Romaniello, R., Signorini, S., Stringini, G., Zanni, G., Romani, M., Valente, E. M. & Emma, F., Nov 6 2018, In : Nephrology Dialysis Transplantation.

Research output: Contribution to journalArticle

Implicit learning deficit in children with Duchenne muscular dystrophy: Evidence for a cerebellar cognitive impairment?

Vicari, S., Piccini, G., Mercuri, E., Battini, R., Chieffo, D., Bulgheroni, S., Pecini, C., Lucibello, S., Lenzi, S., Moriconi, F., Pane, M., D'Amico, A., Astrea, G., Baranello, G., Riva, D., Cioni, G. & Alfieri, P., Jan 16 2018, In : PLoS One. 13, 1, p. e0191164 10 p.

Research output: Contribution to journalArticle

Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental Syndrome

Bauer, C. K., Calligari, P., Radio, F. C., Caputo, V., Dentici, M. L., Falah, N., High, F., Pantaleoni, F., Barresi, S., Ciolfi, A., Pizzi, S., Bruselles, A., Person, R., Richards, S., Cho, M. T., Claps Sepulveda, D. J., Pro, S., Battini, R., Zampino, G., Digilio, M. C. & 4 others, Bocchinfuso, G., Dallapiccola, B., Stella, L. & Tartaglia, M., Oct 4 2018, In : American Journal of Human Genetics. 103, 4, p. 621-630 10 p.

Research output: Contribution to journalArticle

Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental Syndrome

Bauer, C. K., Calligari, P., Radio, F. C., Caputo, V., Dentici, M. L., Falah, N., High, F., Pantaleoni, F., Barresi, S., Ciolfi, A., Pizzi, S., Bruselles, A., Person, R., Richards, S., Cho, M. T., Claps Sepulveda, D. J., Pro, S., Battini, R., Zampino, G., Digilio, M. C. & 4 others, Bocchinfuso, G., Dallapiccola, B., Stella, L. & Tartaglia, M., 2018, In : American Journal of Human Genetics. 103, 4, p. 621-630 10 p.

Research output: Contribution to journalArticle

Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study

D'Amore, A., Tessa, A., Casali, C., Dotti, M. T., Filla, A., Silvestri, G., Antenora, A., Astrea, G., Barghigiani, M., Battini, R., Battisti, C., Bruno, I., Cereda, C., Dato, C., Di Iorio, G., Donadio, V., Felicori, M., Fini, N., Fiorillo, C., Gallone, S. & 33 others, Gemignani, F., Gigli, G. L., Graziano, C., Guerrini, R., Gurrieri, F., Kariminejad, A., Lieto, M., Marques LourenḈo, C., Malandrini, A., Mandich, P., Marcotulli, C., Mari, F., Massacesi, L., Melone, M. A. B., Mignarri, A., Milone, R., Musumeci, O., Pegoraro, E., Perna, A., Petrucci, A., Pini, A., Pochiero, F., Pons, M. R., Ricca, I., Rossi, S., Seri, M., Stanzial, F., Tinelli, F., Toscano, A., Valente, M., Federico, A., Rubegni, A. & Santorelli, F. M., 2018, In : Frontiers in Neurology. 9, p. 981

Research output: Contribution to journalArticle

Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study

D'Amore, A., Tessa, A., Casali, C., Dotti, M. T., Filla, A., Silvestri, G., Antenora, A., Astrea, G., Barghigiani, M., Battini, R., Battisti, C., Bruno, I., Cereda, C., Dato, C., Di Iorio, G., Donadio, V., Felicori, M., Fini, N., Fiorillo, C., Gallone, S. & 33 others, Gemignani, F., Gigli, G. L., Graziano, C., Guerrini, R., Gurrieri, F., Kariminejad, A., Lieto, M., Marques LourenḈo, C., Malandrini, A., Mandich, P., Marcotulli, C., Mari, F., Massacesi, L., Melone, M. A. B., Mignarri, A., Milone, R., Musumeci, O., Pegoraro, E., Perna, A., Petrucci, A., Pini, A., Pochiero, F., Pons, M. R., Ricca, I., Rossi, S., Seri, M., Stanzial, F., Tinelli, F., Toscano, A., Valente, M., Federico, A., Rubegni, A. & Santorelli, F. M., 2018, In : Frontiers in Neurology. 9, p. 981 1 p.

Research output: Contribution to journalArticle

Next generation sequencing technologies for a successful diagnosis in a cold case of Leigh syndrome

Aretini, P., Mazzanti, C. M., La Ferla, M., Franceschi, S., Lessi, F., De Gregorio, V., Nesti, C., Valetto, A., Bertini, V., Toschi, B., Battini, R. & Caligo, M. A., Jul 20 2018, In : BMC Neurology. 18, 1, 99.

Research output: Contribution to journalArticle

R106C TFG variant causes infantile neuroaxonal dystrophy “plus” syndrome

Catania, A., Battini, R., Pippucci, T., Pasquariello, R., Chiapparini, M. L., Seri, M., Garavaglia, B., Zorzi, G., Nardocci, N., Ghezzi, D. & Tiranti, V., Aug 1 2018, In : Neurogenetics. 19, 3, p. 179-187 9 p.

Research output: Contribution to journalArticle

Upper limb function in Duchenne muscular dystrophy: 24 month longitudinal data

Pane, M., Coratti, G., Brogna, C., Mazzone, E. S., Mayhew, A., Fanelli, L., Messina, S., D'Amico, A., Catteruccia, M., Scutifero, M., Frosini, S., Lanzillotta, V., Colia, G., Cavallaro, F., Rolle, E., De Sanctis, R., Forcina, N., Petillo, R., Barp, A., Gardani, A. & 19 others, Pini, A., Monaco, G., D'Angelo, M. G., Zanin, R., Vita, G. L., Bruno, C., Mongini, T., Ricci, F., Pegoraro, E., Bello, L., Berardinelli, A., Battini, R., Sansone, V., Albamonte, E., Baranello, G., Bertini, E., Politano, L., Sormani, M. P. & Mercuri, E., 2018, In : PLoS One. 13, 6, p. e0199223

Research output: Contribution to journalArticle

Upper limb function in Duchenne muscular dystrophy: 24 month longitudinal data

Pane, M., Coratti, G., Brogna, C., Mazzone, E. S., Mayhew, A., Fanelli, L., Messina, S., Amico, A. D., Catteruccia, M., Scutifero, M., Frosini, S., Lanzillotta, V., Colia, G., Cavallaro, F., Rolle, E., De Sanctis, R., Forcina, N., Petillo, R., Barp, A., Gardani, A. & 19 others, Pini, A., Monaco, G., Angelo, M. G. D., Zanin, R., Vita, G. L., Bruno, C., Mongini, T., Ricci, F., Pegoraro, E., Bello, L., Berardinelli, A., Battini, R., Sansone, V., Albamonte, E., Baranello, G., Bertini, E., Politano, L., Sormani, M. P. & Mercuri, E., 2018, In : PLoS One. 13, 6

Research output: Contribution to journalArticle

Upper limb function in Duchenne muscular dystrophy: 24 month longitudinal data

Pane, M., Coratti, G., Brogna, C., Mazzone, E. S., Mayhew, A., Fanelli, L., Messina, S., Amico, A. D., Catteruccia, M., Scutifero, M., Frosini, S., Lanzillotta, V., Colia, G., Cavallaro, F., Rolle, E., De Sanctis, R., Forcina, N., Petillo, R., Barp, A., Gardani, A. & 19 others, Pini, A., Monaco, G., Angelo, M. G. D., Zanin, R., Vita, G. L., Bruno, C., Mongini, T., Ricci, F., Pegoraro, E., Bello, L., Berardinelli, A., Battini, R., Sansone, V., Albamonte, E., Baranello, G., Bertini, E., Politano, L., Sormani, M. P. & Mercuri, E., 2018, In : PLoS One. 13, 6

Research output: Contribution to journalArticle

Upper limb function in Duchenne muscular dystrophy: 24 month longitudinal data

Pane, M., Coratti, G., Brogna, C., Mazzone, E. S., Mayhew, A., Fanelli, L., Messina, S., Amico, A. D., Catteruccia, M., Scutifero, M., Frosini, S., Lanzillotta, V., Colia, G., Cavallaro, F., Rolle, E., De Sanctis, R., Forcina, N., Petillo, R., Barp, A., Gardani, A. & 19 others, Pini, A., Monaco, G., Angelo, M. G. D., Zanin, R., Vita, G. L., Bruno, C., Mongini, T., Ricci, F., Pegoraro, E., Bello, L., Berardinelli, A., Battini, R., Sansone, V., Albamonte, E., Baranello, G., Bertini, E., Politano, L., Sormani, M. P. & Mercuri, E., 2018, In : PLoS One. 13, 6

Research output: Contribution to journalArticle

2017

Cognitive profile in Duchenne muscular dystrophy boys without intellectual disability: The role of executive functions

Battini, R., Chieffo, D., Bulgheroni, S., Piccini, G., Pecini, C., Lucibello, S., Lenzi, S., Moriconi, F., Pane, M., Astrea, G., Baranello, G., Alfieri, P., Vicari, S., Riva, D., Cioni, G. & Mercuri, E., Dec 6 2017, In : Neuromuscular Disorders. 28, 2, p. 122-128 7 p.

Research output: Contribution to journalArticle

Cognitive profile in Duchenne muscular dystrophy boys without intellectual disability: The role of executive functions

Battini, R., Chieffo, D., Bulgheroni, S., Piccini, G., Pecini, C., Lucibello, S., Lenzi, S., Moriconi, F., Pane, M., Astrea, G., Baranello, G., Alfieri, P., Vicari, S., Riva, D., Cioni, G. & Mercuri, E., Nov 29 2017, (Accepted/In press) In : Neuromuscular Disorders.

Research output: Contribution to journalArticle

Deletion Extents Are Not the Cause of Clinical Variability in 22q11.2 Deletion Syndrome: Does the Interaction between DGCR8 and miRNA-CNVs Play a Major Role?

Bertini, V., Azzara, A., Legitimo, A., Milone, R., Battini, R., Consolini, R. & Valetto, A., May 1 2017, In : Frontiers in Genetics. 8

Research output: Contribution to journalArticle

Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements

D'Amico, A., Catteruccia, M., Baranello, G., Politano, L., Govoni, A., Previtali, SC., Pane, M., D'Angelo, MG., Bruno, C., Messina, S., Ricci, F., Pegoraro, E., Pini, A., Berardinelli, A., Gorni, K., Battini, R., Vita, G., Trucco, F., Scutifero, M., Petillo, R. & 8 others, D'Ambrosio, P., Ardissone, A., Pasanisi, B., Mongini, T., Moggio, M., Comi, GP., Mercuri, E. & Bertini, E., 2017, In : Neuromuscular Disorders. 27, 5, p. 447-451 5 p.

Research output: Contribution to journalArticle

Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements

D'Amico, A., Catteruccia, M., Baranello, G., Politano, L., Govoni, A., Previtali, S. C., Pane, M., D'Angelo, M. G., Bruno, C., Messina, S., Ricci, F., Pegoraro, E., Pini, A., Berardinelli, A., Gorni, K., Battini, R., Vita, G., Trucco, F., Scutifero, M., Petillo, R. & 8 others, D'Ambrosio, P., Ardissone, A., Pasanisi, B., Mongini, T., Moggio, M., Comi, G. P., Mercuri, E. & Bertini, E., May 27 2017, In : Neuromuscular Disorders. 27, 5, p. 447-451 5 p.

Research output: Contribution to journalArticle

Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements

D'Amico, A., Catteruccia, M., Baranello, G., Politano, L., Govoni, A., Previtali, S. C., Pane, M., D'Angelo, M. G., Bruno, C., Messina, S., Ricci, F., Pegoraro, E., Pini, A., Berardinelli, A., Gorni, K., Battini, R., Vita, G. L., Trucco, F., Scutifero, M., Petillo, R. & 9 others, D'Ambrosio, P., Ardissone, A., Pasanisi, B., Vita, G., Mongini, T., Moggio, M., Comi, G. P., Mercuri, E. & Bertini, E., 2017, In : Neuromuscular Disorders. 27, 5, p. 447-451 5 p.

Research output: Contribution to journalArticle

Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements

D'Amico, A., Catteruccia, M., Baranello, G., Politano, L., Govoni, A., Previtali, S. C., Pane, M., D'Angelo, M. G., Bruno, C., Messina, S., Ricci, F., Pegoraro, E., Pini, A., Berardinelli, A., Gorni, K., Battini, R., Vita, G., Trucco, F., Scutifero, M., Petillo, R. & 9 others, D'Ambrosio, P., Ardissone, A., Pasanisi, B., Vita, G., Mongini, T., Moggio, M., Comi, G. P., Mercuri, E. & Bertini, E., 2017, In : Neuromuscular Disorders. 27, 5, p. 447-451 5 p.

Research output: Contribution to journalArticle

Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements

D'Amico, A., Catteruccia, M., Baranello, G., Politano, L., Govoni, A., Previtali, S. C., Pane, M., D'Angelo, M. G., Bruno, C., Messina, S., Ricci, F., Pegoraro, E., Pini, A., Berardinelli, A., Gorni, K., Battini, R., Vita, G., Trucco, F., Scutifero, M., Petillo, R. & 8 others, D'Ambrosio, P., Ardissone, A., Pasanisi, B., Mongini, T., Moggio, M., Comi, G. P., Mercuri, E. & Bertini, E., 2017, In : Neuromuscular Disorders. 27, 5, p. 447-451 5 p.

Research output: Contribution to journalArticle

Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements

D'Amico, A., Catteruccia, M., Baranello, G., Politano, L., Govoni, A., Previtali, S. C., Pane, M., D'Angelo, M. G., Bruno, C., Messina, S., Ricci, F., Pegoraro, E., Pini, A., Berardinelli, A., Gorni, K., Battini, R., Vita, G., Trucco, F., Scutifero, M., Petillo, R. & 8 others, D'Ambrosio, P., Ardissone, A., Pasanisi, B., Mongini, T., Moggio, M., Comi, G. P., Mercuri, E. & Bertini, E., 2017, In : Neuromuscular Disorders. 27, 5, p. 447-451 5 p.

Research output: Contribution to journalArticle

Implicit learning deficit in children with Duchenne muscular dystrophy: Evidence for a cerebellar cognitive impairment?

Vicari, S., Piccini, G., Mercuri, E., Battini, R., Chieffo, D., Bulgheroni, S., Pecini, C., Lucibello, S., Lenzi, S., Moriconi, F., Pane, M., D’Amico, A., Astrea, G., Baranello, G., Riva, D., Cioni, G. & Alfieri, P., Dec 31 2017, (Accepted/In press) In : PLoS One. 13, 1, e0191164.

Research output: Contribution to journalArticle