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Author/Creator Pedemonte, M.

2. A 5-center experience with intrathecal administration of nusinersen in SMA1 in Italy letter to the editor of european journal of pediatric neurology regarding the manuscript "single-center experience with intrathecal administration of nusinersen in children with spinal muscular atrophy type 1" written by pechmann and colleagues". (July 2018)

Authors:
Sansone, V.A.; Pane, M.; Messina, S.; Bruno, C.; D'Amico, A.; Albamonte, E.; Catteruccia, M.; Sframeli, M.; Pedemonte, M.; Vita, G.; Bertini, E.; Mercuri, E.; Leone, Daniela; de Sanctis, Roberto; Forcina, Nicola; Piastra, Marco; Genovese, Orazio; Pedicelli, Alessandro; Versaci, Antonio; Rulli, Imma
Journal:
European journal of paediatric neurology
Issue:
Volume 22:Number 4(2018:Jul.)
Page Start:
729
Record Type:
Journal Article
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3. Beyond spinal muscular atrophy with lower extremity dominance: cerebellar hypoplasia associated with a novel mutation in BICD2. (April 2016)

Authors:
Fiorillo, C.; Moro, F.; Brisca, G.; Accogli, A.; Trucco, F.; Trovato, R.; Pedemonte, M.; Severino, M.; Catala, M.; Capra, V.; Santorelli, F. M.; Bruno, C.; Rossi, A.; Minetti, C.
Journal:
European journal of neurology
Issue:
Volume 23:Number 4(2016:Apr.)
Page Start:
e19
Record Type:
Journal Article
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4. Expanding the histopathological spectrum of CFL2‐related myopathies. Issue 6 (25th March 2018)

Authors:
Fattori, F.; Fiorillo, C.; Rodolico, C.; Tasca, G.; Verardo, M.; Bellacchio, E.; Pizzi, S.; Ciolfi, A.; Fagiolari, G.; Lupica, A.; Broda, P.; Pedemonte, M.; Moggio, M.; Bruno, C.; Tartaglia, M.; Bertini, E.; D'Amico, A.
Journal:
Clinical genetics
Issue:
Volume 93:Issue 6(2018)
Page Start:
1234
Record Type:
Journal Article
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6. MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients. Issue 1 (December 2016)

Authors:
Fiorillo, C.; Astrea, G.; Savarese, M.; Cassandrini, D.; Brisca, G.; Trucco, F.; Pedemonte, M.; Trovato, R.; Ruggiero, L.; Vercelli, L.; D'Amico, A.; Tasca, G.; Pane, M.; Fanin, M.; Bello, L.; Broda, P.; Musumeci, O.; Rodolico, C.; Messina, S.; Vita, G.
Journal:
Orphanet journal of rare diseases
Issue:
Volume 11:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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7. Onasemnogene abeparvovec gene therapy for symptomatic infantile-onset spinal muscular atrophy type 1 (STR1VE-EU): an open-label, single-arm, multicentre, phase 3 trial. Issue 10 (October 2021)

Authors:
Mercuri, Eugenio; Muntoni, Francesco; Baranello, Giovanni; Masson, Riccardo; Boespflug-Tanguy, Odile; Bruno, Claudio; Corti, Stefania; Daron, Aurore; Deconinck, Nicolas; Servais, Laurent; Straub, Volker; Ouyang, Haojun; Chand, Deepa; Tauscher-Wisniewski, Sitra; Mendonca, Nuno; Lavrov, Arseniy; Se...
Journal:
Lancet neurology
Issue:
Volume 20:Issue 10(2021)
Page Start:
832
Record Type:
Journal Article
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8. Sometimes they come back: New and old spinal muscular atrophy adults in the era of nusinersen. (31st October 2020)

Authors:
Sansone, V. A.; Coratti, G.; Pera, M. C.; Pane, M.; Messina, S.; Salmin, F.; Albamonte, E.; De Sanctis, R.; Sframeli, M.; Di Bella, V.; Morando, S.; d'Amico, A.; Frongia, A. L.; Antonaci, L.; Pirola, A.; Pedemonte, M.; Bertini, E.; Bruno, C.; Mercuri, E.
Other Names:
Di Bari Alessandra investigator.; Signorino Amelia investigator.; Longo Antonella investigator.; Tacchetti Paola investigator.; Brolatti Noemi investigator.; Rossi Diletta investigator.; Bravetti Chiara investigator.; Lucibello Simona investigator.; Fanelli Lavinia investigator.; Forcina Nicola i...
Journal:
European journal of neurology
Issue:
Volume 28:Number 2(2021)
Page Start:
602
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗