10 results on '"Lamperti, C."'
Search Results
2. Neuro-telehealth for fragile patients in a tertiary referral neurological institute during the COVID-19 pandemic in Milan, Lombardy
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Pareyson D., Pantaleoni C., Eleopra R., De Filippis G., Moroni I., Freri E., Zibordi F., Bulgheroni S., Pagliano E., Sarti D., Silvani A., Grazzi L., Tiraboschi P., Didato G., Anghileri E., Bersano A., Valentini L., Piacentini S., Muscio C., Leonardi M., Mariotti C., Eoli M., Nuzzo S., Tagliavini F., Confalonieri P., De Giorgi F., Antozzi C., Ardissone A., Bersano E., Boncoraglio G., Bonvegna S., Botturi A., Brambilla L., Canafoglia L., Caputi L., Caroppo P., Carriero M. R., Casali C., Casazza M., Catania A., Ciaccio C., Cilia R., DallaBella E., D'Amico D., Danti F. R., D'Arrigo S., DeCurtis M., Deleo F., Devigili G., DiFede G., DiGiacomo R., Elia A., Esposito S., Estienne M., Fenu S., Fichera M., Finocchiaro G., Frangiamore R., Gatti M., Gaviani P., Giaccone G., Giani L., Giovagnoli A. R., Andreasi N. G., Granata T., Granocchio E., Lamperti C., Lamperti E., Leone M., Masson R., Nanetti L., Nardocci N., Pastori C., Pisciotta C., Cecchini A. P., Ragona F., Redaelli V., Saletti V., Salsano E., Scelzo E., Solazzi R., Tozzo A., Usai S., Zorzi G., Arnoldi M. T., Foscan M., Marchi A., Pedrinelli I., Zanin R., Gazzola S., Magazu S., Scopelliti M. R., Casalino T., DeSalvatore M., Mazzanti S., Taddei M., Fedeli A., Sattin D., Galimberti L., Zagari R., Bombonato M., Fonte L., Floridia S., Pareyson, D, Pantaleoni, C, Eleopra, R, De Filippis, G, Moroni, I, Freri, E, Zibordi, F, Bulgheroni, S, Pagliano, E, Sarti, D, Silvani, A, Grazzi, L, Tiraboschi, P, Didato, G, Anghileri, E, Bersano, A, Valentini, L, Piacentini, S, Muscio, C, Leonardi, M, Mariotti, C, Eoli, M, Nuzzo, S, Tagliavini, F, Confalonieri, P, De Giorgi, F, Antozzi, C, Ardissone, A, Bersano, E, Boncoraglio, G, Bonvegna, S, Botturi, A, Brambilla, L, Canafoglia, L, Caputi, L, Caroppo, P, Carriero, M, Casali, C, Casazza, M, Catania, A, Ciaccio, C, Cilia, R, Dallabella, E, D'Amico, D, Danti, F, D'Arrigo, S, Decurtis, M, Deleo, F, Devigili, G, Difede, G, Digiacomo, R, Elia, A, Esposito, S, Estienne, M, Fenu, S, Fichera, M, Finocchiaro, G, Frangiamore, R, Gatti, M, Gaviani, P, Giaccone, G, Giani, L, Giovagnoli, A, Andreasi, N, Granata, T, Granocchio, E, Lamperti, C, Lamperti, E, Leone, M, Masson, R, Nanetti, L, Nardocci, N, Pastori, C, Pisciotta, C, Cecchini, A, Ragona, F, Redaelli, V, Saletti, V, Salsano, E, Scelzo, E, Solazzi, R, Tozzo, A, Usai, S, Zorzi, G, Arnoldi, M, Foscan, M, Marchi, A, Pedrinelli, I, Zanin, R, Gazzola, S, Magazu, S, Scopelliti, M, Casalino, T, Desalvatore, M, Mazzanti, S, Taddei, M, Fedeli, A, Sattin, D, Galimberti, L, Zagari, R, Bombonato, M, Fonte, L, and Floridia, S
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Adult ,medicine.medical_specialty ,Telemedicine ,Neurology ,Referral ,Dermatology ,Telehealth ,03 medical and health sciences ,0302 clinical medicine ,Pandemic ,medicine ,Humans ,Outpatient clinic ,030212 general & internal medicine ,Medical prescription ,Child ,Pandemics ,Referral and Consultation ,SARS-CoV-2 ,business.industry ,Teleneurorehabilitation ,COVID-19 ,General Medicine ,medicine.disease ,Televisit ,Psychiatry and Mental health ,Italy ,Neuro-telehealth ,Neurology (clinical) ,Neurosurgery ,Medical emergency ,business ,030217 neurology & neurosurgery - Abstract
Background: Lombardy was severely hit by the COVID-19 pandemic since February 2020 and the Health System underwent rapid reorganization. Outpatient clinics were stopped for non-urgent patients: it became a priority to manage hundreds of fragile neurological patients who suddenly had less reference points. In Italy, before the pandemic, Televisits were neither recognized nor priced. Methods: At the Fondazione IRCCS Istituto Neurologico C. Besta, we reorganized outpatient clinics to deliver Neuro-telemedicine services, including Televisits and Teleneurorehabilitation, since March 2020. A dedicated Working Group prepared the procedure, tested the system, and designed satisfaction questionnaires for adults and children. Results: After a pilot phase, we prepared a procedure for Telemedicine outpatient clinics which was approved by hospital directions. It included prescription, booking, consenting, privacy and data protection, secure connection with patients (Teams Microsoft 365), electronic report preparation and delivery, reporting, and accountability of the services. During the March–September 2020 period, we delivered 3167 Telemedicine services, including 1618 Televisits, to 1694 patients (972 adults, 722 children) with a wide range of chronic neurological disorders. We successfully administered different clinical assessment and scales. Satisfaction among patients and caregivers was very high. Conclusions: During the dramatic emergency, we were able to take care of more than 1600 patients by organizing Neuro-telehealth in a few weeks, lessening the impact of the pandemic on fragile patients with chronic neurological disorders; this strategy is now stably embedded in our care pathways. In Italy, Telehealth is at present recognized and priced and is becoming a stable pillar of the health system.
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- 2021
3. Adult-onset mitochondrial movement disorders: a national picture from the Italian Network
- Author
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Montano, V., primary, Orsucci, D., additional, Carelli, V., additional, La Morgia, C., additional, Valentino, M. L., additional, Lamperti, C., additional, Marchet, S., additional, Musumeci, O., additional, Toscano, A., additional, Primiano, G., additional, Santorelli, F. M., additional, Ticci, C., additional, Filosto, M., additional, Rubegni, A., additional, Mongini, T., additional, Tonin, P., additional, Servidei, S., additional, Ceravolo, R., additional, Siciliano, G., additional, and Mancuso, Michelangelo, additional
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- 2021
- Full Text
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4. AAV9-based gene therapy partially ameliorates the clinical phenotype of a mouse model of Leigh syndrome
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Di Meo, I, primary, Marchet, S, additional, Lamperti, C, additional, Zeviani, M, additional, and Viscomi, C, additional
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- 2017
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5. Revisiting mitochondrial ocular myopathies: a study from the Italian Network
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Orsucci, D., primary, Angelini, C., additional, Bertini, E., additional, Carelli, V., additional, Comi, G. P., additional, Federico, A., additional, Minetti, C., additional, Moggio, M., additional, Mongini, T., additional, Santorelli, F. M., additional, Servidei, S., additional, Tonin, P., additional, Ardissone, A., additional, Bello, L., additional, Bruno, C., additional, Ienco, E. Caldarazzo, additional, Diodato, D., additional, Filosto, M., additional, Lamperti, C., additional, Moroni, I., additional, Musumeci, O., additional, Pegoraro, E., additional, Primiano, G., additional, Ronchi, D., additional, Rubegni, A., additional, Salvatore, S., additional, Sciacco, M., additional, Valentino, M. L., additional, Vercelli, L., additional, Toscano, A., additional, Zeviani, M., additional, Siciliano, G., additional, and Mancuso, M., additional
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- 2017
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6. Evaluation of muscle biopsy in late-onset GSDII patients before and after enzyme replacement therapy (ERT)
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Violano, R, primary, Ripolone, M, additional, Lucchini, V, additional, Villa, L, additional, Sciacco, M, additional, Comi, G, additional, Tonin, P, additional, Filosto, M, additional, Previtali, S, additional, Mongini, T, additional, Vercelli, L, additional, Vittonatto, E, additional, Toscano, A, additional, Musumeci, O, additional, Barca, E, additional, Angelini, C, additional, Ravaglia, S, additional, Lamperti, C, additional, Mora, M, additional, Morandi, L, additional, and Moggio, M, additional
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- 2013
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7. A case of Leber hereditary optic neuropathy plus dystonia caused by G14459A mitochondrial mutation
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Saracchi, Enrico, primary, DiFrancesco, J. C., additional, Brighina, L., additional, Marzorati, L., additional, Curtò, N. A., additional, Lamperti, C., additional, Carrara, F., additional, Zeviani, M., additional, and Ferrarese, C., additional
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- 2012
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8. An apparently sporadic case of oculopharyngeal muscular dystrophy: the first Italian report
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Tremolizzo, L., primary, Galbussera, A., additional, Tagliabue, E., additional, Fermi, S., additional, Bruttini, M., additional, Lamperti, C., additional, Moggio, M., additional, Curtò, N., additional, Appollonio, I., additional, and Ferrarese, C., additional
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- 2008
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9. An apparently sporadic case of oculopharyngeal muscular dystrophy: the first Italian report
- Author
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Tremolizzo, L., primary, Galbussera, A., additional, Tagliabue, E., additional, Fermi, S., additional, Bruttini, M., additional, Lamperti, C., additional, Moggio, M., additional, Appollonio, I., additional, and Ferrarese, C., additional
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- 2007
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10. Redefining phenotypes associated with mitochondrial DNA single deletion
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Carlo Minetti, Enrico Bertini, Elena Cardaioli, Elena Pegoraro, Filippo M. Santorelli, Liliana Vercelli, Donato Sauchelli, Michelangelo Mancuso, Paola Da Pozzo, Giacomo P. Comi, Maurizio Moggio, Daniele Orsucci, Mauro Scarpelli, Valerio Carelli, M. Sciacco, Serenella Servidei, Elena Caldarazzo Ienco, Corrado Angelini, Massimiliano Filosto, Paola Tonin, Isabella Moroni, Massimo Zeviani, Gabriele Siciliano, Claudio Bruno, Maria Lucia Valentino, Costanza Lamperti, Tiziana Mongini, Maria Alice Donati, Michela Catteruccia, Dario Ronchi, Luca Bello, Antonio Toscano, Olimpia Musumeci, Antonio Federico, Mancuso, M., Orsucci, D., Angelini, C., Bertini, E., Carelli, V., Comi, G.P., Donati, M.A., Federico, A., Minetti, C., Moggio, M., Mongini, T., Santorelli, F.M., Servidei, S., Tonin, P., Toscano, A., Bruno, C., Bello, L., Caldarazzo Ienco, E., Cardaioli, E., Catteruccia, M., Da Pozzo, P., Filosto, M., Lamperti, C., Moroni, I., Musumeci, O., Pegoraro, E., Ronchi, D., Sauchelli, D., Scarpelli, M., Sciacco, M., Valentino, M.L., Vercelli, L., Zeviani, M., and Siciliano, G.
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Male ,Ophthalmoplegia, Chronic Progressive External ,Mitochondrial Diseases ,Databases, Factual ,Kearns-Sayre Syndrome ,mitochondrial DNA ,Disease ,CPEO ,KSS ,Mitochondrial disorders ,mtDNA ,Pearson syndrome ,Single deletion ,Neurology (clinical) ,Neurology ,Bioinformatics ,Acyl-CoA Dehydrogenase ,Kearns–Sayre syndrome ,Congenital Bone Marrow Failure Syndromes ,Genetics ,Ophthalmoplegia ,Inborn Errors ,Medicine (all) ,Acyl-CoA Dehydrogenase, Long-Chain ,Middle Aged ,Heteroplasmy ,Mitochondrial ,Settore MED/26 - NEUROLOGIA ,Phenotype ,Female ,Cohort study ,Adult ,musculoskeletal diseases ,Mitochondrial DNA ,Mitochondrial disease ,Biology ,DNA, Mitochondrial ,Lipid Metabolism, Inborn Errors ,Databases ,Young Adult ,Muscular Diseases ,medicine ,Humans ,Factual ,Retrospective Studies ,Retrospective cohort study ,DNA ,Lipid Metabolism ,medicine.disease ,progressive external ophthalmoplegia ,PEO ,Chronic Progressive External ,Long-Chain ,Gene Deletion - Abstract
Progressive external ophthalmoplegia (PEO), Kearns–Sayre syndrome (KSS) and Pearson syndrome are the three sporadic clinical syndromes classically associated with single large-scale deletions of mitochondrial DNA (mtDNA). PEO plus is a term frequently utilized in the clinical setting to identify patients with PEO and some degree of multisystem involvement, but a precise definition is not available. The purpose of the present study is to better define the clinical phenotypes associated with a single mtDNA deletion, by a retrospective study on a large cohort of 228 patients from the database of the “Nation-wide Italian Collaborative Network of Mitochondrial Diseases”. In our database, single deletions account for about a third of all patients with mtDNA-related disease, more than previously recognized. We elaborated new criteria for the definition of PEO and “KSS spectrum” (a category of which classic KSS represents the most severe extreme). The criteria for “KSS spectrum” include the resulting multisystem clinical features associated with the KSS features, and which therefore can predict their presence or subsequent development. With the new criteria, we were able to classify nearly all our single-deletion patients: 64.5% PEO, 31.6% KSS spectrum (including classic KSS 6.6%) and 2.6% Pearson syndrome. The deletion length was greater in KSS spectrum than in PEO, whereas heteroplasmy was inversely related with age at onset. We believe that the new phenotype definitions implemented here may contribute to a more homogeneous patient categorization, which will be useful in future cohort studies of natural history and clinical trials. © 2015, Springer-Verlag Berlin Heidelberg.
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- 2015
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