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Research Output 1988 2019

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Article
2019

A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs)

Pareyson, D., Stojkovic, T., Reilly, M. M., Leonard-Louis, S., Laurà, M., Blake, J., Parman, Y., Battaloglu, E., Tazir, M., Bellatache, M., Bonello-Palot, N., Lévy, N., Sacconi, S., Guimarães-Costa, R., Attarian, S., Latour, P., Solé, G., Megarbane, A., Horvath, R., Ricci, G. & 22 others, Choi, B. O., Schenone, A., Gemelli, C., Geroldi, A., Sabatelli, M., Luigetti, M., Santoro, L., Manganelli, F., Quattrone, A., Valentino, P., Murakami, T., Scherer, S. S., Dankwa, L., Shy, M. E., Bacon, C. J., Herrmann, D. N., Zambon, A., Tramacere, I., Pisciotta, C., Magri, S., Previtali, S. C. & Bolino, A., Jul 1 2019, In : Annals of Neurology. 86, 1, p. 55-67 13 p.

Research output: Contribution to journalArticle

Multicenter Studies
Retrospective Studies
Mutation
Proteins
Neural Conduction
Longitudinal Studies
Outcome Assessment (Health Care)
Multicenter Studies
Quality of Life
Pharmacology

Expanding the spectrum of genes responsible for hereditary motor neuropathies

Previtali, S. C., Zhao, E., Lazarevic, D., Pipitone, G. B., Fabrizi, G. M., Manganelli, F., Mazzeo, A., Pareyson, D., Schenone, A., Taroni, F., Vita, G., Bellone, E., Ferrarini, M., Garibaldi, M., Magri, S., Padua, L., Pennisi, E., Pisciotta, C., Riva, N., Scaioli, V. & 11 others, Scarlato, M., Tozza, S., Geroldi, A., Jordanova, A., Ferrari, M., Molineris, I., Reilly, M. M., Comi, G., Carrera, P., Devoto, M. & Bolino, A., Oct 1 2019, In : Journal of Neurology, Neurosurgery and Psychiatry. 90, 10, p. 1171-1179 9 p.

Research output: Contribution to journalArticle

Charcot-Marie-Tooth Disease
Genes
Exome
Phenotype
Neuromuscular Diseases

Leukoencephalopathy With Predominant Infratentorial Involvement Caused by a Novel ABCD1 Mutation: Does the Spinocerebellar Variant of Adrenoleukodystrophy Exist?

Benzoni, C., Farina, L., Pensato, V., Marotta, G., Kuqo, A., Mauro, E., Pareyson, D. & Salsano, E., Nov 1 2019, In : The neurologist. 24, 6, p. 194-197 4 p.

Research output: Contribution to journalArticle

Adrenoleukodystrophy
Leukoencephalopathies
Mutation
Brain Stem
Phenotype

Longitudinal quantitative magnetic resonance imaging in adrenomyeloneuropathy

Politi, L. S., Castellano, A., Papinutto, N., Mauro, E., Pareyson, D., Henry, R. G., Falini, A. & Salsano, E., Oct 1 2019, In : European Journal of Neurology. 26, 10, p. 1341-1344 4 p.

Research output: Contribution to journalArticle

Adrenoleukodystrophy
Magnetic Resonance Imaging
Diffusion Tensor Imaging
Spinal Cord
Hereditary Spastic Paraplegia

Mutation update for myelin protein zero-related neuropathies and the increasing role of variants causing a late-onset phenotype

Callegari, I., Gemelli, C., Geroldi, A., Veneri, F., Mandich, P., D’Antonio, M., Pareyson, D., Shy, M. E., Schenone, A., Prada, V. & Grandis, M., Nov 1 2019, In : Journal of Neurology. 266, 11, p. 2629-2645 17 p.

Research output: Contribution to journalArticle

Myelin P0 Protein
Neural Conduction
Phenotype
Mutation
Genes

Outcome measures in the clinical evaluation of ambulatory Charcot-Marie-Tooth 1A subjects

Mori, L., Prada, V., Signori, A., Pareyson, D., Piscosquito, G., Padua, L., Pazzaglia, C., Fabrizi, G. M., Smania, N., Picelli, A., Schenone, A., Accogli, S., Bolla, S., Brugnera, A., Casati, E., Cattaneo, D., Crimi, E., Fontana, C., Francini, L., Maggi, G. & 8 others, Marinelli, L., Montesano, A., Monti Bragadin, M., Munari, D., Salerno, A., Scorsone, D., Zuccarino, R. & Grp, TPE. S., Feb 1 2019, In : European Journal of Physical and Rehabilitation Medicine. 55, 1, p. 47-55 9 p.

Research output: Contribution to journalArticle

Single-Blind Method
Outcome Assessment (Health Care)
Exercise
Evidence-Based Medicine
Therapeutics
2018

Adult leukoencephalopathies with prominent infratentorial involvement can be caused by Erdheim–Chester disease

Chiapparini, L., Cavalli, G., Langella, T., Venerando, A., de Luca, G., Raspante, S., Marotta, G., Pollo, B., Lauria, G., Cangi, M. G., Gerevini, S., Botturi, A., Pareyson, D., Dagna, L. & Salsano, E., 2018, In : Journal of Neurology. 265, 2, p. 273-284 12 p.

Research output: Contribution to journalArticle

Leukoencephalopathies
Radionuclide Imaging
Non-Langerhans-Cell Histiocytosis
Leg Bones
Cerebellar Ataxia

Altered TDP-43-dependent splicing in HSPB8-related distal hereditary motor neuropathy and myofibrillar myopathy

Cortese, A., Laurà, M., Casali, C., Nishino, I., Hayashi, Y. K., Magri, S., Taroni, F., Stuani, C., Saveri, P., Moggio, M., Ripolone, M., Prelle, A., Pisciotta, C., Sagnelli, A., Pichiecchio, A., Reilly, M. M., Buratti, E. & Pareyson, D., Jan 2018, In : European Journal of Neurology. 25, 1, p. 154-163 10 p.

Research output: Contribution to journalArticle

Muscles
Distal Myopathies
Small Heat-Shock Proteins
Charcot-Marie-Tooth Disease
Biopsy

Altered TDP-43-dependent splicing in HSPB8-related distal hereditary motor neuropathy and myofibrillar myopathy

Cortese, A., Laurà, M., Casali, C., Nishino, I., Hayashi, Y. K., Magri, S., Taroni, F., Stuani, C., Saveri, P., Moggio, M., Ripolone, M., Prelle, A., Pisciotta, C., Sagnelli, A., Pichiecchio, A., Reilly, M. M., Buratti, E. & Pareyson, D., Jan 1 2018, In : European Journal of Neurology. 25, 1, p. 154-163 10 p.

Research output: Contribution to journalArticle

Muscles
Distal Myopathies
Small Heat-Shock Proteins
Charcot-Marie-Tooth Disease
Biopsy

Development and validation of the Charcot-Marie-Tooth Disease Infant Scale

Mandarakas, M. R., Menezes, M. P., Rose, K. J., Shy, R., Eichinger, K., Foscan, M., Estilow, T., Kennedy, R., Herbert, K., Bray, P., Refshauge, K., Ryan, M. M., Yiu, E. M., Farrar, M., Sampaio, H., Moroni, I., Pagliano, E., Pareyson, D., Yum, S. W., Herrmann, D. N. & 4 others, Acsadi, G., Shy, M. E., Burns, J. & Sanmaneechai, O., Dec 1 2018, In : Brain : a journal of neurology. 141, 12, p. 3319-3330 12 p.

Research output: Contribution to journalArticle

Charcot-Marie-Tooth Disease
Riboflavin Deficiency
Outcome Assessment (Health Care)
Confidence Intervals
Pediatrics

Different nerve ultrasound patterns in charcot-marie-tooth types and hereditary neuropathy with liability to pressure palsies

Padua, L., Coraci, D., Lucchetta, M., Paolasso, I., Pazzaglia, C., Granata, G., Cacciavillani, M., Luigetti, M., Manganelli, F., Pisciotta, C., Piscosquito, G., Pareyson, D. & Briani, C., 2018, In : Muscle and Nerve. 57, 1, p. E18-E23

Research output: Contribution to journalArticle

Different nerve ultrasound patterns in charcot-marie-tooth types and hereditary neuropathy with liability to pressure palsies

Padua, L., Coraci, D., Lucchetta, M., Paolasso, I., Pazzaglia, C., Granata, G., Cacciavillani, M., Luigetti, M., Manganelli, F., Pisciotta, C., Piscosquito, G., Pareyson, D. & Briani, C., Jan 1 2018, In : Muscle and Nerve. 57, 1, p. E18-E23

Research output: Contribution to journalArticle

Charcot-Marie-Tooth Disease
Upper Extremity
Tibial Nerve
Sural Nerve
Peroneal Nerve
Negotiating
Tooth
Walking
Healthy Volunteers
Muscle Weakness
Negotiating
Tooth
Walking
Healthy Volunteers
Muscle Weakness
Walking
Tooth
Outcome Assessment (Health Care)
Charcot-Marie-Tooth Disease
Aptitude

PFN2 and GAMT as common molecular determinants of axonal Charcot-Marie-Tooth disease

Juneja, M., Azmi, A., Baets, J., Roos, A., Jennings, M. J., Saveri, P., Pisciotta, C., Bernard-Marissal, N., Schneider, B. L., Verfaillie, C., Chrast, R., Seeman, P., Hahn, A. F., De Jonghe, P., Maudsley, S., Horvath, R., Pareyson, D. & Timmerman, V., Aug 1 2018, In : Journal of Neurology, Neurosurgery and Psychiatry. 89, 8, p. 870-878 9 p.

Research output: Contribution to journalArticle

Guanidinoacetate N-Methyltransferase
Profilins
Charcot-Marie-Tooth Disease
Tooth
Motor Neurons

Prevalence and orthopedic management of foot and ankle deformities in Charcot–Marie–Tooth disease

Laurá, M., Singh, D., Ramdharry, G., Morrow, J., Skorupinska, M., Pareyson, D., Burns, J., Lewis, R. A., Scherer, S. S., Herrmann, D. N., Cullen, N., Bradish, C., Gaiani, L., Martinelli, N., Gibbons, P., Pfeffer, G., Phisitkul, P., Wapner, K., Sanders, J., Flemister, S. & 3 others, Shy, M. E., Reilly, M. M. & on behalf of the Inherited Neuropathies Consortium, Feb 1 2018, In : Muscle and Nerve. 57, 2, p. 255-259 5 p.

Research output: Contribution to journalArticle

Foot Deformities
Ankle
Orthopedics
Disease Management
Foot

The Italian neuromuscular registry: A coordinated platform where patient organizations and clinicians collaborate for data collection and multiple usage

Ambrosini, A., Calabrese, D., Avato, F. M., Catania, F., Cavaletti, G., Pera, M. C., Toscano, A., Vita, G., Monaco, L. & Pareyson, D., Oct 4 2018, In : Orphanet Journal of Rare Diseases. 13, 1, 176.

Research output: Contribution to journalArticle

Neuromuscular Diseases
Registries
Organizations
Patient Participation
Atrophic Muscular Disorders
2017

221st ENMC International Workshop:: Foot Surgery in Charcot-Marie-Tooth disease. 10–12 June 2016, Naarden, The Netherlands

Reilly, M. M., Pareyson, D., Burns, J., Laurá, M., Shy, M. E., Singh, D., Agren, P. H., Altmann, V., Baets, J., Briggs, P., Burns, J., Butcher, K., Gaiani, L., Genovese, F., Gibbons, P., Laurá, M., Louwerens, J. W., Manzur, A., Moroni, I., Martinelli, N. & 9 others, Pareyson, D., Pfeffer, G., Ramdharry, G., Reilly, M. M., Shy, M., Singh, D., van der Linden, M., Wenz, W. & ENMC CMT Foot Surgery Study Group, Dec 1 2017, In : Neuromuscular Disorders. 27, 12, p. 1138-1142 5 p.

Research output: Contribution to journalArticle

A novel NDRG1 mutation in a non-Romani patient with CMT4D/HMSN-Lom

Piscosquito, G., Magri, S., Saveri, P., Milani, M., Ciano, C., Farina, L., Taroni, F. & Pareyson, D., Mar 1 2017, In : Journal of the Peripheral Nervous System. 22, 1, p. 47-50 4 p.

Research output: Contribution to journalArticle

Hereditary Sensory and Motor Neuropathy
Roma
Mutation
Genes
Medulla Oblongata

Biomarkers predict outcome in Charcot-Marie-Tooth disease 1A

Fledrich, R., Mannil, M., Leha, A., Ehbrecht, C., Solari, A., Pelayo-Negro, A. L., Berciano, J., Schlotter-Weigel, B., Schnizer, T. J., Prukop, T., Garcia-Angarita, N., Czesnik, D., Haberlová, J., Mazanec, R., Paulus, W., Beissbarth, T., Walter, M. C., Hogrel, J. Y., Dubourg, O., Schenone, A. & 8 others, Baets, J., De Jonghe, P., Shy, M. E., Horvath, R., Pareyson, D., Seeman, P., Young, P. & Sereda, M. W., Nov 1 2017, In : Journal of Neurology, Neurosurgery and Psychiatry. 88, 11, p. 941-952 12 p.

Research output: Contribution to journalArticle

Charcot-Marie-Tooth Disease
Biomarkers
Disease Progression
Skin
Biopsy

Cross-sectional analysis of a large cohort with X-linked Charcot-Marie-Tooth disease (CMTX1)

Panosyan, F. B., Laura, M., Rossor, A. M., Pisciotta, C., Piscosquito, G., Burns, J., Li, J., Yum, S. W., Lewis, R. A., Day, J., Horvath, R., Herrmann, D. N., Shy, M. E., Pareyson, D., Reilly, M. M. & Scherer, S. S., Aug 29 2017, In : Neurology. 89, 9, p. 927-935 9 p.

Research output: Contribution to journalArticle

Charcot-Marie-Tooth Disease
Cross-Sectional Studies
Ulnar Nerve
Mutation
Radial Nerve

Hereditary gelsolin amyloidosis (HGA): a neglected cause of bilateral progressive or recurrent facial palsy

Sagnelli, A., Piscosquito, G., Di Bella, D., Fadda, L., Melzi, L., Morico, A., Ciano, C., Taroni, F., Facchetti, D., Salsano, E. & Pareyson, D., Mar 1 2017, In : Journal of the Peripheral Nervous System. 22, 1, p. 59-63 5 p.

Research output: Contribution to journalArticle

Familial Amyloidosis
Gelsolin
Facial Paralysis
Mothers
Facial Nerve

Mutations in noncoding regions of GJB1 are a major cause of X-linked CMT

Tomaselli, P. J., Rossor, A. M., Horga, A., Jaunmuktane, Z., Carr, A., Saveri, P., Piscosquito, G., Pareyson, D., Laura, M., Blake, J. C., Poh, R., Polke, J., Houlden, H. & Reilly, M. M., Apr 11 2017, In : Neurology. 88, 15, p. 1445-1453 9 p.

Research output: Contribution to journalArticle

Charcot-Marie-Tooth Disease
Mutation
3' Untranslated Regions
Gap Junctions
DNA

Natural history of Charcot-Marie-Tooth disease during childhood

Cornett, K. M. D., Menezes, M. P., Shy, R. R., Moroni, I., Pagliano, E., Pareyson, D., Estilow, T., Yum, S. W., Bhandari, T., Muntoni, F., Laura, M., Reilly, M. M., Finkel, R. S., Eichinger, K. J., Herrmann, D. N., Bray, P., Halaki, M., Shy, M. E., Burns, J., Cornett, K. M. D. & 27 others, Menezes, M. P., Ouvrier, R., Acsadi, G., Shy, R. R., Calabrese, D., Foscan, M., Sala, R., Moroni, I., Pagliano, E., Pareyson, D., Estilow, T., Yum, S. W., Bhandari, T., Muntoni, F., Laura, M., Reilly, M. M., Finkel, R. S., Eichinger, K. J., Herrmann, D. N., Bray, P., Rose, K., Halaki, M., Pallant, J., Lek, M., Shy, M. E., Burns, J. & for the CMTPedS Study Group, Sep 1 2017, In : Annals of Neurology. 82, 3, p. 353-359 7 p.

Research output: Contribution to journalArticle

Charcot-Marie-Tooth Disease
Confidence Intervals
Pediatrics
Tooth
Mutation

Peripheral neuropathy in complex inherited diseases: An approach to diagnosis

Rossor, A. M., Carr, A. S., Devine, H., Chandrashekar, H., Pelayo-Negro, A. L., Pareyson, D., Shy, M. E., Scherer, S. S. & Reilly, M. M., Oct 1 2017, In : Journal of Neurology, Neurosurgery and Psychiatry. 88, 10, p. 846-863 18 p.

Research output: Contribution to journalArticle

Peripheral Nervous System Diseases
Ataxia
Cardiomyopathies
Phenotype

Responsiveness of gait analysis parameters in a cohort of 71 CMT subjects

Lencioni, T., Piscosquito, G., Rabuffetti, M., Bovi, G., Di Sipio, E., Diverio, M., Moroni, I., Padua, L., Pagliano, E., Schenone, A., Pareyson, D. & Ferrarin, M., Nov 2017, In : Neuromuscular Disorders. 27, 11, p. 1029-1037 9 p.

Research output: Contribution to journalArticle

Charcot-Marie-Tooth Disease
Gait
Outcome Assessment (Health Care)
Biomechanical Phenomena
Muscle Strength

Responsiveness of gait analysis parameters in a cohort of 71 CMT subjects

Lencioni, T., Piscosquito, G., Rabuffetti, M., Bovi, G., Di Sipio, E., Diverio, M., Moroni, I., Padua, L., Pagliano, E., Schenone, A., Pareyson, D. & Ferrarin, M., Aug 2017, In : Neuromuscular Disorders.

Research output: Contribution to journalArticle

Charcot-Marie-Tooth Disease
Gait
Outcome Assessment (Health Care)
Biomechanical Phenomena
Muscle Strength

Transcriptional role of androgen receptor in the expression of long non-coding RNA Sox2OT in neurogenesis

Tosetti, V., Sassone, J., Ferri, A. L. M., Taiana, M., Bedini, G., Nava, S., Brenna, G., Resta, C. D., Pareyson, D., Giulio, A. M. D., Carelli, S., Parati, E. A. & Gorio, A., Jul 1 2017, In : PLoS One. 12, 7, e0180579.

Research output: Contribution to journalArticle

Long Noncoding RNA
neurogenesis
Neurogenesis
Androgen Receptors
Transcription

Transcriptional role of androgen receptor in the expression of long non-coding RNA Sox2OT in neurogenesis

Tosetti, V., Sassone, J., Ferri, ALM., Taiana, M., Bedini, G., Nava, S., Brenna, G., Di Resta, C., Pareyson, D., Di Giulio, AM., Carelli, S., Parati, EA. & Gorio, A., 2017, In : PLoS One. 12, 7, e0180579.

Research output: Contribution to journalArticle

Long Noncoding RNA
neurogenesis
Neurogenesis
Androgen Receptors
Transcription
2016

Alternative Splicing in the Human PMP22 Gene: Implications in CMT1A Neuropathy

Visigalli, D., Castagnola, P., Capodivento, G., Geroldi, A., Bellone, E., Mancardi, G. L., Pareyson, D., Schenone, A. & Nobbio, L., Jan 1 2016, In : Human Mutation. 37, 1, p. 98-109 12 p.

Research output: Contribution to journalArticle

Alternative Splicing
Messenger RNA
Genes
Sural Nerve
Endoplasmic Reticulum

Alternative Splicing in the Human PMP22 Gene: Implications in CMT1A Neuropathy

Visigalli, D., Castagnola, P., Capodivento, G., Geroldi, A., Bellone, E., Mancardi, G., Pareyson, D., Schenone, A. & Nobbio, L., Jan 1 2016, In : Human Mutation. 37, 1, p. 98-109 12 p.

Research output: Contribution to journalArticle

Alternative Splicing
Messenger RNA
Genes
Sural Nerve
Endoplasmic Reticulum

Clinical Trials in Spinal and Bulbar Muscular Atrophy—Past, Present, and Future

Weydt, P., Sagnelli, A., Rosenbohm, A., Fratta, P., Pradat, P. F., Ludolph, A. C. & Pareyson, D., Mar 1 2016, In : Journal of Molecular Neuroscience. 58, 3, p. 379-387 9 p.

Research output: Contribution to journalArticle

Atrophic Muscular Disorders
Clinical Trials
X-Linked Bulbo-Spinal Atrophy
Inheritance Patterns
X-Linked Genes

Combined central and peripheral demyelination: Clinical features, diagnostic findings, and treatment

Cortese, A., Franciotta, D., Alfonsi, E., Visigalli, N., Zardini, E., Diamanti, L., Prunetti, P., Osera, C., Gastaldi, M., Berzero, G., Pichiecchio, A., Piccolo, G., Lozza, A., Piscosquito, G., Salsano, E., Ceroni, M., Moglia, A., Bono, G., Pareyson, D. & Marchioni, E., Apr 15 2016, In : Journal of the Neurological Sciences. 363, p. 182-187 6 p.

Research output: Contribution to journalArticle

Demyelinating Diseases
Chronic Inflammatory Demyelinating Polyradiculoneuropathy
Peripheral Nervous System Diseases
Multiple Sclerosis
Therapeutics

Combined central and peripheral demyelination: Clinical features, diagnostic findings, and treatment

Cortese, A., Franciotta, D., Alfonsi, E., Visigalli, N., Zardini, E., Diamanti, L., Prunetti, P., Osera, C., Gastaldi, M., Berzero, G., Pichiecchio, A., Piccolo, G., Lozza, A., Piscosquito, G., Salsano, E., Ceroni, M., Moglia, A., Bono, G., Pareyson, D. & Marchioni, E., Apr 15 2016, In : Journal of the Neurological Sciences. 363, p. 182-187 6 p.

Research output: Contribution to journalArticle

Demyelinating Diseases
Chronic Inflammatory Demyelinating Polyradiculoneuropathy
Peripheral Nervous System Diseases
Multiple Sclerosis
Therapeutics

Combined central and peripheral demyelination: Clinical features, diagnostic findings, and treatment

Cortese, A., Franciotta, D., Alfonsi, E., Visigalli, N., Zardini, E., Diamanti, L., Prunetti, P., Osera, C., Gastaldi, M., Berzero, G., Pichiecchio, A., Piccolo, G., Lozza, A., Piscosquito, G., Salsano, E., Ceroni, M., Moglia, A., Bono, G., Pareyson, D. & Marchioni, E., Apr 15 2016, In : Journal of the Neurological Sciences. 363, p. 182-187 6 p.

Research output: Contribution to journalArticle

Demyelinating Diseases
Chronic Inflammatory Demyelinating Polyradiculoneuropathy
Peripheral Nervous System Diseases
Multiple Sclerosis
Therapeutics

Early-onset progressive spastic paraplegia caused by a novel TUBB4A mutation: brain MRI and FDG-PET findings

Sagnelli, A., Magri, S., Farina, L., Chiapparini, L., Marotta, G., Tonduti, D., Consonni, M., Scigliuolo, G. M., Benti, R., Pareyson, D., Taroni, F., Salsano, E. & Di Bella, D., Mar 1 2016, In : Journal of Neurology. 263, 3, p. 591-593 3 p.

Research output: Contribution to journalArticle

Early-onset progressive spastic paraplegia caused by a novel TUBB4A mutation: brain MRI and FDG-PET findings

Sagnelli, A., Magri, S., Farina, L., Chiapparini, L., Marotta, G., Tonduti, D., Consonni, M., Scigliuolo, G., Benti, R., Pareyson, D., Taroni, F., Salsano, E. & Di Bella, D., Mar 1 2016, In : Journal of Neurology. 263, 3, p. 591-593 3 p.

Research output: Contribution to journalArticle

Erratum to: Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area (Journal of Neurology, DOI: 10.1007/s00415-016-8064-9)

Cortese, A., Vita, G., Luigetti, M., Russo, M., Bisogni, G., Sabatelli, M., Manganelli, F., Santoro, L., Cavallaro, T., Fabrizi, G. M., Schenone, A., Grandis, M., Gemelli, C., Mauro, A., Pradotto, L. G., Gentile, L., Stancanelli, C., Lozza, A., Perlini, S., Piscosquito, G. & 4 others, Calabrese, D., Mazzeo, A., Obici, L. & Pareyson, D., May 1 2016, In : Journal of Neurology. 263, 5, p. 925-926 2 p.

Research output: Contribution to journalArticle

Erratum to: Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area (Journal of Neurology, DOI: 10.1007/s00415-016-8064-9)

Cortese, A., Vita, G., Luigetti, M., Russo, M., Bisogni, G., Sabatelli, M., Manganelli, F., Santoro, L., Cavallaro, T., Fabrizi, G. M., Schenone, A., Grandis, M., Gemelli, C., Mauro, A., Pradotto, L., Gentile, L., Stancanelli, C., Lozza, A., Perlini, S., Piscosquito, G. & 4 others, Calabrese, D., Mazzeo, A., Obici, L. P. & Pareyson, D., May 1 2016, In : Journal of Neurology. 263, 5, p. 925-926 2 p.

Research output: Contribution to journalArticle

Erratum to: Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area (Journal of Neurology, DOI: 10.1007/s00415-016-8064-9)

Cortese, A., Vita, G., Luigetti, M., Russo, M., Bisogni, G., Sabatelli, M., Manganelli, F., Santoro, L., Cavallaro, T., Fabrizi, G. M., Schenone, A., Grandis, M., Gemelli, C., Mauro, A., Pradotto, L., Gentile, L., Stancanelli, C., Lozza, A., Perlini, S., Piscosquito, G. & 4 others, Calabrese, D., Mazzeo, A., Obici, L. P. & Pareyson, D., May 1 2016, In : Journal of Neurology. 263, 5, p. 925-926 2 p.

Research output: Contribution to journalArticle

Laryngeal and phrenic nerve involvement in a patient with hereditary neuropathy with liability to pressure palsies (HNPP)

Cortese, A., Piccolo, G., Lozza, A., Schreiber, A., Callegari, I., Moglia, A., Alfonsi, E. & Pareyson, D., Jul 2016, In : Neuromuscular Disorders. 26, 7, p. 455-458 4 p.

Research output: Contribution to journalArticle

Laryngeal Nerves
Phrenic Nerve
Diaphragm
Laryngeal Muscles
Weight Loss

Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area

Cortese, A., Vita, G., Luigetti, M., Russo, M., Bisogni, G., Sabatelli, M., Manganelli, F., Santoro, L., Cavallaro, T., Fabrizi, G. M., Schenone, A., Grandis, M., Gemelli, C., Mauro, A., Pradotto, L., Gentile, L., Stancanelli, C., Lozza, A., Perlini, S., Piscosquito, G. & 4 others, Calabrese, D., Mazzeo, A., Obici, L. P. & Pareyson, D., Mar 16 2016, (Accepted/In press) In : Journal of Neurology. p. 1-9 9 p.

Research output: Contribution to journalArticle

Italy
Multicenter Studies
Longitudinal Studies
Safety
Mutation

Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area

Cortese, A., Vita, G., Luigetti, M., Russo, M., Bisogni, G., Sabatelli, M., Manganelli, F., Santoro, L., Cavallaro, T., Fabrizi, G. M., Schenone, A., Grandis, M., Gemelli, C., Mauro, A., Pradotto, L., Gentile, L., Stancanelli, C., Lozza, A., Perlini, S., Piscosquito, G. & 4 others, Calabrese, D., Mazzeo, A., Obici, L. P. & Pareyson, D., Mar 16 2016, (Accepted/In press) In : Journal of Neurology. p. 1-9 9 p.

Research output: Contribution to journalArticle

Italy
Multicenter Studies
Longitudinal Studies
Safety
Mutation

Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area

Cortese, A., Vita, G., Luigetti, M., Russo, M., Bisogni, G., Sabatelli, M., Manganelli, F., Santoro, L., Cavallaro, T., Fabrizi, G. M., Schenone, A., Grandis, M., Gemelli, C., Mauro, A., Pradotto, L., Gentile, L., Stancanelli, C., Lozza, A., Perlini, S., Piscosquito, G. & 4 others, Calabrese, D., Mazzeo, A., Obici, L. P. & Pareyson, D., Mar 16 2016, (Accepted/In press) In : Journal of Neurology. p. 1-9 9 p.

Research output: Contribution to journalArticle

Italy
Multicenter Studies
Longitudinal Studies
Safety
Mutation

Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area

Cortese, A., Vita, G., Luigetti, M., Russo, M., Bisogni, G., Sabatelli, M., Manganelli, F., Santoro, L., Cavallaro, T., Fabrizi, G. M., Schenone, A., Grandis, M., Gemelli, C., Mauro, A., Pradotto, L., Gentile, L., Stancanelli, C., Lozza, A., Perlini, S., Piscosquito, G. & 4 others, Calabrese, D., Mazzeo, A., Obici, L. P. & Pareyson, D., Mar 16 2016, (Accepted/In press) In : Journal of Neurology. p. 1-9 9 p.

Research output: Contribution to journalArticle

Italy
Multicenter Studies
Longitudinal Studies
Safety
Mutation

Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area

Cortese, A., Vita, G., Luigetti, M., Russo, M., Bisogni, G., Sabatelli, M., Manganelli, F., Santoro, L., Cavallaro, T., Fabrizi, G. M., Schenone, A., Grandis, M., Gemelli, C., Mauro, A., Pradotto, L. G., Gentile, L., Stancanelli, C., Lozza, A., Perlini, S., Piscosquito, G. & 4 others, Calabrese, D., Mazzeo, A., Obici, L. & Pareyson, D., Mar 16 2016, (Accepted/In press) In : Journal of Neurology. p. 1-9 9 p.

Research output: Contribution to journalArticle

Italy
Multicenter Studies
Longitudinal Studies
Safety
Mutation