Search Results - "Ciano, C."

Observation of phonon-polaritons in thin flakes of hexagonal boron nitride on gold by Ciano, C., Giliberti, V., Ortolani, M., Baldassarre, L.

“…Hexagonal Boron Nitride (hBN) is a layered van der Waals material able to sustain hyperbolic phonon-polaritons within its mid-infrared reststrahlen bands. We…”
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Amyotrophic lateral sclerosis causes small fiber pathology by Dalla Bella, E., Lombardi, R., Porretta-Serapiglia, C., Ciano, C., Gellera, C., Pensato, V., Cazzato, D., Lauria, G.

“…Background and purpose Our aim was to address the correlation between small fiber loss and amyotrophic lateral sclerosis (ALS) for disease onset, phenotype,…”
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Design and simulation of losses in Ge/SiGe terahertz quantum cascade laser waveguides by Gallacher, K, Ortolani, M, Rew, K, Ciano, C, Baldassarre, L, Virgilio, M, Scalari, G, Faist, J, Di Gaspare, L, De Seta, M, Capellini, G, Grange, T, Birner, S, Paul, D J

“…The waveguide losses from a range of surface plasmon and double metal waveguides for Ge/Si Ge THz quantum cascade laser gain media are investigated at 4.79 THz…”
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Supratentorial and pontine MRI abnormalities characterize recessive spastic ataxia of Charlevoix-Saguenay. A comprehensive study of an Italian series by Prodi, E., Grisoli, M., Panzeri, M., Minati, L., Fattori, F., Erbetta, A., Uziel, G., D'Arrigo, S., Tessa, A., Ciano, C., Santorelli, F. M., Savoiardo, M., Mariotti, C.

“…Background and purpose The autosomal recessive spastic ataxia of Charlevoix‐Saguenay (ARSACS) is an early‐onset neurodegenerative disorder caused by mutations…”
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Monomelic amyotrophy in cervical myelopathy associated with anterior dural sac displacement induced by neck flexion by Brambilla, Laura, Erbetta, A., Ciano, C., Maggi, L.

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Dynasore enhances the formation of mitochondrial antiviral signalling aggregates and endocytosis‐independent NF‐κB activation by Ailenberg, M, Di Ciano‐Oliveira, C, Szaszi, K, Dan, Q, Rozycki, M, Kapus, A, Rotstein, O D

“…Background and Purpose Dynasore has been used extensively as an inhibitor of clathrin‐mediated endocytosis. While studying the role of endocytosis in…”
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Giant SEPs and SEP-recovery function in Unverricht–Lundborg disease by Visani, E, Canafoglia, L, Rossi Sebastiano, D, Agazzi, P, Panzica, F, Scaioli, V, Ciano, C, Franceschetti, S

“…Highlights ► In progressive myoclonic epilepsy 1A patients with giant SEPs had a delayed SEP recovery (SEP-R). ► The delayed SEP-R affected the “gigantisms” of…”
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Osmotic stress and the cytoskeleton: the R(h)ole of Rho GTPases by Di Ciano-Oliveira, C., Thirone, A. C. P., Szászi, K., Kapus, A.

“…Hyperosmotic stress initiates a variety of compensatory and adaptive responses, which either serve to restore near‐normal volume or remodel and reinforce the…”
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Sensorimotor cortex excitability in Unverricht-Lundborg disease and Lafora body disease by CANAFOGLIA, L, CIANO, C, PANZICA, F, SCAIOLI, V, ZUCCA, C, AGAZZI, P, VISANI, E, AVANZINI, G, FRANCESCHETTI, S

“…To investigate whether Unverricht-Lundborg disease (ULD) and Lafora body disease (LBD) can be differentiated on the basis of their neurophysiologic profiles…”
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Movement-activated myoclonus in genetically defined progressive myoclonic epilepsies: EEG–EMG relationship estimated using autoregressive models by Panzica, F, Canafoglia, L, Franceschetti, S, Binelli, S, Ciano, C, Visani, E, Avanzini, G

“…Objective: To study electroencephalography–electromyography (EEG–EMG) relationships in patients with different forms of progressive myoclonic epilepsies (PME)…”
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Movement-related desynchronization-synchronization (ERD/ERS) in patients with Unverricht–Lundborg disease by Visani, E., Agazzi, P., Canafoglia, L., Panzica, F., Ciano, C., Scaioli, V., Avanzini, G., Franceschetti, S.

“…We studied changes in event-related desynchronization/synchronization (ERD/ERS) patterns in patients with Unverricht–Lundborg disease (ULD), presenting with…”
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POEMS syndrome: relapse after successful autologous peripheral blood stem cell transplantation by Giglia, F, Chiapparini, L, Fariselli, L, Barbui, T, Ciano, C, Scarlato, M, Pareyson, D

“…Abstract We report a patient with POEMS syndrome (Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal gammopathy, Skin changes) treated with high dose…”
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Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation by PAREYSON, D, TARONI, F, BOTTI, S, MORBIN, M, BARATTA, S, LAURIA, G, CIANO, C, SGHIRLANZONI, A

“…Mutations in the gene coding for the Schwann cell transcription factor early growth response 2 (EGR2), which seems to regulate myelinogenesis and hindbrain…”
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P14-7 Somatosensory evoked potentials recovery function in patients with cortical myoclonus by Visani, E, Canafoglia, L, Ciano, C, Agazzi, P, Panzica, F, Scaioli, V, Varotto, G, Franceschetti, S

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P23-14 Action myoclonus in sialidosis: a comparative study with Unverricht-Lundborg disease by Canafoglia, L, Franceschetti, S, Uziel, G, Ciano, C, Scaioli, V, Visani, E, Varotto, G, Guerrini, R, Panzica, F

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Propriospinal myoclonus with life threatening tonic spasms as paraneoplastic presentation of breast cancer by Salsano, E, Ciano, C, Romano, S, Cornelio, F, Di Donato, S, Pareyson, D

“…[...]hyperekplexia, a hereditary or sporadic disorder with abnormal startle response, was also ruled out. [...]although paraneoplastic syndromes expedite…”
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Childhood-onset multifocal motor neuropathy with conduction blocks by MORONI, I, BUGIANI, M, CIANO, C, BONO, R, PAREYSON, D

“…Multifocal motor neuropathy (MMN) is an acquired disorder with onset in adulthood. The authors describe a patient with a slowly progressing distal upper limb…”
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Sequential antibodies to potassium channels and glutamic acid decarboxylase in neuromyotonia by ANTOZZI, C, FRASSONI, C, MANTEGAZZA, R, VINCENT, A, REGONDI, M. C, ANDREETTA, F, BERNASCONI, P, CIANO, C, CHANG, T, CORNELIO, F, SPREAFICO, R

“…A patient with thymoma-associated neuromyotonia and voltage-gated potassium channel (Kv1.2 and Kv1.6) antibodies by immunoprecipitation and rat brain…”
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Polymyography in the diagnosis of childhood onset movement disorders by Canavese, C, Ciano, C, Zorzi, G, Zibordi, F, Costa, C, Nardocci, N

“…Abstract We report on the results of a clinical and polymyographic retrospective study of 61 paediatric patients with tremor, dystonia and/or myoclonus. Aim of…”
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Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion by PAREYSON, D, SCAIOLI, V, TARONI, F, BOTTI, S, LORENZETTI, D, SOLARI, A, CIANO, C, SGHIRLANZONI, A

“…Hereditary neuropathy with liability to pressure palsies (HNPP) is commonly associated with a 1.5-megabase deletion on chromosome 17p11.2-12. We analyzed the…”
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