Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Ilaria Trezzi"'
Autor:
Angelica Carandina, Giulia Lazzeri, Gabriel Dias Rodrigues, Giulia Franco, Edoardo Monfrini, Federica Arienti, Emanuele Frattini, Ilaria Trezzi, Pedro Paulo da Silva Soares, Chiara Bellocchi, Ludovico Furlan, Nicola Montano, Alessio Di Fonzo, Eleonora Tobaldini
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2022)
Evidence from clinical practice suggests that PD patients with the Glucocerebrosidase gene mutations (GBA-PD) are characterized by more severe dysautonomic symptoms than patients with idiopathic PD (iPD). Therefore, an accurate assessment of cardiova
Externí odkaz:
https://doaj.org/article/cd4a3b6e81254f72913b68683bbdec92
Autor:
Lucia Corrado, Fabiola De Marchi, Sara Tunesi, Gaia Donata Oggioni, Miryam Carecchio, Luca Magistrelli, Silvana Tesei, Giulio Riboldazzi, Alessio Di Fonzo, Clarissa Locci, Ilaria Trezzi, Roberta Zangaglia, Cristina Cereda, Sandra D’Alfonso, Corrado Magnani, Giacomo P. Comi, Giorgio Bono, Claudio Pacchetti, Roberto Cantello, Stefano Goldwurm, Cristoforo Comi
Publikováno v:
Frontiers in Neurology, Vol 9 (2018)
BackgroundAlpha-synuclein is a constituent of Lewy bodies and mutations of its gene cause familial Parkinson’s disease (PD). A previous study showed that a variant of the alpha-synuclein gene (SNCA), namely the 263 bp allele of Rep1 was associated
Externí odkaz:
https://doaj.org/article/774f3424aaa043409a9ea78888eb221a
Autor:
Linda Borellini, Silvia Lanfranconi, Sara Bonato, Ilaria Trezzi, Giulia Franco, Lorella Torretta, Nereo Bresolin, Alessio Barnaba Di Fonzo
Publikováno v:
Frontiers in Neurology, Vol 8 (2017)
IntroductionA 60-year-old man presented with a 6-month history of low back pain and progressive rigidity of the trunk and lower limbs, followed by pruritus, dysphonia, hyperhydrosis, and urinary retention. Brain and spinal imaging were normal. EMG sh
Externí odkaz:
https://doaj.org/article/8f95558d96034de4a9757cf872a94dc0
Autor:
Silvia Lanfranconi, Paola Basilico, Ilaria Trezzi, Linda Borellini, Giulia Franco, Vittorio Civelli, Francesco Pallotti, Nereo Bresolin, Pierluigi Baron
Publikováno v:
Neurology Research International, Vol 2013 (2013)
Introduction. Leptomeningeal carcinomatosis occurs in about 5% of cancer patients. Ocular involvement is a common clinical manifestation and often the presenting clinical feature. Materials and Methods. We report the case of a 52-year old lady with o
Externí odkaz:
https://doaj.org/article/acd29f607cf0478d911af374e7742e19
Autor:
Megi Meneri, Giulia Lazzeri, Tiziana Carandini, Domenica Saccomanno, Giacomo P. Comi, Nereo Bresolin, Silvia Lanfranconi, Ilaria Trezzi, M.C. Saetti, Edoardo Monfrini, Daniele Velardo, Alessio Di Fonzio, Giulia Franco, Federica Arienti, Delia Gagliardi, Maria Vizziello, Stefania Corti
Publikováno v:
Journal of the Neurological Sciences. 429:119599
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22670835762f557080a85509bac7441c
https://doi.org/10.1016/j.jns.2021.119599
https://doi.org/10.1016/j.jns.2021.119599
Autor:
Lucia, Corrado, Fabiola, De Marchi, Sara, Tunesi, Gaia Donata, Oggioni, Miryam, Carecchio, Luca, Magistrelli, Silvana, Tesei, Giulio, Riboldazzi, Alessio, Di Fonzo, Clarissa, Locci, Ilaria, Trezzi, Roberta, Zangaglia, Cristina, Cereda, Sandra, D'Alfonso, Corrado, Magnani, Giacomo P, Comi, Giorgio, Bono, Claudio, Pacchetti, Roberto, Cantello, Stefano, Goldwurm, Cristoforo, Comi
Publikováno v:
Frontiers in Neurology
Background Alpha-synuclein is a constituent of Lewy bodies and mutations of its gene cause familial Parkinson’s disease (PD). A previous study showed that a variant of the alpha-synuclein gene (SNCA), namely the 263 bp allele of Rep1 was associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7e4f20133e46bea11584b7c209bc3d32
https://pubmed.ncbi.nlm.nih.gov/29662465
https://pubmed.ncbi.nlm.nih.gov/29662465
Autor:
Comi Giacomo Pietro, Sara Tunesi, Claudio Pacchetti, Silvana Tesei, Corrado Magnani, Cristoforo Comi, Clarissa Locci, Ilaria Trezzi, G.D. Oggioni, Sandra D'Alfonso, Roberta Zangaglia, Roberto Cantello, Stefano Goldwurm, Lucia Corrado, Miryam Carecchio, Giulio Riboldazzi, Fabiola De Marchi, Alessio Di Fonzo, Cristina Cereda, Luca Magistrelli, Giorgio Bono
α-synuclein is a constituent of Lewy bodies and mutations of its gene cause familial PD. A previous study showed that a variant of α-synuclein gene (SNCA), namely the 263bp allele of Rep1 was associated to faster motor progression in PD. On the con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf751c3280a15e912957266a70ff3d6c
Autor:
Sabrina Salani, Silvano Bosari, Gabriele Mora, Ilaria Trezzi, Eduardo Nobile-Orazio, Mafalda Rizzuti, G. Micieli, Alessio Di Fonzo, Elisa Fassone, Stefania Corti, Francesca Gallia, Mauro Ceroni, Ivana Ricca, Fulvia Milena Cribiù, Ivan Limongelli, Francesco Fortunato, Nereo Bresolin, Annalisa Vetro, Orsetta Zuffardi, Andreina Bordoni, Giacomo P. Comi, Dario Ronchi, Riccardo Bellazzi, Erika Della Mina
Publikováno v:
Neurology. 82:1990-1998
Objective: To investigate the molecular defect underlying a large Italian kindred with progressive adult-onset respiratory failure, proximal weakness of the upper limbs, and evidence of lower motor neuron degeneration. Methods: We describe the clinic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ede09d97830d756810c1115bcb2f2ac5
https://doi.org/10.1212/wnl.0000000000000476
https://doi.org/10.1212/wnl.0000000000000476
Autor:
Giulia Franco, Anna Chiara Di Caprio, Ilaria Trezzi, Giacomo Monzio Compagnoni, Stefania Corti, Giacomo P. Comi, Emanuele Frattini, Edoardo Monfrini, Alessio Di Fonzo, Valentina Melzi, Gianluca Ardolino, Filippo Cogiamanian, Gabriele Buongarzone, Nereo Bresolin, Dario Ronchi, Linda Borellini
Publikováno v:
Parkinsonismrelated disorders. 39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e756b7a4f008c676e7c67d046137665e
https://pubmed.ncbi.nlm.nih.gov/28318986
https://pubmed.ncbi.nlm.nih.gov/28318986
Autor:
Chiara Barzaghi, Alessio Di Fonzo, Antonio E. Elia, Barbara Garavaglia, Sara Bonato, Giulia Franco, Gianluca Ardolino, Filippo Cogiamanian, Christian Bergamini, Valentina Melzi, Stefania Corti, Gabriele Mora, Alberto Priori, Francesco Fortunato, Ilaria Trezzi, Linda Borellini, Giacomo Monzio Compagnoni, Ernesto Di Biase, Dario Ronchi, Giacomo P. Comi, Emanuele Frattini, Roberto Del Bo, Edoardo Monfrini, Nereo Bresolin, Romana Fato, Francesca Del Sorbo
COQ2 mutations have been implicated in the etiology of multiple system atrophy (MSA) in Japan. However, several genetic screenings have not confirmed the role of its variants in the disease. We performed COQ2 sequence analysis in 87 probable MSA. A h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b2a4b3cdc357a0c48e9b90eec45dc5d
http://hdl.handle.net/11585/587913
http://hdl.handle.net/11585/587913