Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Chiara Terracciano"'
Autor:
Erika Poggiali, Nicola Morelli, Chiara Terracciano, Claudia Caborni, Benedetta Pergolotti, Pietro Gavioli, Andrea Vercelli
Publikováno v:
Emergency Care Journal (2024)
We report the case of a young male patient who presented to our emergency department complaining of a transient headache and a feeling of motor impairment in his right lower limb, both of which completely resolved spontaneously. After a few minutes o
Externí odkaz:
https://doaj.org/article/f371740d53e445849f08a191e1366c8f
Autor:
Paolo Immovilli, Nicola Morelli, Chiara Terracciano, Eugenia Rota, Elena Marchesi, Stefano Vollaro, Paola De Mitri, Domenica Zaino, Veronica Bazzurri, Donata Guidetti
Publikováno v:
Neurology International, Vol 14, Iss 2, Pp 368-377 (2022)
The COVID-19 pandemic poses an ongoing global challenge, and several risk factors make people with multiple sclerosis (pwMS) particularly susceptible to running a severe disease course. Although the literature does report numerous articles on the ris
Externí odkaz:
https://doaj.org/article/18b7babd27454bf8944f68b008e767f3
Autor:
Giorgia Borio, Chiara Terracciano, Federico Buttafava, Andrea Vercelli, Laura Pagani, Chiara Zanzani, Alessandra Manicardi, Andrea Magnacavallo, Erika Poggiali
Publikováno v:
European Journal of Case Reports in Internal Medicine (2021)
We report the case of a 62-year-old male patient fully vaccinated for COVID-19, admitted to our emergency room for persistent fever associated with exertional dyspnoea, skin lesions, diffuse myalgias and arthralgias not responsive to broad-spectrum a
Externí odkaz:
https://doaj.org/article/d1b412bf6a4a4c31874886b768fbafe7
Autor:
Clemente Dato, MD, Guglielmo Capaldo, MD, Chiara Terracciano, MD, PhD, Filomena Napolitano, MSc, PhD, Alessandra D'Amico, MD, Sabina Pappatà, MD, Filippo Maria Santorelli, MD, PhD, Giuseppe Di Iorio, MD, Simone Sampaolo, MD, PhD, Mariarosa AB Melone, MD
Publikováno v:
Radiology Case Reports, Vol 14, Iss 3, Pp 309-314 (2019)
X-linked adrenoleukodystrophy (X-ALD) is a rare inherited metabolic disease affecting the nervous system and the adrenal glands. It is caused by a mutation of the ABCD1 gene, resulting in the impaired degradation of very long-chain fatty acids and th
Externí odkaz:
https://doaj.org/article/ed127b731df447ce8531e6667e418bcd
Autor:
Innocenzo Rainero, Amalia C. Bruni, Camillo Marra, Annachiara Cagnin, Laura Bonanni, Chiara Cupidi, Valentina Laganà, Elisa Rubino, Alessandro Vacca, Raffaele Di Lorenzo, Paolo Provero, Valeria Isella, Nicola Vanacore, Federica Agosta, Ildebrando Appollonio, Paolo Caffarra, Cinzia Bussè, Renato Sambati, Davide Quaranta, Valeria Guglielmi, Giancarlo Logroscino, Massimo Filippi, Gioacchino Tedeschi, Carlo Ferrarese, the SINdem COVID-19 Study Group, Erica Gallo, Alberto Grassini, Andrea Marcinnò, Fausto Roveta, Paola De Martino, Francesca Frangipane, Gianfranco Puccio, Rosanna Colao, Maria Mirabelli, Chiara Terracciano, Federica Lino, Stefano Mozzetta, Gianmarco Gazzola, Giulia Camporese, Simona Sacco, Maria Carmela Lechiara, Claudia Carrarini, Mirella Russo, Alfonsina Casa lena, Patrizia Sucapane, Pietro Tiraboschi, Paola Caroppo, Veronica Redaelli, Giuseppe Di Fede, Daniela Coppa, Lenino Peluso, Pasqualina Insarda, Matteo De Bartolo, Sabrina Esposito, Alessandro Iavarone, Carmine Fuschillo, Elena Salvatore, Chiara Criscuolo, Luisa Sambati, Rossella Santoro, Daniela Gragnaniello, Ilaria Pedriali, Livia Ludovico, Annalisa Chiari, Andrea Fabbo, Petra Bevilacqua, Chiara Galli, Silvia Magarelli, Gianfranco Spalletta, Nerisa Banaj, Giulia Caruso, Desirée Estela Porcari, Franco Giubilei, Anna Rosa Casini, Francesca Ursini, Giuseppe Bruno, Stefano Boffelli, Michela Brambilla, Giuseppe Magnani, Francesca Caso, Edoardo G. Spinelli, Elena Sinforiani, Alfredo Costa, Simona Luzzi, Gabriella Cacchiò, A.I.M.A. –sez Parma, Marta Perini, Rossano Angeloni, Cinzia Giuli, Katia Fabi, Marco Guidi, Cristina Paci, Annaelisa Castellano, Elena Carapelle, Rossella Petrucci, Miriam Accogli, Giovanna Nicoletta Trevisi, Serena Renna, Antonella Vasquez Giuliano, Fulvio Da Re, Antonio Milia, Giuseppina Pilia, Maria Giuseppina Mascia, Valeria Putzu, Tommaso Piccoli, Luca Cuffaro, Roberto Monastero, Antonella Battaglia, Valeria Blandino, Federica Lupo, Eduardo Cumbo, Antonina Luca, Giuseppe Caravaglios, Annalisa Vezzosi, Valentina Bessi, Gloria Tognoni, Valeria Calsolaro, Giulia Lucarelli, Serena Amici, Alberto Trequattrini, Salvatore Pezzuto, Patrizia Mecocci, Giulia Caironi, Barbara Boselli, Marino Formilan, Alessandra Coin, Laura De Togni, Francesca Sala, Giulia Sandri, Maurizio Gallucci, Anna Paola Mazzarolo, Cristina Bergamelli, Serena Passoni
Publikováno v:
Frontiers in Aging Neuroscience, Vol 12 (2021)
IntroductionPrevious studies showed that quarantine for pandemic diseases is associated with several psychological and medical effects. The consequences of quarantine for COVID-19 pandemic in patients with dementia are unknown. We investigated the cl
Externí odkaz:
https://doaj.org/article/fb09b8d6b5f247759120b4e3b554efb4
Autor:
Paolo Immovilli, Elena Marchesi, Chiara Terracciano, Nicola Morelli, Veronica Bazzurri, Fabiola Magnifico, Domenica Zaino, Emilio Terlizzi, Paola De Mitri, Stefano Vollaro, Nicola Mometto, Donata Guidetti
Publikováno v:
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association. 31(11)
To assess whether COVID-19 could be a concurrent factor in the genesis and/or worsening of stroke and to provide data on COVID-19 -associated stroke patients during the first pandemic wave and comparative data on COVID-19 negative stroke patients in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42dd22d5b5cd44b72241b3c715079729
https://pubmed.ncbi.nlm.nih.gov/36087377
https://pubmed.ncbi.nlm.nih.gov/36087377
Autor:
Giulia Losi, Alessandro Dacrema, Luca Rovero, Andrea Vercelli, Marzia Nuccetelli, Erika Poggiali, Sergio Bernardini, Giovanni Battista Vadacca, Andrea Magnacavallo, Paolo Immovilli, Donata Guidetti, Domenica Zaino, Chiara Terracciano
Publikováno v:
Clinica Chimica Acta; International Journal of Clinical Chemistry
Clinica Chimica Acta
Clinica Chimica Acta
Highlights • Elevated LDH and CRP serum concentrations are associated to respiratory failure in CoVID-19 patients.
Objective The dramatic worldwide CoVID-19 infection requires the identification of a reliable and inexpensive tool to quickly di
Objective The dramatic worldwide CoVID-19 infection requires the identification of a reliable and inexpensive tool to quickly di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::743682d2524dafd43fd8e85497462da5
https://doi.org/10.1016/j.cca.2020.06.012
https://doi.org/10.1016/j.cca.2020.06.012
Autor:
Filomena, Napolitano, Milena, Dell'Aquila, Chiara, Terracciano, Giuseppina, Franzese, Maria Teresa, Gentile, Giulio, Piluso, Claudia, Santoro, Davide, Colavito, Anna, Patanè, Paolo, De Blasiis, Simone, Sampaolo, Simona, Paladino, Mariarosa Anna Beatrice, Melone
Publikováno v:
Genes. 13(7)
Neurofibromatosis type 1 (NF1) is one of the most common genetic tumor predisposition syndrome, caused by mutations in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d73350d3eda9390775a007cf38ecb46c
https://pubmed.ncbi.nlm.nih.gov/35885913
https://pubmed.ncbi.nlm.nih.gov/35885913
Autor:
Filomena Napolitano, Milena Dell’Aquila, Chiara Terracciano, Giuseppina Franzese, Maria Teresa Gentile, Giulio Piluso, Claudia Santoro, Davide Colavito, Anna Patanè, Paolo De Blasiis, Simone Sampaolo, Simona Paladino, Mariarosa Anna Beatrice Melone
Publikováno v:
Genes; Volume 13; Issue 7; Pages: 1130
Neurofibromatosis type 1 (NF1) is one of the most common genetic tumor predisposition syndrome, caused by mutations in the NF1. To date, few genotype-phenotype correlations have been discerned in NF1, due to a highly variable clinical presentation. W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f26cba46d5ed1a55ebacbcbab13d3065
http://hdl.handle.net/11588/897605
http://hdl.handle.net/11588/897605
Autor:
Giorgia Bruno, Simone Sampaolo, U Barillari, Filippo M. Santorelli, Teresa Esposito, Filomena Napolitano, Claudia Nesti, Mariarosa A. B. Melone, Chiara Terracciano, Maria Rosaria Barillari
Publikováno v:
American journal of medical genetics
(2019). doi:10.1002/ajmg.a.61381
info:cnr-pdr/source/autori:Napolitano F, Terracciano C, Bruno G, Nesti C, Barillari MR, Barillari U, Santorelli FM, Melone MAB, Esposito T, Sampaolo S./titolo:Intrafamilial "DOA-plus" phenotype variability related to different OMI%2FHTRA2 expression./doi:10.1002%2Fajmg.a.61381/rivista:American journal of medical genetics (Print)/anno:2019/pagina_da:/pagina_a:/intervallo_pagine:/volume
(2019). doi:10.1002/ajmg.a.61381
info:cnr-pdr/source/autori:Napolitano F, Terracciano C, Bruno G, Nesti C, Barillari MR, Barillari U, Santorelli FM, Melone MAB, Esposito T, Sampaolo S./titolo:Intrafamilial "DOA-plus" phenotype variability related to different OMI%2FHTRA2 expression./doi:10.1002%2Fajmg.a.61381/rivista:American journal of medical genetics (Print)/anno:2019/pagina_da:/pagina_a:/intervallo_pagine:/volume
Dominant Optic Atrophy and Deafness (DOAD) may be associated with one or more of the following disorders such as myopathy, progressive external ophthalmoplegia, peripheral neuropathy, and cerebellar atrophy ("DOA-plus"). Intra- and interfamilial vari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::392779b482c1f916a2c1e4c7246ce1fd
https://doi.org/10.1002/ajmg.a.61381
https://doi.org/10.1002/ajmg.a.61381