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Your search keyword '"Arighi A."' showing total 10 results
Start Over Author "Arighi A." Journal neurology
10 results on '"Arighi A."'

1. Spontaneous ARIA-like Events in Cerebral Amyloid Angiopathy–Related Inflammation: A Multicenter Prospective Longitudinal Cohort Study

Author

Antolini, Laura, DiFrancesco, Jacopo C., Zedde, Marialuisa, Basso, Gianpaolo, Arighi, Andrea, Shima, Atsushi, Cagnin, Annachiara, Caulo, Massimo, Carare, Roxana O., Charidimou, Andreas, Cirillo, Mario, Di Lazzaro, Vincenzo, Ferrarese, Carlo, Giossi, Alessia, Inzitari, Domenico, Marcon, Michela, Marconi, Roberto, Ihara, Masafumi, Nitrini, Ricardo, Orlandi, Berardino, Padovani, Alessandro, Pascarella, Rosario, Perini, Francesco, Perini, Giulia, Sessa, Maria, Scarpini, Elio, Tagliavini, Fabrizio, Valenti, Raffaella, Vázquez-Costa, Juan Francisco, Villarejo-Galende, Alberto, Hagiwara, Yuta, Ziliotto, Nicole, and Piazza, Fabrizio

Published
2021
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2. Characterizing the Clinical Features and Atrophy Patterns of MAPT-Related Frontotemporal Dementia With Disease Progression Modeling

Author

Young, Alexandra L., Bocchetta, Martina, Russell, Lucy L., Convery, Rhian S., Peakman, Georgia, Todd, Emily, Cash, David M., Greaves, Caroline V., van Swieten, John, Jiskoot, Lize, Seelaar, Harro, Moreno, Fermin, Sanchez-Valle, Raquel, Borroni, Barbara, Laforce, Robert, Jr, Masellis, Mario, Tartaglia, Maria Carmela, Graff, Caroline, Galimberti, Daniela, Rowe, James B., Finger, Elizabeth, Synofzik, Matthis, Vandenberghe, Rik, de Mendonça, Alexandre, Tagliavini, Fabrizio, Santana, Isabel, Ducharme, Simon, Butler, Chris, Gerhard, Alex, Levin, Johannes, Danek, Adrian, Otto, Markus, Sorbi, Sandro, Williams, Steven C.R., Alexander, Daniel C., Rohrer, Jonathan D., Rossor, Martin N., Fox, Nick C., Warren, Jason D., Woollacott, Ione, Shafei, Rachelle, Heller, Carolin, Swift, Imogen J, Moore, Katrina, Guerreiro, Rita, Bras, Jose, Thomas, David L., Nicholas, Jennifer, Mead, Simon, Meeter, Lieke, Panman, Jessica, Papma, Janne M., Poos, Jackie, van Minkelen, Rick, Pijnenburg, Yolande, Barandiaran, Myriam, Indakoetxea, Begoña, Gabilondo, Alazne, Tainta, Mikel, de Arriba, María, Gorostidi, Ana, Zulaica, Miren, Villanua, Jorge, Díaz, Zigor, Borrego-Ecija, Sergi, Olives, Jaume, Lladó, Albert, Balasa, Mircea, Antonell, Anna, Bargalló, Nuria, Premi, Enrico, Cosseddu, Maura, Gazzina, Stefano, Padovani, Alessandro, Gasparotti, Roberto, Archetti, Silvana, Black, Sandra, Mitchell, Sara, Rogaeva, Ekaterina, Freedman, Morris, Keren, Ron, Tang-Wai, David, Öijerstedt, Linn, Andersson, Christin, Jelic, Vesna, Thonberg, Hakan, Arighi, Andrea, Fenoglio, Chiara, Scarpini, Elio, Fumagalli, Giorgio, Cope, Thomas, Timberlake, Carolyn, Rittman, Timothy, Shoesmith, Christen, Bartha, Robart, Rademakers, Rosa, Wilke, Carlo, Karnath, Hans Otto, Bender, Benjamin, Bruffaerts, Rose, Van Damme, Philip, Vandenbulcke, Mathieu, Ferreira, Catarina B., Miltenberger, Gabriel, Maruta, Carolina, Verdelho, Ana, Afonso, Sónia, Taipa, Ricardo, Caroppo, Paola, Di Fede, Giuseppe, Giaccone, Giorgio, Prioni, Sara, Redaelli, Veronica, Rossi, Giacomina, Tiraboschi, Pietro, Duro, Diana, Almeida, Maria Rosario, Branco, Miguel Castelo, Leitão, Maria João, Pereira, Miguel Tábuas, Santiago, Beatriz, Gauthier, Serge, Neto, Pedro Rosa, Veldsman, Michele, Thompson, Paul, Prix, Catharina, Hoegen, Tobias, Mag.rer.nat, Elisabeth Wlasich, Loosli, Sandra, Schönecker, Sonja, Dr.hum.bio, Elisa Semler, Psych, Dipl., Anderl-Straub, Sarah, Psych, Dipl., Nacmias, Benedetta, Ferrari, Camilla, Polito, Cristina, Lombardi, Gemma, and Bessi, Valentina

Published
2021
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4. Teaching NeuroImage: Crowned Dens Syndrome

Author

Francia, Alessandro, primary, Conte, Giorgio, additional, Platania, Giulia, additional, Arighi, Andrea, additional, Pietroboni, Anna Margherita, additional, Fumagalli, Giorgio Giulio, additional, Floro, Stefano, additional, Scarpini, Elio, additional, Galimberti, Daniela, additional, Saetti, Maria Cristina, additional, and Carandini, Tiziana, additional

Published
2022
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5. Evidence of CNS β-amyloid deposition in Nasu-Hakola disease due to the TREM2 Q33X mutation

Author

Riccardo Benti, Laura Ghezzi, Tiziana Carandini, Marina Arcaro, Giorgio G. Fumagalli, Elio Scarpini, Paola Basilico, Marta Scarioni, Andrea Arighi, Milena De Riz, Alberto Calvi, Daniela Galimberti, Anna M. Pietroboni, Chiara Fenoglio, Annalisa Colombi, M Serpente, and Giorgio Marotta

Subjects
0301 basic medicine, Mutation, Pathology, medicine.medical_specialty, Myeloid, business.industry, TREM2, Disease, medicine.disease_cause, medicine.disease, Leukoencephalopathy, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, medicine.anatomical_structure, medicine, Dementia, Neurology (clinical), business, Receptor, 030217 neurology & neurosurgery, Nasu-Hakola disease
Abstract

Nasu-Hakola disease (NHD), also known as polycystic lipomembranous osteodysplasia and sclerosing leukoencephalopathy, is an autosomal recessive disorder characterized by dementia and multifocal bone cysts. NHD is associated with the loss-of-function mutation of triggering receptor expressed on myeloid cells-2 gene ( TREM2 ), leading to an aberrant form of TREM2.1

Published
2017

6. Evidence of CNS β-amyloid deposition in Nasu-Hakola disease due to the

Author

Laura, Ghezzi, Tiziana, Carandini, Andrea, Arighi, Chiara, Fenoglio, Marina, Arcaro, Milena, De Riz, Anna M, Pietroboni, Giorgio G, Fumagalli, Paola, Basilico, Alberto, Calvi, Marta, Scarioni, Annalisa, Colombi, Maria, Serpente, Giorgio, Marotta, Riccardo, Benti, Elio, Scarpini, and Daniela, Galimberti

Subjects
Adult, Amyloid beta-Peptides, Membrane Glycoproteins, Lipodystrophy, Mutation, Humans, Female, Occipital Lobe, Subacute Sclerosing Panencephalitis, Receptors, Immunologic, Mental Status and Dementia Tests, Osteochondrodysplasias, Frontal Lobe
Published
2017

7. A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation

Author

Milena De Riz, Mario Rango, Andrea Arighi, Daniela Galimberti, Erika Tenderini, Elio Scarpini, Maria Teresa Bassi, Francesca Jacini, Giorgio G. Fumagalli, Laura Ghezzi, Anna M. Pietroboni, and Nereo Bresolin

Subjects
medicine.medical_specialty, Eukaryotic Initiation Factor-2B, Physiology, Biology, medicine.disease_cause, White matter, Leukoencephalopathy, Vanishing white matter disease, Leukoencephalopathies, Internal medicine, medicine, Humans, Clinical severity, Primary amenorrhea, Aged, Mutation, Alanine, Valine, medicine.disease, Premature ovarian failure, medicine.anatomical_structure, Endocrinology, Female, Neurology (clinical)
Abstract

Vanishing white matter (VWM; OMIM # 603896) is one of the most prevalent inherited childhood leukoencephalopathies. It has, however, become evident that VWM has a wider clinical spectrum, with age at onset inversely related to clinical severity. Many affected women experience a combination of leukoencephalopathy and primary amenorrhea or premature ovarian failure, a condition named ovarioleukodystrophy. Mutations in any of the genes encoding the 5 subunits of the Eukaryotic Initiation Factor 2B gene (EIF2B1, 2, 3, 4, and 5) can independently cause VWM.(1).

Published
2012

8. A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation

Author

Ghezzi, Laura, primary, Scarpini, Elio, additional, Rango, Mario, additional, Arighi, Andrea, additional, Bassi, Maria Teresa, additional, Tenderini, Erika, additional, De Riz, Milena, additional, Jacini, Francesca, additional, Fumagalli, Giorgio G., additional, Pietroboni, Anna M., additional, Galimberti, Daniela, additional, and Bresolin, Nereo, additional

Published
2012
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10. Clinical/Scientific Notes.

Author

Ghezzi, Laura, Carandini, Tiziana, Arighi, Andrea, Fenoglio, Chiara, Arcaro, Marina, De Riz, Milena, Pietroboni, Anna M., Fumagalli, Giorgio G., Basilico, Paola, Calvi, Alberto, Scarioni, Marta, Colombi, Annalisa, Serpente, Maria, Marotta, Giorgio, Benti, Riccardo, Scarpini, Elio, and Galimberti, Daniela

Published
2017

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