19972020

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Article
2020

Discovering the Italian phenotype of cerebral amyloid angiopathy (CAA): the SENECA project

on behalf of SENECA project, Jan 1 2020, (Accepted/In press) In : Neurological Sciences.

Research output: Contribution to journalArticle

Plasma neurofilament light chain: an early biomarker for hereditary ATTR amyloid polyneuropathy

Maia, L. F., Maceski, A., Conceição, I., Obici, L., Magalhães, R., Cortese, A., Leppert, D., Merlini, G., Kuhle, J. & Saraiva, M. J., Jan 1 2020, (Accepted/In press) In : Amyloid.

Research output: Contribution to journalArticle

Quality of life outcomes in APOLLO, the phase 3 trial of the RNAi therapeutic patisiran in patients with hereditary transthyretin-mediated amyloidosis

Obici, L., Berk, J. L., González-Duarte, A., Coelho, T., Gillmore, J., Schmidt, H. H. J., Schilling, M., Yamashita, T., Labeyrie, C., Brannagan, T. H., Ajroud-Driss, S., Gorevic, P., Kristen, A. V., Franklin, J., Chen, J., Sweetser, M. T., Wang, J. J. & Adams, D., Jan 1 2020, (Accepted/In press) In : Amyloid.

Research output: Contribution to journalArticle

Open Access
2019

An International Delphi Survey for the Definition of New Classification Criteria for Familial Mediterranean Fever, Mevalonate Kinase Deficiency, TNF Receptortextendashassociated Periodic Fever Syndromes, and Cryopyrin-associated Periodic Syndrome

Federici, S., Vanoni, F., Ben-Chetrit, E., Cantarini, L., Frenkel, J., Goldbach-Mansky, R., Gul, A., Hoffman, H., Koné-Paut, I., Kuemmerle-Deschner, J., Lachmann, H. J., Martini, A., Obici, L., Ozen, S., Simon, A., Hofer, M., Ruperto, N. & Gattorno, M., 2019, In : The Journal of rheumatology. 46, 4, p. 429-436 8 p.

Research output: Contribution to journalArticle

A novel knock-in mouse model of cryopyrin-associated periodic syndromes with development of amyloidosis: Therapeutic efficacy of proton pump inhibitors

Bertoni, A., Carta, S., Baldovini, C., Penco, F., Balza, E., Borghini, S., Di Duca, M., Ognio, E., Signori, A., Nozza, P., Schena, F., Castellani, P., Pastorino, C., Perrone, C., Obici, L., Martini, A., Ceccherini, I., Gattorno, M., Rubartelli, A. & Chiesa, S., Jan 1 2019, In : Journal of Allergy and Clinical Immunology.

Research output: Contribution to journalArticle

Burden of hereditary transthyretin amyloidosis on quality of life

Yarlas, A., Gertz, M. A., Dasgupta, N. R., Obici, L., Pollock, M., Ackermann, E. J., Lovley, A., Kessler, A. S., Patel, P. A., White, M. K. & Guthrie, S. D., Aug 1 2019, In : Muscle and Nerve. 60, 2, p. 169-175 7 p.

Research output: Contribution to journalArticle

Open Access

Classification criteria for autoinflammatory recurrent fevers

Gattorno, M., Hofer, M., Federici, S., Vanoni, F., Bovis, F., Aksentijevich, I., Anton, J., Arostegui, J. I., Barron, K., Ben-Cherit, E., Brogan, P. A., Cantarini, L., Ceccherini, I., De Benedetti, F., Dedeoglu, F., Demirkaya, E., Frenkel, J., Goldbach-Mansky, R., Gul, A., Hentgen, V. & 23 others, Hoffman, H., Kallinich, T., Kone-Paut, I., Kuemmerle-Deschner, J., Lachmann, H. J., Laxer, R. M., Livneh, A., Obici, L., Ozen, S., Rowczenio, D., Russo, R., Shinar, Y., Simon, A., Toplak, N., Touitou, I., Uziel, Y., van Gijn, M., Foell, D., Garassino, C., Kastner, D., Martini, A., Sormani, M. P. & Ruperto, N., Apr 24 2019, In : Annals of the Rheumatic Diseases.

Research output: Contribution to journalArticle

Classification criteria for autoinflammatory recurrent fevers

Gattorno, M., Hofer, M., Federici, S., Vanoni, F., Bovis, F., Aksentijevich, I., Anton, J., Arostegui, J. I., Barron, K., Ben-Cherit, E., Brogan, P. A., Cantarini, L., Ceccherini, I., De Benedetti, F., Dedeoglu, F., Demirkaya, E., Frenkel, J., Goldbach-Mansky, R., Gul, A., Hentgen, V. & 23 others, Hoffman, H., Kallinich, T., Kone-Paut, I., Kuemmerle-Deschner, J., Lachmann, H. J., Laxer, R. M., Livneh, A., Obici, L., Ozen, S., Rowczenio, D., Russo, R., Shinar, Y., Simon, A., Toplak, N., Touitou, I., Uziel, Y., Van Gijn, M., Foell, D., Garassino, C., Kastner, D., Martini, A., Sormani, M. P. & Ruperto, N., Aug 1 2019, In : Annals of the Rheumatic Diseases. 78, 8, p. 1025-1032 8 p.

Research output: Contribution to journalArticle

Open Access

Classification criteria for autoinflammatory recurrent fevers

Gattorno, M., Hofer, M., Federici, S., Vanoni, F., Bovis, F., Aksentijevich, I., Anton, J., Arostegui, J. I., Barron, K., Ben-Cherit, E., Brogan, P. A., Cantarini, L., Ceccherini, I., De Benedetti, F., Dedeoglu, F., Demirkaya, E., Frenkel, J., Goldbach-Mansky, R., Gul, A., Hentgen, V. & 24 others, Hoffman, H., Kallinich, T., Kone-Paut, I., Kuemmerle-Deschner, J., Lachmann, H. J., Laxer, R. M., Livneh, A., Obici, L., Ozen, S., Rowczenio, D., Russo, R., Shinar, Y., Simon, A., Toplak, N., Touitou, I., Uziel, Y., van Gijn, M., Foell, D., Garassino, C., Kastner, D., Martini, A., Sormani, M. P., Ruperto, N. & (PRINTO), E. R. A. T. P. R. I. T. O., Aug 2019, In : Annals of the Rheumatic Diseases. 78, 8, p. 1025-1032 8 p.

Research output: Contribution to journalArticle

Inotersen for the treatment of adults with polyneuropathy caused by hereditary transthyretin-mediated amyloidosis

Gertz, M. A., Scheinberg, M., Waddington-Cruz, M., Heitner, S. B., Karam, C., Drachman, B., Khella, S., Whelan, C. & Obici, L., Jan 1 2019, In : Expert Review of Clinical Pharmacology.

Research output: Contribution to journalArticle

Open Access

Inotersen preserves or improves quality of life in hereditary transthyretin amyloidosis

Coelho, T., Yarlas, A., Waddington-Cruz, M., White, M. K., Sikora Kessler, A., Lovley, A., Pollock, M., Guthrie, S., Ackermann, E. J., Hughes, S. G., Karam, C., Khella, S., Gertz, M., Merlini, G., Obici, L., Schmidt, H. H., Polydefkis, M., Dyck, P. J. B., Brannagan, T. H., Conceição, I. & 2 others, Benson, M. D. & Berk, J. L., Jan 1 2019, (Accepted/In press) In : Journal of Neurology.

Research output: Contribution to journalArticle

Open Access

Patisiran, an RNAi therapeutic for the treatment of hereditary transthyretin-mediated amyloidosis

Kristen, A. V., Ajroud-Driss, S., Conceição, I., Gorevic, P., Kyriakides, T. & Obici, L., Feb 1 2019, In : Neurodegenerative disease management. 9, 1, p. 5-23 19 p.

Research output: Contribution to journalArticle

Transthyretin deposition in the eye in the era of effective therapy for hereditary ATTRV30M amyloidosis

Buxbaum, J. N., Brannagan, T., Buades-Reinés, J., Cisneros, E., Conceicao, I., Kyriakides, T., Merlini, G., Obici, L., Plante-Bordeneuve, V., Rousseau, A., Sekijima, Y., Imai, A., Waddington Cruz, M. & Yamada, M., Jan 2 2019, In : Amyloid. 26, 1, p. 10-14 5 p.

Research output: Contribution to journalArticle

2018

Becoming familiar with hereditary transthyretin amyloidosis, a treatable neuropathy

Obici, L., Sep 1 2018, In : Arquivos de Neuro-Psiquiatria. 76, p. 573 - 574

Research output: Contribution to journalArticle

Canakinumab for the treatment of autoinflammatory recurrent fever syndromes

De Benedetti, F., Gattorno, M., Anton, J., Eldad, B. C., Frenkel, J., Hoffman, H. M., Isabelle, K. P., Lachmann, H. J., Ozen, S., Simon, A., Zeft, A., Penades, I. C., Moutschen, M., Quartier, P., Kasapcopur, O., Shcherbina, A., Hofer, M., Hashkes, P. J., Van der Hilst, J., Hara, R. & 10 others, Segundo, B. R., Constantin, T., Gul, A., Livneh, A., Brogan, P., Cattalini, M., Obici, L., Lheritier, K., Speziale, A. & Junge, G., May 17 2018, In : New England Journal of Medicine. 378, 20, p. 1908-1919 12 p.

Research output: Contribution to journalArticle

Canakinumab for the treatment of autoinflammatory recurrent fever syndromes

De Benedetti, F., Gattorno, M., Anton, J., Eldad, B-C., Frenkel, J., Hoffman, H. M., Isabelle, K-P., Lachmann, H. J., Ozen, S., Simon, A., Zeft, A., Penades, I. C., Moutschen, M., Quartier, P., Kasapcopur, O., Shcherbina, A., Hofer, M., Hashkes, P. J., Van der Hilst, J., Hara, R. & 10 others, Segundo, B-R., Constantin, T., Gul, A., Livneh, A., Brogan, P., Cattalini, M., Obici, L., Lheritier, K., Speziale, A. & Junge, G., 2018, In : New England Journal of Medicine. 378, 20, p. 1908-1919 12 p.

Research output: Contribution to journalArticle

Canakinumab for the treatment of autoinflammatory recurrent fever syndromes

De Benedetti, F., Gattorno, M., Anton, J., Eldad, B. C., Frenkel, J., Hoffman, H. M., Isabelle, K. P., Lachmann, H. J., Ozen, S., Simon, A., Zeft, A., Penades, I. C., Moutschen, M., Quartier, P., Kasapcopur, O., Shcherbina, A., Hofer, M., Hashkes, P. J., Van der Hilst, J., Hara, R. & 10 others, Segundo, B. R., Constantin, T., Gul, A., Livneh, A., Brogan, P., Cattalini, M., Obici, L., Lheritier, K., Speziale, A. & Junge, G., May 17 2018, In : New England Journal of Medicine. 378, 20, p. 1908-1919 12 p.

Research output: Contribution to journalArticle

Inotersen treatment for patients with Hereditary transthyretin amyloidosis

Benson, M. D., Waddington-Cruz, M., Berk, J. L., Polydefkis, M., Dyck, P. J., Wang, A. K., Planté-Bordeneuve, V., Barroso, F. A., Merlini, G., Obici, L., Scheinberg, M., Brannagan, T. H., Litchy, W. J., Whelan, C., Drachman, B. M., Adams, D., Heitner, S. B., Conceição, I., Schmidt, H. H., Vita, G. & 15 others, Campistol, J. M., Gamez, J., Gorevic, P. D., Gane, E., Shah, A. M., Solomon, S. D., Monia, B. P., Hughes, S. G., Jesse Kwoh, T., McEvoy, B. W., Jung, S. W., Baker, B. F., Ackermann, E. J., Gertz, M. A. & Coelho, T., Jul 5 2018, In : New England Journal of Medicine. 379, 1, p. 22-31 10 p.

Research output: Contribution to journalArticle

Plasminogen activation triggers transthyretin amyloidogenesis in vitro

Mangione, P. P., Verona, G., Corazza, A., Marcoux, J., Canetti, D., Giorgetti, S., Raimondi, S., Stoppini, M., Esposito, M., Relini, A., Canale, C., Valli, M., Marchese, L., Faravelli, G., Obici, L., Hawkins, P. N., Taylor, G. W., Gillmore, J. D., Pepys, M. B. & Bellotti, V., Jan 1 2018, In : Journal of Biological Chemistry. 293, 37, p. 14192-14199 8 p.

Research output: Contribution to journalArticle

Progressive axonal polyneuropathy in a mitochondrial disorder: an uncommon association with familial amyloid neuropathy

Luigetti, M., Primiano, G., Bisogni, G., Cuccagna, C., Carrozzo, R., Obici, L., Bernardo, D., Sancricca, C. & Servidei, S., Jan 1 2018, (Accepted/In press) In : Amyloid.

Research output: Contribution to journalArticle

Progressive axonal polyneuropathy in a mitochondrial disorder: an uncommon association with familial amyloid neuropathy

Luigetti, M., Primiano, G., Bisogni, G., Cuccagna, C., Carrozzo, R., Obici, L., Bernardo, D., Sancricca, C. & Servidei, S., 2018, In : Amyloid. 25, 4, p. 261-262 2 p.

Research output: Contribution to journalArticle

Progressive axonal polyneuropathy in a mitochondrial disorder: an uncommon association with familial amyloid neuropathy

Luigetti, M., Primiano, G., Bisogni, G., Cuccagna, C., Carrozzo, R., Obici, L., Bernardo, D., Sancricca, C. & Servidei, S., 2018, In : Amyloid.

Research output: Contribution to journalArticle

The role of clinical and neuroimaging features in the diagnosis of CADASIL

on behalf of Lombardia GENS-group, 2018, In : Journal of Neurology. 265, 12, p. 2934-2943

Research output: Contribution to journalArticle

Updated overview of molecular pathways involved in the most common monogenic autoinflammatory diseases

Lucherini, O. M., Rigante, D., Sota, J., Fabiani, C., Obici, L., Cattalini, M., Gattorno, M. & Cantarini, L., Jan 1 2018, In : Clinical and Experimental Rheumatology. 36, 1, p. 3-9 7 p.

Research output: Contribution to journalArticle

Updated overview of molecular pathways involved in the most common monogenic autoinflammatory diseases

Lucherini, O. M., Rigante, D., Sota, J., Fabiani, C., Obici, L., Cattalini, M., Gattorno, M. & Cantarini, L., 2018, In : Clinical and Experimental Rheumatology. 36, p. S3-S9

Research output: Contribution to journalArticle

2017

Canakinumab reverses overexpression of inflammatory response genes in tumour necrosis factor receptor-associated periodic syndrome

Torene, R., Nirmala, N., Obici, L., Cattalini, M., Tormey, V., Caorsi, R., Starck-Schwertz, S., Letzkus, M., Hartmann, N., Abrams, K., Lachmann, H. & Gattorno, M., Jan 1 2017, In : Annals of the Rheumatic Diseases. 76, 1, p. 303-309 7 p.

Research output: Contribution to journalArticle

Canakinumab treatment for patients with active recurrent or chronic TNF receptor-associated periodic syndrome (TRAPS): an open-label, phase II study

Gattorno, M., Obici, L., Cattalini, M., Tormey, V., Abrams, K., Davis, N., Speziale, A., Bhansali, S. G., Martini, A. & Lachmann, H. J., Jan 1 2017, In : Annals of the Rheumatic Diseases. 76, 1, p. 173-178 6 p.

Research output: Contribution to journalArticle

Cryopyrin-associated periodic syndromes in Italian Patients: Evaluation of the rate of somatic NLRP3 mosaicism and phenotypic characterization

Lasigliè, D., Mensa-Vilaro, A., Ferrera, D., Caorsi, R., Penco, F., Santamaria, G., Di Duca, M., Amico, G., Nakagawa, K., Antonini, F., Tommasini, A., Consolini, R., Insalaco, A., Cattalini, M., Obici, L., Gallizzi, R., Santarelli, F., Del Zotto, G., Severino, M., Rubartelli, A. & 7 others, Ravazzolo, R., Martini, A., Ceccherini, I., Nishikomori, R., Gattorno, M., Arostegui, J. I. & Borghini, S., Nov 1 2017, In : Journal of Rheumatology. 44, 11, p. 1667-1673 7 p.

Research output: Contribution to journalArticle

Cryopyrin-associated Periodic Syndromes in Italian Patients

Lasigliè, D., Mensa-Vilaro, A., Ferrera, D., Caorsi, R., Penco, F., Santamaria, G., Di Duca, M., Amico, G., Nakagawa, K., Antonini, F., Tommasini, A., Consolini, R., Insalaco, A., Cattalini, M., Obici, L., Gallizzi, R., Santarelli, F., Del Zotto, G., Severino, M., Rubartelli, A. & 7 others, Ravazzolo, R., Martini, A., Ceccherini, I., Nishikomori, R., Gattorno, M., Arostegui, J. I. & Borghini, S., Nov 2017, In : Journal of Rheumatology. 44, 11, p. 1667-1673 7 p.

Research output: Contribution to journalArticle

Cryopyrin-associated periodic syndromes in Italian Patients: Evaluation of the rate of somatic NLRP3 mosaicism and phenotypic characterization

Lasigliè, D., Mensa-Vilaro, A., Ferrera, D., Caorsi, R., Penco, F., Santamaria, G., Di Duca, M., Amico, G., Nakagawa, K., Antonini, F., Tommasini, A., Consolini, R., Insalaco, A., Cattalini, M., Obici, L., Gallizzi, R., Santarelli, F., Del Zotto, G., Severino, M., Rubartelli, A. & 7 others, Ravazzolo, R., Martini, A., Ceccherini, I., Nishikomori, R., Gattorno, M., Arostegui, J. I. & Borghini, S., 2017, In : Journal of Rheumatology. 44, 11, p. 1667-1673 7 p.

Research output: Contribution to journalArticle

Differential expression of Cathepsin E in transthyretin amyloidosis: From neuropathology to the immune system

Gonçalves, N. P., Moreira, J., Martins, D., Vieira, P., Obici, L., Merlini, G., Saraiva, M. & Saraiva, M. J., Jun 6 2017, In : Journal of Neuroinflammation. 14, 1, 115.

Research output: Contribution to journalArticle

2016

Canakinumab reverses overexpression of inflammatory response genes in tumour necrosis factor receptor-associated periodic syndrome

Torene, R., Nirmala, N., Obici, L. P., Cattalini, M., Tormey, V., Caorsi, R., Starck-Schwertz, S., Letzkus, M., Hartmann, N., Abrams, K., Lachmann, H. & Gattorno, M., Jul 29 2016, (Accepted/In press) In : Annals of the Rheumatic Diseases.

Research output: Contribution to journalArticle

Canakinumab reverses overexpression of inflammatory response genes in tumour necrosis factor receptor-associated periodic syndrome

Torene, R., Nirmala, N., Obici, L., Cattalini, M., Tormey, V., Caorsi, R., Starck-Schwertz, S., Letzkus, M., Hartmann, N., Abrams, K., Lachmann, H. & Gattorno, M., Jul 29 2016, (Accepted/In press) In : Annals of the Rheumatic Diseases.

Research output: Contribution to journalArticle

Canakinumab treatment for patients with active recurrent or chronic TNF receptor-associated periodic syndrome (TRAPS): An open-label, phase II study

Gattorno, M., Obici, L., Cattalini, M., Tormey, V., Abrams, K., Davis, N., Speziale, A., Bhansali, S. G., Martini, A. & Lachmann, H. J., Jun 7 2016, (Accepted/In press) In : Annals of the Rheumatic Diseases.

Research output: Contribution to journalArticle

Canakinumab treatment for patients with active recurrent or chronic TNF receptor-associated periodic syndrome (TRAPS): An open-label, phase II study

Gattorno, M., Obici, L. P., Cattalini, M., Tormey, V., Abrams, K., Davis, N., Speziale, A., Bhansali, S. G., Martini, A. & Lachmann, H., Jun 7 2016, (Accepted/In press) In : Annals of the Rheumatic Diseases.

Research output: Contribution to journalArticle

Clinical characteristics of patients carrying the Q703K variant of the NLRP3 Gene: A 10-year multicentric national study

Naselli, A., Penco, F., Cantarini, L., Insalaco, A., Alessio, M., Tommasini, A., Maggio, C., Obici, L., Gallizi, R., Cimmino, M., Signa, S., Lucherini, O. M., Carta, S., Caroli, F., Martini, A., Rubartelli, A., Ceccherini, I. & Gattorno, M., Jun 1 2016, In : Journal of Rheumatology. 43, 6, p. 1093-1100 8 p.

Research output: Contribution to journalArticle

Clinical characteristics of patients carrying the Q703K variant of the NLRP3 Gene: A 10-year multicentric national study

Naselli, A., Penco, F., Cantarini, L., Insalaco, A., Alessio, M., Tommasini, A., Maggio, C., Obici, L. P., Gallizi, R., Cimmino, M. A., Signa, S., Lucherini, O. M., Carta, S., Caroli, F., Martini, A., Rubartelli, A., Ceccherini, I. & Gattorno, M., Jun 1 2016, In : Journal of Rheumatology. 43, 6, p. 1093-1100 8 p.

Research output: Contribution to journalArticle

Clinical characteristics of patients carrying the Q703K variant of the NLRP3 Gene: A 10-year multicentric national study

Naselli, A., Penco, F., Cantarini, L., Insalaco, A., Alessio, M., Tommasini, A., Maggio, C., Obici, L. P., Gallizi, R., Cimmino, M. A., Signa, S., Lucherini, O. M., Carta, S., Caroli, F., Martini, A., Rubartelli, A., Ceccherini, I. & Gattorno, M., Jun 1 2016, In : Journal of Rheumatology. 43, 6, p. 1093-1100 8 p.

Research output: Contribution to journalArticle

Clinical pregenetic screening for stroke monogenic diseases: Results from lombardia GENS registry

Bersano, A., Markus, H. S., Quaglini, S., Arbustini, E., Lanfranconi, S., Micieli, G., Boncoraglio, G. B., Taroni, F., Gellera, C., Baratta, S., Penco, S., Mosca, L., Grasso, M., Carrera, P., Ferrari, M., Cereda, C., Grieco, G., Corti, S. P., Ronchi, D., Bassi, M. T. & 42 others, Obici, L. P., Parati, E. A., Pezzini, A., De Lodovici, M. L., Verrengia, E. P., Bono, G., Mazucchelli, F., Zarcone, D., Calloni, M. V., Perrone, P., Bordo, B. M., Colombo, A., Padovani, A., Cavallini, A., Beretta, S., Ferrarese, C., Motto, C., Agostoni, E., Molini, G., Sasanelli, F., Corato, M., Marcheselli, S., Sessa, M., Comi, G., Checcarelli, N., Guidotti, M., Uccellini, D., Capitani, E., Tancredi, L., Arnaboldi, M., Incorvaia, B., Tadeo, C. S., Fusi, L., Grampa, G., Merlini, G., Trobia, N., Comi, G. P., Braga, M., Vitali, P., Baron, P., Grond-Ginsbach, C. & Candelise, L., Jul 1 2016, In : Stroke. 47, 7, p. 1702-1709 8 p.

Research output: Contribution to journalArticle

Clinical pregenetic screening for stroke monogenic diseases: Results from lombardia GENS registry

Bersano, A., Markus, H. S., Quaglini, S., Arbustini, E., Lanfranconi, S., Micieli, G., Boncoraglio, G. B., Taroni, F., Gellera, C., Baratta, S., Penco, S., Mosca, L., Grasso, M., Carrera, P., Ferrari, M., Cereda, C., Grieco, G., Corti, S. P., Ronchi, D., Bassi, M. T. & 42 others, Obici, L. P., Parati, E. A., Pezzini, A., De Lodovici, M. L., Verrengia, E. P., Bono, G., Mazucchelli, F., Zarcone, D., Calloni, M. V., Perrone, P., Bordo, B. M., Colombo, A., Padovani, A., Cavallini, A., Beretta, S., Ferrarese, C., Motto, C., Agostoni, E., Molini, G., Sasanelli, F., Corato, M., Marcheselli, S., Sessa, M., Comi, G., Checcarelli, N., Guidotti, M., Uccellini, D., Capitani, E., Tancredi, L., Arnaboldi, M., Incorvaia, B., Tadeo, C. S., Fusi, L., Grampa, G., Merlini, G., Trobia, N., Comi, G. P., Braga, M., Vitali, P., Baron, P., Grond-Ginsbach, C. & Candelise, L., Jul 1 2016, In : Stroke. 47, 7, p. 1702-1709 8 p.

Research output: Contribution to journalArticle

Clinical pregenetic screening for stroke monogenic diseases: Results from lombardia GENS registry

Bersano, A., Markus, H. S., Quaglini, S., Arbustini, E., Lanfranconi, S., Micieli, G., Boncoraglio, G. B., Taroni, F., Gellera, C., Baratta, S., Penco, S., Mosca, L., Grasso, M., Carrera, P., Ferrari, M., Cereda, C., Grieco, G., Corti, S. P., Ronchi, D., Bassi, M. T. & 42 others, Obici, L. P., Parati, E. A., Pezzini, A., De Lodovici, M. L., Verrengia, E. P., Bono, G., Mazucchelli, F., Zarcone, D., Calloni, M. V., Perrone, P., Bordo, B. M., Colombo, A., Padovani, A., Cavallini, A., Beretta, S., Ferrarese, C., Motto, C., Agostoni, E., Molini, G., Sasanelli, F., Corato, M., Marcheselli, S., Sessa, M., Comi, G., Checcarelli, N., Guidotti, M., Uccellini, D., Capitani, E., Tancredi, L., Arnaboldi, M., Incorvaia, B., Tadeo, C. S., Fusi, L., Grampa, G., Merlini, G., Trobia, N., Comi, G. P., Braga, M., Vitali, P., Baron, P., Grond-Ginsbach, C. & Candelise, L., Jul 1 2016, In : Stroke. 47, 7, p. 1702-1709 8 p.

Research output: Contribution to journalArticle

Clinical pregenetic screening for stroke monogenic diseases: Results from lombardia GENS registry

Bersano, A., Markus, H. S., Quaglini, S., Arbustini, E., Lanfranconi, S., Micieli, G., Boncoraglio, G. B., Taroni, F., Gellera, C., Baratta, S., Penco, S., Mosca, L., Grasso, M., Carrera, P., Ferrari, M., Cereda, C., Grieco, G., Corti, S. P., Ronchi, D., Bassi, M. T. & 42 others, Obici, L. P., Parati, E. A., Pezzini, A., De Lodovici, M. L., Verrengia, E. P., Bono, G., Mazucchelli, F., Zarcone, D., Calloni, M. V., Perrone, P., Bordo, B. M., Colombo, A., Padovani, A., Cavallini, A., Beretta, S., Ferrarese, C., Motto, C., Agostoni, E., Molini, G., Sasanelli, F., Corato, M., Marcheselli, S., Sessa, M., Comi, G., Checcarelli, N., Guidotti, M., Uccellini, D., Capitani, E., Tancredi, L., Arnaboldi, M., Incorvaia, B., Tadeo, C. S., Fusi, L., Grampa, G., Merlini, G., Trobia, N., Comi, G. P., Braga, M., Vitali, P., Baron, P., Grond-Ginsbach, C. & Candelise, L., Jul 1 2016, In : Stroke. 47, 7, p. 1702-1709 8 p.

Research output: Contribution to journalArticle

Clinical pregenetic screening for stroke monogenic diseases: Results from lombardia GENS registry

Bersano, A., Markus, H. S., Quaglini, S., Arbustini, E., Lanfranconi, S., Micieli, G., Boncoraglio, G. B., Taroni, F., Gellera, C., Baratta, S., Penco, S., Mosca, L., Grasso, M., Carrera, P., Ferrari, M., Cereda, C., Grieco, G., Corti, S., Ronchi, D., Bassi, M. T. & 42 others, Obici, L., Parati, E. A., Pezzini, A., De Lodovici, M. L., Verrengia, E. P., Bono, G., Mazucchelli, F., Zarcone, D., Calloni, M. V., Perrone, P., Bordo, B. M., Colombo, A., Padovani, A., Cavallini, A., Beretta, S., Ferrarese, C., Motto, C., Agostoni, E., Molini, G., Sasanelli, F., Corato, M., Marcheselli, S., Sessa, M., Comi, G., Checcarelli, N., Guidotti, M., Uccellini, D., Capitani, E., Tancredi, L., Arnaboldi, M., Incorvaia, B., Tadeo, C. S., Fusi, L., Grampa, G., Merlini, G., Trobia, N., Comi, G. P., Braga, M., Vitali, P., Baron, P., Grond-Ginsbach, C. & Candelise, L., Jul 1 2016, In : Stroke. 47, 7, p. 1702-1709 8 p.

Research output: Contribution to journalArticle

Clinical pregenetic screening for stroke monogenic diseases: Results from lombardia GENS registry

Bersano, A., Markus, H. S., Quaglini, S., Arbustini, E., Lanfranconi, S., Micieli, G., Boncoraglio, G. B., Taroni, F., Gellera, C., Baratta, S., Penco, S., Mosca, L., Grasso, M., Carrera, P., Ferrari, M., Cereda, C., Grieco, G., Corti, S. P., Ronchi, D., Bassi, M. T. & 42 others, Obici, L. P., Parati, E. A., Pezzini, A., De Lodovici, M. L., Verrengia, E. P., Bono, G., Mazucchelli, F., Zarcone, D., Calloni, M. V., Perrone, P., Bordo, B. M., Colombo, A., Padovani, A., Cavallini, A., Beretta, S., Ferrarese, C., Motto, C., Agostoni, E., Molini, G., Sasanelli, F., Corato, M., Marcheselli, S., Sessa, M., Comi, G., Checcarelli, N., Guidotti, M., Uccellini, D., Capitani, E., Tancredi, L., Arnaboldi, M., Incorvaia, B., Tadeo, C. S., Fusi, L., Grampa, G., Merlini, G., Trobia, N., Comi, G. P., Braga, M., Vitali, P., Baron, P., Grond-Ginsbach, C. & Candelise, L., Jul 1 2016, In : Stroke. 47, 7, p. 1702-1709 8 p.

Research output: Contribution to journalArticle