• 2981 Citations
  • 30 h-Index
1981 …2019
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Research Output 1981 2019

2019

Efficacy and Adverse Events During Janus Kinase Inhibitor Treatment of SAVI Syndrome

Volpi, S., Insalaco, A., Caorsi, R., Santori, E., Messia, V., Sacco, O., Terheggen-Lagro, S., Cardinale, F., Scarselli, A., Pastorino, C., Moneta, G., Cangemi, G., Passarelli, C., Ricci, M., Girosi, D., Derchi, M., Bocca, P., Diociaiuti, A., El Hachem, M., Cancrini, C. & 7 others, Tomà, P., Granata, C., Ravelli, A., Candotti, F., Picco, P., DeBenedetti, F. & Gattorno, M., Jul 2019, In : Journal of Clinical Immunology. 39, 5, p. 476-485 10 p.

Research output: Contribution to journalArticle

Janus Kinases
Therapeutics
Virus Diseases
Respiratory Tract Infections
Interferon Type I
2018

ABCC6 mutations and early onset stroke: Two cases of a typical Pseudoxanthoma Elasticum

Gaslini Pediatric Stroke Group, Jul 2018, In : European Journal of Paediatric Neurology. 22, 4, p. 725-728 4 p.

Research output: Contribution to journalArticle

Pseudoxanthoma Elasticum
Eye Manifestations
Angioid Streaks
Stroke
Skin Manifestations
3 Citations (Scopus)
Epstein-Barr Virus Infections
Human Herpesvirus 4
Lymphadenitis
Fever
Mutation
8 Citations (Scopus)

High-dose ustekinumab for severe childhood deficiency of interleukin-36 receptor antagonist (DITRA)

Bonekamp, N., Caorsi, R., Viglizzo, G. M., De Graaf, M., Minoia, F., Grossi, A., Picco, P., Ceccherini, I., Frenkel, J. & Gattorno, M., Aug 1 2018, In : Annals of the Rheumatic Diseases. 77, 8, p. 1241-1243 3 p.

Research output: Contribution to journalLetter

Inflammatory myopathy in a patient with collagen VI mutations

Papa, R., Fiorillo, C., Malattia, C., Minoia, F., Caorsi, R., Assereto, S., Iacomino, M., Savarese, M., Nigro, V., Bruno, C., Minetti, C. & Picco, P., Mar 4 2018, In : Scandinavian Journal of Rheumatology. 47, 2, p. 166-167 2 p.

Research output: Contribution to journalLetter

Loss of tubulin deglutamylase CCP1 causes infantile-onset neurodegeneration

Undiagnosed Diseases Network, Dec 3 2018, In : EMBO Journal. 37, 23

Research output: Contribution to journalArticle

Tubulin
Neurons
Purkinje Cells
Motor Neurons
Post Translational Protein Processing

T-cell defects in patients with ARPC1B germline mutations account for combined immunodeficiency

Brigida, I., Zoccolillo, M., Cicalese, MP., Pfajfer, L., Barzaghi, F., Scala, S., Oleaga-Quintas, C., Álvarez-Álvarez, JA., Sereni, L., Giannelli, S., Sartirana, C., Dionisio, F., Pavesi, L., Benavides-Nieto, M., Basso-Ricci, L., Capasso, P., Mazzi, B., Rosain, J., Marcus, N., Lee, YN. & 26 others, Somech, R., Degano, M., Raiola, G., Caorsi, R., Picco, P., Velez, MM., Khourieh, J., Arias, AA., Bousfiha, A., Issekutz, T., Issekutz, A., Boisson, B., Dobbs, K., Villa, A., Lombardo, A., Neven, B., Moshous, D., Casanova, JL., Franco, JL., Notarangelo, LD., Scielzo, C., Volpi, S., Dupré, L., Bustamante, J., Gattorno, M. & Aiuti, A., 2018, In : Blood. 132, 22, p. 2362-2374 13 p.

Research output: Contribution to journalArticle

T-cells
Germ-Line Mutation
T-Lymphocytes
Defects
T-Cell Antigen Receptor

T-cell defects in patients with ARPC1B germline mutations account for combined immunodeficiency

Brigida, I., Zoccolillo, M., Cicalese, M. P., Pfajfer, L., Barzaghi, F., Scala, S., Oleaga-Quintas, C., Álvarez-Álvarez, J. A., Sereni, L., Giannelli, S., Sartirana, C., Dionisio, F., Pavesi, L., Benavides-Nieto, M., Basso-Ricci, L., Capasso, P., Mazzi, B., Rosain, J., Marcus, N., Lee, Y. N. & 26 others, Somech, R., Degano, M., Raiola, G., Caorsi, R., Picco, P., Moncada Velez, M., Khourieh, J., Arias, A. A., Bousfiha, A., Issekutz, T., Issekutz, A., Boisson, B., Dobbs, K., Villa, A., Lombardo, A., Neven, B., Moshous, D., Casanova, J-L., Franco, J. L., Notarangelo, L. D., Scielzo, C., Volpi, S., Dupré, L., Bustamante, J., Gattorno, M. & Aiuti, A., Nov 29 2018, In : Blood. 132, 22, p. 2362-2374 13 p.

Research output: Contribution to journalArticle

Germ-Line Mutation
T-Lymphocytes
T-Cell Antigen Receptor
Actins
Immunological Synapses
19 Citations (Scopus)

Type I interferon pathway activation in COPA syndrome

Volpi, S., Tsui, J., Mariani, M., Pastorino, C., Caorsi, R., Sacco, O., Ravelli, A., Shum, A. K., Gattorno, M. & Picco, P., Feb 1 2018, In : Clinical Immunology. 187, p. 33-36 4 p.

Research output: Contribution to journalArticle

Interferon Type I
Interstitial Lung Diseases
Arthritis
Joints
Mutation
2017
52 Citations (Scopus)

ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: a multicentre national study

Caorsi, R., Penco, F., Grossi, A., Insalaco, A., Omenetti, A., Alessio, M., Conti, G., Marchetti, F., Picco, P., Tommasini, A., Martino, S., Malattia, C., Gallizi, R., Podda, R. A., Salis, A., Falcini, F., Schena, F., Garbarino, F., Morreale, A., Pardeo, M. & 11 others, Ventrici, C., Passarelli, C., Zhou, Q., Severino, M., Gandolfo, C., Damonte, G., Martini, A., Ravelli, A., Aksentijevich, I., Ceccherini, I. & Gattorno, M., Oct 2017, In : Annals of the Rheumatic Diseases. 76, 10, p. 1648-1656 9 p.

Research output: Contribution to journalArticle

Polyarteritis Nodosa
Adenosine Deaminase
Multicenter Studies
Stroke
Mutation
52 Citations (Scopus)

ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: A multicentre national study

Caorsi, R., Penco, F., Grossi, A., Insalaco, A., Omenetti, A., Alessio, M., Conti, G., Marchetti, F., Picco, P., Tommasini, A., Martino, S., Malattia, C., Gallizi, R., Podda, R. A., Salis, A., Falcini, F., Schena, F., Garbarino, F., Morreale, A., Pardeo, M. & 11 others, Ventrici, C., Passarelli, C., Zhou, Q., Severino, M., Gandolfo, C., Damonte, G., Martini, A., Ravelli, A., Aksentijevich, I., Ceccherini, I. & Gattorno, M., Oct 1 2017, In : Annals of the Rheumatic Diseases. 76, 10, p. 1648-1656 9 p.

Research output: Contribution to journalArticle

Polyarteritis Nodosa
Adenosine Deaminase
Multicenter Studies
Stroke
Mutation
52 Citations (Scopus)

ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: A multicentre national study

Caorsi, R., Penco, F., Grossi, A., Insalaco, A., Omenetti, A., Alessio, M., Conti, G., Marchetti, F., Picco, P., Tommasini, A., Martino, S., Malattia, C., Gallizi, R., Podda, R. A., Salis, A., Falcini, F., Schena, F., Garbarino, F., Morreale, A., Pardeo, M. & 11 others, Ventrici, C., Passarelli, C., Zhou, Q., Severino, M., Gandolfo, C., Damonte, G., Martini, A., Ravelli, A., Aksentijevich, I., Ceccherini, I. & Gattorno, M., 2017, In : Annals of the Rheumatic Diseases. 76, 10, p. 1648-1656 9 p.

Research output: Contribution to journalArticle

52 Citations (Scopus)

ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: A multicentre national study

Caorsi, R., Penco, F., Grossi, A., Insalaco, A., Omenetti, A., Alessio, M., Conti, G., Marchetti, F., Picco, P., Tommasini, A., Martino, S., Malattia, C., Gallizi, R., Podda, R. A., Salis, A., Falcini, F., Schena, F., Garbarino, F., Morreale, A., Pardeo, M. & 11 others, Ventrici, C., Passarelli, C., Zhou, Q., Severino, M., Gandolfo, C., Damonte, G., Martini, A., Ravelli, A., Aksentijevich, I., Ceccherini, I. & Gattorno, M., 2017, In : Annals of the Rheumatic Diseases. 76, 10, p. 1648-1656 9 p.

Research output: Contribution to journalArticle

Periostitis
Hyperostosis
Bone and Bones
Acute-Phase Proteins
Streptococcus
19 Citations (Scopus)

Intra-articular corticosteroids versus intra-articular corticosteroids plus methotrexate in oligoarticular juvenile idiopathic arthritis: a multicentre, prospective, randomised, open-label trial

Ravelli, A., Davì, S., Bracciolini, G., Pistorio, A., Consolaro, A., van Dijkhuizen, E. H. P., Lattanzi, B., Filocamo, G., Verazza, S., Gerloni, V., Gattinara, M., Pontikaki, I., Insalaco, A., De Benedetti, F., Civino, A., Presta, G., Breda, L., Marzetti, V., Pastore, S., Magni-Manzoni, S. & 11 others, Maggio, M. C., Garofalo, F., Rigante, D., Gattorno, M., Malattia, C., Picco, P., Viola, S., Lanni, S., Ruperto, N., Martini, A. & Italian Pediatric Rheumatology Study Group, Mar 4 2017, In : The Lancet. 389, 10072, p. 909-916 8 p.

Research output: Contribution to journalArticle

Juvenile Arthritis
Methotrexate
Adrenal Cortex Hormones
Joints
Therapeutics
19 Citations (Scopus)

Intra-articular corticosteroids versus intra-articular corticosteroids plus methotrexate in oligoarticular juvenile idiopathic arthritis

Ravelli, A., Davì, S., Bracciolini, G., Pistorio, A., Consolaro, A., van Dijkhuizen, E. H. P., Lattanzi, B., Filocamo, G., Verazza, S., Gerloni, V., Gattinara, M., Pontikaki, I., Insalaco, A., De Benedetti, F., Civino, A., Presta, G., Breda, L., Marzetti, V., Pastore, S., Magni-Manzoni, S. & 11 others, Maggio, M. C., Garofalo, F., Rigante, D., Gattorno, M., Malattia, C., Picco, P., Viola, S., Lanni, S., Ruperto, N., Martini, A. & Group, I. P. R. S., Mar 4 2017, In : The Lancet. 389, 10072, p. 909-916 8 p.

Research output: Contribution to journalArticle

Juvenile Arthritis
Methotrexate
Adrenal Cortex Hormones
Joints
Therapeutics
19 Citations (Scopus)

Intra-articular corticosteroids versus intra-articular corticosteroids plus methotrexate in oligoarticular juvenile idiopathic arthritis: a multicentre, prospective, randomised, open-label trial

Ravelli, A., Davì, S., Bracciolini, G., Pistorio, A., Consolaro, A., van Dijkhuizen, E. H. P., Lattanzi, B., Filocamo, G., Verazza, S., Gerloni, V., Gattinara, M., Pontikaki, I., Insalaco, A., De Benedetti, F., Civino, A., Presta, G., Breda, L., Marzetti, V., Pastore, S., Magni-Manzoni, S. & 11 others, Maggio, M. C., Garofalo, F., Rigante, D., Gattorno, M., Malattia, C., Picco, P., Viola, S., Lanni, S., Ruperto, N., Martini, A. & Italian Pediatric Rheumatology Study Group, Mar 4 2017, In : The Lancet. 389, 10072, p. 909-916 8 p.

Research output: Contribution to journalArticle

Juvenile Arthritis
Methotrexate
Adrenal Cortex Hormones
Joints
Therapeutics
19 Citations (Scopus)

Intra-articular corticosteroids versus intra-articular corticosteroids plus methotrexate in oligoarticular juvenile idiopathic arthritis: a multicentre, prospective, randomised, open-label trial

Ravelli, A., Davì, S., Bracciolini, G., Pistorio, A., Consolaro, A., van Dijkhuizen, E. H. P., Lattanzi, B., Filocamo, G., Verazza, S., Gerloni, V., Gattinara, M., Pontikaki, I., Insalaco, A., De Benedetti, F., Civino, A., Presta, G., Breda, L., Marzetti, V., Pastore, S., Magni-Manzoni, S. & 10 others, Maggio, M. C., Garofalo, F., Rigante, D., Gattorno, M., Malattia, C., Picco, P., Viola, S., Lanni, S., Ruperto, N. & Martini, A., 2017, In : The Lancet. 389, 10072, p. 909-916 8 p.

Research output: Contribution to journalArticle

Juvenile Arthritis
Methotrexate
Adrenal Cortex Hormones
Joints
Therapeutics
36 Citations (Scopus)

Type i interferon-mediated autoinflammation due to DNase II deficiency

Rodero, M. P., Tesser, A., Bartok, E., Rice, G. I., Della Mina, E., Depp, M., Beitz, B., Bondet, V., Cagnard, N., Duffy, D., Dussiot, M., Frémond, M. L., Gattorno, M., Guillem, F., Kitabayashi, N., Porcheray, F., Rieux-Laucat, F., Seabra, L., Uggenti, C., Volpi, S. & 37 others, Zeef, L. A. H., Alyanakian, M. A., Beltrand, J., Bianco, A. M., Boddaert, N., Brouzes, C., Candon, S., Caorsi, R., Charbit, M., Fabre, M., Faletra, F., Girard, M., Harroche, A., Hartmann, E., Lasne, D., Marcuzzi, A., Neven, B., Nitschke, P., Pascreau, T., Pastore, S., Picard, C., Picco, P., Piscianz, E., Polak, M., Quartier, P., Rabant, M., Stocco, G., Taddio, A., Uettwiller, F., Valencic, E., Vozzi, D., Hartmann, G., Barchet, W., Hermine, O., Bader-Meunier, B., Tommasini, A. & Crow, Y. J., Dec 1 2017, In : Nature Communications. 8, 1, 2176.

Research output: Contribution to journalArticle

interferon
Deoxyribonucleases
Interferons
Nucleic Acids
Neonatal Anemia
36 Citations (Scopus)

Type I interferon-mediated autoinflammation due to DNase II deficiency

Rodero, M. P., Tesser, A., Bartok, E., Rice, G. I., Della Mina, E., Depp, M., Beitz, B., Bondet, V., Cagnard, N., Duffy, D., Dussiot, M., Frémond, M-L., Gattorno, M., Guillem, F., Kitabayashi, N., Porcheray, F., Rieux-Laucat, F., Seabra, L., Uggenti, C., Volpi, S. & 37 others, Zeef, L. A. H., Alyanakian, M-A., Beltrand, J., Bianco, A. M., Boddaert, N., Brouzes, C., Candon, S., Caorsi, R., Charbit, M., Fabre, M., Faletra, F., Girard, M., Harroche, A., Hartmann, E., Lasne, D., Marcuzzi, A., Neven, B., Nitschke, P., Pascreau, T., Pastore, S., Picard, C., Picco, P., Piscianz, E., Polak, M., Quartier, P., Rabant, M., Stocco, G., Taddio, A., Uettwiller, F., Valencic, E., Vozzi, D., Hartmann, G., Barchet, W., Hermine, O., Bader-Meunier, B., Tommasini, A. & Crow, Y. J., Dec 19 2017, In : Nature Communications. 8, 1, p. 2176

Research output: Contribution to journalArticle

interferon
Interferon Type I
Deoxyribonucleases
Interferons
Nucleic Acids
2016
4 Citations (Scopus)

A long-term psychological observation in an adolescent affected with Gardner diamond syndrome

Bizzi, F., Sciarretta, L., D'alessandro, M. & Picco, P., Jan 1 2016, In : Indian Journal of Psychological Medicine. 38, 1, p. 74-77 4 p.

Research output: Contribution to journalArticle

Observation
Psychology
Ecchymosis
Skin Tests
Erythrocytes
16 Citations (Scopus)

Disease activity accounts for long-term efficacy of IL-1 blockers in pyogenic sterile arthritis pyoderma gangrenosum and severe acne syndrome

Omenetti, A., Carta, S., Caorsi, R., Finetti, M., Marotto, D., Lattanzi, B., Jorini, M., Delfino, L., Penco, F., Picco, P., Buoncompagni, A., Martini, A., Rubartelli, A. & Gattorno, M., Jul 1 2016, In : Rheumatology. 55, 7, p. 1325-1335 11 p., kew031.

Research output: Contribution to journalArticle

Interleukin-1
Protein Phosphatase 1
Monocytes
Phosphoprotein Phosphatases
Pyogenic arthritis, pyoderma gangrenosum, and acne

Erratum: Mutations in CDCA7 and HELLS cause immunodeficiency-centromeric instability-facial anomalies syndrome (Nature Communications (2015) 6 (7870) DOI: 10.1038/ncomms8870)

Thijssen, P. E., Ito, Y., Grillo, G., Wang, J., Velasco, G., Nitta, H., Unoki, M., Yoshihara, M., Suyama, M., Sun, Y., Lemmers, R. J. L. F., De Greef, J. C., Gennery, A., Picco, P., Kloeckener-Gruissem, B., Güngör, T., Reisli, I., Picard, C., Kebaili, K., Roquelaure, B. & 9 others, Iwai, T., Kondo, I., Kubota, T., Van Ostaijen-Ten Dam, M. M., Van Tol, M. J. D., Weemaes, C., Francastel, C., Van Der Maarel, S. M. & Sasaki, H., Jun 22 2016, In : Nature Communications. 7, 12003.

Research output: Contribution to journalComment/debate

1 Citation (Scopus)

Interstitial de novo 18q22.3q23 deletion: clinical, neuroradiological and molecular characterization of a new case and review of the literature

Tassano, E., Severino, M., Rosina, S., Papa, R., Tortora, D., Gimelli, G., Cuoco, C. & Picco, P., Oct 10 2016, In : Molecular Cytogenetics. 9, 1, p. 1-7 7 p.

Research output: Contribution to journalArticle

Chromosomes
Genes
Flatfoot
Phenotype
Chromosomes, Human, Pair 18
4 Citations (Scopus)
Skin Abnormalities
Eosinophilia
Upper Extremity
Pediatrics
Skin
32 Citations (Scopus)

Type I interferonopathies in pediatric rheumatology

Volpi, S., Picco, P., Caorsi, R., Candotti, F. & Gattorno, M., Jun 4 2016, In : Pediatric Rheumatology. 14, 1, 35.

Research output: Contribution to journalReview article

Rheumatology
Pediatrics
Chilblains
Livedo Reticularis
Panniculitis
2015

B cells characterization in ADA2 Deficiency patients

Schena, F., Volpi, S., Caorsi, R., Pastorino, C., Penco, F., Kalli, F., Omenetti, A., Chiesa, S., Bertoni, A., Picco, P., Filaci, G., Aksentijevich, I., Grossi, A., Ceccherini, I., Martini, A., Traggiai, E. & Gattorno, M., Sep 28 2015, (Accepted/In press) In : Pediatric Rheumatology.

Research output: Contribution to journalArticle

29 Citations (Scopus)

Dissecting the heterogeneity of macrophage activation syndrome complicating systemic juvenile idiopathic arthritis

Minoia, F., Davì, S., Horne, A., Bovis, F., Demirkaya, E., Akikusa, J., Ayaz, N. A., Al-Mayouf, S. M., Barone, P., Bica, B., Bolt, I., Breda, L., De Cunto, C., Enciso, S., Gallizzi, R., Griffin, T., Hennon, T., Horneff, G., Jeng, M., Kapovic, A. M. & 19 others, Lipton, J. M., Manzoni, S. M., Rozenfelde, R. I., Magalhaes, C. S., Sewairi, W. M., Stine, K. C., Vougiouka, O., Weaver, L. K., Davidsone, Z., De Inocencio, J., Ioseliani, M., Lattanzi, B., Tezer, H., Buoncompagni, A., Picco, P., Ruperto, N., Martini, A., Cron, R. Q. & Ravelli, A., Jun 1 2015, In : Journal of Rheumatology. 42, 6, p. 994-1001 8 p.

Research output: Contribution to journalArticle

Macrophage Activation Syndrome
Juvenile Arthritis
Pediatrics
Etoposide
Cyclosporine

Enlarging the clinical spectrum of SAVI syndrome

Caorsi, R., Rice, G., Volpi, S., Cardinale, F., Buoncompagni, A., Crow, Y., Martini, A., Gattorno, M. & Picco, P., Sep 28 2015, (Accepted/In press) In : Pediatric Rheumatology.

Research output: Contribution to journalArticle

Identification of type I interferonopathies using blood interferon signature: The experience of a pediatric rheumatology center

Volpi, S., Santori, E., Picco, P., Rice, G., Caorsi, R., Martini, A., Crow, Y., Candotti, F. & Gattorno, M., Sep 28 2015, (Accepted/In press) In : Pediatric Rheumatology.

Research output: Contribution to journalArticle

Juvenile eosinophilic fasciitis: Report of three cases with a review of the literature

Papa, R., Nozza, P., Granata, C., Caorsi, R., Gattorno, M., Martini, A. & Picco, P., Sep 28 2015, (Accepted/In press) In : Pediatric Rheumatology.

Research output: Contribution to journalArticle

1 Citation (Scopus)

Long-term efficacy of IL-1 blockers in PAPA patients

Finetti, M., Caorsi, R., Marotto, D., Buoncompagni, A., Omenetti, A., Lattanzi, B., Minoia, F., Picco, P., Jorini, M., Martini, A. & Gattorno, M., Sep 28 2015, In : Pediatric Rheumatology. 13, 1, P207.

Research output: Contribution to journalArticle

45 Citations (Scopus)

Mutations in CDCA7 and HELLS cause immunodeficiency-centromeric instability-facial anomalies syndrome

Thijssen, P. E., Ito, Y., Grillo, G., Wang, J., Velasco, G., Nitta, H., Unoki, M., Yoshihara, M., Suyama, M., Sun, Y., Lemmers, R. J. L. F., De Greef, J. C., Gennery, A., Picco, P., Kloeckener-Gruissem, B., Güngör, T., Reisli, I., Picard, C., Kebaili, K., Roquelaure, B. & 9 others, Iwai, T., Kondo, I., Kubota, T., Van Ostaijen-Ten Dam, M. M., Van Tol, M. J. D., Weemaes, C., Francastel, C., Van Der Maarel, S. M. & Sasaki, H., Jul 28 2015, In : Nature Communications. 6, 7870.

Research output: Contribution to journalArticle

mutations
genes
Genes
anomalies
Mutation

Rapid and sustained effect of anti-TNF treatment in patients with ADA2 deficiency

Caorsi, R., Omenetti, A., Morreale, A., Insalaco, A., Buoncompagni, A., Picco, P., Malattia, C., Gandolfo, C., Aksentievic, I., Martini, A. & Gattorno, M., Sep 28 2015, (Accepted/In press) In : Pediatric Rheumatology.

Research output: Contribution to journalArticle

2014
4 Citations (Scopus)

Cytomegalovirus-related necrotising vasculitis mimicking henoch-schönlein syndrome

D'Alessandro, M., Buoncompagni, A., Minoia, F., Coccia, M. C., Martini, A. & Picco, P., 2014, In : Clinical and Experimental Rheumatology. 32, SUPPL.82, p. 73-75 3 p.

Research output: Contribution to journalArticle

Vasculitis
Cytomegalovirus
Steroids
Schoenlein-Henoch Purpura
Systemic Vasculitis
253 Citations (Scopus)

Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type i interferon signaling

Rice, G. I., Del Toro Duany, Y., Jenkinson, E. M., Forte, G. M. A., Anderson, B. H., Ariaudo, G., Bader-Meunier, B., Baildam, E. M., Battini, R., Beresford, M. W., Casarano, M., Chouchane, M., Cimaz, R., Collins, A. E., Cordeiro, N. J. V., Dale, R. C., Davidson, J. E., De Waele, L., Desguerre, I., Faivre, L. & 33 others, Fazzi, E., Isidor, B., Lagae, L., Latchman, A. R., Lebon, P., Li, C., Livingston, J. H., Lourenço, C. M., Mancardi, M. M., Masurel-Paulet, A., McInnes, I. B., Menezes, M. P., Mignot, C., O'Sullivan, J., Orcesi, S., Picco, P. P., Riva, E., Robinson, R. A., Rodriguez, D., Salvatici, E., Scott, C., Szybowska, M., Tolmie, J. L., Vanderver, A., Vanhulle, C., Vieira, J. P., Webb, K., Whitney, R. N., Williams, S. G., Wolfe, L. A., Zuberi, S. M., Hur, S. & Crow, Y. J., 2014, In : Nature Genetics. 46, 5, p. 503-509 7 p.

Research output: Contribution to journalArticle

Interferon Type I
Interferons
Aicardi Syndrome
Phenotype
Mutation
55 Citations (Scopus)

Long-term efficacy of interleukin-1 receptor antagonist (Anakinra) in corticosteroid-dependent and colchicine-resistant recurrent pericarditis

Finetti, M., Insalaco, A., Cantarini, L., Meini, A., Breda, L., Alessio, M., D'Alessandro, M., Picco, P., Martini, A. & Gattorno, M., 2014, In : Journal of Pediatrics. 164, 6

Research output: Contribution to journalArticle

Interleukin 1 Receptor Antagonist Protein
Pericarditis
Interleukin-1 Receptors
Colchicine
Adrenal Cortex Hormones
11 Citations (Scopus)

Osteolytic lesion in PAPA syndrome responding to anti-interleukin 1 treatment

Caorsi, R., Picco, P., Buoncompagni, A., Martini, A. & Gattorno, M., Nov 1 2014, In : Journal of Rheumatology. 41, 11, p. 2333-2334 2 p.

Research output: Contribution to journalArticle

61 Citations (Scopus)

Whole-body MRI in the assessment of disease activity in juvenile dermatomyositis

Malattia, C., Damasio, M. B., Madeo, A., Pistorio, A., Providenti, A., Pederzoli, S., Viola, S., Buoncompagni, A., Mattiuz, C., Beltramo, A., Consolaro, A., Ravelli, A., Ruperto, N., Picco, P., Magnano, G. M. & Martini, A., 2014, In : Annals of the Rheumatic Diseases. 73, 6, p. 1083-1090 8 p.

Research output: Contribution to journalArticle

Magnetic resonance imaging
Muscle
Muscles
Inflammation
Sequence Inversion
2013
33 Citations (Scopus)

Factors associated with achievement of inactive disease in children with juvenile idiopathic arthritis treated with etanercept

Solari, N., Palmisani, E., Consolaro, A., Pistorio, A., Viola, S., Buoncompagni, A., Gattorno, M., Picco, P., Ruperto, N., Malattia, C., Martini, A. & Ravelli, A., Feb 2013, In : Journal of Rheumatology. 40, 2, p. 192-200 9 p.

Research output: Contribution to journalArticle

Juvenile Arthritis
Wrist
Etanercept
Regression Analysis
Age of Onset

Massive calcinosis and severe osteoporosis in paediatric-onset overlap syndrome

Picco, P., Papa, R., Minoia, F., Leoni, M., Consolini, R. & Buoncompagni, A., Nov 2013, In : Clinical and Experimental Rheumatology. 31, 6, p. 991 1 p.

Research output: Contribution to journalArticle

3 Citations (Scopus)

Primary red ear syndrome associated with cochleo-vestibular symptomatology: A paediatric case report

Picco, P. P., D'Alessandro, M., Leoni, M., Doglio, M. & Martini, A., Nov 2013, In : Cephalalgia. 33, 15, p. 1277-1280 4 p.

Research output: Contribution to journalArticle

Ear
Pediatrics
Blood Vessels
Headache Disorders
Migraine Disorders

Recurrent Pericarditis in Myhre Syndrome

Picco, P., Naselli, A., Pala, G., Marsciani, A., Buoncompagni, A. & Martini, A., May 2013, In : American Journal of Medical Genetics, Part A. 161, 5, p. 1164-1166 3 p.

Research output: Contribution to journalArticle

Pericarditis
Mixed Conductive-Sensorineural Hearing Loss
Brachydactyly
Prognathism
Somatotypes

Recurrent Pericarditis in Myhre Syndrome

Picco, P., Naselli, A., Pala, G., Marsciani, A., Buoncompagni, A. & Martini, A., 2013, (Accepted/In press) In : American Journal of Medical Genetics, Part A. 9999

Research output: Contribution to journalArticle

Pericarditis
Mixed Conductive-Sensorineural Hearing Loss
Brachydactyly
Prognathism
Somatotypes
2011
9 Citations (Scopus)

Candidate genes in patients with autoinflammatory syndrome resembling tumor necrosis factor receptor-associated periodic syndrome without mutations in the TNFRSF1A gene

Borghini, S., Fiore, M., Di Duca, M., Caroli, F., Finetti, M., Santamaria, G., Ferlito, F., Bua, F., Picco, P., Obici, L., Martini, A., Gattorno, M. & Ceccherini, I., Jul 2011, In : Journal of Rheumatology. 38, 7, p. 1378-1384 7 p.

Research output: Contribution to journalArticle

Tumor Necrosis Factor Receptors
Mutation
Receptors, Tumor Necrosis Factor, Type I
Genes
Tumor Necrosis Factor-alpha
2009
1 Citation (Scopus)

Reply

Picco, P. & Martini, A., Aug 2009, In : Arthritis and Rheumatism. 60, 8, p. 2543-2544 2 p.

Research output: Contribution to journalArticle

93 Citations (Scopus)
Interleukin 1 Receptor Antagonist Protein
Pericarditis
Interleukin-1 Receptors
Therapeutics
Steroids
2008

L'artrite idiopatica giovanile

Translated title of the contribution: Juvenile idiopathic arthritisBuoncompagni, A., Loy, A., Picco, P., Viola, S. & Martini, A., Feb 2008, In : Area Pediatrica. 9, 2

Research output: Contribution to journalArticle

2006
13 Citations (Scopus)
Osteopontin
Juvenile Arthritis
Genes
Association reactions
Polymerase chain reaction
117 Citations (Scopus)

Neutrophils from patients with TNFRSF1A mutations display resistance to tumor necrosis factor-induced apoptosis: Pathogenetic and clinical implications

D'Osualdo, A., Ferlito, F., Prigione, I., Obici, L., Meini, A., Zulian, F., Pontillo, A., Corona, F., Barcellona, R., Di Duca, M., Santamaria, G., Traverso, F., Picco, P., Baldi, M., Plebani, A., Ravazzolo, R., Ceccherini, I., Martini, A. & Gattorno, M., Mar 2006, In : Arthritis and Rheumatism. 54, 3, p. 998-1008 11 p.

Research output: Contribution to journalArticle

Neutrophils
Tumor Necrosis Factor-alpha
Apoptosis
Mutation
Cycloheximide