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Items: 1 to 50 of 117

1.

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

Bertamino M, Severino M, Grossi A, Rusmini M, Tortora D, Gandolfo C, Pederzoli S, Malattia C, Picco P, Striano P, Ceccherini I, Di Rocco M; Gaslini Pediatric Stroke Group.

Eur J Paediatr Neurol. 2018 Jul;22(4):725-728. doi: 10.1016/j.ejpn.2018.04.002. Epub 2018 Apr 12.

PMID:
29709427
2.

CD70 Deficiency due to a Novel Mutation in a Patient with Severe Chronic EBV Infection Presenting As a Periodic Fever.

Caorsi R, Rusmini M, Volpi S, Chiesa S, Pastorino C, Sementa AR, Uva P, Grossi A, Lanino E, Faraci M, Minoia F, Signa S, Picco P, Martini A, Ceccherini I, Gattorno M.

Front Immunol. 2018 Jan 29;8:2015. doi: 10.3389/fimmu.2017.02015. eCollection 2017.

3.

Type I interferon-mediated autoinflammation due to DNase II deficiency.

Rodero MP, Tesser A, Bartok E, Rice GI, Della Mina E, Depp M, Beitz B, Bondet V, Cagnard N, Duffy D, Dussiot M, Frémond ML, Gattorno M, Guillem F, Kitabayashi N, Porcheray F, Rieux-Laucat F, Seabra L, Uggenti C, Volpi S, Zeef LAH, Alyanakian MA, Beltrand J, Bianco AM, 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 YJ.

Nat Commun. 2017 Dec 19;8(1):2176. doi: 10.1038/s41467-017-01932-3.

4.

Type I interferon pathway activation in COPA syndrome.

Volpi S, Tsui J, Mariani M, Pastorino C, Caorsi R, Sacco O, Ravelli A, Shum AK, Gattorno M, Picco P.

Clin Immunol. 2018 Feb;187:33-36. doi: 10.1016/j.clim.2017.10.001. Epub 2017 Oct 10.

PMID:
29030294
5.

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

Bonekamp N, Caorsi R, Viglizzo GM, Graaf M, Minoia F, Grossi A, Picco P, Ceccherini I, Frenkel J, Gattorno M.

Ann Rheum Dis. 2018 Aug;77(8):1241-1243. doi: 10.1136/annrheumdis-2017-211805. Epub 2017 Sep 2. No abstract available.

PMID:
28866646
6.

Reconstruction of Hind and Mid-Foot Defects after Melanoma Resection Using the Reverse Sural Flap: A Case Series.

Larrañaga JJ, Picco PI, Yanzon A, Figari M.

Surg J (N Y). 2017 Aug 3;3(3):e124-e127. doi: 10.1055/s-0037-1604473. eCollection 2017 Jul.

7.

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 RA, Salis A, Falcini F, Schena F, Garbarino F, Morreale A, Pardeo M, Ventrici C, Passarelli C, Zhou Q, Severino M, Gandolfo C, Damonte G, Martini A, Ravelli A, Aksentijevich I, Ceccherini I, Gattorno M.

Ann Rheum Dis. 2017 Oct;76(10):1648-1656. doi: 10.1136/annrheumdis-2016-210802. Epub 2017 May 18.

PMID:
28522451
8.

Critical role of STIR MRI in early detection of post-streptococcal periostitis with dysproteinaemia (Goldbloom's syndrome).

Papa R, Consolaro A, Minoia F, Caorsi R, Magnano G, Gattorno M, Ravelli A, Picco P.

Clin Exp Rheumatol. 2017 May-Jun;35(3):516-517. Epub 2017 Mar 23. Review.

PMID:
28339360
9.

Widening the Heterogeneity of Leigh Syndrome: Clinical, Biochemical, and Neuroradiologic Features in a Patient Harboring a NDUFA10 Mutation.

Minoia F, Bertamino M, Picco P, Severino M, Rossi A, Fiorillo C, Minetti C, Nesti C, Santorelli FM, Di Rocco M.

JIMD Rep. 2017;37:37-43. doi: 10.1007/8904_2017_9. Epub 2017 Mar 1.

10.

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 EHP, 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, Maggio MC, Garofalo F, Rigante D, Gattorno M, Malattia C, Picco P, Viola S, Lanni S, Ruperto N, Martini A; Italian Pediatric Rheumatology Study Group.

Lancet. 2017 Mar 4;389(10072):909-916. doi: 10.1016/S0140-6736(17)30065-X. Epub 2017 Feb 3.

PMID:
28162781
11.

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.

Scand J Rheumatol. 2018 Mar;47(2):166-167. doi: 10.1080/03009742.2016.1274423. Epub 2017 Jan 18. No abstract available.

PMID:
28097933
12.

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.

Mol Cytogenet. 2016 Oct 10;9:78. eCollection 2016.

13.

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

Thijssen PE, Ito Y, Grillo G, Wang J, Velasco G, Nitta H, Unoki M, Yoshihara M, Suyama M, Sun Y, Lemmers RJ, de Greef JC, Gennery A, Picco P, Kloeckener-Gruissem B, Güngör T, Reisli I, Picard C, Kebaili K, Roquelaure B, Iwai T, Kondo I, Kubota T, van Ostaijen-Ten Dam MM, van Tol MJ, Weemaes C, Francastel C, van der Maarel SM, Sasaki H.

Nat Commun. 2016 Jun 22;7:12003. doi: 10.1038/ncomms12003. No abstract available.

14.

Juvenile eosinophilic fasciitis: three case reports with review of the literature.

Papa R, Nozza P, Granata C, Caorsi R, Gattorno M, Martini A, Picco P.

Clin Exp Rheumatol. 2016 May-Jun;34(3):527-30. Epub 2016 May 30.

PMID:
27268780
15.

Type I interferonopathies in pediatric rheumatology.

Volpi S, Picco P, Caorsi R, Candotti F, Gattorno M.

Pediatr Rheumatol Online J. 2016 Jun 4;14(1):35. doi: 10.1186/s12969-016-0094-4. Review.

16.

A Long-Term Psychological Observation in an Adolescent Affected with Gardner Diamond Syndrome.

Bizzi F, Sciarretta L, D'Alessandro M, Picco P.

Indian J Psychol Med. 2016 Jan-Feb;38(1):74-7. doi: 10.4103/0253-7176.175129.

17.

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.

Rheumatology (Oxford). 2016 Jul;55(7):1325-35. doi: 10.1093/rheumatology/kew031. Epub 2016 Mar 17.

PMID:
26989109
18.

Management Issues in the Treatment of an Ameloblastoma with an Atypical Presentation.

Larrañaga JJ, Sahovaler A, Picco PI, Mazzaro EL, Figari MF.

Craniomaxillofac Trauma Reconstr. 2015 Sep;8(3):257-61. doi: 10.1055/s-0035-1549012. Epub 2015 Mar 19.

19.

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

Thijssen PE, Ito Y, Grillo G, Wang J, Velasco G, Nitta H, Unoki M, Yoshihara M, Suyama M, Sun Y, Lemmers RJ, de Greef JC, Gennery A, Picco P, Kloeckener-Gruissem B, Güngör T, Reisli I, Picard C, Kebaili K, Roquelaure B, Iwai T, Kondo I, Kubota T, van Ostaijen-Ten Dam MM, van Tol MJ, Weemaes C, Francastel C, van der Maarel SM, Sasaki H.

Nat Commun. 2015 Jul 28;6:7870. doi: 10.1038/ncomms8870.

20.

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 NA, Al-Mayouf SM, Barone P, Bica B, Bolt I, Breda L, De Cunto C, Enciso S, Gallizzi R, Griffin T, Hennon T, Horneff G, Jeng M, Kapovic AM, Lipton JM, Magni Manzoni S, Rumba-Rozenfelde I, Magalhaes CS, Sewairi WM, Stine KC, Vougiouka O, Weaver LK, Davidsone Z, De Inocencio J, Ioseliani M, Lattanzi B, Tezer H, Buoncompagni A, Picco P, Ruperto N, Martini A, Cron RQ, Ravelli A; Pediatric Rheumatology International Trials Organization; Childhood Arthritis and Rheumatology Research Alliance; Pediatric Rheumatology Collaborative Study Group; Histiocyte Society.

J Rheumatol. 2015 Jun;42(6):994-1001. doi: 10.3899/jrheum.141261. Epub 2015 Apr 15.

PMID:
25877504
21.

Whole-body MRI as an unconventional diagnostic tool in a pediatric patient with systemic infection.

Picco P, Naselli A, Pala G, Rizzo F, Damasio B, Buoncompagni A, Martini A.

Acta Radiol Short Rep. 2014 Dec 4;3(11):2047981614549571. doi: 10.1177/2047981614549571. eCollection 2014 Dec.

22.

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

Caorsi R, Picco P, Buoncompagni A, Martini A, Gattorno M.

J Rheumatol. 2014 Nov;41(11):2333-4. doi: 10.3899/jrheum.140060. No abstract available.

PMID:
25362725
23.

Cytomegalovirus-related necrotising vasculitis mimicking Henoch-Schönlein syndrome.

D'Alessandro M, Buoncompagni A, Minoia F, Coccia MC, Martini A, Picco P.

Clin Exp Rheumatol. 2014 May-Jun;32(3 Suppl 82):S73-5. Epub 2014 May 16.

PMID:
24854375
24.

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

Rice GI, Del Toro Duany Y, Jenkinson EM, Forte GM, Anderson BH, Ariaudo G, Bader-Meunier B, Baildam EM, Battini R, Beresford MW, Casarano M, Chouchane M, Cimaz R, Collins AE, Cordeiro NJ, Dale RC, Davidson JE, De Waele L, Desguerre I, Faivre L, Fazzi E, Isidor B, Lagae L, Latchman AR, Lebon P, Li C, Livingston JH, Lourenço CM, Mancardi MM, Masurel-Paulet A, McInnes IB, Menezes MP, Mignot C, O'Sullivan J, Orcesi S, Picco PP, Riva E, Robinson RA, Rodriguez D, Salvatici E, Scott C, Szybowska M, Tolmie JL, Vanderver A, Vanhulle C, Vieira JP, Webb K, Whitney RN, Williams SG, Wolfe LA, Zuberi SM, Hur S, Crow YJ.

Nat Genet. 2014 May;46(5):503-509. doi: 10.1038/ng.2933. Epub 2014 Mar 30.

25.

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.

J Pediatr. 2014 Jun;164(6):1425-31.e1. doi: 10.1016/j.jpeds.2014.01.065. Epub 2014 Mar 12.

PMID:
24630353
26.

Treatment of edentulous mandibular fractures with rigid internal fixation: case series and literature review.

Franciosi E, Mazzaro E, Larranaga J, Rios A, Picco P, Figari M.

Craniomaxillofac Trauma Reconstr. 2014 Mar;7(1):35-42. doi: 10.1055/s-0033-1364195. Epub 2014 Jan 14.

27.

Groove pancreatitis vs groove pancreatic adenocarcinoma. Report of two cases and review of the literature.

Goransky J, Alvarez FA, Picco P, Spina JC, Santibañes Md, Mazza O.

Acta Gastroenterol Latinoam. 2013 Sep;43(3):248-53. Review.

PMID:
24303693
28.

Massive calcinosis and severe osteoporosis in paediatric-onset overlap syndrome.

Picco P, Papa R, Minoia F, Leoni M, Consolini R, Buoncompagni A.

Clin Exp Rheumatol. 2013 Nov-Dec;31(6):991. Epub 2013 Nov 14. No abstract available.

PMID:
24238236
29.

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

Picco PP, D'Alessandro M, Leoni M, Doglio M, Martini A.

Cephalalgia. 2013 Nov;33(15):1277-80. doi: 10.1177/0333102413493527. Epub 2013 Jun 25.

PMID:
23800828
30.

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

Malattia C, Damasio MB, 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 GM, Martini A.

Ann Rheum Dis. 2014 Jun;73(6):1083-90. doi: 10.1136/annrheumdis-2012-202915. Epub 2013 May 1.

PMID:
23636654
31.

Recurrent pericarditis in Myhre syndrome.

Picco P, Naselli A, Pala G, Marsciani A, Buoncompagni A, Martini A.

Am J Med Genet A. 2013 May;161A(5):1164-6. doi: 10.1002/ajmg.a.35892.

PMID:
23610053
32.

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.

J Rheumatol. 2013 Feb;40(2):192-200. doi: 10.3899/jrheum.120842. Epub 2012 Dec 1.

PMID:
23204218
33.

Coxarthritis as the presenting symptom of Gaucher disease type 1.

Brisca G, Di Rocco M, Picco P, Damasio MB, Martini A.

Arthritis. 2011;2011:361279. doi: 10.1155/2011/361279. Epub 2011 Mar 30.

34.

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.

J Rheumatol. 2011 Jul;38(7):1378-84. doi: 10.3899/jrheum.101260. Epub 2011 Apr 1.

PMID:
21459945
35.

Successful treatment of idiopathic recurrent pericarditis in children with interleukin-1beta receptor antagonist (anakinra): an unrecognized autoinflammatory disease?

Picco P, Brisca G, Traverso F, Loy A, Gattorno M, Martini A.

Arthritis Rheum. 2009 Jan;60(1):264-8. doi: 10.1002/art.24174.

36.

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.

Arthritis Rheum. 2006 Mar;54(3):998-1008.

37.

A polymorphic variant inside the osteopontin gene shows association with disease course in oligoarticular juvenile idiopathic arthritis.

Marciano R, Giacopelli F, Divizia MT, Gattorno M, Felici E, Pistorio A, Martini A, Ravazzolo R, Picco P.

Ann Rheum Dis. 2006 May;65(5):662-5. Epub 2005 Sep 8.

38.

MVK mutations and associated clinical features in Italian patients affected with autoinflammatory disorders and recurrent fever.

D'Osualdo A, Picco P, Caroli F, Gattorno M, Giacchino R, Fortini P, Corona F, Tommasini A, Salvi G, Specchia F, Obici L, Meini A, Ricci A, Seri M, Ravazzolo R, Martini A, Ceccherini I.

Eur J Hum Genet. 2005 Mar;13(3):314-20.

39.

Cytokine flexibility of early and differentiated memory T helper cells in juvenile idiopathic arthritis.

Chiesa S, Prigione I, Morandi F, Buoncompagni A, Picco P, Bocca P, Martini A, Pistoia V, Gattorno M.

J Rheumatol. 2004 Oct;31(10):2048-54.

PMID:
15468374
40.

First report of systemic reactive (AA) amyloidosis in a patient with the hyperimmunoglobulinemia D with periodic fever syndrome.

Obici L, Manno C, Muda AO, Picco P, D'Osualdo A, Palladini G, Avanzini MA, Torres D, Marciano S, Merlini G.

Arthritis Rheum. 2004 Sep;50(9):2966-9.

41.

Synovial expression of osteopontin correlates with angiogenesis in juvenile idiopathic arthritis.

Gattorno M, Gregorio A, Ferlito F, Gerloni V, Parafioriti A, Felici E, Sala E, Gambini C, Picco P, Martini A.

Rheumatology (Oxford). 2004 Sep;43(9):1091-6. Epub 2004 Jun 15.

PMID:
15199218
42.

Neonatal lupus and a seronegative mother.

Gattorno M, Di Rocco M, Buoncompagni A, Picco P, Meroni PL, Martini A.

Lancet. 2004 Mar 27;363(9414):1038. No abstract available.

PMID:
15051284
43.

Chronic infantile neurological cutaneous articular syndrome: CD10 over-expression in neutrophils is a possible key to the pathogenesis of the disease.

Leone V, Presani G, Perticarari S, Tommasini A, Crovella S, Lenhardt A, Picco P, Lepore L.

Eur J Pediatr. 2003 Oct;162(10):669-73. Epub 2003 Aug 20.

PMID:
12928894
44.

Primary Sjögren syndrome in the paediatric age: a multicentre survey.

Cimaz R, Casadei A, Rose C, Bartunkova J, Sediva A, Falcini F, Picco P, Taglietti M, Zulian F, Ten Cate R, Sztajnbok FR, Voulgari PV, Drosos AA.

Eur J Pediatr. 2003 Oct;162(10):661-5. Epub 2003 Jul 29.

PMID:
12898241
45.

Outcome of primary antiphospholipid syndrome in childhood.

Gattorno M, Falcini F, Ravelli A, Zulian F, Buoncompagni A, Martini G, Resti M, Picco P, Martini A.

Lupus. 2003;12(6):449-53.

PMID:
12873046
46.

Electron energy constancy verification using a double-wedge phantom.

Wells DM, Picco PJ, Ansbacher W.

J Appl Clin Med Phys. 2003 Summer;4(3):204-8.

47.

Levels of soluble CD27 in sera and synovial fluid and its expression on memory T cells in patients with juvenile idiopathic arthritides.

Gattorno M, Prigione I, Vignola S, Falcini F, Chiesa S, Morandi F, Picco P, Buoncompagni A, Martini A, Pistoia V.

Clin Exp Rheumatol. 2002 Nov-Dec;20(6):863-6.

PMID:
12508783
48.

MICA gene polymorphisms in an Italian paediatric series of juvenile Behçet disease.

Picco P, Porfirio B, Gattorno M, Buoncompagni A, Falcini F, Cusano R, Bordo D, Pistoia V, Ravazzolo R, Seri M.

Int J Mol Med. 2002 Nov;10(5):575-8.

PMID:
12373294
49.

Synovial membrane expression of matrix metalloproteinases and tissue inhibitor 1 in juvenile idiopathic arthritides.

Gattorno M, Gerloni V, Morando A, Comanducci F, Buoncompagni A, Picco P, Fantini F, Pistoia V, Gambini C.

J Rheumatol. 2002 Aug;29(8):1774-9.

PMID:
12180743
50.

Involvement of the hypothalamic-pituitary-adrenal axis in children with oligoarticular-onset idiopathic arthritis.

Picco P, Gattorno M, Sormani MP, Vignola S, Buoncompagni A, Battilana N, Pistoia V, Ravazzolo R.

Ann N Y Acad Sci. 2002 Jun;966:369-72.

PMID:
12114294

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