P. Picco

E. Castagnola, P. Picco, A. Cama, 1998, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

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

G. Merlini, M. Avanzini, A. O. Muda, 2004, Arthritis and rheumatism.

A child with a novel ACAN missense variant mimicking a septic arthritis

R. Papa, M. Gattorno, P. Picco, 2019, Italian Journal of Pediatrics.

Anti-GAD epileptic encephalopathy in a toddler with Parry-Romberg syndrome

S. Sotgiu, F. Graus, P. Picco, 2019, Neurological Sciences.

Recurrent Pericarditis in Myhre Syndrome

A. Martini, P. Picco, A. Naselli, 2013, American journal of medical genetics. Part A.

Common variable immunodeficiency presenting in a girl as lung infiltrates and mediastinal adenopathies leading to severe "superior vena caval" syndrome.

V. Pistoia, M. Faraci, G. Rossi, 1996, The European respiratory journal.

Mesangial glomerulonephritis and transient SLE manifestations in an adolescent with dermatomyositis

A. Trivelli, V. Pistoia, P. Picco, 1997, Lupus.

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

P. Striano, M. Severino, D. Tortora, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

A combined immunodeficiency with severe infections, inflammation, and allergy caused by ARPC1B deficiency.

Ivan K. Chinn, J. Lupski, U. Pannicke, 2019, The Journal of allergy and clinical immunology.

Intracranial calcifications and nephrogenic diabetes insipidius

M. Rocco, P. Picco, P. Gandullia, 1991, European Journal of Pediatrics.

Serum luteinizing hormone concentrations, as measured by a sensitive immunoradiometric assay, in children with normal, precocious or delayed pubertal development.

S. Magier, P. Picco, L. Garibaldi, 1991, The Journal of clinical endocrinology and metabolism.

Primary Sjögren syndrome in the paediatric age: a multicentre survey

A. Šedivá, M. Taglietti, P. Voulgari, 2003, European Journal of Pediatrics.

Diagnostic difficulties and positive therapeutic response in a patient with sinus histiocytosis with massive lymphadenopathy

V. Pistoia, M. Rocco, P. Picco, 1993, European Journal of Pediatrics.

Report on two patients with Costello syndrome and sialuria.

M. Di Rocco, A. Barabino, P. Picco, 1993, American journal of medical genetics.

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

A. Martini, A. Rubartelli, A. Omenetti, 2016, Rheumatology.

Osteolytic Lesion in PAPA Syndrome Responding to Anti-interleukin 1 Treatment

A. Martini, M. Gattorno, P. Picco, 2014, The Journal of Rheumatology.

Clinical and biological characteristics of immunopathological disease-related erythema nodosum in children.

V. Pistoia, A. Barabino, M. Gattorno, 1999, Scandinavian journal of rheumatology.

In utero virilization by danazol: Effects on adrenal steroidogenesis

M. Rocco, E. Podesta, S. Pang, 1995 .

Increased gut permeability in juvenile chronic arthritides. A multivariate analysis of the diagnostic parameters.

M. Sormani, A. Barabino, M. Gattorno, 2000, Clinical and experimental rheumatology.

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

J. Casanova, L. Notarangelo, J. Franco, 2018, Blood.

Type I interferonopathies in pediatric rheumatology

F. Candotti, S. Volpi, M. Gattorno, 2016, Pediatric Rheumatology.

Role of busulfan and total body irradiation on growth of prepubertal children receiving bone marrow transplantation and results of treatment with recombinant human growth hormone.

G. Dini, M. Cisternino, F. Locatelli, 1995, Blood.

Cytomegalovirus-related necrotising vasculitis mimicking Henoch-Schönlein syndrome.

A. Martini, P. Picco, A. Buoncompagni, 2014, Clinical and experimental rheumatology.

JIMD Reports, Volume 37

F. Santorelli, C. Minetti, M. Severino, 2017, JIMD Reports.

Next generation sequencing panel in undifferentiated autoinflammatory diseases identify patients with colchicine-responder recurrent fevers.

M. van Gijn, I. Ceccherini, L. Obici, 2019, Rheumatology.

Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy.

M. Devoto, V. Morra, R. Cusano, 1999, American journal of human genetics.

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

L. Lagae, A. Vanderver, J. Tolmie, 2014, Nature Genetics.

The expanding pathways of autoinflammation: a lesson from the first 100 genes related to autoinflammatory manifestations.

R. Papa, M. Gattorno, P. Picco, 2020, Advances in protein chemistry and structural biology.

Type I interferon-mediated autoinflammation due to DNase II deficiency

F. Rieux-Laucat, C. Picard, Y. Crow, 2017, Nature Communications.

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

A. Martini, C. Gandolfo, A. Omenetti, 2015, Pediatric Rheumatology.

Role of haematological, pulmonary and renal complications in the long-term prognosis of patients with lysinuric protein intolerance

G. Garibotto, G. Rossi, P. Picco, 1993, European Journal of Pediatrics.

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

M. Suyama, C. Picard, A. Gennery, 2015, Nature Communications.

Inflammatory myopathy in a patient with collagen VI mutations

C. Bruno, C. Minetti, M. Iacomino, 2018, Scandinavian journal of rheumatology.

Severe hypoalbuminaemia in a systemic lupus erythematosus-like patient

P. Tomà, A. Barabino, M. Gattorno, 2002, European Journal of Pediatrics.

Factors Associated with Achievement of Inactive Disease in Children with Juvenile Idiopathic Arthritis Treated with Etanercept

A. Martini, A. Pistorio, C. Malattia, 2013, The Journal of Rheumatology.

Brain perfusion spect in juvenile neuro-Behçet's disease.

P. Vitali, G. Mariani, G. Rodriguez, 2001, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

Complications of lysinuric protein intolerance must be treated with immunosuppressive drugs

M. Di Rocco, P. Picco, A. Buoncompagni, 1998, Journal of Inherited Metabolic Disease.

Neonatal lupus and a seronegative mother

A. Martini, M. Gattorno, P. Picco, 2004, The Lancet.

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions.

G. Gimelli, M. Di Rocco, P. Picco, 1998, Journal of medical genetics.

Brother and sister with different vasculitides

M. Gattorno, P. Picco, A. Buoncompagni, 1999, The Lancet.

Kawasaki's disease in northern Italy: a multicenter retrospective study of 250 patients.

R. Cimaz, F. Zulian, P. Picco, 2002, Clinical and experimental rheumatology.

Insulin like growth factor I (IGF1) in children with neural tube closure defects: a preliminary report.

A. Barreca, P. Picco, A. Cama, 1993, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

Growth and endocrine assessment in children undergoing bone marrow transplant: the 'G. Gaslini' experience.

G. Dini, E. Lanino, A. Garaventa, 1991, Bone marrow transplantation.

Tumor necrosis factor induced adhesion molecule serum concentrations in Henoch-Schönlein purpura and pediatric systemic lupus erythematosus.

M. Sormani, V. Pistoia, M. Gattorno, 2000, The Journal of rheumatology.

Non-steroidal anti-inflammatory drugs in the treatment of hyper-IgD syndrome.

M. Di Rocco, M. Gattorno, P. Picco, 2001, Annals of the rheumatic diseases.

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

P. Picco, F. Bizzi, L. Sciarretta, 2016, Indian Journal of Psychological Medicine.

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

I. Ceccherini, M. Gattorno, P. Picco, 2017, Annals of the rheumatic diseases.

Dissecting the Heterogeneity of Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis

T. Griffin, A. Martini, J. Lipton, 2015, The Journal of Rheumatology.

Mevalonate kinase deficiency in a child with periodic fever and without hyperimmunoglobulinaemia D

H. Waterham, R. Wanders, P. Picco, 2001, Journal of Inherited Metabolic Disease.

6-methylprednisolone 'mini-pulses': a new modality of glucocorticoid treatment in systemic onset juvenile chronic arthritis.

V. Pistoia, M. Gattorno, P. Picco, 1996, Scandinavian Journal of Rheumatology.

Early treatment of systemic onset juvenile chronic arthritis with low-dose cyclosporin A.

V. Pistoia, M. Faraci, M. Gattorno, 1995, Clinical and experimental rheumatology.

Corticosterone methyl oxidase type II deficiency: a cause of failure to thrive and recurrent dehydration in early infancy

M. Rocco, P. Picco, L. Garibaldi, 1992, European Journal of Pediatrics.

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

A. Martini, A. Pistorio, M. B. Damasio, 2013, Annals of the rheumatic diseases.

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

Y. Crow, A. Martini, G. Rice, 2015, Pediatric Rheumatology.

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

A. Martini, A. Pistorio, M. Gattinara, 2017, The Lancet.

Next generation sequencing panel in undifferentiated autoinflammatory diseases identifies patients with colchicine-responder recurrent fevers.

M. van Gijn, I. Ceccherini, L. Obici, 2019, Rheumatology.

Involvement of the Hypothalamic‐Pituitary‐Adrenal Axis in Children with Oligoarticular‐Onset Idiopathic Arthritis

R. Ravazzolo, V. Pistoia, M. Gattorno, 2002, Annals of the New York Academy of Sciences.

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

V. Leone, A. Tommasini, S. Crovella, 2003, European Journal of Pediatrics.

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

G. Gimelli, M. Severino, D. Tortora, 2016, Molecular Cytogenetics.

Central precocious puberty in children affected by myelomeningocele

M. Gattorno, P. Picco, A. Cama, 1995 .

FRI0526 Long-Term Efficacy of IL-1 Blockers in Papa Patients

A. Martini, A. Omenetti, M. Gattorno, 2015 .

Immotile cilia syndrome associated with hydrocephalus and precocious puberty: a case report.

E. Zammarchi, M. Donati, M. Gattorno, 1993, European journal of pediatric surgery.

Oral Administration of S-Adenosylmethionine (SAMe) and Lactobacillus Plantarum HEAL9 Improves the Mild-To-Moderate Symptoms of Depression: A Randomized, Double-Blind, Placebo-Controlled Study.

I. Schiavetti, R. Montisci, P. Picco, 2020, The primary care companion for CNS disorders.

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

C. Cancrini, F. Candotti, C. Granata, 2019, Journal of Clinical Immunology.

Prolactin and interleukin 6 in prepubertal girls with juvenile chronic arthritis.

V. Pistoia, M. Gattorno, P. Picco, 1998, The Journal of rheumatology.

Interactions between Prolactin and the Proinflammatory Cytokine Network in Juvenile Chronic Arthritis

V. Pistoia, M. Gattorno, P. Picco, 1999, Annals of the New York Academy of Sciences.

Antiphospholipid antibodies in paediatric systemic lupus erythematosus, juvenile chronic arthritis and overlap syndromes: SLE patients with both lupus anticoagulant and high-titre anticardiolipin antibodies are at risk for clinical manifestations related to the antiphospholipid syndrome.

V. Pistoia, A. Molinari, M. Gattorno, 1995, British journal of rheumatology.

Tumor necrosis factor receptor p75 correlates better than p55 with disease activity in juvenile rheumatoid arthritis: comment on the article by Mangge et al.

V. Pistoia, M. Gattorno, P. Picco, 1996, Arthritis and rheumatism.

Serum p 55 and p 75 tumour necrosis factor receptors as markers of disease activity in juvenile chronic arthritis

M. Sormani, V. Pistoia, P. Picco, 2022 .

A case of paediatric discoid lupus erythematosus evolving into SLE.

V. Pistoia, M. Gattorno, P. Picco, 1998, Clinical and experimental rheumatology.

99mTc-white cell scanning to detect gut inflammation in children with inflammatory bowel diseases or spondyloarthropathies.

M. Sormani, G. Villavecchia, A. Barabino, 1998, Clinical and experimental rheumatology.

Type I interferon-mediated autoinflammation due to DNase II deficiency

F. Rieux-Laucat, C. Picard, Naoki Kitabayashi, 2017, Nature Communications.

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

F. Santorelli, C. Minetti, M. Severino, 2017, JIMD reports.

Coxarthritis as the Presenting Symptom of Gaucher Disease Type 1

A. Martini, M. B. Damasio, M. Di Rocco, 2011, Arthritis.

Long-term follow-up of systemic onset juvenile idiopathic arthritis patients treated with Anakinra

A. Martini, A. Accogli, M. Gattorno, 2011, Pediatric Rheumatology Online Journal.

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

R. Ravazzolo, B. Porfirio, R. Cusano, 2002, International journal of molecular medicine.