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1.
The Italian Registry for Primary Immunodeficiencies (Italian Primary Immunodeficiency Network; IPINet): Twenty Years of Experience (1999-2019).
J Clin Immunol
; 40(7): 1026-1037, 2020 10.
Article
in English
| MEDLINE | ID: mdl-32803625
2.
An immune-molecular hypothesis supporting infectious aetiopathogenesis of Kawasaki disease in children.
Eur J Immunol
; 48(3): 543-545, 2018 03.
Article
in English
| MEDLINE | ID: mdl-29193035
3.
Clinical features and follow-up in patients with 22q11.2 deletion syndrome.
J Pediatr
; 164(6): 1475-80.e2, 2014 Jun.
Article
in English
| MEDLINE | ID: mdl-24657119
4.
Non invasive assessment of lung disease in ataxia telangiectasia by high-field magnetic resonance imaging.
J Clin Immunol
; 33(7): 1185-91, 2013 Oct.
Article
in English
| MEDLINE | ID: mdl-23975689
5.
Long-term follow-up in common variable immunodeficiency: the pediatric-onset and adult-onset landscape.
Front Pediatr
; 11: 1125994, 2023.
Article
in English
| MEDLINE | ID: mdl-37435172
6.
Long term longitudinal follow-up of an AD-HIES cohort: the impact of early diagnosis and enrollment to IPINet centers on the natural history of Job's syndrome.
Allergy Asthma Clin Immunol
; 19(1): 32, 2023 Apr 20.
Article
in English
| MEDLINE | ID: mdl-37081481
7.
Hereditary deficiency of gp91(phox) is associated with enhanced arterial dilatation: results of a multicenter study.
Circulation
; 120(16): 1616-22, 2009 Oct 20.
Article
in English
| MEDLINE | ID: mdl-19805647
8.
Nutritional Status in Agammaglobulinemia: An Italian Multicenter Study.
J Clin Immunol
; 35(7): 595-7, 2015 Oct.
Article
in English
| MEDLINE | ID: mdl-26384979
9.
Atopy in preschool Italian children with recurrent respiratory infections.
Pediatr Med Chir
; 31(4): 161-4, 2009.
Article
in English
| MEDLINE | ID: mdl-19839398
10.
Kawasaki disease: guidelines of Italian Society of Pediatrics, part II - treatment of resistant forms and cardiovascular complications, follow-up, lifestyle and prevention of cardiovascular risks.
Ital J Pediatr
; 44(1): 103, 2018 Aug 30.
Article
in English
| MEDLINE | ID: mdl-30157893
11.
Kawasaki disease: guidelines of the Italian Society of Pediatrics, part I - definition, epidemiology, etiopathogenesis, clinical expression and management of the acute phase.
Ital J Pediatr
; 44(1): 102, 2018 Aug 30.
Article
in English
| MEDLINE | ID: mdl-30157897
12.
Invasive meningococcal disease in three siblings with hereditary deficiency of the 8(th) component of complement: evidence for the importance of an early diagnosis.
Orphanet J Rare Dis
; 11(1): 64, 2016 05 17.
Article
in English
| MEDLINE | ID: mdl-27183977
13.
Intra-erythrocyte infusion of dexamethasone reduces neurological symptoms in ataxia teleangiectasia patients: results of a phase 2 trial.
Orphanet J Rare Dis
; 9: 5, 2014 Jan 09.
Article
in English
| MEDLINE | ID: mdl-24405665
14.
Different degrees of NADPH oxidase 2 regulation and in vivo platelet activation: lesson from chronic granulomatous disease.
J Am Heart Assoc
; 3(3): e000920, 2014 Jun 27.
Article
in English
| MEDLINE | ID: mdl-24973227
15.
Autosomal-dominant hyper-IgE syndrome is associated with appearance of infections early in life and/or neonatal rash: Evidence from the Italian cohort of 61 patients with elevated IgE.
J Allergy Clin Immunol Pract
; 7(6): 2072-2075.e4, 2019.
Article
in English
| MEDLINE | ID: mdl-30797078
16.
Invasive Aspergillus nidulans infection in a patient with chronic granulomatous disease.
Mycoses
; 51(5): 458-60, 2008 Sep.
Article
in English
| MEDLINE | ID: mdl-18783555
17.
Does NADPH oxidase deficiency cause artery dilatation in humans?
Antioxid Redox Signal
; 18(12): 1491-6, 2013 Apr 20.
Article
in English
| MEDLINE | ID: mdl-23216310
18.
Hyper-IgE syndrome: dental implications.
Oral Surg Oral Med Oral Pathol Oral Radiol
; 114(2): 147-53, 2012 Aug.
Article
in English
| MEDLINE | ID: mdl-22769403
19.
Outcome of tonsillectomy in selected patients with PFAPA syndrome.
Arch Otolaryngol Head Neck Surg
; 135(6): 548-53, 2009 Jun.
Article
in English
| MEDLINE | ID: mdl-19528401
20.
The hyper-IgE syndrome is not caused by a microdeletion syndrome.
Immunogenetics
; 59(12): 913-26, 2007 Dec.
Article
in English
| MEDLINE | ID: mdl-18000661
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