Mycophenolic Acid

Una dermatomiosite complessa

Morreale DM, Carlino C, Taverniti M, Maggio MC, Alizzi C, Allegra M, Corsello G

2026/5 — pag. 111-112 — DOI

The paper presents the case of an 8-year-old girl that was admitted to the hospital with pruritic, erythematous and scaling skin lesions on her limbs, chest, back and fingers (Gottron’s papules), along with a malar (‘butterfly’) rash. She also had mu...

Terapie genetiche inarrestabili (parte prima): prime editing per la CGD Terapie genetiche inarrestabili (parte seconda): tornare a sentire Novità nella sindrome nefrosica: micofenolato sempre prima? Bambini con PCI, attenzione al percentile Ancora FPIAP: meno è meglio Mutilazione genitale femminile: parliamone e riconosciamola

2026/4 — pag. 213 — DOI

Prima l'epatite autoimmune e poi la MICI... dopo tanto tempo

Izzo BP, Mainetti M, Aprile MR, Foschi F, Buzzi A, Marchetti F

2024/26 — pag. 4-5 — DOI

The authors describe the case of a girl with IBD that manifested 10 years after the diagnosis of seronegative hepatitis. ...

Una diagnosi complementare: la C3-glomerulopathy

Amoroso S

2022/6 — pag. 134-134 — DOI

The case of a 10-year-old boy with macrohaematuria is presented. The diagnosis of C3-glomerulopathy was eventually made. The author remarks the main clinical and diagnostic aspects of C3-glomerulopathy....

Le interferonopatie di tipo I

Tommasini A, Bruno I, Morelli ME, Lepore L

2021/8 — pag. 509-514 — DOI

Type I interferonopathies are autoinflammatory monogenic disorders arising from excessive production of interferons. Some manifestations like chilblains, neurologic involvement, arthritis and lipodystrophy may be shared by several diseases. Measure o...

Glomerulopatia da depositi di C3

S. Amoroso, M. Pennesi, A. Ventura

2018/2 — pag. 119-122

C3-glomerulopathy includes several nephropathy charac-terised by almost only C3 deposits without immunoglobu-lins with a mesangial proliferative or membrano-proliferative pattern on light microscopy. C3-glomerulopathy is determined by a dysregulation...

Glomerulopatia da depositi di C3

S. Amoroso, M. Pennesi, A. Ventura

2018/2

C3-glomerulopathy includes several nephropathy charac-terised by almost only C3 deposits without immunoglobu-lins with a mesangial proliferative or membrano-proliferative pattern on light microscopy. C3-glomerulopathy is determined by a dysregulation...

Una morfea pansclerotica: nulla è servito

S. Della Paolera, S. Pastore, M. Minute, M. Rabusin, L. Lepore, A. Ventura

2017/8 — pag. 531-532

The paper presents the case of a 12-year-old boy affected by circumscribed morphea that started with multiple skin lesions on both feet and hands. Despite different therapeutic approaches the disease evolved to an extremely disabling form of panscler...

Trattamento della sindrome nefrosica idiopatica corticosensibile

C. Romanello

2005/9 — pag. 580-586

The steroid treatment of Idiopathic Nephrotic Syndrome (ISN) should be continued for at least 3 months, as there is evidence of an inverse correlation between the duration and the total dosage of steroids and the risk of relapses. The tendency to r...