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Journal Article
Celsi F, Piscianz E, Romano M, Crovella S. Knockdown of MVK does not lead to changes in NALP3 expression or activation. J Inflamm (Lond) 2015;12:7.
Rocca MS, Pecile V, Cleva L, Speltra E, Selice R, Di Mambro A, Foresta C, Ferlin A. The Klinefelter syndrome is associated with high recurrence of copy number variations on the X chromosome with a potential role in the clinical phenotype. Andrology 2016;4(2):328-34.
Zanella G, Tornese G, Mascheroni E, Faleschini E, Ventura A, Barbi E. A Klinefelter boy with congenital adrenal hyperplasia: too much or too little androgens?. Ital J Pediatr 2018;44(1):43.
Tisato V, Perri P, Rimondi E, Melloni E, Lamberti G, Milani D, Secchiero P, Zauli G. Kinetic Profiles of Inflammatory Mediators in the Conjunctival Sac Fluid of Patients upon Photorefractive Keratectomy. Mediators Inflamm 2015;2015:942948.
Ayub Q, Mezzavilla M, Pagani L, Haber M, Mohyuddin A, Khaliq S, Mehdi SQasim, Tyler-Smith C. The Kalash genetic isolate: ancient divergence, drift, and selection. Am J Hum Genet 2015;96(5):775-83.

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