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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.
Rocca MSanta, Fabretto A, Faletra F, Carlet O, Skabar A, Gasparini P, Pecile V. Contribution of SNP arrays in diagnosis of deletion 2p11.2-p12. Gene 2012;492(1):315-8.
Roia A, Paviotti E, Ferluga V, Montico M, Monasta L, Ronfani L, Tamburlini G. Promoting effective child development practices in the first year of life: does timing make a difference?. BMC Pediatr 2014;14:222.
Romano C, Oliva S, Martellossi S, Miele E, Arrigo S, Graziani MGiovanna, Cardile S, Gaiani F, de'Angelis GLuigi, Torroni F. Pediatric gastrointestinal bleeding: Perspectives from the Italian Society of Pediatric Gastroenterology. World J Gastroenterol 2017;23(8):1328-1337.
Rondelli R, Dini G, De Rosa M, Quarello P, Bisogno G, Aricò M, Vasconcelos C, Tamaro P, Casazza G, Zecca M, De Laurentis C, Porta F, Pession A. Foreign children with cancer in Italy. Ital J Pediatr 2011;37:44.
Rosati A, Ilvento L, L'Erario M, De Masi S, Biggeri A, Fabbro G, Bianchi R, Stoppa F, Fusco L, Pulitanò S, Battaglia D, Pettenazzo A, Sartori S, Biban P, Fontana E, Cesaroni E, Mora D, Costa P, Meleleo R, Vittorini R, Conio A, Wolfler A, Mastrangelo M, Mondardini MCristina, Franzoni E, McGreevy KS, Di Simone L, Pugi A, Mirabile L, Vigevano F, Guerrini R. Efficacy of ketamine in refractory convulsive status epilepticus in children: a protocol for a sequential design, multicentre, randomised, controlled, open-label, non-profit trial (KETASER01). BMJ Open 2016;6(6):e011565.
Rossetto E, Matarazzo L, Maschio M, Taddio A, Costa P, Ventura A. A Child with Severe Developmental Delay and Growth Retardation. J Pediatr 2016;175:241-241.e1.
Rubinato E, Morgan A, D'Eustacchio A, Pecile V, Gortani G, Gasparini P, Faletra F. A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta. Gene 2014;545(2):290-2.
Rudan I, Arifeen SEl, Bhutta ZA, Black RE, Brooks A, Chan KYee, Chopra M, Duke T, Marsh D, Pio A, Simoes EAF, Tamburlini G, Theodoratou E, Weber MW, Whitney CG, Campbell H, Qazi SA. Setting research priorities to reduce global mortality from childhood pneumonia by 2015. PLoS Med 2011;8(9):e1001099.
Ruggenenti P, Ruggiero B, Cravedi P, Vivarelli M, Massella L, Marasà M, Chianca A, Rubis N, Ene-Iordache B, Rudnicki M, Pollastro RMaria, Capasso G, Pisani A, Pennesi M, Emma F, Remuzzi G. Rituximab in steroid-dependent or frequently relapsing idiopathic nephrotic syndrome. J Am Soc Nephrol 2014;25(4):850-63.
Ruggiero B, Vivarelli M, Gianviti A, Pecoraro C, Peruzzi L, Benetti E, Ventura G, Pennesi M, Murer L, Coppo R, Emma F. Outcome of childhood-onset full-house nephropathy. Nephrol Dial Transplant 2017;32(7):1194-1204.
Rupel K, Zupin L, Colliva A, Kamada A, Poropat A, Ottaviani G, Gobbo M, Fanfoni L, Gratton R, Santoro M, Di Lenarda R, Biasotto M, Zacchigna S. Photobiomodulation at Multiple Wavelengths Differentially Modulates Oxidative Stress and . Oxid Med Cell Longev 2018;2018:6510159.

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