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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.
. Contribution of SNP arrays in diagnosis of deletion 2p11.2-p12. Gene 2012;492(1):315-8.
. Promoting effective child development practices in the first year of life: does timing make a difference?. BMC Pediatr 2014;14:222.
. Pediatric gastrointestinal bleeding: Perspectives from the Italian Society of Pediatric Gastroenterology. World J Gastroenterol 2017;23(8):1328-1337.
. Foreign children with cancer in Italy. Ital J Pediatr 2011;37:44.
. 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.
. A Child with Severe Developmental Delay and Growth Retardation. J Pediatr 2016;175:241-241.e1.
. A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta. Gene 2014;545(2):290-2.
. Setting research priorities to reduce global mortality from childhood pneumonia by 2015. PLoS Med 2011;8(9):e1001099.
. Rituximab in steroid-dependent or frequently relapsing idiopathic nephrotic syndrome. J Am Soc Nephrol 2014;25(4):850-63.
. Outcome of childhood-onset full-house nephropathy. Nephrol Dial Transplant 2017;32(7):1194-1204.
. Photobiomodulation at Multiple Wavelengths Differentially Modulates Oxidative Stress and . Oxid Med Cell Longev 2018;2018:6510159.
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