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Common variants in CLDN14 are associated with differential excretion of magnesium over calcium in urine. Pflugers Arch 2017;469(1):91-103.
. A complete duplication of X chromosome resulting in a tricentric isochromosome originated by centromere repositioning. Mol Cytogenet 2017;10:22.
. A congenital purplish tumour. Arch Dis Child Educ Pract Ed 2017;102(2):79-81.
. A congenital purplish tumour. Arch Dis Child Educ Pract Ed 2017;102(2):79-81.
. CYP3A genes and the association between prenatal methylmercury exposure and neurodevelopment. Environ Int 2017;105:34-42.
. DEFB1 polymorphisms and salivary hBD-1 concentration in Oral Lichen Planus patients and healthy subjects. Arch Oral Biol 2017;73:161-165.
. Defects in mitochondrial energetic function compels Fanconi Anaemia cells to glycolytic metabolism. Biochim Biophys Acta Mol Basis Dis 2017;1863(6):1214-1221.
. Diagnosis and management of newly diagnosed childhood autoimmune haemolytic anaemia. Recommendations from the Red Cell Study Group of the Paediatric Haemato-Oncology Italian Association. Blood Transfus 2017;15(3):259-267.
. Dynamic quadripolar radiofrequency treatment of vaginal laxity/menopausal vulvo-vaginal atrophy: 12-month efficacy and safety. Minerva Ginecol 2017;69(4):342-349.
. Early-life nutritional exposures and lifelong health: immediate and long-lasting impacts of probiotics, vitamin D, and breastfeeding. Nutr Rev 2017;75(2):83-97.
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