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Long-term clinical profile of children with the low-penetrance R92Q mutation of the TNFRSF1A gene. Arthritis Rheum 2011;63(4):1141-50.
. Subcutaneous Granuloma Annulare: A Diagnostic Conundrum-Learning From Mistakes. Pediatr Emerg Care 2017;33(8):e30-e31.
. Laparoscopic orchiopexy: short term outcomes. Experience of a single centre. Minerva Pediatr 2015;
. Handlebar injury in children: The hidden danger. Surgery 2015;
. An asymptomatic multiple magnet ingestion with transmesenteric entero-enteric fistula. APSP J Case Rep 2014;5(2):16.
. Fainting Starting Parenteral Nutrition. Pediatr Emerg Care 2015;31(9):648.
. MYH9: Structure, functions and role of non-muscle myosin IIA in human disease. Gene 2018;664:152-167.
. MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations. Hum Mutat 2014;35(2):236-47.
. Alteration of liver enzymes is a feature of the MYH9-related disease syndrome. PLoS One 2012;7(4):e35986.
. Eltrombopag for the treatment of the inherited thrombocytopenia deriving from MYH9 mutations. Blood 2010;116(26):5832-7.
. Higher growth, fat and fat-free masses correlate with larger cerebellar volumes in preterm infants at term. Acta Paediatr 2017;106(6):918-925.
. Making the first days of life safer: time for a new protocol?. J Perinatol 2014;34(12):957.
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