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Pediatric idiopathic intracranial hypertension and the underlying endocrine-metabolic dysfunction: a pilot study.
Salpietro V, Mankad K, Kinali M, Adams A, Valenzise M, Tortorella G, Gitto E, Polizzi A, Chirico V, Nicita F, David E, Romeo AC, Squeri CA, Savasta S, Marseglia GL, Arrigo T, Johanson CE, Ruggieri M. Salpietro V, et al. Among authors: arrigo t. J Pediatr Endocrinol Metab. 2014 Jan;27(1-2):107-15. doi: 10.1515/jpem-2013-0156. J Pediatr Endocrinol Metab. 2014. PMID: 24025722
A de novo 0.63 Mb 6q25.1 deletion associated with growth failure, congenital heart defect, underdeveloped cerebellar vermis, abnormal cutaneous elasticity and joint laxity.
Salpietro V, Ruggieri M, Mankad K, Di Rosa G, Granata F, Loddo I, Moschella E, Calabro MP, Capalbo A, Bernardini L, Novelli A, Polizzi A, Seidler DG, Arrigo T, Briuglia S. Salpietro V, et al. Among authors: arrigo t. Am J Med Genet A. 2015 Sep;167A(9):2042-51. doi: 10.1002/ajmg.a.37118. Epub 2015 May 1. Am J Med Genet A. 2015. PMID: 25940952
High-mobility group box 1 (HMGB1) in childhood: from bench to bedside.
Chirico V, Lacquaniti A, Salpietro V, Munafò C, Calabrò MP, Buemi M, Arrigo T, Salpietro C. Chirico V, et al. Among authors: arrigo t. Eur J Pediatr. 2014 Sep;173(9):1123-36. doi: 10.1007/s00431-014-2327-1. Epub 2014 May 9. Eur J Pediatr. 2014. PMID: 24809802 Review.
232 results