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Diagnosis, treatment, and follow-up of a case of Wolman disease with hemophagocytic lymphohistiocytosis.
Baronio F, Conti F, Miniaci A, Carfagnini F, Di Natale V, Di Donato G, Testi M, Totaro C, De Fanti A, Boenzi S, Dionisi-Vici C, Esposito S, Pession A. Baronio F, et al. Among authors: pession a. Mol Genet Metab Rep. 2021 Dec 20;30:100833. doi: 10.1016/j.ymgmr.2021.100833. eCollection 2022 Mar. Mol Genet Metab Rep. 2021. PMID: 35242567 Free PMC article.
Cerebral ischemic involvement in Vogt-Koyanagi-Harada disease.
Vergaro R, Cordelli DM, Miniaci A, Tassinari D, Spinardi L, Pession A, Franzoni E. Vergaro R, et al. Among authors: pession a. Pediatr Neurol. 2014 Jul;51(1):119-22. doi: 10.1016/j.pediatrneurol.2014.03.004. Epub 2014 Mar 15. Pediatr Neurol. 2014. PMID: 24830768
Letter to the Editors: Concerning "Divergent clinical outcomes of alphaglucosidase enzyme replacement therapy in two siblings with infantile-onset Pompe disease treated in the symptomatic or pre-symptomatic state" by Takashi M et al.
Ortolano R, Baronio F, Masetti R, Prete A, Cassio A, Pession A. Ortolano R, et al. Among authors: pession a. Mol Genet Metab Rep. 2017 Mar 7;11:1. doi: 10.1016/j.ymgmr.2017.02.003. eCollection 2017 Jun. Mol Genet Metab Rep. 2017. PMID: 28316933 Free PMC article. No abstract available.
The autoimmune burden in juvenile idiopathic arthritis.
Tronconi E, Miniaci A, Pession A. Tronconi E, et al. Among authors: pession a. Ital J Pediatr. 2017 Jun 14;43(1):56. doi: 10.1186/s13052-017-0373-9. Ital J Pediatr. 2017. PMID: 28615030 Free PMC article.
687 results