Sestito S - Search Results

1

Risk of autoimmune diseases in patients with RASopathies: systematic study of humoral and cellular immunity.

Siano MA, Marchetti V, Pagano S, Di Candia F, Alessio M, De Brasi D, De Luca A, Pinna V, Sestito S, Concolino D, Tartaglia M, Strisciuglio P, D'Esposito V, Cabaro S, Perruolo G, Formisano P, Melis D. Siano MA, et al. Among authors: sestito s. Orphanet J Rare Dis. 2021 Oct 2;16(1):410. doi: 10.1186/s13023-021-02050-6. Orphanet J Rare Dis. 2021. PMID: 34600590 Free PMC article.

2

Gastrointestinal Symptoms of Patients with Fabry Disease.

Pensabene L, Sestito S, Nicoletti A, Graziano F, Strisciuglio P, Concolino D. Pensabene L, et al. Among authors: sestito s. Gastroenterol Res Pract. 2016;2016:9712831. doi: 10.1155/2016/9712831. Epub 2015 Dec 31. Gastroenterol Res Pract. 2016. PMID: 26880903 Free PMC article.

3

Clericuzio-type poikiloderma with neutropenia syndrome in three sibs with mutations in the C16orf57 gene: delineation of the phenotype.

Concolino D, Roversi G, Muzzi GL, Sestito S, Colombo EA, Volpi L, Larizza L, Strisciuglio P. Concolino D, et al. Among authors: sestito s. Am J Med Genet A. 2010 Oct;152A(10):2588-94. doi: 10.1002/ajmg.a.33600. Am J Med Genet A. 2010. PMID: 20734427

4

Long-term treatment with recombinant insulin-like growth factor 1 (IGF-1) in a child with IGF-1 gene mutation.

Concolino D, Muzzi G, Sestito S, Vega G, Bonapace G, Strisciuglio P. Concolino D, et al. Among authors: sestito s. Eur J Pediatr. 2010 Feb;169(2):245-7. doi: 10.1007/s00431-009-1004-2. Epub 2009 Jun 11. Eur J Pediatr. 2010. PMID: 19517134

5

Cardiac involvement in MPS patients: incidence and response to therapy in an Italian multicentre study.

Sestito S, Rinninella G, Rampazzo A, D'Avanzo F, Zampini L, Santoro L, Gabrielli O, Fiumara A, Barone R, Volpi N, Scarpa M, Tomanin R, Concolino D. Sestito S, et al. Orphanet J Rare Dis. 2022 Jun 29;17(1):251. doi: 10.1186/s13023-022-02396-5. Orphanet J Rare Dis. 2022. PMID: 35768874 Free PMC article.

6

Co-existence of phenylketonuria and Fabry disease on a 3 year-old boy: case report.

Concolino D, Rapsomaniki M, Disabella E, Sestito S, Pascale MG, Moricca MT, Bonapace G, Arbustini E, Strisciuglio P. Concolino D, et al. Among authors: sestito s. BMC Pediatr. 2010 May 17;10:32. doi: 10.1186/1471-2431-10-32. BMC Pediatr. 2010. PMID: 20478016 Free PMC article.

7

Anderson-Fabry disease in children.

Sestito S, Ceravolo F, Concolino D. Sestito S, et al. Curr Pharm Des. 2013;19(33):6037-45. doi: 10.2174/13816128113199990345. Curr Pharm Des. 2013. PMID: 23448455 Review.

8

Evolution of congenital hypothyroidism in a cohort of preterm born children.

Scavone M, Giancotti L, Anastasio E, Pensabene L, Sestito S, Concolino D. Scavone M, et al. Among authors: sestito s. Pediatr Neonatol. 2020 Dec;61(6):629-636. doi: 10.1016/j.pedneo.2020.07.014. Epub 2020 Jul 23. Pediatr Neonatol. 2020. PMID: 32771362 Free article.

9

Beneficial Effects of Slow-Release Large Neutral Amino Acids after a Phenylalanine Oral Load in Patients with Phenylketonuria.

Scala I, Concolino D, Nastasi A, Esposito G, Crisci D, Sestito S, Ferraro S, Albano L, Ruoppolo M, Parenti G, Strisciuglio P. Scala I, et al. Among authors: sestito s. Nutrients. 2021 Nov 10;13(11):4012. doi: 10.3390/nu13114012. Nutrients. 2021. PMID: 34836270 Free PMC article.

10

Genetics and Gene Therapy in Hunter Disease.

Sestito S, Falvo F, Scozzafava C, Apa R, Pensabene L, Bonapace G, Moricca MT, Concolino D. Sestito S, et al. Curr Gene Ther. 2018;18(2):90-95. doi: 10.2174/1566523218666180404155759. Curr Gene Ther. 2018. PMID: 29618310 Review.

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