Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

112 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Mitochondrial DNA haplogroups may influence Fabry disease phenotype.
Simoncini C, Chico L, Concolino D, Sestito S, Fancellu L, Boadu W, Sechi GP, Feliciani C, Gnarra M, Zampetti A, Salviati A, Scarpelli M, Orsucci D, Bonuccelli U, Siciliano G, Mancuso M. Simoncini C, et al. Among authors: sestito s. Neurosci Lett. 2016 Aug 26;629:58-61. doi: 10.1016/j.neulet.2016.06.051. Epub 2016 Jun 27. Neurosci Lett. 2016. PMID: 27365132
Oxidative stress biomarkers in Fabry disease: is there a room for them?
Simoncini C, Torri S, Montano V, Chico L, Gruosso F, Tuttolomondo A, Pinto A, Simonetta I, Cianci V, Salviati A, Vicenzi V, Marchi G, Girelli D, Concolino D, Sestito S, Zedde M, Siciliano G, Mancuso M. Simoncini C, et al. Among authors: sestito s. J Neurol. 2020 Dec;267(12):3741-3752. doi: 10.1007/s00415-020-10044-w. Epub 2020 Jul 27. J Neurol. 2020. PMID: 32719972 Free PMC article.
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.
Urine bikunin as a marker of renal impairment in Fabry's disease.
Lepedda AJ, Fancellu L, Zinellu E, De Muro P, Nieddu G, Deiana GA, Canu P, Concolino D, Sestito S, Formato M, Sechi G. Lepedda AJ, et al. Among authors: sestito s. Biomed Res Int. 2013;2013:205948. doi: 10.1155/2013/205948. Epub 2013 Jun 12. Biomed Res Int. 2013. PMID: 23841057 Free PMC article.
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.
Renal involvement in paediatric Fabry disease.
Sestito S, Falvo F, Sallemi A, Petrisano M, Scuderi MG, Tarsitano F, D'Angelo G, Betta P, Roppa K, Parisi F, Pensabene L, Fede C, Chimenz R, Concolino D. Sestito S, et al. J Biol Regul Homeost Agents. 2019 Sep-Oct;33(5 Suppl. 1):59-63. Special Issue: Focus on Pediatric Nephrology. J Biol Regul Homeost Agents. 2019. PMID: 31630715
The heart in Anderson-Fabry disease.
Sestito S, Roppa K, Parisi F, Moricca MT, Pensabene L, Chimenz R, Ceravolo MD, Cucinotta U, Ceravolo G, Calabrò MP, Cuppari C, Mondello P, Musolino D, Tallarico V, Concolino D. Sestito S, et al. J Biol Regul Homeost Agents. 2020 Jul-Aug;34(4 Suppl. 2):63-69. SPECIAL ISSUE: FOCUS ON PEDIATRIC CARDIOLOGY. J Biol Regul Homeost Agents. 2020. PMID: 33000603 No abstract available.
Genetic variants associated with gastrointestinal symptoms in Fabry disease.
Di Martino MT, Scionti F, Sestito S, Nicoletti A, Arbitrio M, Hiram Guzzi P, Talarico V, Altomare F, Sanseviero MT, Agapito G, Pisani A, Riccio E, Borrelli O, Concolino D, Pensabene L. Di Martino MT, et al. Among authors: sestito s. Oncotarget. 2016 Dec 27;7(52):85895-85904. doi: 10.18632/oncotarget.13135. Oncotarget. 2016. PMID: 27825144 Free PMC article.
Norrbottnian clinical variant of Gaucher disease in Southern Italy.
Sestito S, Filocamo M, Ceravolo F, Falvo F, Grisolia M, Moricca MT, Cantaffa R, Grossi S, Strisciuglio P, Concolino D. Sestito S, et al. J Hum Genet. 2017 Apr;62(4):507-511. doi: 10.1038/jhg.2016.158. Epub 2016 Dec 22. J Hum Genet. 2017. PMID: 28003644
112 results