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149 results

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Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up study.
Iapadre G, Zagaroli L, Cimini N, Belcastro V, Concolino D, Coppola G, Del Giudice E, Farello G, Iezzi ML, Margari L, Matricardi S, Orsini A, Parisi P, Piccioli M, Di Donato G, Savasta S, Siliquini S, Spalice A, Striano S, Striano P, Verrotti A. Iapadre G, et al. Among authors: concolino d. Epilepsy Behav. 2020 Feb;103(Pt A):106578. doi: 10.1016/j.yebeh.2019.106578. Epub 2019 Nov 1. Epilepsy Behav. 2020. PMID: 31680025
Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15).
Matricardi S, Darra F, Spalice A, Basti C, Fontana E, Dalla Bernardina B, Elia M, Giordano L, Accorsi P, Cusmai R, De Liso P, Romeo A, Ragona F, Granata T, Concolino D, Carotenuto M, Pavone P, Pruna D, Striano P, Savasta S, Verrotti A. Matricardi S, et al. Among authors: concolino d. Acta Neurol Scand. 2018 Jun;137(6):575-581. doi: 10.1111/ane.12902. Epub 2018 Jan 23. Acta Neurol Scand. 2018. PMID: 29363096
Epilepsy, electroclinical features, and long-term outcomes in Pitt-Hopkins syndrome due to pathogenic variants in the TCF4 gene.
Matricardi S, Bonanni P, Iapadre G, Elia M, Cesaroni E, Danieli A, Negrin S, Zagaroli L, Operto FF, Carotenuto M, Pisani F, Turco EC, Orsini A, Bonuccelli A, Savasta S, Concolino D, Di Cara G, Striano P, Verrotti A. Matricardi S, et al. Among authors: concolino d. Eur J Neurol. 2022 Jan;29(1):19-25. doi: 10.1111/ene.15104. Epub 2021 Oct 7. Eur J Neurol. 2022. PMID: 34519126
Postinfectious functional gastrointestinal disorders in children: a multicenter prospective study.
Pensabene L, Talarico V, Concolino D, Ciliberto D, Campanozzi A, Gentile T, Rutigliano V, Salvatore S, Staiano A, Di Lorenzo C; Post-Infectious Functional Gastrointestinal Disorders Study Group of Italian Society for Pediatric Gastroenterology, Hepatology and Nutrition. Pensabene L, et al. Among authors: concolino d. J Pediatr. 2015 Apr;166(4):903-7.e1. doi: 10.1016/j.jpeds.2014.12.050. Epub 2015 Feb 4. J Pediatr. 2015. PMID: 25661403
Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy.
Parini R, De Lorenzo P, Dardis A, Burlina A, Cassio A, Cavarzere P, Concolino D, Della Casa R, Deodato F, Donati MA, Fiumara A, Gasperini S, Menni F, Pagliardini V, Sacchini M, Spada M, Taurisano R, Valsecchi MG, Di Rocco M, Bembi B. Parini R, et al. Among authors: concolino d. Orphanet J Rare Dis. 2018 Feb 8;13(1):32. doi: 10.1186/s13023-018-0771-0. Orphanet J Rare Dis. 2018. PMID: 29422078 Free PMC article.
Unusual presentation of Henoch-Schönlein purpura.
Chimenz R, Cannavò L, Spinuzza A, Fede C, Cucinotta U, Pensabene L, Betta P, Gitto E, Concolino D, Cuppari C. Chimenz R, et al. Among authors: concolino d. J Biol Regul Homeost Agents. 2019 Sep-Oct;33(5 Suppl. 1):69-74. Special Issue: Focus on Pediatric Nephrology. J Biol Regul Homeost Agents. 2019. PMID: 31630717
GAPO syndrome associated with vestibular dysfunction and hearing loss.
Rapsomaniki M, Chiarella G, Mascaro I, Ceravolo F, Cassandro E, Strisciuglio P, Concolino D. Rapsomaniki M, et al. Among authors: concolino d. Am J Med Genet A. 2013 Aug;161A(8):2102-4. doi: 10.1002/ajmg.a.35992. Epub 2013 Jun 21. Am J Med Genet A. 2013. PMID: 23794220 No abstract available.
149 results