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CECCHERINI I
Collezione AOU Alessandria

  

Items : 7

A unicentric cross-sectional observational study on chronic intestinal inflammation in total colonic aganglionosis: beware of an underestimated condition. in Orphanet journal of rare diseases / Orphanet J Rare Dis. 2023 Oct 27;18(1):339. doi: 10.1186/s13023-023-02958-1.
2023
AOU Alessandria

Erculiani M; Poluzzi F; Mottadelli G; Felici E; Ml N; Caraccia M; Grandi A; Casella S; Giacometti L; Montobbio G; Ceccherini I; Di Marco E; Bonaretti C; Biassoni R; Squillario M; Pietrantoni A; Villanacci V; Pini Prato A;

Multi-disciplinary Insights from the First European Forum on Visceral Myopathy 2022 Meeting. in Digestive diseases and sciences / Dig Dis Sci. 2023 Oct;68(10):3857-3871. doi: 10.1007/s10620-023-08066-1. Epub 2023 Aug 31.
2023
AOU Alessandria

Viti F; De Giorgio R; Ceccherini I; Ahluwalia A; Alves MM; Baldo C; Baldussi G; Bonora E; Borrelli O; Dall'Oglio L; De Coppi P; De Filippo C; de Santa Barbara P; Diamanti A; Di Lorenzo C; Di Maulo R; Galeone A; Gandullia P; Hashmi SK; Lacaille F; Lancon L; Leone S; Mahé MM; Molnar MJ; Palmitelli A; Perin S; Prato AP; Thapar N; Vassalli M; et alii...

Congenital anomalies of the kidney and urinary tract in a cohort of 280 consecutive patients with Hirschsprung disease. in Pediatric nephrology (Berlin, Germany) / Pediatr Nephrol. 2021 Oct;36(10):3151-3158. doi: 10.1007/s00467-021-05061-4. Epub 2021 Apr 9.
2021
AOU Alessandria

Pini Prato A; Arnoldi R; Falconi I; Dusio MP; Ceccherini I; Tentori A; Felici E; Nozza P;

Novel ACTG2 variants disclose allelic heterogeneity and bi-allelic inheritance in pediatric chronic intestinal pseudo-obstruction. in Clinical genetics / Clin Genet. 2021 Mar;99(3):430-436. doi: 10.1111/cge.13895. Epub 2020 Dec 14.
2021
AOU Alessandria

Alberti D; Pini Prato A; Spagnuolo MI; Diamanti A; Lezo A; Pongiglione M; Santamaria G; Lerone M; Di Duca M; Bordo D; Matera I; Mattioli G; Gandullia P; Ceccherini I;

The OSMR Gene Is Involved in Hirschsprung Associated Enterocolitis Susceptibility through an Altered Downstream Signaling. in International journal of molecular sciences / Int J Mol Sci. 2021 Apr 7;22(8):3831. doi: 10.3390/ijms22083831.
2021
AOU Alessandria

Bachetti T; Rosamilia F; Bartolucci M; Santamaria G; Mosconi M; Sartori S; De Filippo MR; Di Duca M; Obino V; Avanzini S; Mavilio D; Candiani S; Petretto A; Pini Prato A; Ceccherini I; Lantieri F;

Copy number variations in candidate genomic regions confirm genetic heterogeneity and parental bias in Hirschsprung disease. in Orphanet journal of rare diseases / Orphanet J Rare Dis. 2019 Nov 25;14(1):270. doi: 10.1186/s13023-019-1205-3.
2019
AOU Alessandria

Lantieri F; Gimelli S; Viaggi C; Stathaki E; Malacarne M; Santamaria G; Grossi A; Mosconi M; Sloan-Béna F; Prato AP; Coviello D; Ceccherini I;

2019
AOU Alessandria

Pini Prato A; Bartow-McKenney C; Hudspeth K; Mosconi M; Rossi V; Avanzini S; Faticato MG; Ceccherini I; Lantieri F; Mattioli G; Larson D; Pavan W; De Filippo C; Di Paola M; Mavilio D; Cavalieri D;

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