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Pediatric IgG4-related lymphadenopathy: A rare condition associated with autoimmunity and lymphoproliferative disorders.
Mainardi C, Pizzi M, Marzollo A, Carraro E, Boaro MP, Mussolin L, Massano D, Tazzoli S, Onofrillo D, Cesaro S, Farruggia P, Putti MC, Alaggio R, Biffi A, d'Amore ESG, Pillon M. Mainardi C, et al. Among authors: biffi a. Pediatr Allergy Immunol. 2020 Apr;31(3):332-336. doi: 10.1111/pai.13182. Epub 2019 Dec 12. Pediatr Allergy Immunol. 2020. PMID: 31770465 No abstract available.
A novel germline variant in PIK3R1 results in SHORT syndrome associated with TAL/LMO T-cell acute lymphoblastic leukemia.
Marzollo A, Maestrini G, La Starza R, Elia L, Malfona F, Pierini T, Tretti Parenzan C, Coppe A, Bortoluzzi S, Biffi A, Mecucci C, Bresolin S, Testi AM. Marzollo A, et al. Among authors: biffi a. Am J Hematol. 2020 Dec;95(12):E335-E338. doi: 10.1002/ajh.25998. Epub 2020 Sep 30. Am J Hematol. 2020. PMID: 32936972 Free article. No abstract available.
Histiocytic sarcoma arising in a child affected by Burkitt lymphoma, with t(8;14)(q24;q32) positivity in both tumors.
d'Amore ESG, Mainardi C, Mussolin L, Carraro E, Alaggio R, Lazzari E, Fusetti S, Ghirotto C, Marzollo A, Biddeci G, Toffolutti T, Massano D, Scarzello G, Zuliani M, Putti MC, Biffi A, Pillon M. d'Amore ESG, et al. Among authors: biffi a. Pediatr Hematol Oncol. 2021 Feb;38(1):1-7. doi: 10.1080/08880018.2020.1871452. Epub 2021 Feb 23. Pediatr Hematol Oncol. 2021. PMID: 33621154 No abstract available.
IFIH1 loss-of-function variants contribute to very early-onset inflammatory bowel disease.
Cananzi M, Wohler E, Marzollo A, Colavito D, You J, Jing H, Bresolin S, Gaio P, Martin R, Mescoli C, Bade S, Posey JE, Dalle Carbonare M, Tung W, Jhangiani SN, Bosa L, Zhang Y, Filho JS, Gabelli M, Kellermayer R, Kader HA, Oliva-Hemker M, Perilongo G, Lupski JR, Biffi A, Valle D, Leon A, de Macena Sobreira NL, Su HC, Guerrerio AL. Cananzi M, et al. Among authors: biffi a. Hum Genet. 2021 Sep;140(9):1299-1312. doi: 10.1007/s00439-021-02300-4. Epub 2021 Jun 29. Hum Genet. 2021. PMID: 34185153 Free PMC article. Clinical Trial.
Ruxolitinib as a Novel Therapeutic Option for Poor Prognosis T-LBL Pediatric Patients.
Veltri G, Silvestri C, Gallingani I, Sandei M, Vencato S, Lovisa F, Cortese G, Pillon M, Carraro E, Bresolin S, Biffi A, Basso G, Accordi B, Mussolin L, Serafin V. Veltri G, et al. Among authors: biffi a. Cancers (Basel). 2021 Jul 24;13(15):3724. doi: 10.3390/cancers13153724. Cancers (Basel). 2021. PMID: 34359628 Free PMC article.
Neonatal Manifestations of Chronic Granulomatous Disease: MAS/HLH and Necrotizing Pneumonia as Unusual Phenotypes and Review of the Literature.
Marzollo A, Conti F, Rossini L, Rivalta B, Leonardi L, Tretti C, Tosato F, Chiriaco M, Ursu GM, Natalucci CT, Martella M, Borghesi A, Mancini C, Ciolfi A, di Matteo G, Tartaglia M, Cancrini C, Dotta A, Biffi A, Finocchi A, Bresolin S. Marzollo A, et al. Among authors: biffi a. J Clin Immunol. 2022 Feb;42(2):299-311. doi: 10.1007/s10875-021-01159-4. Epub 2021 Oct 31. J Clin Immunol. 2022. PMID: 34718934 Review.
GNE-related thrombocytopenia: evidence for a mutational hotspot in the ADP/substrate domain of the GNE bifunctional enzyme.
Bottega R, Marzollo A, Marinoni M, Athanasakis E, Persico I, Bianco AM, Faleschini M, Valencic E, Simoncini D, Rossini L, Corsolini F, La Bianca M, Robustelli G, Gabelli M, Agosti M, Biffi A, Grotto P, Bozzi V, Noris P, Burlina AB, D'Adamo AP, Tommasini A, Faletra F, Pastore A, Savoia A. Bottega R, et al. Among authors: biffi a. Haematologica. 2022 Mar 1;107(3):750-754. doi: 10.3324/haematol.2021.279689. Haematologica. 2022. PMID: 34788986 Free PMC article. No abstract available.
512 results