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Page 1
Unrelated hematopoietic stem cell transplantation for Cernunnos-XLF deficiency.
Faraci M, Lanino E, Micalizzi C, Morreale G, Di Martino D, Banov L, Comoli P, Locatelli F, Soresina A, Plebani A. Faraci M, et al. Among authors: soresina a. Pediatr Transplant. 2009 Sep;13(6):785-9. doi: 10.1111/j.1399-3046.2008.01028.x. Epub 2008 Nov 26. Pediatr Transplant. 2009. PMID: 19067926
Long term longitudinal follow-up of an AD-HIES cohort: the impact of early diagnosis and enrollment to IPINet centers on the natural history of Job's syndrome.
Carrabba M, Dellepiane RM, Cortesi M, Baselli LA, Soresina A, Cirillo E, Giardino G, Conti F, Dotta L, Finocchi A, Cancrini C, Milito C, Pacillo L, Cinicola BL, Cossu F, Consolini R, Montin D, Quinti I, Pession A, Fabio G, Pignata C, Pietrogrande MC, Badolato R. Carrabba M, et al. Among authors: soresina a. Allergy Asthma Clin Immunol. 2023 Apr 20;19(1):32. doi: 10.1186/s13223-023-00776-5. Allergy Asthma Clin Immunol. 2023. PMID: 37081481 Free PMC article.
COVID-19 Pneumonia with Migratory Pattern in Agammaglobulinemic Patients: A Report of Two Cases and Review of Literature.
Degli Antoni M, Crosato V, Pennati F, Borghesi A, Cristini G, Allegri R, Capone S, Bergamasco A, Soresina A, Badolato R, Maroldi R, Quiros-Roldan E, Matteelli A, Castelli F, Focà E. Degli Antoni M, et al. Among authors: soresina a. Tomography. 2023 Apr 23;9(3):894-900. doi: 10.3390/tomography9030073. Tomography. 2023. PMID: 37218933 Free PMC article. Review.
A case report of a patient with microcephaly, facial dysmorphism, chromosomal radiosensitivity and telomere length alterations closely resembling "Nijmegen breakage syndrome" phenotype.
Berardinelli F, di Masi A, Salvatore M, Banerjee S, Myung K, De Villartay JP, Revy P, Plebani A, Soresina A, Taruscio D, Tanzarella C, Antoccia A. Berardinelli F, et al. Among authors: soresina a. Eur J Med Genet. 2007 May-Jun;50(3):176-87. doi: 10.1016/j.ejmg.2007.01.006. Epub 2007 Feb 21. Eur J Med Genet. 2007. PMID: 17395558
Mutations of the Igbeta gene cause agammaglobulinemia in man.
Ferrari S, Lougaris V, Caraffi S, Zuntini R, Yang J, Soresina A, Meini A, Cazzola G, Rossi C, Reth M, Plebani A. Ferrari S, et al. Among authors: soresina a. J Exp Med. 2007 Sep 3;204(9):2047-51. doi: 10.1084/jem.20070264. Epub 2007 Aug 20. J Exp Med. 2007. PMID: 17709424 Free PMC article.
Sensorineural hearing loss in primary antibody deficiency disorders.
Berlucchi M, Soresina A, Redaelli De Zinis LO, Valetti L, Valotti R, Lougaris V, Meini A, Salsi D, Nicolai P, Plebani A. Berlucchi M, et al. Among authors: soresina a. J Pediatr. 2008 Aug;153(2):293-6. doi: 10.1016/j.jpeds.2008.03.008. J Pediatr. 2008. PMID: 18639734
X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease.
Booth C, Gilmour KC, Veys P, Gennery AR, Slatter MA, Chapel H, Heath PT, Steward CG, Smith O, O'Meara A, Kerrigan H, Mahlaoui N, Cavazzana-Calvo M, Fischer A, Moshous D, Blanche S, Pachlopnik Schmid J, Latour S, de Saint-Basile G, Albert M, Notheis G, Rieber N, Strahm B, Ritterbusch H, Lankester A, Hartwig NG, Meyts I, Plebani A, Soresina A, Finocchi A, Pignata C, Cirillo E, Bonanomi S, Peters C, Kalwak K, Pasic S, Sedlacek P, Jazbec J, Kanegane H, Nichols KE, Hanson IC, Kapoor N, Haddad E, Cowan M, Choo S, Smart J, Arkwright PD, Gaspar HB. Booth C, et al. Among authors: soresina a. Blood. 2011 Jan 6;117(1):53-62. doi: 10.1182/blood-2010-06-284935. Epub 2010 Oct 6. Blood. 2011. PMID: 20926771 Free PMC article.
124 results