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Natural history of Ras-associated autoimmune leukoproliferative disorder: A 20-year follow-up of a NRAS-mutated patient excluding a malignant progression.
Rivalta B, Attardi E, Cifaldi C, Rosti V, Pacillo L, Hajrullaj H, Di Cesare S, Amodio D, Algeri M, Luciani M, Barzaghi F, Finocchi A, Di Matteo G, Aiuti A, Locatelli F, Voso MT, Palumbo G, Cancrini C. Rivalta B, et al. Among authors: cancrini c. Br J Haematol. 2024 Jan;204(1):e6-e10. doi: 10.1111/bjh.19150. Epub 2023 Nov 3. Br J Haematol. 2024. PMID: 37921255 No abstract available.
[Perinatal infections of B19 Parvoviruses].
Di Domenico C, Moschese V, Chini L, Zirletta E, Cancrini C, Di Paolo A, Rossi P, Scalamandrè A. Di Domenico C, et al. Among authors: cancrini c. Ig Sanita Pubbl. 2002 May-Jun;LVIII(3):155-162. Ig Sanita Pubbl. 2002. PMID: 12616272 Italian.
Pediatric renal transplantation: personal experience.
Berloco P, Pretagostini R, Poli L, Rossi M, Iappelli M, Di Nicuolo A, Venettoni S, De Simone P, Cancrini C, Novelli G, Alfani D, Cortesini R, Lubrano R, Castello MA. Berloco P, et al. Among authors: cancrini c. Transplant Proc. 1996 Feb;28(1):282-3. Transplant Proc. 1996. PMID: 8644225 No abstract available.
Role of immunity in maternal-infant HIV-1 transmission.
Jansson M, Orlandi P, Scarlatti G, Moschese V, Romiti ML, Cancrini C, Mancia L, Livadiotti S, Castelli-Gattinara G, Rossi P, Halapi E. Jansson M, et al. Among authors: cancrini c. Acta Paediatr Suppl. 1997 Jun;421:39-45. doi: 10.1111/j.1651-2227.1997.tb18318.x. Acta Paediatr Suppl. 1997. PMID: 9240856 Review.
Schimke immunoosseous dysplasia: suggestions of genetic diversity.
Clewing JM, Fryssira H, Goodman D, Smithson SF, Sloan EA, Lou S, Huang Y, Choi K, Lücke T, Alpay H, André JL, Asakura Y, Biebuyck-Gouge N, Bogdanovic R, Bonneau D, Cancrini C, Cochat P, Cockfield S, Collard L, Cordeiro I, Cormier-Daire V, Cransberg K, Cutka K, Deschenes G, Ehrich JH, Fründ S, Georgaki H, Guillen-Navarro E, Hinkelmann B, Kanariou M, Kasap B, Kilic SS, Lama G, Lamfers P, Loirat C, Majore S, Milford D, Morin D, Ozdemir N, Pontz BF, Proesmans W, Psoni S, Reichenbach H, Reif S, Rusu C, Saraiva JM, Sakallioglu O, Schmidt B, Shoemaker L, Sigaudy S, Smith G, Sotsiou F, Stajic N, Stein A, Stray-Pedersen A, Taha D, Taque S, Tizard J, Tsimaratos M, Wong NA, Boerkoel CF. Clewing JM, et al. Among authors: cancrini c. Hum Mutat. 2007 Mar;28(3):273-83. doi: 10.1002/humu.20432. Hum Mutat. 2007. PMID: 17089404
Intergenerational and intrafamilial phenotypic variability in 22q11.2 deletion syndrome subjects.
Cirillo E, Giardino G, Gallo V, Puliafito P, Azzari C, Bacchetta R, Cardinale F, Cicalese MP, Consolini R, Martino S, Martire B, Molinatto C, Plebani A, Scarano G, Soresina A, Cancrini C, Rossi P, Digilio MC, Pignata C. Cirillo E, et al. Among authors: cancrini c. BMC Med Genet. 2014 Jan 2;15:1. doi: 10.1186/1471-2350-15-1. BMC Med Genet. 2014. PMID: 24383682 Free PMC article.
168 results