Isolated Congenital Asplenia (ICA) and Mutations in RPSA
Author:
Murguia-Favela Luis
Publisher
Springer New York
Reference11 articles.
1. Ahmed SA, Zengeya S, Kini U, Pollard AJ. Familial isolated congenital asplenia: case report and literature review. Eur J Pediatr. 2010;169:315–8. 2. Almoznino-Sarafian D, Dotan E, Sandbank J, Gorelik O, Chachashvily S, Shteinshnaider M, Cohen N. Unusual manifestations of myelofibrosis in a patient with congenital asplenia. Acta Haematol. 2007;118(4):226–30. 3. Ben-Shem A, Garreau de Loubresse N, Melnikov S, Jenner L, Yusupova G, Yusupov M. The structure of the eukaryotic ribosome at 3.0 Å resolution. Science. 2011;334(6062):1524–9. 4. Bolze A, Mahlaoui N, Bruyn M, Turner B, Trede N, Elis S, Abhyankar A, Itan Y, Patin E, Brebner S, Sackstein P, Puel A, Picard C, Abel L, Quintana-Murci L, Faust SN, Williams AP, Baretto R, Duddridge M, Kini U, Pollard AJ, Gaud C, Frange P, Orbach D, Emile JF, Stephan JL, Sorensen R, Plebani A, Hammarstrom L, Conley ME, Selleri L, Casanova JL. Ribosomal protein SA haploinsufficiency in humans with isolated congenital Asplenia. Science. 2013;340:96–978. 5. Imashuku S, Kudo N, Kubo K, Takahashi N, Tohyama K. Persistent thrombocytosis in elderly patients with rare hyposplenias that mimic essential thrombocythemia. Int J Hematol. 2012;95(6):702–5.
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