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Page 1
Clonally unrelated Richter syndrome are truly de novo diffuse large B-cell lymphomas with a mutational profile reminiscent of clonally related Richter syndrome.
Favini C, Talotta D, Almasri M, Andorno A, Rasi S, Adhinaveni R, Kogila S, Awikeh B, Schipani M, Boggione P, Mouhssine S, Ghanej J, Al Essa W, Mahmoud AM, Dondolin R, Alessa N, Margiotta Casaluci G, Boldorini R, Gattei V, Gaidano G, Moia R. Favini C, et al. Among authors: almasri m. Br J Haematol. 2022 Sep;198(6):1016-1022. doi: 10.1111/bjh.18352. Epub 2022 Jul 13. Br J Haematol. 2022. PMID: 35829664 Free PMC article.
XPO1 mutations identify early-stage CLL characterized by shorter time to first treatment and enhanced BCR signalling.
Moia R, Terzi di Bergamo L, Talotta D, Bomben R, Forestieri G, Spina V, Bruscaggin A, Cosentino C, Almasri M, Dondolin R, Bittolo T, Zucchetto A, Baldoni S, Del Giudice I, Mauro FR, Maffei R, Chiarenza A, Tafuri A, Laureana R, Del Principe MI, Zaja F, D'Arena G, Olivieri J, Rasi S, Mahmoud A, Al Essa W, Awikeh B, Kogila S, Bellia M, Mouhssine S, Sportoletti P, Marasca R, Scarfò L, Ghia P, Gattei V, Foà R, Rossi D, Gaidano G. Moia R, et al. Among authors: almasri m. Br J Haematol. 2023 Nov;203(3):416-425. doi: 10.1111/bjh.19052. Epub 2023 Aug 14. Br J Haematol. 2023. PMID: 37580908
Immunoglobulin light chain mutational status refines IGHV prognostic value in identifying chronic lymphocytic leukemia patients with early treatment requirement.
Nabki J, Al Deeban B, Sium AM, Cosentino C, Almasri M, Awikeh B, Maher N, Bellia M, Dondolin R, Mouhssine S, Talotta D, Secomandi E, Kogila S, Ghanej J, Maiellaro F, Cividini L, Rasi S, Chiarenza A, Olivieri J, Gentile M, Zaja F, Del Principe MI, Laurenti L, Bomben R, Vit F, Bittolo T, Zucchetto A, Gattei V, Gaidano G, Moia R. Nabki J, et al. Among authors: almasri m. Leukemia. 2024 Dec 17. doi: 10.1038/s41375-024-02499-x. Online ahead of print. Leukemia. 2024. PMID: 39690182
Molecular clustering on ctDNA improves the prognostic stratification of DLBCL patients compared to ctDNA levels.
Moia R, Talotta D, Terzi di Bergamo L, Almasri M, Dondolin R, Salehi M, Cosentino C, Soscia R, Della Starza I, Bruscaggin A, Andorno AG, Mercalli F, Cresta S, Bomben R, Bittolo T, Vit F, Bulian P, Zucchetto A, Bruna R, Rivolta GM, Schipani M, Secomandi E, Kogila S, Bellia M, Mouhssine S, Nabki J, Al Deeban B, Ghanej J, Cividini L, Maher N, Melle F, Motta G, Leutner M, Lorenzi A, Mahmoud AM, Al Essa W, Deambrog C, Rasi S, Petrucci L, Boldorini R, Di Rocco A, Del Giudice I, Spina M, Palazzolo S, Canal F, Canzonieri V, Martelli M, Pileri SA Professor, Gattei V, Foà R, Rossi D, Gaidano G. Moia R, et al. Among authors: almasri m. Blood Adv. 2025 Jan 18:bloodadvances.2024014136. doi: 10.1182/bloodadvances.2024014136. Online ahead of print. Blood Adv. 2025. PMID: 39825831
Congenital heart defects and consanguinity: An analysis of the Sidra cardiac registry data in Qatar.
Manyama M, Al Sayegh D, Al-Sulaiti K, Almasri M, Sharma O, El Jerbi A, Al-Riyami Z, Sarada PK, Gupta S, Al-Saloos H, Al-Shafai KN. Manyama M, et al. Among authors: almasri m. Int J Cardiol Congenit Heart Dis. 2024 Jul 20;17:100529. doi: 10.1016/j.ijcchd.2024.100529. eCollection 2024 Sep. Int J Cardiol Congenit Heart Dis. 2024. PMID: 39711761 Free PMC article. No abstract available.
277 results