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Publisher: Wiley-Blackwell

Volume 88, Number 4, 1 April 2012

Lenalidomide in multiple myeloma: current experimental and clinical data
pp. 279-291(13)
Authors: Cives, Mauro; Milano, Annalisa; Dammacco, Franco; Silvestris, Franco

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CD68 and CD163 as prognostic factors for Korean patients with Hodgkin lymphoma
pp. 292-305(14)
Authors: Yoon, Dok Hyun; Koh, Young Wha; Kang, Hyo Jeong; Kim, Shin; Park, Chan‐Sik; Lee, Sang‐wook; Suh, Cheolwon; Huh, Jooryung

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Prognostic value of PINI index in patients with multiple myeloma
pp. 306-313(8)
Authors: Dupire, Sophie; Wemeau, Mathieu; Debarri, Houria; Pascal, Laurent; Hivert, Benedicte; Willekens, Christophe; Boyle, Eileen; Manier, Salomon; Béatrice, Thielemans; Onraed, Brigitte; Faucompré, Jean‐Luc; Hennache, Bernadette; Dumontet, Charles; Facon, Thierry; Leleu, Xavier

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Y654 of β‐catenin is essential for FLT3/ITD‐related tyrosine phosphorylation and nuclear localization of β‐catenin
pp. 314-320(7)
Authors: Kajiguchi, Tomohiro; Katsumi, Akira; Tanizaki, Ryohei; Kiyoi, Hitoshi; Naoe, Tomoki

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Clinical bleeding events and laboratory coagulation profiles in acute promyelocytic leukemia
pp. 321-328(8)
Authors: Chang, Hung; Kuo, Ming‐Chung; Shih, Lee‐Yung; Dunn, Po; Wang, Po‐Nan; Wu, Jin‐Hou; Lin, Tung‐Liang; Hung, Yu‐Shin; Tang, Tzung‐Chih

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Hereditary protein C deficiency and thrombosis risk: genotype and phenotype relation in a large Italian family
pp. 336-339(4)
Authors: Cafolla, Arturo; D’Andrea, Giovanna; Baldacci, Erminia; Margaglione, Maurizio; Mazzucconi, Maria Gabriella; Foà, Robin

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Circulating plasmacytoid dendritic cells in patients with primary and Helicobacter pylori‐associated immune thrombocytopenia
pp. 340-349(10)
Authors: Saito, Akio; Yokohama, Akihiko; Osaki, Yohei; Ogawa, Yoshiyuki; Nakahashi, Hirotaka; Toyama, Kohtaro; Mitsui, Takeki; Hashimoto, Yoko; Koiso, Hiromi; Uchiumi, Hideki; Saitoh, Takayuki; Handa, Hiroshi; Sawamura, Morio; Karasawa, Masamitsu; Murakami, Hirokazu; Tsukamoto, Norifumi; Nojima, Yoshihisa

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dRTA and hemolytic anemia: first detailed description of SLC4A1 A858D mutation in homozygous state
pp. 350-355(6)
Authors: Fawaz, Naglaa A.; Beshlawi, Ismail O.; Al Zadjali, Shoaib; Al Ghaithi, Hamed K.; Elnaggari, Mohamed A.; Elnour, Ibtisam; Wali, Yasser A.; Al‐Said, Bushra B.; Rehman, Jalil U.; Pathare, Anil V.; Knox‐Macaulay, Huxley; Alkindi, Salam S.

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A novel α0‐thalassemia deletion in a Greek patient with HbH disease and β‐thalassemia trait
pp. 356-362(7)
Authors: Phylipsen, Marion; Traeger‐Synodinos, Jan; van der Kraan, Martijn; van Delft, Peter; Bakker, Greet; Geerts, Mariska; Kanavakis, Emmanuel; Stamoulakatou, Alexandra; Karagiorga, Markissia; Giordano, Piero C.; Harteveld, Cornelis L.

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Recurrent ischemic colitis in a young female with the prothrombin G20210A mutation
pp. 367-368(2)
Authors: Albert, Nicole E.; Rudolph, David S.; Zitin, Marc A.; Mezey, Alan

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Plasmacytoma of the skull
pp. 369-369(1)
Authors: Gozzetti, Alessandro; Cerase, Alfonso; Defina, Marzia; Bocchia, Monica

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Association of homozygous sickle cell anemia and glucose‐6‐phosphate dehydrogenase deficiency
pp. 370-370(1)
Authors: Lesesve, Jean‐François; Perrin, Julien

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