Literature DB >> 18596743

Simultaneous occurrence of acute myeloid leukaemia with mutated nucleophosmin (NPM1) in the same family.

G Cazzaniga, L Lo Nigro, I Cifola, G Milone, S Schnittger, T Haferlach, E Mirabile, F Costantino, M P Martelli, E Mastrodicasa, F Di Raimondo, F Aversa, A Biondi, B Falini.   

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Year:  2008        PMID： 18596743     DOI： 10.1038/leu.2008.170

Source DB:  PubMed          Journal:  Leukemia        ISSN： 0887-6924            Impact factor:   11.528


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  4 in total

Review 1.  Familial leukemias.

Authors:  Peter H Wiernik
Journal:  Curr Treat Options Oncol       Date:  2015-02

2.  Examination of the FLT3 and NPM1 mutational status in patients with acute myeloid leukemia from southeastern Poland.

Authors:  Dorota Koczkodaj; Szymon Zmorzyński; Małgorzata Michalak-Wojnowska; Ewa Wąsik-Szczepanek; Agata A Filip
Journal:  Arch Med Sci       Date:  2016-02-02       Impact factor: 3.318

3.  [Investigation and clinical analysis of a family with germline CEBPA mutations in acute myeloid leukemia].

Authors:  J P Zhang; D Lin; S C Wang; Y Li; Y M Chen; Y Wang; H Wei; Y C Mi; J X Wang
Journal:  Zhonghua Xue Ye Xue Za Zhi       Date:  2020-12-14

4.  Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism.

Authors:  Maria Carla Proverbio; Eleonora Mangano; Alessandra Gessi; Roberta Bordoni; Roberta Spinelli; Rosanna Asselta; Paola Sogno Valin; Stefania Di Candia; Ilaria Zamproni; Cecilia Diceglie; Stefano Mora; Manuela Caruso-Nicoletti; Alessandro Salvatoni; Gianluca De Bellis; Cristina Battaglia
Journal:  PLoS One       Date:  2013-07-15       Impact factor: 3.240
  4 in total

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