Moassass相关文献与解析，生知库 | 链接生命科学的每一步

日期影响因子

The Clinical Impact of NPM1 Mutations and the Effect of Concurrent Mutations in Acute Myeloid Leukemia: Unraveling the Prognostic Significance

NPM1 突变的临床影响及伴随突变对急性髓系白血病的影响：揭示其预后意义

期刊:Health Science Reports

影响因子:2.1

doi:10.1002/hsr2.70231

Moassass, Faten; Moualla, Yahia; Al-Halabi, Bassel; Khamis, Atieh; Al-Achkar, Walid

发表日期：2024

文献求助收藏

Evaluating the clinical significance of FLT3 mutation status in Syrian newly diagnosed acute myeloid leukemia patients with normal karyotype

评估FLT3突变状态在叙利亚新诊断的、核型正常的急性髓系白血病患者中的临床意义

影响因子:3.6

doi:10.1016/j.heliyon.2022.e11858

Moualla, Yahia; Moassass, Faten; Al-Halabi, Bassel; Al-Achkar, Walid; Georgeos, Michael; Yazigi, Haissam; Khamis, Atieh

发表日期：2022

文献求助收藏

Acute myeloid leukemia due to germline CEBPA mutation in a Syrian family

叙利亚家族中由生殖系CEBPA突变引起的急性髓系白血病

期刊:Molecular Genetics & Genomic Medicine

影响因子:1.6

doi:10.1002/mgg3.1854

Wafa, Abdulsamad; Ali, Belal; Moassass, Faten; Kheder, Maged; Aljapawe, Abdulmunim; Al-Halabi, Bassel; Mrasek, Kristin; Liehr, Thomas; Al-Achkar, Walid

发表日期：2022

文献求助收藏

Prognostic Relevance of DNMT3A, FLT3 and NPM1 Mutations in Syrian Acute Myeloid Leukemia Patients.

DNMT3A、FLT3 和 NPM1 突变在叙利亚急性髓系白血病患者中的预后意义

期刊:Asian Pacific Journal of Cancer Prevention

doi:10.31557/APJCP.2022.23.4.1387

Moualla Yahia, Moassass Faten, Al-Halbi Bassel, Al-Achkar Walid, Georgeos Michael, Yazigi Haissam, Khamis Atieh

发表日期：2022

文献求助收藏

De novo adult acute myeloid leukemia with two new mutations in juxtatransmembrane domain of the FLT3 gene: a case report

一例伴有FLT3基因跨膜区两个新突变的成人原发性急性髓系白血病：病例报告

期刊:Journal of Medical Case Reports

影响因子:0.8

doi:10.1186/s13256-020-02587-3

Alarbeed, Ismael F; Wafa, Abdulsamad; Moassass, Faten; Al-Halabi, Bassel; Al-Achkar, Walid; Liehr, Thomas; Aboukhamis, Imad

发表日期：2021

文献求助收藏

Frequency of FLT3 Internal Tandem Duplications in Adult Syrian Patients with Acute Myeloid Leukemia and Normal Karyotype

叙利亚成年急性髓系白血病患者中FLT3内部串联重复的频率及核型

期刊:Asian Pacific Journal of Cancer Prevention

doi:10.31557/APJCP.2021.22.10.3245

Al-Arbeed, Ismael F; Wafa, Abdulsamad; Moassass, Faten; Al-Halabi, Bassel; Al-Achkar, Walid; Abou-Khamis, Imad

发表日期：2021

文献求助收藏

Down syndrome associated childhood myeloid leukemia with yet unreported acquired chromosomal abnormalities and a new potential adverse marker: dup(1)(q25q44)

唐氏综合征相关儿童髓系白血病伴有尚未报道的获得性染色体异常和新的潜在不良标志物：dup(1)(q25q44)

期刊:Molecular Cytogenetics

影响因子:1.4

doi:10.1186/s13039-018-0370-8

Moassass, Faten; Wafa, Abdulsamad; Liehr, Thomas; Al-Ablog, Ayman; Al Achkar, Walid

发表日期：2018

文献求助收藏

A high complex karyotype involving eleven chromosomes including three novel chromosomal aberrations and monoallelic loss of TP53 in case of follicular lymphoma transformed into B-cell lymphoblastic leukemia

滤泡性淋巴瘤转化为B细胞淋巴母细胞白血病时，存在高度复杂的核型，涉及11条染色体，包括3个新的染色体畸变和TP53单等位基因缺失。

期刊:Molecular Cytogenetics

影响因子:1.4

doi:10.1186/s13039-016-0300-6

Wafa, Abdulsamad; Moassass, Faten; Liehr, Thomas; Bhatt, Samarth; Aljapawe, Abdulmunim; Al Achkar, Walid

细胞生物学

免疫/内分泌

发表日期：2016

文献求助收藏

Acute promyelocytic leukemia with the translocation t(15;17)(q22;q21) associated with t(1;2)(q42~43;q11.2~12): a case report

伴有 t(15;17)(q22;q21) 易位和 t(1;2)(q42~43;q11.2~12) 的急性早幼粒细胞白血病：病例报告

期刊:Journal of Medical Case Reports

影响因子:0.8

doi:10.1186/s13256-016-0982-8

Wafa, Abdulsamad; Moassass, Faten; Liehr, Thomas; Al-Ablog, Ayman; Al-Achkar, Walid

细胞生物学

发表日期：2016

文献求助收藏

Hyperdiploidy associated with T315I mutation in BCR-ABL kinase domain in an accelerated phase-chronic myeloid leukemia case

在加速期慢性粒细胞白血病病例中，BCR-ABL激酶结构域T315I突变相关的超二倍体

期刊:Molecular Cytogenetics

影响因子:1.4

doi:10.1186/s13039-014-0089-0

Al-Achkar, Walid; Moassass, Faten; Ikhtiar, Adnan; Liehr, Thomas; Othman, Moneeb Abdullah Kassem; Wafa, Abdulsamad

细胞生物学

发表日期：2014

文献求助收藏