Partial trisomy 9p22 to 9p24.2 in combination with partial monosomy 9pter in a Syrian girl

por Al Achkar, Walid, Wafa, Abdulsamad, Moassass, Faten, Liehr, Thomas
Publicado 2010

Novel complex translocation involving 5 different chromosomes in a chronic myeloid leukemia with Philadelphia chromosome: a case report

por Al Achkar, Walid, Wafa, Abdulsamad, Mkrtchyan, Hasmik, Moassass, Faten, Liehr, Thomas
Publicado 2009

A rare case of chronic myeloid leukemia with secondary chromosomal changes including partial trisomy 17q21 to 17qter and partial monosomy of 16p13.3

por Al Achkar, Walid, Wafa, Abdulsamad, Mkrtchyan, Hasmik, Moassass, Faten, Liehr, Thomas
Publicado 2010

A novel dic (17;18) (p13.1;q11.2) with loss of TP53 and BCR/ABL rearrangement in an Imatinib resistant chronic myeloid leukemia

por Al-achkar, Walid, Wafa, Abdulsamad, Moassass, Faten, Othman, Moneeb Abdullah Kassem
Publicado 2012

Multiple copies of BCR-ABL fusion gene on two isodicentric Philadelphia chromosomes in an imatinib mesylate-resistant chronic myeloid leukemia patient

por AL-ACHKAR, WALID, WAFA, ABDULSAMAD, MOASSASS, FATEN, KLEIN, ELISABETH, LIEHR, THOMAS
Publicado 2013

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

por Wafa, Abdulsamad, Moassass, Faten, Liehr, Thomas, Al-Ablog, Ayman, Al-Achkar, Walid
Publicado 2016

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

por Moassass, Faten, Wafa, Abdulsamad, Liehr, Thomas, Al-Ablog, Ayman, AL Achkar, Walid
Publicado 2018

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-c...

por Wafa, Abdulsamad, Moassass, Faten, Liehr, Thomas, Bhatt, Samarth, Aljapawe, Abdulmunim, Al Achkar, Walid
Publicado 2016

Two Novel Mutations of the NPM1 Gene in Syrian Adult Patients with Acute Myeloid Leukemia and Normal Karyotype

por Alarbeed, Ismael F., Wafa, Abdulsamad, Moassass, Faten, Al-Halabi, Balssel, Alachkar, Walid, Aboukhamis, Imad
Publicado 2021

An adult B-cell precursor acute lymphoblastic leukemia with multiple secondary cytogenetic aberrations

por AL-Achkar, Walid, Wafa, Abdulsamad, Othman, Moneeb Abdullah Kassem, Moassass, Faten, Aljapawe, Abdulmunim, Liehr, Thomas
Publicado 2014

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

por Al-Achkar, Walid, Moassass, Faten, Ikhtiar, Adnan, Liehr, Thomas, Othman, Moneeb Abdullah Kassem, Wafa, Abdulsamad
Publicado 2014

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

por Moualla, Yahia, Moassass, Faten, AL-Halabi, Bassel, Al-Achkar, Walid, Georgeos, Michael, Yazigi, Haissam, Khamis, Atieh
Publicado 2022

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

por Moualla, Yahia, Moassass, Faten, AL-Halabi, Bassel, Al-achkar, Walid, Georgeos, Michael, Yazigi, Haissam, Khamis, Atieh
Publicado 2022

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

por Alarbeed, Ismael F., Wafa, Abdulsamad, Moassass, Faten, Al-Halabi, Bassel, Al-Achkar, Walid, Liehr, Thomas, Aboukhamis, Imad
Publicado 2021

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

por Al-Arbeed, Ismael F, Wafa, Abdulsamad, Moassass, Faten, AL-Halabi, Bassel, Al-Achkar, Walid, Abou-Khamis, Imad
Publicado 2021

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

por Wafa, Abdulsamad, Ali, Belal, Moassass, Faten, Kheder, Maged, Aljapawe, Abdulmunim, Al‐Halabi, Bassel, Mrasek, Kristin, Liehr, Thomas, Al‐Achkar, Walid
Publicado 2022