De novo adult acute myeloid leukemia with two new mutations in juxtatransmembrane domain of the FLT3 gene: a case report
Alarbeed, Ismael F, Wafa, Abdulsamad, Moassass, Faten, Al-Halabi, Bassel, Al-Achkar, Walid, Liehr, Thomas, Aboukhamis, Imad
Published in Journal of medical case reports (26.01.2021)
Published in Journal of medical case reports (26.01.2021)
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Journal Article
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
Wafa, Abdulsamad, Moassass, Faten, Liehr, Thomas, Bhatt, Samarth, Aljapawe, Abdulmunim, Al Achkar, Walid
Published in Molecular cytogenetics (20.12.2016)
Published in Molecular cytogenetics (20.12.2016)
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Journal Article
Acute myeloid leukemia due to germline CEBPA mutation in a Syrian family
Wafa, Abdulsamad, Ali, Belal, Moassass, Faten, Kheder, Maged, Aljapawe, Abdulmunim, Al‐Halabi, Bassel, Mrasek, Kristin, Liehr, Thomas, Al‐Achkar, Walid
Published in Molecular genetics & genomic medicine (01.02.2022)
Published in Molecular genetics & genomic medicine (01.02.2022)
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Journal Article
Down syndrome associated childhood myeloid leukemia with yet unreported acquired chromosomal abnormalities and a new potential adverse marker: dup(1)(q25q44)
Moassass, Faten, Wafa, Abdulsamad, Liehr, Thomas, Al-Ablog, Ayman, Al Achkar, Walid
Published in Molecular cytogenetics (13.03.2018)
Published in Molecular cytogenetics (13.03.2018)
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Journal Article
An acquired stable variant of a dicentric dic(9;20) and complex karyotype in a Syrian childhood B-acute lymphoblastic leukemia case
Wafa, Abdulsamad, Jarjour, Rami A, Aljapawe, Abdulmunim, ALmedania, Suher, Liehr, Thomas, Melo, Joana B, Carreira, Isabel M, Othman, Moneeb A K, Al-Achkar, Walid
Published in Molecular cytogenetics (10.07.2020)
Published in Molecular cytogenetics (10.07.2020)
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Journal Article
A new childhood ALL case with an extremely complex karyotype and acute spontaneous tumor lysis syndrome
Wafa, Abdulsamad, Jarjour, Rami A, Alolabi, Doaa, Liehr, Thomas, Hamdan, Othman, Melo, Joana B, Carreira, Isabel M, Othman, Moneeb A K, Al-Achkar, Walid
Published in Molecular cytogenetics (11.09.2020)
Published in Molecular cytogenetics (11.09.2020)
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Journal Article
Childhood pre-B cell acute lymphoblastic leukemia with translocation t(1;19)(q21.1;p13.3) and two additional chromosomal aberrations involving chromosomes 1, 6, and 13: a case report
Wafa, Abdulsamad, As'sad, Manar, Liehr, Thomas, Aljapawe, Abdulmunim, Al Achkar, Walid
Published in Journal of medical case reports (07.04.2017)
Published in Journal of medical case reports (07.04.2017)
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Journal Article
A new adult AML case with an extremely complex karyotype, remission and relapse combined with high hyperdiploidy of a normal chromosome set in secondary AML
Wafa, Abdulsamad, ALmedania, Suher, Aljapawe, Abdulmunim, Liehr, Thomas, Soulaiman, Soulaiman E, Mouna, Raja, Othman, Moneeb A K, ALachkar, Walid
Published in BMC blood disorders (31.08.2018)
Published in BMC blood disorders (31.08.2018)
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Journal Article
Partial trisomy 9p22 to 9p24.2 in combination with partial monosomy 9pter in a Syrian girl
Al Achkar, Walid, Wafa, Abdulsamad, Moassass, Faten, Liehr, Thomas
Published in Molecular cytogenetics (04.10.2010)
Published in Molecular cytogenetics (04.10.2010)
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Journal Article
Novel complex translocation involving 5 different chromosomes in a chronic myeloid leukemia with Philadelphia chromosome: a case report
Al Achkar, Walid, Wafa, Abdulsamad, Mkrtchyan, Hasmik, Moassass, Faten, Liehr, Thomas
Published in Molecular cytogenetics (09.11.2009)
Published in Molecular cytogenetics (09.11.2009)
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Journal Article
A rare case of chronic myeloid leukemia with secondary chromosomal changes including partial trisomy 17q21 to 17qter and partial monosomy of 16p13.3
Al Achkar, Walid, Wafa, Abdulsamad, Mkrtchyan, Hasmik, Moassass, Faten, Liehr, Thomas
Published in Molecular cytogenetics (16.03.2010)
Published in Molecular cytogenetics (16.03.2010)
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Journal Article
Association of Methylenetetrahydrofolate Reductase C677T and A1298C Gene Polymorphisms With Recurrent Pregnancy Loss in Syrian Women
Al-Achkar, Walid, Wafa, Abdulsamad, Ammar, Samer, Moassass, Faten, Jarjour, Rami A.
Published in Reproductive sciences (Thousand Oaks, Calif.) (01.09.2017)
Published in Reproductive sciences (Thousand Oaks, Calif.) (01.09.2017)
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Journal Article
Frequency of FLT3 Internal Tandem Duplications in Adult Syrian Patients with Acute Myeloid Leukemia and Normal Karyotype
Al-Arbeed, Ismael F, Wafa, Abdulsamad, Moassass, Faten, Al-Halabi, Bassel, Al-Achkar, Walid, Abou-Khamis, Imad
Published in Asian Pacific journal of cancer prevention : APJCP (01.10.2021)
Published in Asian Pacific journal of cancer prevention : APJCP (01.10.2021)
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