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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Prognostic Relevance of DNMT3A, FLT3 and NPM1 Mutations in Syrian Acute Myeloid Leukemia Patients
Moualla, Yahia, Moassass, Faten, Al-Halbi, Bassel, Al-Achkar, Walid, Georgeos, Michael, Yazigi, Haissam, Khamis, Atieh
Published in Asian Pacific journal of cancer prevention : APJCP (01.04.2022)
Published in Asian Pacific journal of cancer prevention : APJCP (01.04.2022)
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Mitochondrial genomes from modern horses reveal the major haplogroups that underwent domestication
Achilli, Alessandro, Olivieri, Anna, Soares, Pedro, Lancioni, Hovirag, Kashani, Baharak Hooshiar, Perego, Ugo A, Nergadze, Solomon G, Carossa, Valeria, Santagostino, Marco, Capomaccio, Stefano, Felicetti, Michela, Al-Achkar, Walid, Penedo, M. Cecilia T, Verini-Supplizi, Andrea, Houshmand, Massoud, Woodward, Scott R, Semino, Ornella, Silvestrelli, Maurizio, Giulotto, Elena, Pereira, Luísa, Bandelt, Hans-Jürgen, Torroni, Antonio
Published in Proceedings of the National Academy of Sciences - PNAS (14.02.2012)
Published in Proceedings of the National Academy of Sciences - PNAS (14.02.2012)
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Evaluating the clinical significance of FLT3 mutation status in Syrian newly diagnosed acute myeloid leukemia patients with normal karyotype
Moualla, Yahia, Moassass, Faten, AL-Halabi, Bassel, Al-achkar, Walid, Georgeos, Michael, Yazigi, Haissam, Khamis, Atieh
Published in Heliyon (01.11.2022)
Published in Heliyon (01.11.2022)
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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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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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A novel heterozygous variant in exon 32 of the CHD7 gene (c.6923C>T) in a Syrian family with Kallmann syndrome
Wafa, Abdulsamad, Moassass, Faten, Almedani, Suher, Liehr, Thomas, Wilhelm, Kathleen, As'sad, Manar, Knippenberg, Sarah, Glaubitz, Ralf, Jarjour, Rami A., Achkar, Walid Al
Published in Research Results in Biomedicine (30.06.2020)
Published in Research Results in Biomedicine (30.06.2020)
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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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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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De novo acute myeloid leukemia subtype-M4 with initial trisomy 8 and later acquired t(3;12)(q26;p12) leading to ETV6/MDS1/EVI1 fusion transcript expression: A case report
ACHKAR, WALID AL, ALJAPAWE, ABDULMUNIM, LIEHR, THOMAS, WAFA, ABDULSAMAD
Published in Oncology letters (01.03.2014)
Published in Oncology letters (01.03.2014)
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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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A rare chronic myeloid leukemia case with Philadelphia chromosome, BCR-ABL e13a3 transcript and complex translocation involving four different chromosomes
ACHKAR, WALID AL, WAFA, ABDULSAMAD, ALI, BASHAR YOUSEF, MANVELYAN, MARINA, LIEHR, THOMAS
Published in Oncology letters (01.09.2010)
Published in Oncology letters (01.09.2010)
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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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Acquired del(9)(p22.3) in a primary plasma cell leukemia
Achkar, Walid Al, Wafa, Abdulsamad, Aljapawe, Abdulmunim, Othman, Moneeb Ak, Alhourani, Eyad, Liehr, Thomas
Published in Molecular cytogenetics (28.08.2013)
Published in Molecular cytogenetics (28.08.2013)
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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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A unique complex translocation involving six different chromosomes in a case of childhood acute lymphoblastic leukemia with the Philadelphia chromosome and adverse prognosis
ACHKAR, WALID AL, WAFA, ABDULSAMAD, MKRTCHYAN, HASMIK, MOASSASS, FATEN, LIEHR, THOMAS
Published in Oncology letters (01.09.2010)
Published in Oncology letters (01.09.2010)
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