Publications by authors named "Walid Alachkar"

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The Clinical Impact of NPM1 Mutations and the Effect of Concurrent Mutations in Acute Myeloid Leukemia: Unraveling the Prognostic Significance.
Faten Moassass, Yahia Moualla, Bassel Al-Halabi, Atieh Khamis, Walid Al-Achkar

Health Sci Rep· December 2024

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Evaluating the clinical significance of mutation status in Syrian newly diagnosed acute myeloid leukemia patients with normal karyotype.
Yahia Moualla, Faten Moassass, Bassel Al-Halabi, Walid Al-Achkar, Michael Georgeos

Heliyon· November 2022

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Prognostic Relevance of DNMT3A, FLT3 and NPM1 Mutations in Syrian Acute Myeloid Leukemia Patients.
Yahia Moualla, Faten Moassass, Bassel Al-Halbi, Walid Al-Achkar, Michael Georgeos

Asian Pac J Cancer Prev· April 2022

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Acute myeloid leukemia due to germline CEBPA mutation in a Syrian family.
Abdulsamad Wafa, Belal Ali, Faten Moassass, Maged Kheder, Abdulmunim Aljapawe

Mol Genet Genomic Med· February 2022

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Frequency of FLT3 Internal Tandem Duplications in Adult Syrian Patients with Acute Myeloid Leukemia and Normal Karyotype.
Ismael F Al-Arbeed, Abdulsamad Wafa, Faten Moassass, Bassel Al-Halabi, Walid Al-Achkar

Asian Pac J Cancer Prev· October 2021

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De novo adult acute myeloid leukemia with two new mutations in juxtatransmembrane domain of the FLT3 gene: a case report.
Ismael F Alarbeed, Abdulsamad Wafa, Faten Moassass, Bassel Al-Halabi, Walid Al-Achkar

J Med Case Rep· January 2021

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Two Novel Mutations of the NPM1 Gene in Syrian Adult Patients with Acute Myeloid Leukemia and Normal Karyotype.
Ismael F Alarbeed, Abdulsamad Wafa, Faten Moassass, Bassel Al-Halabi, Walid Alachkar

Asian Pac J Cancer Prev· January 2021

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A new childhood ALL case with an extremely complex karyotype and acute spontaneous tumor lysis syndrome.
Abdulsamad Wafa, Rami A Jarjour, Doaa Alolabi, Thomas Liehr, Othman Hamdan

Mol Cytogenet· September 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.
Abdulsamad Wafa, Rami A Jarjour, Abdulmunim Aljapawe, Suher ALmedania, Thomas Liehr

Mol Cytogenet· July 2020

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Bloom syndrome with myelodysplastic syndrome that was converted into acute myeloid leukaemia, with new ophthalmologic manifestations: the first report from Syria.
Sara Aljarad, Ahmad Alhamid, Ahmad Rami Rahmeh, Abdelaziz Alibraheem, Abdulsamad Wafa, Walid Alachkar

Oxf Med Case Reports· December 2018

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Geographical distribution of β-globin gene mutations in Syria.
Hossam Murad, Faten Moasses, Amir Dabboul, Yasser Mukhalalaty, Ahmad Omar Bakoor

Hematology· October 2018

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Investigation of the mtDNA mutations in Syrian families with non-syndromic sensorineural hearing loss.
Faten Moassass, Bassel Al-Halabi, Mohamad Sayah Nweder, Walid Al-Achkar

Int J Pediatr Otorhinolaryngol· October 2018

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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.
Abdulsamad Wafa, Suher ALmedania, Abdulmunim Aljapawe, Thomas Liehr, Soulaiman E Soulaiman, Walid ALachkar

BMC Hematol· August 2018

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De novo Balanced Robertsonian Translocation rob(22;22)(q10;q10) in a Woman with Recurrent Pregnancy Loss: A Rare Case.
Nawras Alhalabi, Walid Al-Achkar, Abdulsamad Wafa, Mazen Kenj, Marwan Alhalabi

J Reprod Infertil· January 2018

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Association of Methylenetetrahydrofolate Reductase C677T and A1298C Gene Polymorphisms With Recurrent Pregnancy Loss in Syrian Women.
Walid Al-Achkar, Abdulsamad Wafa, Samer Ammar, Faten Moassass, Rami A Jarjour

Reprod Sci· September 2017

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First report of prevalence c.IVS1+1G>A and del (GJB6-13S1854) mutations in Syrian families with non-syndromic sensorineural hearing loss.
Walid Al-Achkar, Bassel Al-Halabi, Bashar Ali, Faten Moassass

Int J Pediatr Otorhinolaryngol· January 2017

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Correlation of p210 BCR-ABL transcript variants with clinical, parameters and disease outcome in 45 chronic myeloid leukemia patients.
Walid Al-Achkar, Faten Moassass, Nagham Youssef, Abdulsamad Wafa

J BUON· July 2016

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Acute promyelocytic leukemia with the translocation t(15;17)(q22;q21) associated with t(1;2)(q42~43;q11.2~12): a case report.
Abdulsamad Wafa, Faten Moassass, Thomas Liehr, Ayman Al-Ablog, Walid Al-Achkar

J Med Case Rep· July 2016

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Masked inv dup(22)(q11.23), tetrasomy 8 and trisomy 19 in a blast crisis-chronic myeloid leukemia after interrupted Imatinib-treatment.
Abdulsamad Wafa, Suher Almedani, Thomas Liehr, Walid Al-Achkar

Mol Cytogenet· December 2015

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Deletion 9p23 to 9p11.1 as sole additional abnormality in a Philadelphia positive chronic myeloid leukemia in blast crisis: a rare event.
Abdulsamad Wafa, Manar Asa'ad, Adnan Ikhtiar, Thomas Liehr, Walid Al-Achkar

Mol Cytogenet· August 2015

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Prenatal molecular diagnosis of β-thalassemia and sickle cell anemia in the Syrian population.
Hossam Murad, Faten Moassas, Rami Jarjour, Yasser Mukhalalaty, Walid Al-Achkar

Hemoglobin· July 2015

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Molecular update of β-thalassemia mutations in the Syrian population: identification of rare β-thalassemia mutations.
Rami A Jarjour, Hossam Murad, Faten Moasses, Walid Al-Achkar

Hemoglobin· March 2015

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Chromosomal aberration leads to recurrent pregnancy loss and partial trisomy of 5p12-15.3 in the offspring: report of a Syrian couple and review of the literature .
Walid Al-Achkar, Faten Moassass, Ayman Al-Ablog, Thomas Liehr, Xiaobo Fan

Zhonghua Nan Ke Xue· March 2015

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Hyperdiploidy associated with T315I mutation in BCR-ABL kinase domain in an accelerated phase-chronic myeloid leukemia case.
Walid Al-Achkar, Faten Moassass, Adnan Ikhtiar, Thomas Liehr, Moneeb Abdullah Kassem Othman

Mol Cytogenet· January 2015

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An adult B-cell precursor acute lymphoblastic leukemia with multiple secondary cytogenetic aberrations.
Walid Al-Achkar, Abdulsamad Wafa, Moneeb Abdullah Kassem Othman, Faten Moassass, Abdulmunim Aljapawe

Mol Cytogenet· September 2014

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