Výsledky vyhledávání - "Wafa Abdulsamad"

Akademický článek

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

Autor: Al-achkar Walid, Wafa Abdulsamad, Moassass Faten, Othman Moneeb Abdullah

Publikováno v: Molecular Cytogenetics, Vol 5, Iss 1, p 36 (2012)

Abstract Background The so-called Philadelphia (Ph) chromosome is present in more than 90% of chronic myeloid leukemia (CML) cases. It results in juxtaposition of the 5′ part of the BCR gene on chromosome 22 to the 3′ part of the ABL gene on chro

Externí odkaz: https://doaj.org/article/313a672aaa584d798c9890ba76f0582d

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Akademický článek

Biclonal myelodysplastic syndrome involving six chromosomes and monoallelic loss of RB1 - A rare case

Autor: Klein Elisabeth, Wafa Abdulsamad, Al-Achkar Walid, Aljapawe Abdulmunim

Publikováno v: Molecular Cytogenetics, Vol 4, Iss 1, p 16 (2011)

Abstract Background Myelodysplastic syndrome (MDS) represents a group of clonal hematological disorders characterized by progressive cytopenia, and reflects to defects in erythroid, myeloid and megakaryocytic maturation. MDS is more frequently observ

Externí odkaz: https://doaj.org/article/233420ea0e48443f9080afd66576b97e

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Akademický článek

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

Autor: Moassass Faten, Wafa Abdulsamad, Al Achkar Walid, Liehr Thomas

Publikováno v: Molecular Cytogenetics, Vol 3, Iss 1, p 18 (2010)

Abstract Background Partial trisomy of the short arm of chromosome 9 is among the most common autosomal structural chromosomal anomalies leading to chromosomal imbalance in human. Clinical characteristics are craniofacial dysmorphism including hypert

Externí odkaz: https://doaj.org/article/c330b71b46144cbc9480b0bb409c19dc

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Akademický článek

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

Autor: Mkrtchyan Hasmik, Wafa Abdulsamad, Al Achkar Walid, Moassass Faten, Liehr Thomas

Publikováno v: Molecular Cytogenetics, Vol 3, Iss 1, p 6 (2010)

Abstract Background The so-called Philadelphia (Ph) chromosome is present in almost all cases with chronic myeloid leukemia (CML). Around 5-10% of these patients show complex translocations involving other chromosomes in addition to and/or besides ch

Externí odkaz: https://doaj.org/article/7eef2e488e23403c870fd0584d99cd50

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Akademický článek

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

Autor: Moassass Faten, Mkrtchyan Hasmik, Wafa Abdulsamad, Al Achkar Walid, Liehr Thomas

Publikováno v: Molecular Cytogenetics, Vol 2, Iss 1, p 21 (2009)

Abstract Background The well-known typical fusion gene BCR/ABL can be observed in connection with a complex translocation event in only 2-10% of cases with chronic myeloid leukemia (CML). As currently most CML cases are treated with Imatinib, variant

Externí odkaz: https://doaj.org/article/ceba7ce6515b4ce78cccbba87cb65230

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