We present a case report of a patient with acute myeloid leukemia (AML) characterized by the simultaneous presence of nucleophosmin 1 (NPM1) mutation and the breakpoint cluster region-Abelson (BCR-ABL) fusion oncogene. Our findings emphasize the importance of routinely including BCR-ABL in the diagnostic workup of AML in order to offer to the patients the most appropriate risk category and treatment options
textabstractMutations in nucleophosmin NPM1 are the most frequent acquired molecular abnormalities i...
Abstract Background Philadelphia (Ph) chromosome results from the reciprocal translocation t(9;22)(q...
Mutations of the nucleophosmin gene (NPM1), in the absence of concurrent FLT3-internal tandem duplic...
We present a case report of a patient with acute myeloid leukemia (AML) characterized by the simulta...
Breakpoint cluster region - Abelson (BCR-ABL1) chimeric protein and mutated Nucleophosmin (NPM1) are...
Background: Philadelphia (Ph) chromosome results from the reciprocal translocation t(9;22)(q34.1;q11...
Acute myeloid leukemia carrying NPM1 mutations and cytoplasmic nucleophosmin (NPMc(+) acute myeloid ...
AbstractPrognosis of acute myeloid leukemia relies heavily on the cytogenetic and molecular abnormal...
The BCR/ABL1 fusion gene, usually carried by the Philadelphia chromosome (Ph) resulting from t(9;22)...
The 2016 WHO classification defines acute undifferentiated leukemia (AUL) as a rare type of acute le...
Nucleophosmin (NPM1) mutations in acute myeloid leukemia (AML) affect exon 12, but also sporadically...
Mutations of Nucleophosmin (NPM1) are the most common genetic abnormalities in adult acute myeloid l...
Acute myeloid leukemia (AML) with t(9;22)(q34;q11), also known as AML with BCR-ABL1, is a rare, prov...
Acute myeloid leukemia (AML) with t(9;22)(q34;q11), also known as AML with BCR-ABL1, is a rare, prov...
BCR-ABL-positive acute myeloid leukemia (AML) is a rare subtype of AML that is now included as a pro...
textabstractMutations in nucleophosmin NPM1 are the most frequent acquired molecular abnormalities i...
Abstract Background Philadelphia (Ph) chromosome results from the reciprocal translocation t(9;22)(q...
Mutations of the nucleophosmin gene (NPM1), in the absence of concurrent FLT3-internal tandem duplic...
We present a case report of a patient with acute myeloid leukemia (AML) characterized by the simulta...
Breakpoint cluster region - Abelson (BCR-ABL1) chimeric protein and mutated Nucleophosmin (NPM1) are...
Background: Philadelphia (Ph) chromosome results from the reciprocal translocation t(9;22)(q34.1;q11...
Acute myeloid leukemia carrying NPM1 mutations and cytoplasmic nucleophosmin (NPMc(+) acute myeloid ...
AbstractPrognosis of acute myeloid leukemia relies heavily on the cytogenetic and molecular abnormal...
The BCR/ABL1 fusion gene, usually carried by the Philadelphia chromosome (Ph) resulting from t(9;22)...
The 2016 WHO classification defines acute undifferentiated leukemia (AUL) as a rare type of acute le...
Nucleophosmin (NPM1) mutations in acute myeloid leukemia (AML) affect exon 12, but also sporadically...
Mutations of Nucleophosmin (NPM1) are the most common genetic abnormalities in adult acute myeloid l...
Acute myeloid leukemia (AML) with t(9;22)(q34;q11), also known as AML with BCR-ABL1, is a rare, prov...
Acute myeloid leukemia (AML) with t(9;22)(q34;q11), also known as AML with BCR-ABL1, is a rare, prov...
BCR-ABL-positive acute myeloid leukemia (AML) is a rare subtype of AML that is now included as a pro...
textabstractMutations in nucleophosmin NPM1 are the most frequent acquired molecular abnormalities i...
Abstract Background Philadelphia (Ph) chromosome results from the reciprocal translocation t(9;22)(q...
Mutations of the nucleophosmin gene (NPM1), in the absence of concurrent FLT3-internal tandem duplic...