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Keywords: Next-generation sequencing
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Journal Articles

“The Long Journey of Unexplained Erythrocytosis”: Erythrocytosis due to High-Oxygen Affinity Hemoglobinopathy – Hemoglobin Variant Little Rock (HBB: c.432C>A) – A Report of a Swiss Family and Review of the Literature

Subject Area:
Hematology , Oncology
Camille Perroud, Naomi Porret, Alicia Rovó
Journal: Acta Haematologica
Acta Haematol (2023) 146 (4): 326–330.
https://doi.org/10.1159/000530240
Published Online: 20 March 2023
... and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. 2023 Erythrocytosis Polycythemia High-oxygen affinity hemoglobinopathies Next-generation sequencing Hb Little Rock...
View article titled, “The Long Journey of Unexplained Erythrocytosis”: Erythrocytosis due to High-Oxygen Affinity Hemoglobinopathy – Hemoglobin Variant Little Rock (HBB: c.432C>A) – A Report of a Swiss Family and Review of the Literature
Open the PDF for “The Long Journey of Unexplained Erythrocytosis”: Erythrocytosis due to High-Oxygen Affinity Hemoglobinopathy – Hemoglobin Variant Little Rock (HBB: c.432C>A) – A Report of a Swiss Family and Review of the Literature in another window
Journal Articles

Adult Acute Myeloid Leukemia with the KMT2A- Mixed Lineage Leukemia T10 Fusion: An Analysis of 10 Cases Showed Common Features and Frequent Mutations in the RAS Signaling Pathway

Subject Area:
Hematology , Oncology
Xiaohui Cai, Jinfei Wang, Jingtao Lu, Zhuxia Jia, Meiyu Chen, Jianfang Liu, Xuzhang Lu, Hongying Chao
Journal: Acta Haematologica
Acta Haematol (2022) 145 (2): 144–151.
https://doi.org/10.1159/000518920
Published Online: 22 September 2021
.... The purpose of the present study was to evaluate KMT2A-MLLT10 AML cases with a next-generation sequencing (NGS)-based mutation panel to assess for patterns of co-mutations. This study was conducted from January 2016 to May 2020 and involved 496 AML patients who received treatment at the medical...
View article titled, Adult Acute Myeloid Leukemia with the KMT2A- Mixed Lineage Leukemia T10 Fusion: An Analysis of 10 Cases Showed Common Features and Frequent Mutations in the RAS Signaling Pathway
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Journal Articles

The Prognostic Ability of RAS Pathway-Related Gene Mutations in Patients with Myeloid Neoplasms Treated with Hypomethylating Agents

Subject Area:
Hematology , Oncology
Hee Sue Park, Bo Ra Son, Kyeong Seob Shin, Seonggyu Byeon, Hee Kyung Kim, Yaewon Yang, Yusook Jeong, Hye Sook Han, Ki Hyeong Lee, Jihyun Kwon
Journal: Acta Haematologica
Acta Haematol (2021) 144 (6): 649–659.
https://doi.org/10.1159/000516793
Published Online: 07 July 2021
... with hypomethylating agents (HMAs). Methods: We performed next-generation sequencing on bone marrow aspiration samples of 59 patients diagnosed with acute myeloid leukemia (AML), myelodysplastic syndrome with excess blasts-2, or chronic myelomonocytic leukemia and treated with decitabine or azacitidine as a frontline...
View article titled, The Prognostic Ability of RAS Pathway-Related Gene Mutations in Patients with Myeloid Neoplasms Treated with Hypomethylating Agents
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Journal Articles

Ankyrin Mutations in Hereditary Spherocytosis

Subject Area:
Hematology , Oncology
Archana M. Agarwal
Journal: Acta Haematologica
Acta Haematol (2019) 141 (2): 63–64.
https://doi.org/10.1159/000495339
Published Online: 02 January 2019
... or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Anemia Hereditary spherocytosis Ankyrin Next-generation sequencing Hereditary...
View article titled, Ankyrin Mutations in Hereditary Spherocytosis
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