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Molecular diagnostics of myeloproliferative neoplasms

European journal of haematology, 2015-10, Vol.95 (4), p.270-279

2015

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Molecular Investigation of a Suspected Myeloproliferative Neoplasm in Patients with Basophilia

Journal of clinical and diagnostic research, 2017-04, Vol.11 (4), p.EL01-EL01

2017

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Protracted Clonal Trajectory of a JAK2 V617F-Positive Myeloproliferative Neoplasm Developing during Long-Term Remission from Acute Myeloid Leukemia

Case reports in hematology, 2018-01, Vol.2018 (2018), p.1-4

2018

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Chronic Myeloid Leukemia with an e6a2 BCR-ABL1 Fusion Transcript: Cooperating Mutations at Blast Crisis and Molecular Monitoring

Case reports in hematology, 2017-01, Vol.2017 (2017), p.1-5

2017

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Incidence of CALR mutations in patients with splanchnic vein thrombosis

British journal of haematology, 2015-02, Vol.168 (3), p.459-460

2015

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Acute Lymphoblastic Leukemia Arising in CALR Mutated Essential Thrombocythemia

Case reports in hematology, 2016-01, Vol.2016 (2016), p.1-5

2016

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Who to screen for CALR mutations? An audit of real-life practice and review of current evidence

European journal of internal medicine, 2017

2017

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Evading Capture by Residual Disease Monitoring: Extramedullary Manifestation of JAK2 V617F-Positive Primary Myelofibrosis After Allogeneic Stem Cell Transplantation

Case reports in hematology, 2015-01, Vol.2015 (2015), p.1-4

2015

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Targeted next‐generation sequencing of familial platelet disorder with predisposition to acute myeloid leukaemia

British journal of haematology, 2016-10, Vol.175 (1), p.161-163

2016

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Allogeneic Hematopoietic Stem Cell Transplantation for a BCR-FGFR1 Myeloproliferative Neoplasm Presenting as Acute Lymphoblastic Leukemia

Case reports in hematology, 2012-01, Vol.2012 (2012), p.1-5

2012

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An acquired NRAS mutation contributes to neutrophilic progression in a patient with primary myelofibrosis

British journal of haematology, 2018-10, Vol.183 (2), p.308-310

2018

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The mutant CALR allele burden in essential thrombocythemia at transformation to acute myeloid leukemia

Blood cells, molecules, & diseases, 2017-06, Vol.65, p.66-67

2017

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Cloning and characterization of spliced fusion transcript variants of synovial sarcoma: SYT/SSX4, SYT/SSX4v, and SYT/SSX2v. Possible regulatory role of the fusion gene product in wild type SYT expression

Gene, 2001-05, Vol.268 (1-2), p.173-182

2001

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False-negative CALR mutation in a suspected myeloproliferative neoplasm: identification, resolution and corrective action

Journal of clinical pathology, 2018-05, Vol.71 (5), p.473-474

2018

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Neutrophilia and the JAK2 V617F Mutation

Pathology oncology research, 2019-01, Vol.25 (1), p.437-438

2019

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Assessment of CALR mutations in myelofibrosis patients, post‐allogeneic stem cell transplantation

British journal of haematology, 2014-09, Vol.166 (5), p.800-802

2014

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Monitoring Minimal Residual Disease in the Myeloproliferative Neoplasms: Current Applications and Emerging Approaches

BioMed research international, 2016-01, Vol.2016 (2016), p.1-6

2016

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CALR mutations are rare in childhood essential thrombocythemia

Pediatric blood & cancer, 2014-08, Vol.61 (8), p.1523-1523

2014

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Showing one’s true CALRs: spleen size and platelet count help refine the molecular diagnostic pathway for patients with splanchnic vein thrombosis

AME medical journal, 2017-08, Vol.2, p.107-107

2017

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Impact of Somatic Mutations on Clinical Outcomes Following Flamsa-Bu Conditioning and Allogenic Stem Cell Transplantation in Patients with Poor-Risk Myeloid Malignancies

Blood, 2016-12, Vol.128 (22), p.2277-2277

2016

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Who to screen for calreticulin mutations? An audit of real-life practice and review of current evidence

European journal of internal medicine, 2017-05, Vol.40, p.e22-e23

2017

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Capricious CALR mutated clones in myeloproliferative neoplasms

Blood cells, molecules, & diseases, 2016-03, Vol.57, p.110-111

2016

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A prenatal origin of childhood essential thrombocythaemia

British journal of haematology, 2013-12, Vol.163 (5), p.676-678

2013

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Isolated erythrocytosis associated with a CALR mutation

Blood cells, molecules, & diseases, 2017-07, Vol.66, p.6-7

2017

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Distinct driver mutation profiles of childhood and adolescent essential thrombocythemia

Pediatric blood & cancer, 2015-01, Vol.62 (1), p.175-176

2015

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Molecular diagnostics of myeloproliferative neoplasms

Molecular Investigation of a Suspected Myeloproliferative Neoplasm in Patients with Basophilia

Protracted Clonal Trajectory of a JAK2 V617F-Positive Myeloproliferative Neoplasm Developing during Long-Term Remission from Acute Myeloid Leukemia

Chronic Myeloid Leukemia with an e6a2 BCR-ABL1 Fusion Transcript: Cooperating Mutations at Blast Crisis and Molecular Monitoring

Incidence of CALR mutations in patients with splanchnic vein thrombosis

Acute Lymphoblastic Leukemia Arising in CALR Mutated Essential Thrombocythemia

Who to screen for CALR mutations? An audit of real-life practice and review of current evidence

Evading Capture by Residual Disease Monitoring: Extramedullary Manifestation of JAK2 V617F-Positive Primary Myelofibrosis After Allogeneic Stem Cell Transplantation

Targeted next‐generation sequencing of familial platelet disorder with predisposition to acute myeloid leukaemia

Allogeneic Hematopoietic Stem Cell Transplantation for a BCR-FGFR1 Myeloproliferative Neoplasm Presenting as Acute Lymphoblastic Leukemia

An acquired NRAS mutation contributes to neutrophilic progression in a patient with primary myelofibrosis

The mutant CALR allele burden in essential thrombocythemia at transformation to acute myeloid leukemia

Cloning and characterization of spliced fusion transcript variants of synovial sarcoma: SYT/SSX4, SYT/SSX4v, and SYT/SSX2v. Possible regulatory role of the fusion gene product in wild type SYT expression

False-negative CALR mutation in a suspected myeloproliferative neoplasm: identification, resolution and corrective action

Neutrophilia and the JAK2 V617F Mutation

Assessment of CALR mutations in myelofibrosis patients, post‐allogeneic stem cell transplantation

Monitoring Minimal Residual Disease in the Myeloproliferative Neoplasms: Current Applications and Emerging Approaches

CALR mutations are rare in childhood essential thrombocythemia

Showing one’s true CALRs: spleen size and platelet count help refine the molecular diagnostic pathway for patients with splanchnic vein thrombosis

Impact of Somatic Mutations on Clinical Outcomes Following Flamsa-Bu Conditioning and Allogenic Stem Cell Transplantation in Patients with Poor-Risk Myeloid Malignancies

Who to screen for calreticulin mutations? An audit of real-life practice and review of current evidence

Capricious CALR mutated clones in myeloproliferative neoplasms

A prenatal origin of childhood essential thrombocythaemia

Isolated erythrocytosis associated with a CALR mutation

Distinct driver mutation profiles of childhood and adolescent essential thrombocythemia

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