An Acquired NRAS Mutation Contributes to Neutrophilic Progression in a Patient With Primary Myelofibrosis

British Journal of Haematology - United Kingdom
doi 10.1111/bjh.14957
Full Text
Abstract

Available in full text

Categories
Hematology
Date
Authors
Publisher

Wiley

Related search

Duplication of ALK F1245 Missense Mutation Due to Acquired Uniparental Disomy Associated With Aggressive Progression in a Patient With Relapsed Neuroblastoma

Oncology Letters
Cancer ResearchOncology
2019English

Azacitidine Causes Prolonged Neutropenia in an Elderly Patient With Primary Myelofibrosis Transformed to Acute Myeloid Leukemia

Journal of Blood & Lymph
2012English

Massive Bone Marrow Necrosis and Postnecrotic Myelofibrosis in a Patient With Primary Thrombocythaemia.

Journal of Clinical Pathology
MedicineForensic MedicinePathology
1994English

P2.13-33 a Case Report of Exceptional Clinical Response to MEK Inhibition in a Patient With NRAS Mutation Positive NSCLC

Journal of Thoracic Oncology
MedicineOncologyRespiratory MedicinePulmonary
2018English

LPIN2 Gene Mutation in a Patient With Overlapping Neutrophilic Disease (Pyoderma Gangrenosum and Aseptic Abscess Syndrome)

JAAD Case Reports
Dermatology
2018English

Dramatic Response to Alectinib in a Lung Cancer Patient With a Novel VKORC1L1-ALK Fusion and an Acquired ALK T1151K Mutation

Lung Cancer: Targets and Therapy
Oncology
2018English

Internuclear Bridging of Erythroid Precursors in the Peripheral Blood Smear in a Patient With Primary Myelofibrosis

Turkish Journal of Haematology
Hematology
2017English

Mayor Erythropoietic Response After Deferasirox Treatment in a Transfusion-Dependent Anemic Patient With Primary Myelofibrosis

Case Reports in Hematology
2013English

Neutrophilic Eccrine Hidradenitis in a Primary CNS Lymphoma Patient Receiving High-Dose Chemotherap

Dermatology Case Reports
2019English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy