Thrombocytosis
What's New
Last Posted: Jan 26, 2024
- One thousand patients with essential thrombocythemia: the Florence-CRIMM experience.
Giuseppe G Loscocco, et al. Blood cancer journal 2024 0 (1) 10 - One thousand patients with essential thrombocythemia: the Mayo Clinic experience.
Naseema Gangat, et al. Blood cancer journal 2024 0 (1) 11 - Haptoglobin gene polymorphism and iron profile in sickle cell disease patients with inflammation in Yaounde, Cameroon.
Romaric De Manfouo Tuono, et al. Molecular genetics & genomic medicine 2023 0 e2302 - Characterization of myeloproliferative neoplasms in the paediatric and young adult population.
Harris Zoey, et al. British journal of haematology 2023 0 - Comparison of Clinical and Molecular Features Between Patients With Essential Thrombocythemia and Early/Prefibrotic Primary Myelofibrosis Presenting With Thrombocytosis in Taiwan.
Kuo Ming-Chung, et al. American journal of clinical pathology 2023 0 - Age- and sex-based ranges of platelet count and cause-specific mortality risk in an adult general population: prospective findings from the Moli-sani study.
Bonaccio Marialaura, et al. Platelets 2017 0 (3) 312-315 - High prevalence of heparin induced thrombocytopenia with thrombosis among patients with essential thrombocytemia carrying V617F mutation.
Castelli Roberto, et al. Journal of thrombosis and thrombolysis 2017 0 (1) 106-113 - Pregnancy and myeloproliferative neoplasms : A retrospective monocentric cohort.
Puyade Mathieu, et al. Obstetric medicine 2017 0 (4) 165-169 - Risk factors of occult malignancy in patients with unprovoked venous thromboembolism.
Robin Philippe, et al. Thrombosis research 2017 0 48-51 - Chronic Myeloid Leukemia with b3a3 (e14a3) Fusion: A Rare BCR/ABL Rearrangement Presenting with Thrombocytosis - Does MTHFR Polymorphism Matter.
Chisti Mohammad Muhsin, et al. Case reports in oncology 2018 0 (2) 485-492 - Skewed ratio between type 1 and type 2 calreticulin mutations in essential thrombocytosis patients with concomitant Janus kinase 2 V617F mutation.
Haunstrup Laura M, et al. Experimental hematology 2018 0 62-65 - [Gene mutation spectrum and clinical characteristics analysis of 178 patients with essential thrombocytosis].
Dong H, et al. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2019 0 (10) 837-842 - Genotypic and phenotypic evolution in a patient with chronic myelomonocytic leukemia.
Geissler Klaus, et al. Leukemia research reports 2019 0 100185 - Genotype/phenotype correlations of childhood-onset congenital sideroblastic anaemia in a European cohort.
Fouquet Cyrielle, et al. British journal of haematology 2019 0 (4) 530-542 - Serologic, but Not Genetic, Markers Are Associated With Impaired Anthropometrics at Diagnosis of Pediatric Crohn's Disease.
Naramore Sara K, et al. Journal of pediatric gastroenterology and nutrition 2019 0 (5) e129-e134 - A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2.
Özen Seza, et al. The Journal of rheumatology 2019 0 (1) 117-125 - Erythrocytosis in the general population: clinical characteristics and association with clonal hematopoiesis.
Wouters Hanneke J C M, et al. Blood advances 2020 0 (24) 6353-6363 - Frequency and characteristics of the JAK2 V617F mutation in 23 cerebral venous sinus thrombosis patients with thrombocytosis.
Ma Qiang, et al. The Journal of international medical research 2020 0 (12) 300060520977729 - Relationship of JAK2 (V617F) Allelic Burden with Clinico- Haematological Manifestations of Philadelphia-Negative Myeloproliferative Neoplasms.
Yow Ka Shing, et al. Asian Pacific journal of cancer prevention : APJCP 2020 0 (9) 2805-2810 - High prevalence of clonal hematopoiesis in the blood and bone marrow of healthy volunteers.
Guermouche Hélène, et al. Blood advances 2020 0 (15) 3550-3557
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HLBS-PopOmics is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other materials that address the translation of genomic and other precision health discoveries into improved health care and prevention related to Heart and Vascular Diseases(H), Lung Diseases(L), Blood Diseases(B), and Sleep Disorders(S)...more
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Mensah GA, Yu W, Barfield WL, Clyne M, Engelgau MM, Khoury MJ. HLBS-PopOmics: an online knowledge base to accelerate dissemination and implementation of research advances in population genomics to reduce the burden of heart, lung, blood, and sleep disorders. Genet Med. 2018 Sep 10. doi: 10.1038/s41436-018-0118-1
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 25, 2024
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