Hans K. Hasselbalch

researcher

Hans K. Hasselbalch is …
instance of (P31):
humanQ5

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P496ORCID iD0000-0003-3936-8032
P1153Scopus author ID35402388700

P734family nameHasselbalchQ35261552
HasselbalchQ35261552
HasselbalchQ35261552
P735given nameHansQ632842
HansQ632842
P106occupationresearcherQ1650915
P21sex or gendermaleQ6581097

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author (P50)
Q28553797A 7-Gene Signature Depicts the Biochemical Profile of Early Prefibrotic Myelofibrosis
Q53338106A der(18)t(9;18)(p13;p11) and a der(9;18)(p10;q10) in polycythemia vera associated with a hyperproliferative phenotype in transformation to postpolycythemic myelofibrosis.
Q69105155A distinct subtype of idiopathic myelofibrosis with bone marrow features mimicking hairy cell leukemia: evidence of an autoimmune pathogenesis
Q34189794A highly sensitive quantitative real-time PCR assay for determination of mutant JAK2 exon 12 allele burden
Q37682689A nationwide population-based cross-sectional survey of health-related quality of life in patients with myeloproliferative neoplasms in Denmark (MPNhealthSurvey): survey design and characteristics of respondents and nonrespondents
Q30992878A new internet-based tool for reporting and analysing patient-reported outcomes and the feasibility of repeated data collection from patients with myeloproliferative neoplasms
Q83258186A novel immunohistochemical sequential multi-labelling and erasing technique enables epitope characterization of bone marrow pericytes in primary myelofibrosis
Q39403830A phase II study of vorinostat (MK-0683) in patients with polycythaemia vera and essential thrombocythaemia.
Q42551329A phase II study of vorinostat (MK-0683) in patients with primary myelofibrosis and post-polycythemia vera myelofibrosis
Q53247635A phase II trial of pegylated interferon alpha-2b therapy for polycythemia vera and essential thrombocythemia: feasibility, clinical and biologic effects, and impact on quality of life.
Q47690234A phase III randomized trial comparing glucocorticoid monotherapy versus glucocorticoid and rituximab in patients with autoimmune haemolytic anaemia.
Q43739631A possible role for STI571 in the treatment of idiopathic myelofibrosis
Q41882404A remarkable hematological and molecular response pattern in a patient with polycythemia vera during combination therapy with simvastatin and alendronate
Q38802882A retrospective analysis of the impact of treatments and blood counts on survival and the risk of vascular events during the course of polycythaemia vera.
Q47816393A role of NF-E2 in chronic inflammation and clonal evolution in essential thrombocythemia, polycythemia vera and myelofibrosis?
Q43237567A unified definition of clinical resistance and intolerance to hydroxycarbamide in polycythaemia vera and primary myelofibrosis: results of a European LeukemiaNet (ELN) consensus process
Q36717896A unified definition of clinical resistance/intolerance to hydroxyurea in essential thrombocythemia: results of a consensus process by an international working group.
Q70162109Aberrations of chromosome 6 in 193 newly diagnosed untreated cases of chronic lymphocytic leukemia
Q42247181Activated platelets enhance IL-10 secretion and reduce TNF-α secretion by monocytes
Q44569638Acute leukemia and myelodysplasia in patients with a Philadelphia chromosome negative chronic myeloproliferative disorder treated with hydroxyurea alone or with hydroxyurea after busulphan
Q38706624Age-Related Macular Degeneration in Patients With Chronic Myeloproliferative Neoplasms
Q68129520Alcohol intolerance in the hypereosinophilic syndrome
Q45107227Anagrelide treatment in 52 patients with chronic myeloproliferative diseases
Q48313037Anemia is present years before myelodysplastic syndrome diagnosis: Results from the pre-diagnostic period.
Q81226465Angiogenesis in pulmonary hypertension with myelofibrosis
Q40157905Antecedent cardiovascular disease and autoimmunity in Philadelphia-negative chronic myeloproliferative neoplasms.
Q41713535Association of the blood eosinophil count with hematological malignancies and mortality
Q79734838B lymphocyte depletion with the monoclonal antibody rituximab in Graves' disease: a controlled pilot study
Q36897408B-cell depletion with rituximab in the treatment of autoimmune diseases. Graves' ophthalmopathy the latest addition to an expanding family
Q73643443B-cell depletion with rituximab-a targeted therapy for Graves' disease and autoimmune thyroiditis
Q91817678B-cell frequencies and immunoregulatory phenotypes in myeloproliferative neoplasms: Influence of ruxolitinib, interferon-α2, or combination treatment
Q57788925Bone marrow histomorphology and JAK2 mutation status in essential thrombocythemia
Q51333593Characterization of blood donors with high haemoglobin concentration.
Q87297788Chronic inflammation and autoimmunity as risk factors for the development of chronic myelomonocytic leukemia?
Q38061746Chronic inflammation as a promotor of mutagenesis in essential thrombocythemia, polycythemia vera and myelofibrosis. A human inflammation model for cancer development?
Q51241783Chronic kidney disease in patients with the Philadelphia-negative chronic myeloproliferative neoplasms.
Q45058582Chronic myeloproliferative neoplasms and subsequent cancer risk: a Danish population-based cohort study
Q42221121Circulating YKL-40 in myelofibrosis a potential novel biomarker of disease activity and the inflammatory state
Q61930297Circulating YKL-40 in patients with essential thrombocythemia and polycythemia vera treated with the novel histone deacetylase inhibitor vorinostat
Q44541251Circulating hyaluronan in the myelofibrosis/osteomyelosclerosis syndrome and other myeloproliferative disorders
Q54008969Collagen metabolism and enzymes of the urokinase plasminogen activator system in chronic myeloproliferative disorders: correlation between plasma-soluble urokinase plasminogen activator receptor and serum markers for collagen metabolism.
Q41998667Combination therapy with interferon and JAK1-2 inhibitor is feasible: Proof of concept with rapid reduction in JAK2V617F-allele burden in polycythemia vera
Q42426410Corrigendum to "Combination therapy with interferon and JAK1-2 inhibitor is feasible. Proof of concept with rapid reduction in JAK2V617F-allele burden in Polycythemia Vera" [Leuk. Res. Rep. 3 (2) (2014) 73-75].
Q92996868Data-driven analysis of JAK2V617F kinetics during interferon-alpha2 treatment of patients with polycythemia vera and related neoplasms
Q88009627Demonstrated Benefit of Continuous Interferon-Alpha-2b Therapy in Hairy Cell Leukemia. A Two-Year Follow-Up
Q33328174Diagnosis, pathogenesis and treatment of the myeloproliferative disorders essential thrombocythemia, polycythemia vera and essential megakaryocytic granulocytic metaplasia and myelofibrosis.
Q36169641Differential Dynamics of CALR Mutant Allele Burden in Myeloproliferative Neoplasms during Interferon Alfa Treatment
Q48228561Discordance between the cortisol response to insulin-hypoglycemia and 30-minute ACTH stimulation test in chronic alcoholic men.
Q37231416Does primary myelofibrosis involve a defective stem cell niche? From concept to evidence.
Q33436570Effect of thrombopoietin-receptor agonists on circulating cytokine and chemokine levels in patients with primary immune thrombocytopenia (ITP).
Q79358236Elevated plasma levels of TIMP-1 correlate with plasma suPAR/uPA in patients with chronic myeloproliferative disorders
Q44148383Elevated soluble urokinase plasminogen activator receptor in plasma from patients with idiopathic myelofibrosis or polycythaemia vera
Q44007100Eosinophilia in routine blood samples and the subsequent risk of hematological malignancies and death
Q53236154Eosinophilia in routine blood samples as a biomarker for solid tumor development - A study based on the Copenhagen Primary Care Differential Count (CopDiff) Database.
Q42339242Epigenetic changes in myelofibrosis: Distinct methylation changes in the myeloid compartments and in cases with ASXL1 mutations
Q54333652Expansion of circulating CD56bright natural killer cells in patients with JAK2-positive chronic myeloproliferative neoplasms during treatment with interferon-α.
Q40448136Extreme neutrophil granulocytosis in a patient with anaplastic large cell lymphoma of T-cell lineage.
Q54597002FLT3-mediated p38-MAPK activation participates in the control of megakaryopoiesis in primary myelofibrosis.
Q33397092Fibroproliferative activity in patients with immune thrombocytopenia (ITP) treated with thrombopoietic agents
Q43916592Frequent occurrence of anticardiolipin antibodies, Factor V Leiden mutation, and perturbed endothelial function in chronic myeloproliferative disorders
Q83796932High expression of carcinoembryonic antigen-related cell adhesion molecule (CEACAM) 6 and 8 in primary myelofibrosis
Q45149702High prevalence of arterial thrombosis in JAK2 mutated essential thrombocythaemia: independence of the V617F allele burden
Q44208224High rate of abnormal blood values and vascular complications before diagnosis of myeloproliferative neoplasms.
Q34171747Hydroxycarbamide: a user's guide for chronic myeloproliferative disorders.
Q68073139Hypercalcemia in idiopathic myelofibrosis: modulation of calcium and collagen homeostasis by 1,25-dihydroxyvitamin D3
Q48960781Hypothalamic-pituitary and thyroid function in chronic alcoholics with neurological complications
Q41414552Hypothesis: a possible role for interferon in the treatment of idiopathic myelofibrosis
Q40859828Idiopathic myelofibrosis--an update with particular reference to clinical aspects and prognosis
Q44667229Imatinib mesylate in idiopathic and postpolycythemic myelofibrosis
Q50664354Incidence, clinical features and outcome of essential thrombocythaemia in a well defined geographical area.
Q61698815Increase in circulating CD4+CD25+Foxp3+ T cells in patients with Philadelphia-negative chronic myeloproliferative neoplasms during treatment with IFN-
Q43605862Increased circulating platelet-leukocyte aggregates in myeloproliferative disorders is correlated to previous thrombosis, platelet activation and platelet count
Q39722432Increased gene expression of histone deacetylases in patients with Philadelphia-negative chronic myeloproliferative neoplasms
Q40808732Increased iron stores prolong the QT interval - a general population study including 20 261 individuals and meta-analysis of thalassaemia major.
Q74129093Increased platelet activation and abnormal membrane glycoprotein content and redistribution in myeloproliferative disorders
Q84114126Interferon alfa in the treatment of Philadelphia-negative chronic myeloproliferative neoplasms
Q46636672Interferon and the treatment of polycythemia vera, essential thrombocythemia and myelofibrosis
Q69912609Interferon in myelofibrosis
Q87353766Interferon in polycythemia vera and related neoplasms. Can it become the treatment of choice without a randomized trial?
Q54245609Interferon-α induces marked alterations in circulating regulatory T cells, NK cell subsets, and dendritic cells in patients with JAK2V617F-positive essential thrombocythemia and polycythemia vera.
Q41313835Is thrombocytosis a valid indicator of advanced stage and high mortality of gynecological cancer?
Q42629080Lack of somatic mutations in the catalytic domains of CREBBP and EP300 genes implies a role for histone deacetylase inhibition in myeloproliferative neoplasms
Q46156541Limited efficacy of hydroxyurea in lowering of the JAK2 V617F allele burden
Q44837107Long term molecular responses in a cohort of Danish patients with essential thrombocythemia, polycythemia vera and myelofibrosis treated with recombinant interferon alpha
Q34775393MPL mutations in myeloproliferative disorders: analysis of the PT-1 cohort.
Q26775996MPNs as Inflammatory Diseases: The Evidence, Consequences, and Perspectives
Q41576528Mathematical modelling as a proof of concept for MPNs as a human inflammation model for cancer development
Q42133965Mediators of Inflammation in Myeloproliferative Neoplasms: State of the Art.
Q40959669Minimal residual disease after long-term interferon-alpha2 treatment: a report on hematological, molecular and histomorphological response patterns in 10 patients with essential thrombocythemia and polycythemia vera
Q57788892Minimal residual disease and normalization of the bone marrow after long-term treatment with alpha-interferon2b in polycythemia vera. A report on molecular response patterns in seven patients in sustained complete hematological remission
Q39237430Minimal residual disease or cure in MPNs? Rationales and perspectives on combination therapy with interferon-alpha2 and ruxolitinib.
Q41325566Molecular mechanisms associated with leukemic transformation of MPL-mutant myeloproliferative neoplasms
Q48127316Molecular profiling as a novel tool to predict response to interferon-α2 in MPNs: The proof of concept in early myelofibrosis
Q84760917Molecular profiling of peripheral blood cells from patients with polycythemia vera and related neoplasms: identification of deregulated genes of significance for inflammation and immune surveillance
Q98632589Myeloproliferative blood cancers as a human neuroinflammation model for development of Alzheimer's disease: evidences and perspectives
Q38725723Myeloproliferative neoplasms and inflammation: whether to target the malignant clone or the inflammatory process or both
Q42847809Myeloproliferative neoplasms in five multiple sclerosis patients
Q92385638Neo-antigen specific memory T-cell responses in healthy individuals
Q77319931Non-invasive imaging of retinal blood flow in myeloproliferative neoplasms
Q67653780On the pathogenesis of angiogenesis in idiopathic myelofibrosis
Q39979643Optimal therapy for polycythemia vera and essential thrombocythemia: Preferred use of interferon therapy based on phase 2 trials
Q83408567Perspectives on chronic inflammation in essential thrombocythemia, polycythemia vera, and myelofibrosis: is chronic inflammation a trigger and driver of clonal evolution and development of accelerated atherosclerosis and second cancer?
Q57159202Perspectives on interferon-alpha in the treatment of Polycythemia vera and related Myeloproliferative neoplasms: minimal residual disease and cure?
Q38187674Perspectives on the impact of JAK-inhibitor therapy upon inflammation-mediated comorbidities in myelofibrosis and related neoplasms.
Q53680800Perspectives on the increased risk of second cancer in patients with essential thrombocythemia, polycythemia vera and myelofibrosis.
Q37163590Philadelphia-negative classical myeloproliferative neoplasms: critical concepts and management recommendations from European LeukemiaNet.
Q40081960Prevalence and clinical significance of neutropenia discovered in routine complete blood cell counts: a longitudinal study
Q92882962Prevalence and phenotypes of JAK2 V617F and calreticulin mutations in a Danish general population
Q57788910Quantitative assessment of the JAK2 V617F allele burden: equivalent levels in peripheral blood and bone marrow
Q37412790Response criteria for essential thrombocythemia and polycythemia vera: result of a European LeukemiaNet consensus conference.
Q40408575Response criteria for myelofibrosis with myeloid metaplasia: results of an initiative of the European Myelofibrosis Network (EUMNET).
Q33734256Risk of lymphoma and solid cancer among patients with rheumatoid arthritis in a primary care setting
Q33405127Rituximab and dexamethasone vs dexamethasone monotherapy in newly diagnosed patients with primary immune thrombocytopenia
Q33365619Rituximab chimeric anti-CD20 monoclonal antibody treatment for adult refractory idiopathic thrombocytopenic purpura
Q33422507Ruxolitinib is manageable in patients with myelofibrosis and severe thrombocytopenia: a report on 12 Danish patients.
Q44530765SU6668 in idiopathic myelofibrosis--a rational therapeutic approach targeting several tyrosine kinases of importance for the myeloproliferation and the development of bone marrow fibrosis and angiogenesis
Q63728939Safety and efficacy of combination therapy of interferon-α2 and ruxolitinib in polycythemia vera and myelofibrosis
Q51608068Second malignancies in hydroxyurea and interferon-treated Philadelphia-negative myeloproliferative neoplasms.
Q54157248Serum hyaluronan is increased in malignant lymphoma.
Q72138908Serum laminin P1 in idiopathic myelofibrosis and related diseases
Q69606775Serum markers for type IV collagen and type III procollagen in the myelofibrosis-osteomyelosclerosis syndrome and other chronic myeloproliferative disorders
Q41348010Smoking and philadelphia-negative chronic myeloproliferative neoplasms
Q38606278Smoking as a contributing factor for development of polycythemia vera and related neoplasms
Q57466753Smoking is associated with increased risk of myeloproliferative neoplasms: A general population-based cohort study
Q92244700Smoking, blood cells and myeloproliferative neoplasms: meta-analysis and Mendelian randomization of 2·3 million people
Q61698758Sorted peripheral blood cells identify CALR mutations in B- and T-lymphocytes
Q91523738Spontaneous T-cell responses against Arginase-1 in the chronic myeloproliferative neoplasms relative to disease stage and type of driver mutation
Q36398850Statins in the treatment of polycythaemia vera and allied disorders: an antithrombotic and cytoreductive potential?
Q44059767Successful treatment of anemia in idiopathic myelofibrosis with recombinant human erythropoietin
Q72488695Survival after a blood alcohol of 1127 mg/dl
Q38384255Survival of patients with chronic myeloproliferative neoplasms and new primary cancers: a population-based cohort study
Q40091659Sustained major molecular response on interferon alpha-2b in two patients with polycythemia vera.
Q33338419Sustained remission of platelet counts following monoclonal anti-CD20 antibody therapy in two cases of idiopathic autoimmune thrombocytopenia and neutropenia.
Q61698772The CALR exon 9 mutations are shared neoantigens in patients with CALR mutant chronic myeloproliferative neoplasms
Q33774105The Copenhagen Primary Care Differential Count (CopDiff) database
Q28067986The Danish National Chronic Myeloid Neoplasia Registry
Q46931482The JAK2 V617F allele burden in essential thrombocythemia, polycythemia vera and primary myelofibrosis--impact on disease phenotype
Q79805830The JAK2 V617F mutation involves B- and T-lymphocyte lineages in a subgroup of patients with Philadelphia-chromosome negative chronic myeloproliferative disorders
Q84545968The JAK2V617F allele burden and STAT3- and STAT5 phosphorylation in myeloproliferative neoplasms: early prefibrotic myelofibrosis compared with essential thrombocythemia, polycythemia vera and myelofibrosis
Q26779929The Role of Reactive Oxygen Species in Myelofibrosis and Related Neoplasms
Q64336965The V617F and exon 9 mutations are shared immunogenic neoantigens in hematological malignancy
Q88895062The impact of interferon-alpha2 on HLA genes in patients with polycythemia vera and related neoplasms
Q51061525The platelet-cancer loop in myeloproliferative cancer. Is thrombocythemia an enhancer of cancer invasiveness and metastasis in essential thrombocythemia, polycythemia vera and myelofibrosis?
Q36462675The rationale for B lymphocyte depletion in Graves' disease. Monoclonal anti-CD20 antibody therapy as a novel treatment option.
Q90481351The red blood cell count and the erythrocyte sedimentation rate in the diagnosis of polycythaemia vera
Q38082073The role of cytokines in the initiation and progression of myelofibrosis.
Q33398815Thrombopoietin-receptor agonists in haematological disorders: the Danish experience
Q41809175Transcriptional profiling of whole blood identifies a unique 5-gene signature for myelofibrosis and imminent myelofibrosis transformation
Q80061323Treatment-resistant severe, active Graves' ophthalmopathy successfully treated with B lymphocyte depletion
Q71378079Urinary free cortisol during pregnancy
Q50747615V617F mutation in JAK2 is associated with poorer survival in idiopathic myelofibrosis.
Q35705470WHO classification 2008 of myeloproliferative neoplasms: a workshop learning effect--the Danish experience
Q59194482Whole blood assay for NK activity in splenectomized and non-splenectomized hairy cell leukemia patients during IFN-α-2b treatment
Q34514329Whole blood transcriptional profiling reveals deregulation of oxidative and antioxidative defence genes in myelofibrosis and related neoplasms. Potential implications of downregulation of Nrf2 for genomic instability and disease progression
Q85862955Whole blood transcriptional profiling reveals significant down-regulation of human leukocyte antigen class I and II genes in essential thrombocythemia, polycythemia vera and myelofibrosis
Q83742042Whole-blood transcriptional profiling of interferon-inducible genes identifies highly upregulated IFI27 in primary myelofibrosis
Q36562094Whole-exome sequencing and genome-wide methylation analyses identify novel disease associated mutations and methylation patterns in idiopathic hypereosinophilic syndrome
Q45884600World Health Organization-defined classification of myeloproliferative neoplasms: morphological reproducibility and clinical correlations--the Danish experience

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