Pallisgaard N - Search Results

1

The JAK2 V617F allele burden in essential thrombocythemia, polycythemia vera and primary myelofibrosis--impact on disease phenotype.

Larsen TS, Pallisgaard N, Møller MB, Hasselbalch HC. Larsen TS, et al. Among authors: pallisgaard n. Eur J Haematol. 2007 Dec;79(6):508-15. doi: 10.1111/j.1600-0609.2007.00960.x. Epub 2007 Oct 23. Eur J Haematol. 2007. PMID: 17961178

2

V617F mutation in JAK2 is associated with poorer survival in idiopathic myelofibrosis.

Campbell PJ, Griesshammer M, Döhner K, Döhner H, Kusec R, Hasselbalch HC, Larsen TS, Pallisgaard N, Giraudier S, Le Bousse-Kerdilès MC, Desterke C, Guerton B, Dupriez B, Bordessoule D, Fenaux P, Kiladjian JJ, Viallard JF, Brière J, Harrison CN, Green AR, Reilly JT. Campbell PJ, et al. Among authors: pallisgaard n. Blood. 2006 Mar 1;107(5):2098-100. doi: 10.1182/blood-2005-08-3395. Epub 2005 Nov 17. Blood. 2006. PMID: 16293597 Free article.

3

[New molecular markers within the chronic myeloproliferative disorders. I: the PRV-1 gene].

Larsen TS, Pallisgaard N, Christensen JH, Gram-Hansen P, Kerndrup GB, Møller MB, Hasselbalch HC. Larsen TS, et al. Among authors: pallisgaard n. Ugeskr Laeger. 2006 Sep 25;168(39):3295-9. Ugeskr Laeger. 2006. PMID: 17032591 Review. Danish.

4

[New molecular markers within the chronic myeloproliferative disorders. II: the JAK2 mutation].

Larsen TS, Pallisgaard N, Christensen JH, Gram-Hansen P, Kerndrup GB, Møller MB, Hasselbalch HC. Larsen TS, et al. Among authors: pallisgaard n. Ugeskr Laeger. 2006 Sep 25;168(39):3299-303. Ugeskr Laeger. 2006. PMID: 17032592 Review. Danish.

5

A 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.

Larsen TS, Hasselbalch HC, Pallisgaard N, Kerndrup GB. Larsen TS, et al. Among authors: pallisgaard n. Cancer Genet Cytogenet. 2007 Jan 15;172(2):107-12. doi: 10.1016/j.cancergencyto.2006.09.015. Cancer Genet Cytogenet. 2007. PMID: 17213018

6

The JAK2 V617F mutation involves B- and T-lymphocyte lineages in a subgroup of patients with Philadelphia-chromosome negative chronic myeloproliferative disorders.

Larsen TS, Christensen JH, Hasselbalch HC, Pallisgaard N. Larsen TS, et al. Among authors: pallisgaard n. Br J Haematol. 2007 Mar;136(5):745-51. doi: 10.1111/j.1365-2141.2007.06497.x. Br J Haematol. 2007. PMID: 17313377 Free article.

7

Bone marrow histomorphology and JAK2 mutation status in essential thrombocythemia.

Stauffer Larsen T, Hasselbalch HC, Pallisgaard N, Møller MB. Stauffer Larsen T, et al. Among authors: pallisgaard n. APMIS. 2007 Nov;115(11):1267-73. doi: 10.1111/j.1600-0643.2007.00807.x. APMIS. 2007. PMID: 18092959

8

High prevalence of arterial thrombosis in JAK2 mutated essential thrombocythaemia: independence of the V617F allele burden.

Larsen TS, Pallisgaard N, Møller MB, Hasselbalch HC. Larsen TS, et al. Among authors: pallisgaard n. Hematology. 2008 Apr;13(2):71-6. doi: 10.1179/102453308X315960. Hematology. 2008. PMID: 18616871 Free article.

9

Limited efficacy of hydroxyurea in lowering of the JAK2 V617F allele burden.

Larsen TS, Pallisgaard N, de Stricker K, Møller MB, Hasselbalch HC. Larsen TS, et al. Among authors: pallisgaard n. Hematology. 2009 Feb;14(1):11-5. doi: 10.1179/102453309X385188. Hematology. 2009. PMID: 19154659 Free article.

10

Ruxolitinib and interferon-α2 combination therapy for patients with polycythemia vera or myelofibrosis: a phase II study.

Sørensen AL, Mikkelsen SU, Knudsen TA, Bjørn ME, Andersen CL, Bjerrum OW, Brochmann N, Patel DA, Gjerdrum LMR, El Fassi D, Kruse TA, Larsen TS, Mourits-Andersen HT, Nielsen CH, Ellervik C, Pallisgaard N, Thomassen M, Kjær L, Skov V, Hasselbalch HC. Sørensen AL, et al. Among authors: pallisgaard n. Haematologica. 2020 Sep 1;105(9):2262-2272. doi: 10.3324/haematol.2019.235648. Haematologica. 2020. PMID: 33054051 Free PMC article. Clinical Trial.

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