Patnaik MM - Search Results

1

Infrequent occurrence of TET1, TET3, and ASXL2 mutations in myelodysplastic/myeloproliferative neoplasms.

Lasho TL, Vallapureddy R, Finke CM, Mangaonkar A, Gangat N, Ketterling R, Tefferi A, Patnaik MM. Lasho TL, et al. Among authors: patnaik mm. Blood Cancer J. 2018 Mar 12;8(3):32. doi: 10.1038/s41408-018-0057-8. Blood Cancer J. 2018. PMID: 29531217 Free PMC article. No abstract available.

2

FIP1L1-PDGFRA in eosinophilic disorders: prevalence in routine clinical practice, long-term experience with imatinib therapy, and a critical review of the literature.

Pardanani A, Ketterling RP, Li CY, Patnaik MM, Wolanskyj AP, Elliott MA, Camoriano JK, Butterfield JH, Dewald GW, Tefferi A. Pardanani A, et al. Among authors: patnaik mm. Leuk Res. 2006 Aug;30(8):965-70. doi: 10.1016/j.leukres.2005.11.011. Epub 2006 Jan 6. Leuk Res. 2006. PMID: 16406016

3

Eosinophilia: secondary, clonal and idiopathic.

Tefferi A, Patnaik MM, Pardanani A. Tefferi A, et al. Among authors: patnaik mm. Br J Haematol. 2006 Jun;133(5):468-92. doi: 10.1111/j.1365-2141.2006.06038.x. Br J Haematol. 2006. PMID: 16681635 Free article. Review.

4

Kit: molecule of interest for the diagnosis and treatment of mastocytosis and other neoplastic disorders.

Patnaik MM, Tefferi A, Pardanani A. Patnaik MM, et al. Curr Cancer Drug Targets. 2007 Aug;7(5):492-503. doi: 10.2174/156800907781386614. Curr Cancer Drug Targets. 2007. PMID: 17691909 Review.

5

The complete evaluation of erythrocytosis: congenital and acquired.

Patnaik MM, Tefferi A. Patnaik MM, et al. Leukemia. 2009 May;23(5):834-44. doi: 10.1038/leu.2009.54. Epub 2009 Mar 19. Leukemia. 2009. PMID: 19295544 Review.

6

Detection of mutant TET2 in myeloid malignancies other than myeloproliferative neoplasms: CMML, MDS, MDS/MPN and AML.

Tefferi A, Lim KH, Abdel-Wahab O, Lasho TL, Patel J, Patnaik MM, Hanson CA, Pardanani A, Gilliland DG, Levine RL. Tefferi A, et al. Among authors: patnaik mm. Leukemia. 2009 Jul;23(7):1343-5. doi: 10.1038/leu.2009.59. Epub 2009 Mar 19. Leukemia. 2009. PMID: 19295549 Free PMC article. No abstract available.

7

Molecular diagnosis of myeloproliferative neoplasms.

Patnaik MM, Tefferi A. Patnaik MM, et al. Expert Rev Mol Diagn. 2009 Jul;9(5):481-92. doi: 10.1586/erm.09.29. Expert Rev Mol Diagn. 2009. PMID: 19580432 Review.

8

JAK2 germline genetic variation affects disease susceptibility in primary myelofibrosis regardless of V617F mutational status: nullizygosity for the JAK2 46/1 haplotype is associated with inferior survival.

Tefferi A, Lasho TL, Patnaik MM, Finke CM, Hussein K, Hogan WJ, Elliott MA, Litzow MR, Hanson CA, Pardanani A. Tefferi A, et al. Among authors: patnaik mm. Leukemia. 2010 Jan;24(1):105-9. doi: 10.1038/leu.2009.225. Epub 2009 Oct 22. Leukemia. 2010. PMID: 19847199

9

Age and platelet count are IPSS-independent prognostic factors in young patients with primary myelofibrosis and complement IPSS in predicting very long or very short survival.

Patnaik MM, Caramazza D, Gangat N, Hanson CA, Pardanani A, Tefferi A. Patnaik MM, et al. Eur J Haematol. 2010 Feb 1;84(2):105-8. doi: 10.1111/j.1600-0609.2009.01373.x. Epub 2009 Nov 6. Eur J Haematol. 2010. PMID: 19895568

10

MPL mutation effect on JAK2 46/1 haplotype frequency in JAK2V617F-negative myeloproliferative neoplasms.

Patnaik MM, Lasho TL, Finke CM, Gangat N, Caramazza D, Siragusa S, Hanson CA, Pardanani A, Tefferi A. Patnaik MM, et al. Leukemia. 2010 Apr;24(4):859-60. doi: 10.1038/leu.2010.1. Epub 2010 Jan 28. Leukemia. 2010. PMID: 20111067 No abstract available.

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