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Items: 1 to 20 of 148

1.

Systemic mastocytosis with associated clonal hematological non-mast-cell lineage disease: analysis of clinicopathologic features and activating c-kit mutations.

Pullarkat VA, Bueso-Ramos C, Lai R, Kroft S, Wilson CS, Pullarkat ST, Bu X, Thein M, Lee M, Brynes RK.

Am J Hematol. 2003 May;73(1):12-7.

2.

Myelomastocytic overlap syndromes: biology, criteria, and relationship to mastocytosis.

Valent P, Sperr WR, Samorapoompichit P, Geissler K, Lechner K, Horny HP, Bennett JM.

Leuk Res. 2001 Jul;25(7):595-602. Review.

PMID:
11377685
3.

Systemic mastocytosis with associated clonal hematologic nonmast cell lineage disease: a clinicopathologic review.

Stoecker MM, Wang E.

Arch Pathol Lab Med. 2012 Jul;136(7):832-8. doi: 10.5858/arpa.2011-0325-RS. Review.

PMID:
22742558
4.

Mastocytosis: state of the art.

Horny HP, Sotlar K, Valent P.

Pathobiology. 2007;74(2):121-32. Review.

PMID:
17587883
5.

Acute myeloid leukaemia with t(8;21) associated with "occult" mastocytosis. Report of an unusual case and review of the literature.

Bernd HW, Sotlar K, Lorenzen J, Osieka R, Fabry U, Valent P, Horny HP.

J Clin Pathol. 2004 Mar;57(3):324-8. Review.

6.

Diagnostic criteria and classification of mastocytosis: a consensus proposal.

Valent P, Horny HP, Escribano L, Longley BJ, Li CY, Schwartz LB, Marone G, Nuñez R, Akin C, Sotlar K, Sperr WR, Wolff K, Brunning RD, Parwaresch RM, Austen KF, Lennert K, Metcalfe DD, Vardiman JW, Bennett JM.

Leuk Res. 2001 Jul;25(7):603-25. Review.

PMID:
11377686
7.

Mastocytosis.

Metcalfe DD.

Novartis Found Symp. 2005;271:232-42; discussion 242-9. Review.

PMID:
16605139
8.

Myelodysplastic syndrome with translocation (8;21): a distinct myelodysplastic syndrome entity or M2-acute myeloid leukemia with extensive myeloid maturation?

Kojima K, Omoto E, Hara M, Sasaki K, Katayama Y, Nawa Y, Kimura Y, Azuma T, Takimoto H, Harada M.

Ann Hematol. 1998 Jun;76(6):279-82. Review.

PMID:
9692817
9.

Pathogenesis, clinical features, and treatment advances in mastocytosis.

Pardanani A, Akin C, Valent P.

Best Pract Res Clin Haematol. 2006;19(3):595-615. Review.

PMID:
16781490
10.

Effects of mutant c-Kit in early myeloid cells.

Ashman LK, Ferrao P, Cole SR, Cambareri AC.

Leuk Lymphoma. 1999 Aug;34(5-6):451-61. Review. Corrected and republished in: Leuk Lymphoma. 2000 Mar;37(1-2):233-43.

PMID:
10492068
11.

Translocation (8;21) in oligoblastic leukemia: is this a true myelodysplastic syndrome?

Xue Y, Yu F, Zhou Z, Guo Y, Xie X, Lin B.

Leuk Res. 1994 Oct;18(10):761-5. Review.

PMID:
7934133
12.

Spectrum of associated clonal hematologic non-mast cell lineage disorders occurring in patients with systemic mastocytosis.

Sperr WR, Horny HP, Valent P.

Int Arch Allergy Immunol. 2002 Feb;127(2):140-2. Review.

PMID:
11919425
13.

Mastocytosis: pathology, genetics, and current options for therapy.

Valent P, Akin C, Sperr WR, Mayerhofer M, Födinger M, Fritsche-Polanz R, Sotlar K, Escribano L, Arock M, Horny HP, Metcalfe DD.

Leuk Lymphoma. 2005 Jan;46(1):35-48. Review.

PMID:
15621779
14.

Diagnosis and classification of mast cell proliferative disorders: delineation from immunologic diseases and non-mast cell hematopoietic neoplasms.

Valent P, Sperr WR, Schwartz LB, Horny HP.

J Allergy Clin Immunol. 2004 Jul;114(1):3-11; quiz 12. Review.

PMID:
15241337
15.

The Kasumi-1 cell line: a t(8;21)-kit mutant model for acute myeloid leukemia.

Larizza L, Magnani I, Beghini A.

Leuk Lymphoma. 2005 Feb;46(2):247-55. Review.

PMID:
15621809
16.

Trisomy 19 as the sole chromosomal anomaly in hematologic neoplasms.

Johansson B, Billström R, Mauritzson N, Mitelman F.

Cancer Genet Cytogenet. 1994 May;74(1):62-5. Review.

PMID:
8194050
17.
18.

8;21 translocation and multilineage involvement.

Kwong YL, Ching LM, Liu HW, Lee CP, Pollock A, Chan LC.

Am J Hematol. 1993 Jul;43(3):212-6. Review.

PMID:
8352238
19.

Systemic mastocytosis: current classification and novel therapeutic options.

Barbie DA, Deangelo DJ.

Clin Adv Hematol Oncol. 2006 Oct;4(10):768-75. Review.

PMID:
17099633
20.

Point mutations in the AML1/RUNX1 gene associated with myelodysplastic syndrome.

Harada H, Harada Y.

Crit Rev Eukaryot Gene Expr. 2005;15(3):183-96. Review.

PMID:
16390315

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