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Items: 1 to 20 of 221

1.

Inherited thrombocytopenias: toward a molecular understanding of disorders of platelet production.

Geddis AE, Kaushansky K.

Curr Opin Pediatr. 2004 Feb;16(1):15-22. Review.

PMID:
14758109
2.

HOXA11 mutation in amegakaryocytic thrombocytopenia with radio-ulnar synostosis syndrome inhibits megakaryocytic differentiation in vitro.

Horvat-Switzer RD, Thompson AA.

Blood Cells Mol Dis. 2006 Jul-Aug;37(1):55-63. Epub 2006 Jun 9.

PMID:
16765069
3.

Linkage between the mechanisms of thrombocytopenia and thrombopoiesis.

Eto K, Kunishima S.

Blood. 2016 Mar 10;127(10):1234-41. doi: 10.1182/blood-2015-07-607903. Epub 2016 Jan 19. Review.

4.

Advances in the understanding of congenital amegakaryocytic thrombocytopenia.

Ballmaier M, Germeshausen M.

Br J Haematol. 2009 Jun;146(1):3-16. doi: 10.1111/j.1365-2141.2009.07706.x. Epub 2009 Apr 21. Review.

PMID:
19388932
5.

Megakaryocytes and platelets in alpha-granule disorders.

Smith MP, Cramer EM, Savidge GF.

Baillieres Clin Haematol. 1997 Feb;10(1):125-48. Review.

PMID:
9154319
6.

Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome.

Deutsch S, Rideau A, Bochaton-Piallat ML, Merla G, Geinoz A, Gabbiani G, Schwede T, Matthes T, Antonarakis SE, Beris P.

Blood. 2003 Jul 15;102(2):529-34. Epub 2003 Mar 20.

7.

Megakaryocytes and inherited thrombocytopenias.

Bellucci S.

Baillieres Clin Haematol. 1997 Feb;10(1):149-62. Review.

PMID:
9154320
9.

Inherited thrombocytopenias: from genes to therapy.

Balduini CL, Iolascon A, Savoia A.

Haematologica. 2002 Aug;87(8):860-80. Review.

10.

Analyses of Genetic and Clinical Parameters for Screening Patients With Inherited Thrombocytopenia with Small or Normal-Sized Platelets.

Ouchi-Uchiyama M, Sasahara Y, Kikuchi A, Goi K, Nakane T, Ikeno M, Noguchi Y, Uike N, Miyajima Y, Matsubara K, Koh K, Sugita K, Imaizumi M, Kure S.

Pediatr Blood Cancer. 2015 Dec;62(12):2082-8. doi: 10.1002/pbc.25668. Epub 2015 Jul 14.

PMID:
26175287
11.

A new familial 'giant platelet syndrome' with structural, metabolic and functional abnormalities of platelets due to a primary megakaryocyte defect.

Greaves M, Pickering C, Martin J, Cartwright I, Preston FE.

Br J Haematol. 1987 Apr;65(4):429-35.

PMID:
3580299
12.

Inherited thrombocytopenias: an approach to diagnosis and management.

Geddis AE.

Int J Lab Hematol. 2013 Feb;35(1):14-25. doi: 10.1111/j.1751-553X.2012.01454.x. Epub 2012 Jul 30. Review.

PMID:
22846067
13.

Amegakaryocytic thrombocytopenia and radio-ulnar synostosis are associated with HOXA11 mutation.

Thompson AA, Nguyen LT.

Nat Genet. 2000 Dec;26(4):397-8. No abstract available.

PMID:
11101832
14.

Low Mpl receptor expression in a pedigree with familial platelet disorder with predisposition to acute myelogenous leukemia and a novel AML1 mutation.

Heller PG, Glembotsky AC, Gandhi MJ, Cummings CL, Pirola CJ, Marta RF, Kornblihtt LI, Drachman JG, Molinas FC.

Blood. 2005 Jun 15;105(12):4664-70. Epub 2005 Mar 1.

15.

Delivering new insight into the biology of megakaryopoiesis and thrombopoiesis.

Battinelli EM, Hartwig JH, Italiano JE Jr.

Curr Opin Hematol. 2007 Sep;14(5):419-26. Review.

PMID:
17934346
16.

Qualitative disorders of platelets and megakaryocytes.

Nurden AT.

J Thromb Haemost. 2005 Aug;3(8):1773-82. Review.

17.

Lonely in Paris: when one gene copy isn't enough.

Shivdasani RA.

J Clin Invest. 2004 Jul;114(1):17-9. Review.

18.

Macrophages of patients with X-linked thrombocytopenia display an attenuated Wiskott-Aldrich syndrome phenotype.

Linder S, Wintergerst U, Bender-Götze C, Schwarz K, Pannicke U, Aepfelbacher M.

Immunol Cell Biol. 2003 Apr;81(2):130-6.

19.

[Murine models of platelet diseases].

Lanza F.

Transfus Clin Biol. 2007 May;14(1):35-40. Epub 2007 May 17. Review. French.

PMID:
17500022
20.

Congenital disorders associated with platelet dysfunctions.

Nurden P, Nurden AT.

Thromb Haemost. 2008 Feb;99(2):253-63. doi: 10.1160/TH07-09-0568. Review.

PMID:
18278172

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