Platelet storage pool deficiency

Revision as of 21:57, 20 February 2009 by Zorkun (talk | contribs) (New page: {{Infobox Disease | Name = {{PAGENAME}} | Image = | Caption = | DiseasesDB = | ICD10 = | ICD9 = | ICDO = | OMIM ...)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigation Jump to search
Platelet storage pool deficiency
OMIM 185050
MeSH D010981

Platelet storage pool deficiency is a type of coagulopathy characterized by defects in the granules in platelets.[1]

Examples include:

References

  1. Alan D. Michelson (2007). Platelets. Burlington, MA: Academic Press/Elsevier. p. 313. ISBN 0-12-369367-5.
  2. Huizing M, Anikster Y, Fitzpatrick DL; et al. (2001). "Hermansky-Pudlak syndrome type 3 in Ashkenazi Jews and other non-Puerto Rican patients with hypopigmentation and platelet storage-pool deficiency". Am. J. Hum. Genet. 69 (5): 1022–32. doi:10.1086/324168. PMC 1274349. PMID 11590544. Unknown parameter |month= ignored (help)
  3. Novak EK, McGarry MP, Swank RT (1985). "Correction of symptoms of platelet storage pool deficiency in animal models for Chediak-Higashi syndrome and Hermansky-Pudlak syndrome". Blood. 66 (5): 1196–201. PMID 3902123. Unknown parameter |month= ignored (help)
  4. Hayward CP, Weiss HJ, Lages B; et al. (2001). "The storage defects in grey platelet syndrome and alphadelta-storage pool deficiency affect alpha-granule factor V and multimerin storage without altering their proteolytic processing". Br. J. Haematol. 113 (4): 871–7. PMID 11442477. Unknown parameter |month= ignored (help)