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Results: 1 to 20 of 30

Select item 229863221.

An infant with aortoiliac thrombosis due to congenital protein C deficiency: anesthetic implications.

Kumar N, Dogra N.

J Clin Anesth. 2012 Sep;24(6):506-7. doi: 10.1016/j.jclinane.2011.08.009. No abstract available.

PMID:: 22986322; [PubMed - indexed for MEDLINE]

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Select item 229844982.

The prothrombotic phenotypes in familial protein C deficiency are differentiated by computational modeling of thrombin generation.

Brummel-Ziedins KE, Orfeo T, Callas PW, Gissel M, Mann KG, Bovill EG.

PLoS One. 2012;7(9):e44378. doi: 10.1371/journal.pone.0044378. Epub 2012 Sep 12.

PMID:: 22984498; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 229511463.

Clinical and genetic features of protein C deficiency in 23 unrelated Chinese patients.

Ding Q, Shen W, Ye X, Wu Y, Wang X, Wang H.

Blood Cells Mol Dis. 2013 Jan;50(1):53-8. doi: 10.1016/j.bcmd.2012.08.004. Epub 2012 Aug 27.

PMID:: 22951146; [PubMed - indexed for MEDLINE]

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Select item 227056204.

Life-saving percutaneous intervention in young patient with massive pulmonary embolism.

Yaakob ZH, Undok AW, Abidin IZ, Wan Ahmad WA.

Ann Saudi Med. 2012 Jul-Aug;32(4):433-6.

PMID:: 22705620; [PubMed - indexed for MEDLINE]

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Select item 225883265.

A novel frameshift mutation Gly239Serfs*8 in the PROC gene results in protein C deficiency in a Korean patient.

Park SH, Jang S, Yang HK, Shim H, Park CJ, Chi HS, Oh YM.

Ann Hematol. 2012 Nov;91(11):1829-30. doi: 10.1007/s00277-012-1484-4. Epub 2012 May 16. No abstract available.

PMID:: 22588326; [PubMed - indexed for MEDLINE]

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Select item 225763106.

Hereditary protein C deficiency in Indian patients with venous thrombosis.

Pai N, Ghosh K, Shetty S.

Ann Hematol. 2012 Sep;91(9):1471-6. doi: 10.1007/s00277-012-1483-5. Epub 2012 May 11.

PMID:: 22576310; [PubMed - indexed for MEDLINE]

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Select item 225451357.

Genetic background analysis of protein C deficiency demonstrates a recurrent mutation associated with venous thrombosis in Chinese population.

Tang L, Guo T, Yang R, Mei H, Wang H, Lu X, Yu J, Wang Q, Hu Y.

PLoS One. 2012;7(4):e35773. doi: 10.1371/journal.pone.0035773. Epub 2012 Apr 24.

PMID:: 22545135; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 225313458.

Homozygous protein C deficiency with late onset venous thrombosis: identification and in vitro expression study of a novel Pro275Ser mutation.

Yu T, Dai J, Liu H, Wang J, Ding Q, Wang H, Wang X, Fu Q.

Pathology. 2012 Jun;44(4):348-53. doi: 10.1097/PAT.0b013e328353a218.

PMID:: 22531345; [PubMed - indexed for MEDLINE]

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Select item 225272939.

Thrombophilic disorders: a real threat to patients with end-stage renal disease on hemodialysis and at the time of renal transplantation.

Klai S, Fekih-Mrissa N, Ghachem A, Baffoun A, Nciri B, Hmida J, Gritli N.

Blood Coagul Fibrinolysis. 2012 Jul;23(5):406-10. doi: 10.1097/MBC.0b013e328353a5fc.

PMID:: 22527293; [PubMed - indexed for MEDLINE]

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Select item 2248799010.

A case of a patient with protein C deficiency presenting with concurrent thromboses in the pulmonary arteries and innominate artery: a suggestive computed tomographic finding of thrombophilia.

Kim JK, Lee HY, Song IS, Yoo SM, Rho JY, Moon JY, White CS.

J Thorac Imaging. 2012 Nov;27(6):W180-1. doi: 10.1097/RTI.0b013e3182475424.

PMID:: 22487990; [PubMed - indexed for MEDLINE]

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Select item 2244137311.

Acroangiodermatitis of Mali in protein C deficiency due to a novel PROC gene mutation.

Wei-Min Tan A, Lee JS, Pramono ZA, Chong WS.

Am J Dermatopathol. 2012 Apr;34(2):e19-21. doi: 10.1097/DAD.0b013e3182169528.

PMID:: 22441373; [PubMed - indexed for MEDLINE]

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Select item 2239843112.

Dabigatran etexilate (Pradaxa®) for preventing warfarin-induced skin necrosis in a patient with severe protein C deficiency.

Hermans C, Eeckhoudt S, Lambert C.

Thromb Haemost. 2012 Jun;107(6):1189-91. doi: 10.1160/TH11-11-0788. Epub 2012 Mar 8. No abstract available.

PMID:: 22398431; [PubMed - indexed for MEDLINE]

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Select item 2232116613.

The phenotypic and genetic assessment of protein C deficiency.

Cooper PC, Hill M, Maclean RM.

Int J Lab Hematol. 2012 Aug;34(4):336-46. doi: 10.1111/j.1751-553X.2012.01401.x. Epub 2012 Feb 9. Review.

PMID:: 22321166; [PubMed - indexed for MEDLINE]

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Select item 2224524414.

Characteristics of fibrin formation and clot stability in individuals with congenital type IIb protein C deficiency.

Foley JH, Ferris L, Brummel-Ziedins KE.

Thromb Res. 2012 Apr;129(4):e142-6. doi: 10.1016/j.thromres.2011.12.020. Epub 2012 Jan 13.

PMID:: 22245244; [PubMed - indexed for MEDLINE]

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Select item 2216845015.

Hereditary protein C deficiency and thrombosis risk: genotype and phenotype relation in a large Italian family.

Cafolla A, D'Andrea G, Baldacci E, Margaglione M, Mazzucconi MG, Foà R.

Eur J Haematol. 2012 Apr;88(4):336-9. doi: 10.1111/j.1600-0609.2011.01742.x. Epub 2012 Jan 10.

PMID:: 22168450; [PubMed - indexed for MEDLINE]

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Select item 2195880516.

Intermittent coronary artery occlusion caused by a floating thrombus in the left coronary sinus of valsalva of a patient with a normal aorta and protein C deficiency.

Hisatomi K, Yamada T, Odate T, Yamashita K.

Ann Thorac Surg. 2011 Oct;92(4):1508-10. doi: 10.1016/j.athoracsur.2011.04.037.

PMID:: 21958805; [PubMed - indexed for MEDLINE]

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Select item 2183969617.

Diagnosis and management of neonatal purpura fulminans.

Price VE, Ledingham DL, Krümpel A, Chan AK.

Semin Fetal Neonatal Med. 2011 Dec;16(6):318-22. doi: 10.1016/j.siny.2011.07.009. Epub 2011 Aug 11. Review.

PMID:: 21839696; [PubMed - indexed for MEDLINE]

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Select item 2173723218.

Severe protein C deficiency is associated with organ dysfunction in patients with severe sepsis.

Shaw AD, Vail GM, Haney DJ, Xie J, Williams MD.

J Crit Care. 2011 Dec;26(6):539-45. doi: 10.1016/j.jcrc.2011.05.006. Epub 2011 Jul 6.

PMID:: 21737232; [PubMed - indexed for MEDLINE]

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Select item 2171841419.

Protein C deficiency with concurrent essential thrombocytosis and orbital compartment syndrome.

Sun MT, Chan W, McRae S, Selva D.

Clin Experiment Ophthalmol. 2012 Apr;40(3):325-6. doi: 10.1111/j.1442-9071.2011.02642.x. Epub 2011 Sep 9. No abstract available.

PMID:: 21718414; [PubMed - indexed for MEDLINE]

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Select item 2162124920.

Genetic defects in Portuguese families with inherited protein C deficiency.

David D, Ferreira C, Ventura C, Freire I, Moreira I, Gago T.

Thromb Res. 2011 Sep;128(3):299-302. doi: 10.1016/j.thromres.2011.05.001. Epub 2011 May 31. No abstract available.

PMID:: 21621249; [PubMed - indexed for MEDLINE]

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5 free full-text articles in PubMed Central

The prothrombotic phenotypes in familial protein C deficiency are differentiated by computational modeling of thrombin generation. [PLoS One. 2012]
The prothrombotic phenotypes in familial protein C deficiency are differentiated by computational modeling of thrombin generation.
Brummel-Ziedins KE, Orfeo T, Callas PW, Gissel M, Mann KG, Bovill EG. PLoS One. 2012; 7(9):e44378. Epub 2012 Sep 12.
Genetic background analysis of protein C deficiency demonstrates a recurrent mutation associated with venous thrombosis in Chinese population. [PLoS One. 2012]
Genetic background analysis of protein C deficiency demonstrates a recurrent mutation associated with venous thrombosis in Chinese population.
Tang L, Guo T, Yang R, Mei H, Wang H, Lu X, Yu J, Wang Q, Hu Y. PLoS One. 2012; 7(4):e35773. Epub 2012 Apr 24.
Genome scan of clot lysis time and its association with thrombosis in a protein C-deficient kindred. [J Thromb Haemost. 2011]
Genome scan of clot lysis time and its association with thrombosis in a protein C-deficient kindred.
Meltzer ME, Hasstedt SJ, Vossen CY, Callas PW, DE Groot PG, Rosendaal FR, Lisman T, Bovill EG. J Thromb Haemost. 2011 Jul; 9(7):1383-90.

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