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Items: 1 to 20 of 95

1.

[A congenital α2-antiplasmin deficiency].

Igala M, Oukkach B, Khoubila N, Faez S, Benchekroun S.

Ann Biol Clin (Paris). 2013 Jan-Feb;71(1):93-5. doi: 10.1684/abc.2012.0775. French.

PMID:
23396430
2.

Alpha2-antiplasmin and its deficiency: fibrinolysis out of balance.

Carpenter SL, Mathew P.

Haemophilia. 2008 Nov;14(6):1250-4. doi: 10.1111/j.1365-2516.2008.01766.x. Review.

PMID:
19141165
3.

A familial hemorrhagic diathesis in a Dutch family: an inherited deficiency of alpha 2-antiplasmin.

Kluft C, Vellenga E, Brommer EJ, Wijngaards G.

Blood. 1982 Jun;59(6):1169-80.

4.

A bleeding disorder due to deficiency of alpha 2-antiplasmin.

Miles LA, Plow EF, Donnelly KJ, Hougie C, Griffin JH.

Blood. 1982 Jun;59(6):1246-51.

5.

A novel mutation of alpha2-plasmin inhibitor gene causes an inherited deficiency and a bleeding tendency.

Maino A, Garagiola I, Artoni A, Al-Humood S, Peyvandi F.

Haemophilia. 2008 Jan;14(1):166. Epub 2007 Oct 24. No abstract available.

PMID:
17961166
6.

Severe hemorrhagic tendency in heterozygous alpha 2-antiplasmin deficiency.

Kordich L, Feldman L, Porterie P, Lago O.

Thromb Res. 1985 Dec 1;40(5):645-51.

PMID:
4089832
7.

alpha 2-Antiplasmin Enschede: dysfunctional alpha 2-antiplasmin molecule associated with an autosomal recessive hemorrhagic disorder.

Kluft C, Nieuwenhuis HK, Rijken DC, Groeneveld E, Wijngaards G, van Berkel W, Dooijewaard G, Sixma JJ.

J Clin Invest. 1987 Nov;80(5):1391-400.

8.

[Congenital deficiency of the fibrinolysis inhibitor alpha 2-antiplasmin as a cause of hemorrhagic diathesis].

Leebeek FW, Knot EA, Kluft C.

Ned Tijdschr Geneeskd. 1988 Jan 23;132(4):167-70. Review. Dutch. No abstract available.

PMID:
3277073
9.

Plasminogen activator inhibitor type 1 deficiency revealed by severe bleeding after prostatectomy in a 76-year-old male.

Bauduer F, Ménard F, Mimoun A.

Blood Coagul Fibrinolysis. 2015 Apr;26(3):350-1. doi: 10.1097/MBC.0000000000000254. No abstract available.

PMID:
25803517
10.

[Blind spots of the diagnostic hemostasis screen].

Levi M, Peters M, Briët E.

Ned Tijdschr Geneeskd. 2000 Mar 4;144(10):457-60. Review. Dutch.

PMID:
10726152
11.

[Congenital deficiency of alpha 2-plasmin inhibitor].

Yoshinaga H, Hirosawa S.

Ryoikibetsu Shokogun Shirizu. 1998;(21 Pt 2):488-90. Review. Japanese. No abstract available.

PMID:
9833551
12.

Severe postadenoidectomy bleeding revealing congenital alpha 2 antiplasmin deficiency in a child.

Paqueron X, Favier R, Richard P, Maillet J, Murat I.

Anesth Analg. 1997 May;84(5):1147-9. No abstract available.

PMID:
9141950
13.

Alpha2-antiplasmin gene deficiency in mice is associated with enhanced fibrinolytic potential without overt bleeding.

Lijnen HR, Okada K, Matsuo O, Collen D, Dewerchin M.

Blood. 1999 Apr 1;93(7):2274-81.

14.

[A homozygous quantitative defect of alpha 2-antiplasmin in a family from central Slovakia].

Zarnovicanova M, Mocikova K.

Bratisl Lek Listy. 2000;101(1):28-30. Slovak.

PMID:
10824409
15.

[Congenital deficiency of alpha 2-antiplasmin in three sisters (author's transl)].

Kamitsuji H, Yoshioka A, Takase T, Mikami S, Iida Y, Tsukada S, Fukui H.

Rinsho Ketsueki. 1981 Jul;22(7):1160-7. Japanese. No abstract available.

PMID:
7328770
16.

A splicing donor site point mutation in intron 6 of the plasmin inhibitor (alpha2 antiplasmin) gene with heterozygous deficiency and a bleeding tendency.

Hanss MM, Farcis M, Ffrench PO, de Mazancourt P, Dechavanne M.

Blood Coagul Fibrinolysis. 2003 Jan;14(1):107-11.

PMID:
12544738
17.

Physiological endogenous fibrinolysis: its congenital abnormalities.

Aoki N.

Nihon Ketsueki Gakkai Zasshi. 1983 Dec;46(7):1367-73. No abstract available.

PMID:
6675397
18.

Fibrinolysis and acquired alpha-2 plasmin inhibitor deficiency in amyloidosis.

Meyer K, Williams EC.

Am J Med. 1985 Sep;79(3):394-6.

PMID:
4036990
19.

Congenital alpha(2)-plasmin inhibitor deficiencies: a review.

Favier R, Aoki N, de Moerloose P.

Br J Haematol. 2001 Jul;114(1):4-10. Review. No abstract available.

PMID:
11472338
20.

Mild haemostatic problems associated with congenital heterozygous alpha 2-antiplasmin deficiency.

Leebeek FW, Stibbe J, Knot EA, Kluft C, Gomes MJ, Beudeker M.

Thromb Haemost. 1988 Feb 25;59(1):96-100.

PMID:
3363537
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