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Items: 1 to 20 of 117

1.

Laboratory diagnosis of dysfibrinogenemia.

Cunningham MT, Brandt JT, Laposata M, Olson JD.

Arch Pathol Lab Med. 2002 Apr;126(4):499-505. Review.

PMID:
11900586
2.

Dusart Syndrome in a Scandinavian family characterized by arterial and venous thrombosis at young age.

Ramanathan R, Gram J, Feddersen S, Nybo M, Larsen A, Sidelmann JJ.

Scand J Clin Lab Invest. 2013 Oct;73(7):585-90. doi: 10.3109/00365513.2013.826818. Epub 2013 Sep 3.

PMID:
24000886
3.

Fibrinogen Alès: a homozygous case of dysfibrinogenemia (gamma-Asp(330)-->Val) characterized by a defective fibrin polymerization site "a".

Lounes KC, Soria C, Mirshahi SS, Desvignes P, Mirshahi M, Bertrand O, Bonnet P, Koopman J, Soria J.

Blood. 2000 Nov 15;96(10):3473-9.

4.

Dysfibrinogenemia associated with hepatoma. Increased carbohydrate content of the fibrinogen molecule.

Gralnick HR, Givelber H, Abrams E.

N Engl J Med. 1978 Aug 3;299(5):221-6.

PMID:
207986
5.
6.

Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC Subcommittee on Fibrinogen.

Haverkate F, Samama M.

Thromb Haemost. 1995 Jan;73(1):151-61. Review.

PMID:
7740487
7.

Fibrinogen Denver: a dysfibrinogenemia associated with an abnormal Reptilase time and significant bleeding.

Walter S, Stabler S, Lefkowitz JB.

Haemophilia. 2006 Jul;12(4):393-7.

PMID:
16834739
8.

Two cases of congenital dysfibrinogenemia associated with thrombosis - Fibrinogen Praha III and Fibrinogen Plzen.

Kotlín R, Reicheltová Z, Malý M, Suttnar J, Sobotková A, Salaj P, Hirmerová J, Riedel T, Dyr JE.

Thromb Haemost. 2009 Sep;102(3):479-86. doi: 10.1160/TH08-11-0771.

PMID:
19718467
9.

Fibrinogen Caracas V, an abnormal fibrinogen with an Aalpha 532 Ser-->Cys substitution associated with thrombosis.

Marchi R, Lundberg U, Grimbergen J, Koopman J, Torres A, de Bosch NB, Haverkate F, Arocha Piñango CL.

Thromb Haemost. 2000 Aug;84(2):263-70.

PMID:
10959699
10.

[Inherited dysfibrinogenemia caused by Arg275His in the beta chain of fibrinogen].

Fang Y, Wang X, Qi H, Wu W, Ding Q, Dai J, Zhou R, Wang W, Xie S, Wang H.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Apr;22(2):201-3. Chinese.

PMID:
15793786
11.

Acquired dysfibrinogenemia caused by monoclonal production of immunoglobulin lambda light chain.

Dear A, Brennan SO, Sheat MJ, Faed JM, George PM.

Haematologica. 2007 Nov;92(11):e111-7.

12.

Fibrinogen and dysfibrinogenemia.

Morse EE.

Ann Clin Lab Sci. 1980 Jul-Aug;10(4):351-5.

PMID:
7447388
13.

Fibrinogen Logroño. A new case of congenital dysfibrinogenemia.

Rocha E, Lasierra J, Narvaiza MJ, Vilades E, Palacios E, Fernandez J.

Ric Clin Lab. 1984 Oct-Dec;14(4):663-72.

PMID:
6522973
14.

Hereditary dysfibrinogenemia.

Bithell TC.

Clin Chem. 1985 Apr;31(4):509-16.

15.

Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group.

Santacroce R, Cappucci F, Pisanelli D, Perricone F, Papa ML, Santoro R, Grandone E, Margaglione M.

Blood Coagul Fibrinolysis. 2006 Jun;17(4):235-40.

PMID:
16651864
16.

[Congenital dysfibrinogenemia. Apropos of 13 cases].

Corrihons G, Soria J, Soria C, Conard J, Horellou MH, Samama M.

Sem Hop. 1983 Oct 13;59(36):2517-23. French.

PMID:
6316508
17.
18.

Fibrinogen Nový Jicín and Praha II: cases of hereditary Aalpha 16 Arg-->Cys and Aalpha 16 Arg-->His dysfibrinogenemia.

Kotlín R, Chytilová M, Suttnar J, Riedel T, Salaj P, Blatný J, Santrůcek J, Klener P, Dyr JE.

Thromb Res. 2007;121(1):75-84. Epub 2007 Apr 3.

PMID:
17408725
19.

Identification of a dysfibrinogenemia of gammaR275C (Fibrinogen Fukushima).

Imafuku Y, Tanaka K, Takahashi K, Ogawa K, Sanpei M, Yamada H, Sato A, Yoshida H.

Clin Chim Acta. 2002 Nov;325(1-2):151-6. Review.

PMID:
12367780
20.

A new dysfibrinogenemia: fibrinogen Oslo IV.

Stormorken H, Brosstad F, Seim H.

Thromb Haemost. 1983 Apr 28;49(2):120-2.

PMID:
6868008

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