Results 111 to 120 of about 900 (164)

Bloodless Surgeries in Pediatric Dentistry: A Review. [PDF]

J Pharm Bioallied Sci
Aggarwal N, Rana V, Srivastava N, Kaushik N, Kaur N.   +4 more
europepmc   +1 more source

Clinical phenotype and laboratory characteristics of 93 patients with congenital fibrinogen disorders from unrelated 36 families. [PDF]

Res Pract Thromb Haemost
Tian D, Liang J, Gao H, Xu X, Nie W, Yin M, Lou J, Shen HQ.   +7 more
europepmc   +1 more source

Molecular Aspects of Rare Coagulation Factor Deficiencies. [PDF]

Cureus
Tourbih H, Harrach A, Bencharef H, Dehbi H, Oukkache B.   +4 more
europepmc   +1 more source

Portal Vein Thrombosis Due to Concomitant Cytomegalovirus and Epstein-Barr Virus Infection: An Underestimated Complication. [PDF]

Am J Case Rep
AlQahtani SY.
europepmc   +1 more source

P423: Recurrent pulmonary hemorrhages as a presenting symptom of congenital dysfibrinogenemia in a hospital patient identified from rapid whole genome sequencing

Genetics in Medicine Open
Rachel Hart, Pi Chun (Jennifer) Cheng, Kerry Hege, Brett Graham   +3 more
doaj   +1 more source

A heterozygous nonsense mutation in the FGB gene (c.1299G > A) causes congenital fibrinogen disorder across four consecutive generations. [PDF]

Thromb J
Chen W, Hu J.
europepmc   +1 more source

A Novel Fibrinogen Assay Using Recombinant Batroxobin and Carboxymethyl Chitosan: Carboxymethyl Chitosan Stimulates the Enzymatic Activity of Recombinant Batroxobin. [PDF]

Ann Lab Med
Kim JA, Ko E, Woo Y, Sohn YD, Kim JT, Song J, Park R.   +6 more
europepmc   +1 more source

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Dysfibrinogenemia and Thrombosis

Seminars in Thrombosis and Hemostasis, 1999
Congenital abnormal fibrinogen molecules (dysfibrinogenemias) are due to structural defects in the molecule. The molecular structure of the fibrinogen molecule is to a great extent known and this has allowed identification of the abnormalities at a molecular level.
Michael W Mosesson
exaly   +3 more sources

Congenital dysfibrinogenemias. A review

La Ricerca in Clinica e in Laboratorio, 1985
Inherited qualitative abnormalities of fibrinogen have been documented in 144 families. These dysfibrinogenemias have been inherited as autosomal dominant traits and usually are clinically silent, but in some cases are associated with bleeding, thrombosis, or defective wound healing. Dysfibrinogenemias may be associated with defects in any of the three
E, Rocha, J A, Páramo, A, Aranda, B, Cuesta, J, Fernández   +4 more
openaire   +2 more sources