about
Treatment for preventing bleeding in people with haemophilia or other congenital bleeding disorders undergoing surgeryTreatment for preventing bleeding in people with congenital bleeding disorders undergoing surgeryFuture of coagulation factor replacement therapyMutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in IndiaFactor VII Deficiency: Clinical Phenotype, Genotype and TherapyRecombinant Factor VIIa Use for Endoscopic Retrograde Cholangiopancreatography With Sphincterotomy in a Patient With Choledocholithiasis and Unusual Coagulopathy.Successful Pregnancy in a Patient with Combined Deficiency of Factor V and Factor VIIIThrombosis in Inherited Fibrinogen Disorders.Current status of Italian Registries on inherited bleeding disorders.Congenital Afibrinogenemia presenting as antenatal intracranial bleed: a case report.Genotype and phenotype correlation in intracranial hemorrhage in neonatal factor VII deficiency among Thai children.Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene.Bleeding disorders in the tribe: result of consanguineous in breeding.The molecular basis of factor V and VIII procofactor activationBlood coagulation factors V and VIII: Molecular Mechanisms of Procofactor Activation.A case of intracranial hemorrhage in a neonate with congenital factor VII deficiency.Use of pharmacokinetic modelling to individualize FFP dosing in factor V deficiency.Cryptic splice site usage in exon 7 of the human fibrinogen Bbeta-chain gene is regulated by a naturally silent SF2/ASF binding site within this exonGenetic sequence analysis of inherited bleeding diseases.Spontaneous splenic rupture in a patient with congenital afibrinogenemia.Blood coagulation and its regulation by anticoagulant pathways: genetic pathogenesis of bleeding and thrombotic diseases.Massive hemoperitoneum due to a ruptured corpus luteum cyst in a patient with congenital hypofibrinogenemiaInherited defects of coagulation factor V: the hemorrhagic side.Clinical profile of patients with rare inherited coagulation disorders: a retrospective analysis of 67 patients from northern India.Bruising and bleeding in infants and children--a practical approach.Rare bleeding disorders.Surgery in patients with congenital factor VII deficiency: A single center experience.The obstetric and gynaecological management of women with inherited bleeding disorders--review with guidelines produced by a taskforce of UK Haemophilia Centre Doctors' Organization.Sustained correction of FVII deficiency in dogs using AAV-mediated expression of zymogen FVIIThe molecular basis of quantitative fibrinogen disorders.The effects of proton radiation on the prothrombin and partial thromboplastin times of irradiated ferrets.Bleeding disorders and periodontology.Blood product support for delivery in severe factor X deficiency: the use of thrombin generation to guide therapy.Hereditary Factor X (Stuart-Prower Factor) DeficiencyA review of transfusion risks and optimal management of perioperative bleeding with cardiac surgery.Congenital afibrinogenemia: a case report of a spontaneous hepatic hematoma.Prophylaxis of bleeding episodes and surgical interventions in patients with rare inherited coagulation disorders.National and international registries of rare bleeding disorders.Genetic aspects and research development in haemostasis.Medical and Surgical Management of Postpartum Hemorrhage in a Woman with Factor XIII Deficiency.
P2860
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P2860
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Recessively inherited coagulation disorders.
@ast
Recessively inherited coagulation disorders.
@en
type
label
Recessively inherited coagulation disorders.
@ast
Recessively inherited coagulation disorders.
@en
prefLabel
Recessively inherited coagulation disorders.
@ast
Recessively inherited coagulation disorders.
@en
P1433
P1476
Recessively inherited coagulation disorders
@en
P2093
Pier Mannuccio Mannucci
P304
P356
10.1182/BLOOD-2004-02-0595
P407
P577
2004-05-11T00:00:00Z