Literature DB >> 5306640

Two types of haemophilia (A+ and A-): a study of 48 cases.

K W Denson, R Biggs, M E Haddon, R Borrett, K Cobb.   

Abstract

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Year:  1969        PMID： 5306640     DOI： 10.1111/j.1365-2141.1969.tb01355.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN： 0007-1048            Impact factor:   6.998


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  13 in total

Review 1.  Hereditary disorders of blood coagulation due to defective and deficient synthesis of protein.

Authors:  D P Jackson
Journal:  Trans Am Clin Climatol Assoc       Date:  1971

2.  The two forms of haemophilia A in a population of Greek haemophiliacs.

Authors:  D Thomopoulos; C Gardikas
Journal:  J Clin Pathol       Date:  1972-05       Impact factor: 3.411

3.  The genetic basis of variation in factor 8 levels among haemophiliacs.

Authors:  D F Roberts
Journal:  J Med Genet       Date:  1971-06       Impact factor: 6.318

4.  Fibrinogen Marburg a new genetic variant of fibrinogen.

Authors:  G Fuchs; R Egbring; K Havemann
Journal:  Blut       Date:  1977-02

5.  Cross-reacting material in genetic variants of haemophilia B.

Authors:  D Meyer; E Bidwell; M J Larrieu
Journal:  J Clin Pathol       Date:  1972-05       Impact factor: 3.411

6.  Immunologic studies in von Willebrand's disease. Evidence that the antihemophilic factor (AHF) produced after transfusions lacks an antigen associated with normal AHF and the inactive material produced by patients with classic hemophilia.

Authors:  B Bennett; O D Ratnoff; J Levin
Journal:  J Clin Invest       Date:  1972-10       Impact factor: 14.808

7.  Immunoradiometric measurement of the factor VIII procoagulant antigen.

Authors:  J Lazarchick; L W Hoyer
Journal:  J Clin Invest       Date:  1978-11       Impact factor: 14.808

8.  Direct characterization of factor VIII in plasma: detection of a mutation altering a thrombin cleavage site (arginine-372----histidine).

Authors:  M Arai; H Inaba; M Higuchi; S E Antonarakis; H H Kazazian; M Fujimaki; L W Hoyer
Journal:  Proc Natl Acad Sci U S A       Date:  1989-06       Impact factor: 11.205

9.  [Clinical studies of familial hereditary factor VII deficiency (author's transl)].

Authors:  E Pilger; H Schenk; J Haralambus; S Sailer
Journal:  Blut       Date:  1981-05

10.  The defect in hemophilic and von Willebrand's disease plasmas studied by a recombination technique.

Authors:  H A Cooper; R H Wagner
Journal:  J Clin Invest       Date:  1974-11       Impact factor: 14.808
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