Literature DB >> 14392404

Hereditary deficiency of proaccelerin (parahemophilia): a family study.

M S SACKS, G RACCUGLIA.   

Abstract

Entities:  

Keywords:  HEMORRHAGIC DIATHESIS

Mesh:

Substances:

Year:  1955        PMID: 14392404

Source DB:  PubMed          Journal:  J Lab Clin Med        ISSN: 0022-2143


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  5 in total

1.  PARAPEMOPHILIA (CONGENITAL FACTOV V DEFICIENCY).

Authors:  C W BAUGH
Journal:  Can Med Assoc J       Date:  1965-05-01       Impact factor: 8.262

2.  Biochemical genetics of blood coagulation.

Authors:  J B GRAHAM
Journal:  Am J Hum Genet       Date:  1956-06       Impact factor: 11.025

3.  The laboratory detection of heterozygotes.

Authors:  D Y HSIA
Journal:  Am J Hum Genet       Date:  1957-06       Impact factor: 11.025

4.  Hemorrhagic varicella in parahemophilia.

Authors:  A Girolami; R Scarpa; P Cadrobbi
Journal:  Blut       Date:  1972-11

5.  Familial intracranial haemorrhage due to factor V deficiency.

Authors:  R S Wadia; S A Sangle; S Kripalaney; M Bafna; S R Karve
Journal:  J Neurol Neurosurg Psychiatry       Date:  1992-03       Impact factor: 10.154

  5 in total

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