Literature DB >> 14273317

THE INHERITANCE OF STUART DISEASE: INVESTIGATION OF A FAMILY WITH FACTOR X DEFICIENCY.

E LECHLER, W P WEBSTER, H R ROBERTS, G D PENICK.   

Abstract

Keywords:  ADOLESCENCE; BLOOD COAGULATION TESTS; DIAGNOSIS; GENETICS, HUMAN; HYPOPROTHROMBINEMIAS

Mesh：

Year:  1965        PMID： 14273317     DOI： 10.1097/00000441-196503000-00006

Source DB:  PubMed          Journal:  Am J Med Sci        ISSN： 0002-9629            Impact factor:   2.378


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  3 in total

1.  Factor X Friuli coagulation disorder. First report of a patient born in Friuli after the description of the disease.

Authors:  A Girolami; A Carli; R Falomo; L De Marco
Journal:  Blut       Date:  1973-09

2.  Severe congenital factor X deficiency with intracranial haemorrhage.

Authors:  T Sumer; M Ahmad; N K Sumer; M I Al-Mouzan
Journal:  Eur J Pediatr       Date:  1986-04       Impact factor: 3.183

3.  Factor X deficiency in the neonatal period.

Authors:  S J Machin; M R Winter; S C Davies; I J Mackie
Journal:  Arch Dis Child       Date:  1980-05       Impact factor: 3.791
  3 in total

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