Literature DB >> 3840917

Protein C deficiency in Austria.

I Pabinger-Fasching, E Deutsch.   

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Year:  1985        PMID： 3840917     DOI： 10.1055/s-2007-1004392

Source DB:  PubMed          Journal:  Semin Thromb Hemost        ISSN： 0094-6176            Impact factor:   4.180


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  4 in total

1.  [Homozygous infant in a family with hereditary protein C deficiency].

Authors:  G Hintz; J Weil; S Buchmann; A Azzam; K Auberger; C Beck
Journal:  Klin Wochenschr       Date:  1987-07-15

Review 2.  Clinical relevance of protein C.

Authors:  I Pabinger
Journal:  Blut       Date:  1986-08

3.  Symptomatic hereditary type-II protein C deficiency caused by a missense mutation in exon IX of the protein C gene (Gly381 to Ser).

Authors:  E Wittmann; J Walter; I Pabinger-Fasching; H H Watzke
Journal:  Ann Hematol       Date:  1994-05       Impact factor: 3.673

4.  Coumarin induced acral skin necrosis associated with hereditary protein C deficiency.

Authors:  I Pabinger; R Karnik; K Lechner; J Slany; H Niessner
Journal:  Blut       Date:  1986-06
  4 in total

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