Literature DB >> 14250111

FAMILIAL GLANZMANN'S THROMBASTHENIA.

L L FRIEDMAN, E J BOWIE, J H THOMPSON, C A OWEN, A L BROWN.   

Abstract

Entities:  

Keywords:  BLOOD COAGULATION DISORDERS; BLOOD COAGULATION TESTS; BLOOD PLATELET DISORDERS; GENETICS, HUMAN; PATHOLOGY

Mesh：

Year:  1964        PMID： 14250111

Source DB:  PubMed          Journal:  Mayo Clin Proc        ISSN： 0025-6196            Impact factor:   7.616


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  6 in total

Review 1.  Ultrastructural features of abnormal blood platelets. A review.

Authors:  J G White; J M Gerrard
Journal:  Am J Pathol       Date:  1976-06       Impact factor: 4.307

2.  [Pregnancy and delivery in familial Glanzmann-Naegeli disease].

Authors:  H Vinazzer; H Bergmann; F Wolf
Journal:  Blut       Date:  1974-10

Review 3.  Genetics of human blood coagulation.

Authors:  C B Kerr
Journal:  J Med Genet       Date:  1965-12       Impact factor: 6.318

4.  Assignment of human platelet GP2B (GPIIb) gene to chromosome 17, region q21.1-q21.3.

Authors:  N V Cong; G Uzan; M S Gross; C Jegou-Foubert; P Frachet; C Boucheix; G Marguerie; J Frézal
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

5.  The ultrastructure of defective human platelets.

Authors:  J G White; J M Gerrard
Journal:  Mol Cell Biochem       Date:  1978-11-01       Impact factor: 3.396

6.  Deletion of the platelet-specific alloantigen PlA1 from platelets in Glanzmann's thrombasthenia.

Authors:  T J Kunicki; R H Aster
Journal:  J Clin Invest       Date:  1978-05       Impact factor: 14.808
  6 in total

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