Literature DB >> 13359054

Vascular hemophilia; a familial hemorrhagic disease in males and females characterized by combined antihemophilic globulin deficiency and vascular abnormality.

M ERLANDSON, E FORT, R E LEE, I SCHULMAN, C H SMITH.   

Abstract

Entities:  

Keywords:  HEMORRHAGIC DIATHESIS

Mesh：

Substances：

Year:  1956        PMID： 13359054

Source DB:  PubMed          Journal:  Pediatrics        ISSN： 0031-4005            Impact factor:   7.124


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  10 in total

1.  [ON THE PATHOGENESIS OF THE VON WILLEBRAND-JUERGENS SYNDROME. A CLINICAL AND SUBMICROSCOPICAL STUDY].

Authors:  R MARX; G JEAN
Journal:  Klin Wochenschr       Date:  1964-05-15

2.  [Dominant mild hemophilia AB with prolonged bleeding time as a subgroup of pseudohemophilias].

Authors:  R MARX; G FRUHMANN
Journal:  Klin Wochenschr       Date:  1958-12-01

3.  [Hereditary hemorrhagic diathesis with prolonged bleeding time, partial deficiency of anti-hemophilic globulin A and a functional disorder of some thrombocyte factors].

Authors:  F KOCH; H E SCHULTZE; G SCHWICK
Journal:  Blut       Date:  1958-02

4.  [Effect of plasma fraction I on hemorrhagic vascular factors].

Authors:  S WITTE; K T SCHRICKER; D BRESSEL
Journal:  Klin Wochenschr       Date:  1957-10-01

5.  [The so-called pseudohemophilia; follow-up of a hemophilic tribe in Saarland after 20 years].

Authors:  R KLESPER; W ACHENBACH
Journal:  Klin Wochenschr       Date:  1957-10-15

6.  The Inheritance of "Vascular Hemophilia": A New and Interesting Problem in Human Genetics.

Authors:  J B Graham
Journal:  Am J Hum Genet       Date:  1959-06       Impact factor: 11.025

Review 7.  Von Willebrand's disease.

Authors:  I M Nilsson; S Lethagen
Journal:  Indian J Pediatr       Date:  1993 Mar-Apr       Impact factor: 1.967

Review 8.  Von Willebrand Disease: Current Status of Diagnosis and Management.

Authors:  Angela C Weyand; Veronica H Flood
Journal:  Hematol Oncol Clin North Am       Date:  2021-08-13       Impact factor: 3.722

9.  [Pseudohemophilia, angiohemophilia, Willebrand-Jurgens' disease and related hemorrhagic diatheses].

Authors:  R GROSS; E MAMMEN
Journal:  Klin Wochenschr       Date:  1958-02-01

10.  Antihaemophilic factor deficiency, capillary defect of von Willebrand type, and idiopathic thrombocytopenia occurring in one family.

Authors:  E K BLACKBURN; J M MACFIE; J H MONAGHAN; A P PAGE
Journal:  J Clin Pathol       Date:  1961-09       Impact factor: 3.411
  10 in total

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