Zobrazeno 1 - 10
of 64
pro vyhledávání: '"M R, Ledford"'
Publikováno v:
Thrombosis and Haemostasis. 71:723-726
SummaryHomozygous protein S (PS) deficiency is a very rare disorder that causes purpura fulminans in affected newborns. This report describes the molecular genetic abnormality of a severe PS deficient child who developed purpura fulminans shortly aft
Publikováno v:
Scopus-Elsevier
A variant of von Willebrand disease (vWD) was identified in six members of a kindred spanning four generations. The proband was a 46-year-old woman with a lifelong history of bleeding, a prolonged bleeding time (> 15 minutes), markedly elevated von W
Autor:
Cole, Rebekah1 rebekah.cole@usuhs.edu, Ward, Christine2, Quintana, Taqueena3, Burgin, Elizabeth4
Publikováno v:
Professional Counselor. 2024, Vol. 14 Issue 1, p83-99. 17p.
Publikováno v:
Thrombosis and haemostasis. 71(6)
Homozygous protein S (PS) deficiency is a very rare disorder that causes purpura fulminans in affected newborns. This report describes the molecular genetic abnormality of a severe PS deficient child who developed purpura fulminans shortly after birt
Publikováno v:
Blood. 82(1)
A variant of von Willebrand disease (vWD) was identified in six members of a kindred spanning four generations. The proband was a 46-year-old woman with a lifelong history of bleeding, a prolonged bleeding time (15 minutes), markedly elevated von Wil
Publikováno v:
Thrombosis and haemostasis. 64(4)
This study was performed to compare three visualization methods for the detection of vWF multimers: autoradiography (125I), electroblot with a horseradish peroxidase system (BLOT-HRP), and an avidin-biotin peroxidase system (AV-BIO). Each method was
Publikováno v:
Medicine & Science in Sports & Exercise. 28:108
Publikováno v:
Journal of Social & Personal Relationships; Mar2023, Vol. 40 Issue 3, p734-772, 39p
Publikováno v:
Human Review; 2023, Vol. 16 Issue 1, p171-187, 17p
Publikováno v:
Journal of Family Communication; Jan-Mar2023, Vol. 23 Issue 1, p1-21, 21p, 3 Charts