Associated Papers
Case Report: Respiratory lesions successfully treated with intravenous plasminogen, human-tvmh, replacement therapy in four patients with plasminogen deficiency type 1.
Nakar C et al.
Frontiers in Pediatrics, 2024
Study of angiopoietin and plasminogen genes in hereditary angioedema.
Kruk T et al.
Revista Da Associacao Medica Brasileira (1992), 2020
Hereditary angioedema in a single family with specific mutations in both plasminogen and SERPING1 genes.
Bork K et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : Jddg, 2020
Bork K et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : Jddg, 2020
Hereditary angioedema with a mutation in the plasminogen gene.
Bork K et al.
Allergy, 2018
Treatment of plasminogen deficiency patients with fresh frozen plasma.
Kızılocak H et al.
Pediatric Blood & Cancer, 2018
Novel plasminogen gene mutations in Turkish patients with type I plasminogen deficiency.
Dönmez-Demir B et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis, 2016
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