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Salder, J.E., Shelton-Inloes, B.B., Sorace, J.M., Harlan, J.M., Titani, K. and Davie, E.W. (1985) Cloning and Caracterization of Two cDNAs Coding for Humain von Willebrand Factor. Proceedings of the National Academy of Sciences of the United States of America, 82, 6394-6398.
https://doi.org/10.1073/pnas.82.19.6394

has been cited by the following article:

• TITLE: First Case of Von Willebrand Disease in Niger

  AUTHORS: Amadou Djibrilla-Almoustapha, Moustapha Maman-Brah, Moustapha Elhadji-Chefou, Maman Rabiou Badé, Amal Al-Azhari, Youssoufa Seydou-Moussa, Maman Aminou Mahamane Sani, Mamane Daou, Souleymane Brah, Badé Malam-Abdou

  KEYWORDS: Willebrand Disease, Onco, Hematology, Niamey, Niger

  JOURNAL NAME: Open Journal of Blood Diseases, Vol.11 No.1, January 21, 2021

  ABSTRACT: Von Willebrand’s disease was first described in 1926 by Erik Von Willebrand. It is a genetic, constitutional defect of hemostasis that is different from hemophilia. It is classified among the rare diseases whose clinical manifestations are dominated by a hemorrhagic profile, which varies from patient to patient. It is an easily diagnosed disease based on a quantitative and qualitative bioassay of VWF. Treatment is multidisciplinary and is based on well-structured prevention. We report the first case of von Willebrand disease in Niger, diagnosed in the Hematology Department of Niamey’s National Hospital.