A Homozygous Deep Intronic Variant Causes Von Willebrand Factor Deficiency and Lack of Endothelial-Specific Secretory Organelles, Weibel–Palade Bodies

por Yadegari, Hamideh, Jamil, Muhammad Ahmer, Marquardt, Natascha, Oldenburg, Johannes
Publicado 2022

Disruption of Structural Disulfides of Coagulation FXIII-B Subunit; Functional Implications for a Rare Bleeding Disorder

por Singh, Sneha, Akhter, Mohammad Suhail, Dodt, Johannes, Sharma, Amit, Kaniyappan, Senthilvelrajan, Yadegari, Hamideh, Ivaskevicius, Vytautas, Oldenburg, Johannes, Biswas, Arijit
Publicado 2019

Multifaceted pathomolecular mechanism of a VWF large deletion involved in the pathogenesis of severe VWD

por Yadegari, Hamideh, Jamil, Muhammad Ahmer, Müller, Jens, Marquardt, Natascha, Rawley, Orla, Budde, Ulrich, El-Maarri, Osman, Lillicrap, David, Oldenburg, Johannes
Publicado 2022

ATZ11 Recognizes Not Only Z-α(1)-Antitrypsin-Polymers and Complexed Forms of Non-Z-α(1)-Antitrypsin but Also the von Willebrand Factor

por Goltz, Diane, Hittetiya, Kanishka, Yadegari, Hamideh, Driesen, Julia, Kirfel, Jutta, Neuhaus, Thomas, Steiner, Susanne, Esch, Christiane, Bedorf, Jörg, Hertfelder, Hans-Jörg, Fischer, Hans-Peter
Publicado 2014

Von Willebrand factor propeptide and pathophysiological mechanisms in European and Iranian patients with type 3 von Willebrand disease enrolled in the 3WINTERS‐IPS study

por Pagliari, Maria Teresa, Rosendaal, Frits R., Ahmadinejad, Minoo, Badiee, Zahra, Baghaipour, Mohammad‐Reza, Baronciani, Luciano, Benítez Hidalgo, Olga, Bodó, Imre, Budde, Ulrich, Castaman, Giancarlo, Eshghi, Peyman, Goudemand, Jenny, Karimi, Mehran, Keikhaei, Bijan, Lassila, Riitta, Leebeek, Frank W. G., Lopez Fernandez, Maria Fernanda, Mannucci, Pier Mannuccio, Marino, Renato, Oldenburg, Johannes, Peake, Ian, Santoro, Cristina, Schneppenheim, Reinhard, Tiede, Andreas, Toogeh, Gholamreza, Tosetto, Alberto, Trossaert, Marc, Yadegari, Hamideh, Zetterberg, Eva M. K., Peyvandi, Flora, Federici, Augusto B., Eikenboom, Jeroen
Publicado 2022