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Cited by in CrossRef
For: Gadisseur A, Berneman Z, Schroyens W, Michiels JJ. Pseudohemophilia of Erik von Willebrand caused by homozygous one nucleotide deletion in exon 18 of the VW-factor gene. World J Hematol 2013; 2(4): 99-108 [DOI: 10.5315/wjh.v2.i4.99]
URL: https://www.wjgnet.com/2218-6204/full/v2/i4/99.htm
Number Citing Articles
1
Stefanie Lehner, Mahnaz Ekhlasi-Hundrieser, Carsten Detering, Hanna Allerkamp, Christiane Pfarrer, Mario von Depka Prondzinski. A 12.3-kb Duplication Within the VWF Gene in Pigs Affected by Von Willebrand Disease Type 3G3 Genes|Genomes|Genetics 2018; 8(2): 577 doi: 10.1534/g3.117.300432
2
Jan Jacques Michiels, Petr Smejkal, Miroslav Penka, Angelika Batorova, Tatiana Pricangova, Ulrich Budde, Inge Vangenechten, Alain Gadisseur. Diagnostic Differentiation of von Willebrand Disease Types 1 and 2 by von Willebrand Factor Multimer Analysis and DDAVP Challenge TestClinical and Applied Thrombosis/Hemostasis 2017; 23(6): 518 doi: 10.1177/1076029616647157
3
Tulasi Geevar, Rutvi Gautam Dave, Nitty Skariah Mathews, Snehil Kumar, Joy John Mammen, Ramya Vijayan, Fouzia N. Aboobacker, Aby Abraham, Alok Srivastava, Sukesh Chandran Nair. Laboratory characterization of obligate carriers of type 3 von Willebrand disease with a potential role for Platelet Function Analyzer (PFA‐200)International Journal of Laboratory Hematology 2022; 44(3): 603 doi: 10.1111/ijlh.13787
4
Emmanuel J. Favaloro. Congenital Bleeding Disorders2023; : 77 doi: 10.1007/978-3-031-43156-2_3