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| 1 |
Molecular Genetics of von Willebrand Disease in Korean Patients: Novel Variants and Limited Diagnostic Utility of Multiplex Ligation-Dependent Probe Amplification Analyses
Hee-Jung Kim, Soon Ki Kim, Ki-Young Yoo, Ki-O Lee, Jae Won Yun, Sun-Hee Kim, Hee-Jin Kim, Sang Kyu Park
Ann Lab Med.2019;39(6):545-551. Published online 2019 June 25
DOI: http://dx.doi.org/10.3343/alm.2019.39.6.545
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| 2 |
Bone Density Status in Bleeding Disorders: Where Are We and What Needs to Be Done?
Hassan Mansouritorghabeh, Zahra Rezaieyazdi
J Bone Metab.2017;24(4):201-206. Published online 2017 November 30
DOI: http://dx.doi.org/10.11005/jbm.2017.24.4.201
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| 3 |
Concurrent Ruptured Pseudoaneurysm of the Internal Carotid Artery and Cerebral Infarction as an Initial Manifestation of Polycythemia Vera
Kyu-Sun Choi, Jae-Min Kim, Je-Il Ryu, Young-Ha Oh
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| 4 |
Erythromelalgia and Livedo Reticularis in a Patient with Essential Thrombocythemia, Acquired von Willebrand Disease, and Elevated Anti-Phospholipid Antibodies
Thilo Gambichler, Rebecca Matip
Ann Dermatol.2012;24(2):214-217. Published online 2012 April 26
DOI: http://dx.doi.org/10.5021/ad.2012.24.2.214
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| 5 |
Acquired von Willebrand Syndrome Associated with Amyloidosis
Hyewon Pakk, In-Ho Kim, Sung-Hye Park, Dong-Soon Lee, Seon-Yang Park, Han-Ik Cho, Hyun Kyung Kim
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| 6 |
von Willebrand disease with G4022A mutation (vWd Sungnam): a case report
Kyung Soon Song, Shin Heh Kang, Myung Seo Kang, Young Sook Park, Jong Rak Choi, Hyun Kyung Kim, Quhen Park
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| 7 |
A Case of Type 2N von Willebrand Disease with Homozygous R816W Mutation of the VWF Gene in a Nepalese Woman
Sook Young Lee, Eun Mi Nam, Soon Nam Lee, Hee-Jin Kim, Ki Sook Hong
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| 8 |
von Willebrand Disease in Childhood Chronic ITP
Sun Min Park, Ji Hye Lee, Kun Soo Lee
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| 9 |
Investigation of von Willebrand Factor Gene Mutations in Korean von Willebrand Disease Patients
Jaewoo Song, Jong Rak Choi, Kyung Soon Song
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