Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

more+
SELECT FILTER
 
Close

PUBLICATION DATE

22 results
Display

Recombinant von Willebrand Factor for Pediatric Patient with von Willebrand Disease: First Report in Korea

Kim S, Park YS

von Willebrand disease (VWD) is the most common hereditary bleeding disorder. The treatment of VWD consists mainly of desmopressin and plasma-derived von Willebrand factor (pd-VWF) concentrate. We report on the...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Significance of Evaluation for von Willebrand Disease in Premenopausal Women with Iron Deficiency Anemia and Menorrhagia

Kim JH, Lee JY, Lee BL, Kim KH, Lee JE, Park JK

Background: In Korea, in the case of patients with significant bleeding symptoms due to unknown causes, there are very few studies that evaluate bleeding disorders, including von Willebrand disease (VWD...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Perioperative Management and Outcomes in Children with Hereditary Bleeding Disorder: a Retrospective Review at a Single Hemophilia Treatment Center

Chon HN, Cho JH, Park YS

Background: Establishing hemostasis for surgical procedures in children with hereditary bleeding disorders is challenging. We evaluated the results of surgical procedures in children with hereditary bleeding disorders at our center...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Multicenter Study on von Willebrand Disease Realities in Yeungnam Region

Kim HJ, Shim YJ, Lee JM, Lim YT, Yang EJ, Park KM, Chueh HW, Park ES, Kim HS, Park JK, Choi EJ, Kong SG, Kim JY, Park SK

BACKGROUND: von Willebrand disease (VWD) is one of the most common inherited bleeding disorders. However, the number of patients who register to the Korea Hemophilia Foundation (KHF) is much lower...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Molecular Genetics of von Willebrand Disease in Korean Patients: Novel Variants and Limited Diagnostic Utility of Multiplex Ligation-Dependent Probe Amplification Analyses

Kim HJ, Kim SK, Yoo KY, Lee KO, Yun JW, Kim SH, Kim HJ, Park SK

BACKGROUND: von Willebrand disease (VWD), characterized by quantitative or qualitative defects of von Willebrand factor (VWF), is the most common inheritable bleeding disorder. Data regarding the genetic background of VWD...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Surgery in Patients with Von Willebrand Disease : A Single Center Experience

Park BY, Park YS

BACKGROUND: Von Willebrand disease (VWD) is the most common inherited bleeding disorder. Surgery, even relatively minor procedures, in patients with moderate to severe qualitative and quantitative deficiencies of von Willebrand...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Bone Density Status in Bleeding Disorders: Where Are We and What Needs to Be Done?

Mansouritorghabeh H, Rezaieyazdi Z

Bleeding disorders, including hemophilia, can be seen in every ethnic population in the world. Among various bleeding disorders, reduced bone density has been addressed in hemophilia A. In recent years,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Multicenter Study on Korean von Willebrand Disease Realities

Seol JH, Kim HJ, Kim SK, Yoo KY, Shim YJ, Baek HJ, Park YS, Choi EJ, Park SK

BACKGROUND: von Willebrand disease (VWD) is the most common inherited bleeding disorder with a prevalence of up to 1%. However in Korea, only 126 VWD patients were registered in Korea...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Concurrent Ruptured Pseudoaneurysm of the Internal Carotid Artery and Cerebral Infarction as an Initial Manifestation of Polycythemia Vera

Choi KS, Kim JM, Ryu JI, Oh YH

The most common neurologic manifestations of polycythemia vera (PV) are cerebral infarction and transient ischemic attacks, while cerebral hemorrhage or intracranial dissection has been rarely associated with PV. Here we...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Prevalence of Possible von Willebrand Disease

Lee MS, Kim DB, Kim SK, Yoo KY, Kim HJ, Lee SH, Park SK

  • KMID: 2279835
  • Clin Pediatr Hematol Oncol.
  • 2014 Apr;21(1):16-22.
BACKGROUND: Definition of possible von Willebrand disease (VWD) included levels of von Willebrand factor antigen (VWF:Ag) or von Willebrand factor ristocetin cofactor activity (VWF:RCo) below 30 U/dL. The purpose of...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Clinical Application and Evaluation of Preoperative Bleeding Tendency using Platelet Function Analyzer (PFA(R))-100

Han J, Do ER, Kim TS, Zhang C, Park DH

Routine preoperative tests such as BT/CT, PT/PTT and CBC, could not test abnormal hemostasis that take drugs and health functional food. We used platelet function analyzer (PFA(R))-100, to evaluate preoperative...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Erythromelalgia and Livedo Reticularis in a Patient with Essential Thrombocythemia, Acquired von Willebrand Disease, and Elevated Anti-Phospholipid Antibodies

Gambichler T, Matip R

  • KMID: 2434691
  • Ann Dermatol.
  • 2012 May;24(2):214-217.
Essential thrombocythemia (ET) is a clonal stem cell disease characterized by isolated thrombocytosis and thrombohemorrhagic complications. We describe an unusual case of ET primarly presenting with skin symptoms including erythromelalgia...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Acquired von Willebrand Syndrome Associated with Amyloidosis

Pakk H, Kim IH, Park SH, Lee DS, Park SY, Cho HI, Kim HK

Acquired von Willebrand syndrome (AvWS) is a relatively rare acquired bleeding disorder similar to inherited von Willebrand disease in terms of laboratory findings, and occurs without a personal or family...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Type 2N von Willebrand Disease with Homozygous R816W Mutation of the VWF Gene in a Nepalese Woman

Lee SY, Nam EM, Lee SN, Kim HJ, Hong KS

Type 2N von Willebrand disease (vWD) can be confused with hemophilia A due to decreased factor VIII levels and a bleeding tendency, and differential diagnosis is of importance for providing...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
von Willebrand Disease in Childhood Chronic ITP

Park SM, Lee JH, Lee KS

BACKGROUND: This study was performed to diagnose von Willebrand disease (vWD) in children with chronic immune thrombocytopenic purpura (ITP). METHODS: Seventeen cases of chronic ITP were included in this study. Screening...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Investigation of von Willebrand Factor Gene Mutations in Korean von Willebrand Disease Patients

Song J, Choi JR, Song KS

BACKGROUND: We intended to find the mutations of von Willebrand factor (VWF) gene as the most important contributing factor of von Willebrand disease (VWD) in Korean patients. METHODS: In...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Detection of Novel C4517G (Ser743Trp) Mutation in a Family with Type 2A von Willebrand Disease

Song KS, Kim HK, Park YS

  • KMID: 1515020
  • Korean J Hematol.
  • 2003 Nov;38(4):274-278.
Quantitative von Willebrand disease (VWD) are divided into partial deficiency (type 1) and total deficiency (type 3). Qualitative VWD are devided further into four subcategories (2A, 2B, 2M, 2N) based...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Subperiosteal Orbital Hematoma Associated with von Willebrand Disease

Huh KC, Kim YD

  • KMID: 2125412
  • J Korean Ophthalmol Soc.
  • 2002 Jan;43(1):213-218.
PURPOSE: Subperiosteal orbital hematoma is rare, and most cases occur in children or young adults after direct facial or orbital trauma. Nontraumatic subperiosteal hemorrhage has been reported in association with...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Subtypes of von Willebrand Disease Based on vWF Multimer Analysis in Korea

Kang SH, Kim EJ

  • KMID: 1979922
  • Korean J Pediatr Hematol Oncol.
  • 2000 Apr;7(1):42-49.
PURPOSE: von Willebrand disease is a common inherited bleeding disorder characterized by high degree of variable clinical presentation due to either quantitative or qualitative defects in von Willebrand factor....
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
von Willebrand disease with G4022A mutation (vWd Sungnam): a case report

Song KS, Kang SH, Kang MS, Park YS, Choi JR, Kim HK, Park Q

A 10-year-old male patient affected by type 2 von Willebrand disease (vWD) and his family members were investigated by hemostatic and molecular genetic studies. The propositus, who experienced frequent bleeding...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2021 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr