- A case of thrombasthenia
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Suh YB, Sohn EK, Choi YM, Ahn CI
- KMID: 1691941
- J Korean Pediatr Soc.
- 1991 Feb;34(2):287-291.
No abstract available. -
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- Two cases of Glanzmann's thrombasthenia in brother
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Yang WM, Ham HK, Namgoong M, Lim BK, Yoon HS, Yoon KJ
- KMID: 1683073
- J Korean Pediatr Soc.
- 1989 Nov;32(11):1574-1580.
No abstract available. -
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- Three Cases of Glanzmann's Thrombasthenia
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Baek SI, Hyun MC, Kim HM, Lee KS, Ahn DH, Chun HJ, Kim JS
- KMID: 1676418
- J Korean Pediatr Soc.
- 1985 Nov;28(11):1153-1157.
No abstract available. -
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- Anesthetic Management of a Patient with Glanzmann's Thrombasthenia: A case report
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Jeong MW, Seo KS, Kim HJ, Yum KW
- KMID: 2039638
- Korean J Anesthesiol.
- 2007 Sep;53(3):407-410.
- doi: 10.4097/kjae.2007.53.3.407
Glanzmann's thrombasthenia is a rare autosomal recessive disorder characterized by bleeding tendency due to decreased coagulation function of platelets. Perioperative adequate blood transfusion including preoperative platelet transfusion seems to be... -
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- A case of Glanzmann's thrombasthenia diagnosed by analysis of glycoprotein on platelet membrane by SDS-PAGE
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Hyun DS, Oh SY, Lim DS, Whang KS, Song KS
- KMID: 1698172
- Korean J Intern Med.
- 1992 Jul;43(1):119-125.
No abstract available. -
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- Analysis of platelet glycoprotein IIIa by flow cytometry and diagnosis of Glanzmann's thrombasthenia
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Kang MS, Chang JY, Yoon KJ, Kim HM
- KMID: 1684999
- Korean J Clin Pathol.
- 1992 Sep;12(3):305-309.
No abstract available. -
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- Anesthetic experience for orthopedic surgery on a patient with Glanzmann's thrombasthenia refractory to platelet transfusion: A case report
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Park JB, Shin YS, Kim SH
- KMID: 1765457
- Korean J Anesthesiol.
- 2009 Oct;57(4):507-510.
- doi: 10.4097/kjae.2009.57.4.507
Glanzmann's thrombasthenia is an autosomal recessive bleeding disorder caused by qualitative or quantitative abnormalities of the platelet glycoprotein IIb/IIIa (GP IIb/IIIa), which can lead to excessive bleeding. Glanzmann thrombasthenia is... -
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- A case of Glanzmann's thrombasthenia disagnosed by SDS-PAGE analysis of platelet membrane glycoprotein
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Oh KE, Park SH, Kang SH, Yang CH, Kim KY, Song KS
- KMID: 1688093
- Korean J Hematol.
- 1991 Jun;26(1):181-188.
No abstract available. -
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- A case of Glanzmann's thrombasthenia diagnosed with flow cytometry and SDS-PAGE analysis of platelet membrane glycoprotein
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Doh YJ, Kim MH, Nahm CH, Song KS, won OH, Kim KY
- KMID: 1688280
- Korean J Hematol.
- 1992 Oct;27(2):443-451.
No abstract available. -
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- A Case of Acquired Glanzmann's Thrombasthenia
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Oh SY, Jang MJ, Kang MS, Oh D, Chong SY
- KMID: 1610813
- Korean J Hematol.
- 2005 Sep;40(3):183-187.
- doi: 10.5045/kjh.2005.40.3.183
Glanzmann's thrombasthenia (GT) is a rare inherited platelet disorder, which is characterized by a complete lack of platelet aggregation due to a deficiency or abnormality of the membrane glycoprotein IIb/IIIa... -
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- A Case of TypeI Glanzmann's Thrombasthenia Diagnosed by Flow Cytometry
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Lee MS, Shin CH, Kim KY, Son DW, Chung HR, Kim DH
- KMID: 1946332
- J Korean Pediatr Soc.
- 1999 Jan;42(1):133-137.
Glanzmann's thrombasthenia is a rare autosomal recessive hemorrhagic disorder of platelet function with missing or abnormal platelet plasma membrane glycoprotein IIb-IIIa, which functions as a receptor for fibrinogen. We have... -
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- A Case of Glanzmann's Thrombasthenia Successfully Managed after Tonsillectomy
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Choi JS, Jung GH, Lim JY, Kim YM, Kim SK
- KMID: 2279837
- Clin Pediatr Hematol Oncol.
- 2014 Apr;21(1):29-32.
Glanzmann's thrombasthenia (GT) is a rare autosomal recessive disease and platelet function disorder, in which platelet membrane GP IIb/ IIIa complex is defective and platelet aggregation is undeveloped. GT is... -
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- Periodontal treatment of a Glanzmann's thrombasthenia patient: A case report
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Lee HC, Han SB, Kim WS, Lee HJ
- KMID: 2045128
- J Korean Acad Periodontol.
- 1997 Sep;27(3):597-602.
- doi: 10.5051/jkape.1997.27.3.597
Glanzmann's thrombasthenia is a qualitative platelet disorder characterized by a deficiency in the platelet membrane glycoproteins IIb/IIIa. It belongs to a group of hereditary platelet disorders typified by normal platelet... -
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- A case of Thrombasthenia
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Cho SS, Kim KT, Ahn DH, Sohn KC
- KMID: 2335040
- J Korean Pediatr Soc.
- 1981 Jan;24(1):88-93.
A 6 year 6month-old boy was admitted with complains of severe spontaneou epistaxis and easy brusability. He was one of five siblings, and two of them died of recurred severe... -
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- Glanzmann Thrombasthenia in a Korean Patient: A Postoperative Intracranial Hemorrhagic Diasthesis in a Patient with a Rupture of a Cerebral Aneurysm
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Choi MS, Lee JH, Lim YC
- KMID: 2405769
- J Neurocrit Care.
- 2017 Dec;10(2):126-128.
- doi: 10.18700/jnc.170025
BACKGROUND: Glanzmann thrombasthenia (GT) is a rare disease with severe insufficiency of platelet function. There are no reports of GT associated with a cerebral hemorrhage. CASE REPORT: A 45-year-old woman had... -
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- Analysis of Platelet Membrane Glycoprotein Iib-IIIa Complex in Whole Blood of Glanzmann's Thrombasthenia by Flow Cytometry
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Lee BG, Kang MC, Park JM, Hwang PH, Kim JS
- KMID: 2208413
- J Korean Pediatr Soc.
- 1994 Nov;37(11):1540-1547.
Glanzmann's thrombasthenia is a rare autosomal recessive hemorrhagic disorder characterized by prolonged bleeding time, ad deficient or absent clot retraction in the presence of normal platelet count. The major underlying... -
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