- A Case of Familial beta-thalassemia Minor
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Kim SH, Han BK, Kim HT, Lee KH, Hwang CH, Cho MK, Choi KR
- KMID: 2208313
- J Korean Pediatr Soc.
- 1995 Apr;38(4):557-560.
Thalassemias are a diverse group of inherited anemias that are characterized by defective synthesis of one or more globin chains. The thalassemias are classified according to the globin chain or... -
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- A Case of Pregnant Woman with beta-Thalassemia in Korean
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Ryu A
- KMID: 2404862
- Soonchunhyang Med Sci.
- 2017 Dec;23(2):143-145.
- doi: 10.0000/sms.2017.23.2.143
Thalassemia is hereditary disease characterized by impaired production of the normal globin peptide. Beta-thalassemia, a common disorder in Central Africa, the Middle East, and Southeast Asia, has been rarely reported... -
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- Delta beta thalassemia: a rare hemoglobin variant
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Mansoori H, Asad S, Rashid A, Karim F
- KMID: 2353507
- Blood Res.
- 2016 Sep;51(3):213-214.
- doi: 10.5045/br.2016.51.3.213
No abstract available. -
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- A case of beta-thalassemia minor
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Kim JH, Jang JS, Lee YY, Kim IS, Jeong TJ, Choi IY, Kim JQ
- KMID: 1688091
- Korean J Hematol.
- 1991 Jun;26(1):171-175.
No abstract available. -
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- A Case of beta Thalassemia Intermedia Due to Hemoglobin Cagliari (beta 60 Val - >Glu)
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Park ES, Han HY, Lim JY, Park SS, Kim SY
- KMID: 2252134
- Korean J Hematol.
- 2009 Sep;44(3):153-156.
- doi: 10.5045/kjh.2009.44.3.153
Beta Thalassemia is a very rare disease in Korea. Only14 mutations have been reported in South Korea to date. This is the first case of beta thalassemia intermedia due to... -
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- A case of vaginal delivery in beta-thalassemia minor pregnant woman
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Shim HJ, Cho EK, Jeon HJ, Lee MR, Kim YS, Bae DH, Kim HJ
- KMID: 2274054
- Korean J Obstet Gynecol.
- 2011 Jul;54(7):381-385.
- doi: 10.5468/KJOG.2011.54.7.381
The thalassemias are a group of autosomal recessive genetic disorders of hemoglobin synthesis. The thalassemias are classified into two main varieties, alpha- and beta-, depending on which of the adult... -
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- A case of familial ?thalassemia minor
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Lim YA, Jeon HS, Chae SL, Cha YJ, Kim HT, Park AJ, Lee SJ, Park SS, Kim JQ
- KMID: 1688320
- Korean J Hematol.
- 1993 May;28(1):165-169.
No abstract available. -
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- A family case of beta-thalassemia minor and hemoglobin Queens: alpha 34 (B15) Leu-Arg
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Lee NY, Cho HI, Kim SI, Kim BK, Ohba Y, Hattori Y
- KMID: 1421944
- J Korean Med Sci.
- 1992 Dec;7(4):385-388.
- doi: 10.3346/jkms.1992.7.4.385
We report a Korean family case of beta-thalassemia minor and Hb Queens. This is the first case report of Hb Queens in Korea. A 43-year-old male and his four... -
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- Three Cases of beta-thalassemia in Children with HBB Gene Mutation
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Kang EY, Lee HJ, Choi SI, Park EH, Kim SY, Hwang PH
- KMID: 2279917
- Clin Pediatr Hematol Oncol.
- 2007 Oct;14(2):192-197.
Beta thalassemia is an inherited anemia characterized by decreased or absent synthesis of beta globin chain and known to be uncommon in Korea, but is recently reported more frequently in... -
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- 2 Cases of Beta-thalassemia Minor in Korea
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Kim EJ, Jeung SW, Yoon HS
- KMID: 2396015
- Clin Pediatr Hematol Oncol.
- 2017 Oct;24(2):136-139.
- doi: 10.15264/cpho.2017.24.2.136
In Korea, recent epidemiologic studies show that the incidence of β-thalassemia is increasing as the influx of South-East Asian population increases and molecular technologies develop. However, many patients are still... -
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- Hematological malignancies complicating beta-thalassemia syndromes: a single center experience
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Alavi S, Safari A, Sadeghi E, Amiri S
- KMID: 2172915
- Blood Res.
- 2013 Jun;48(2):149-151.
- doi: 10.5045/br.2013.48.2.149
No abstract available. -
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- A Korean Family with Thalassemia Intermedia due to Co-inheritance of Triplicated alpha-Globin Genes (alphaalpha/alphaalphaalphaanti3.7) and beta-Thalassemia Trait (IVSII-1 G -> A)
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Han JY, Kim TG, Kim KH, Kim IH, Lee EY, Cho GJ, Ren ZR, Huang SZ, Zeng YT, Rodgers GP
- KMID: 2083384
- Korean J Hematol.
- 1999 May;34(2):338-343.
We report a Korean family in which the interaction of a triplicated alpha-globin locus and a heterozygous beta-thalassemia gives rise to a clinical phenotype of thalassemia intermedia. The propositus, a... -
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- RFLP Haplotypes of beta-Globin Gene Complex of beta-Thalassemic Chromosomes in Koreans
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Lee YJ, Park SS, Kim JY, Cho HI
- KMID: 1109754
- J Korean Med Sci.
- 2002 Aug;17(4):475-478.
- doi: 10.3346/jkms.2002.17.4.475
Korea is in the low-prevalence area of beta-thalassemia and the Korean population has relatively homogenous racial characteristics. Recently, we identified some causative mutations of the Korean beta-thalassemia patients. In order... -
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- Immunity to tetanus in major beta thalassemia patients
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Jahromi AS, Rahmanian
- KMID: 1965403
- Clin Exp Vaccine Res.
- 2015 Jul;4(2):184-188.
- doi: 10.7774/cevr.2015.4.2.184
PURPOSE: Patients with beta thalassemia major are at increased risk for bacterial infections specially splenectomized patients. The aim of this study was to determine the anti-tetanus antibody concentration among patients... -
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- Role of iron deficiency anemia in the propagation of beta thalssemia gene
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Usman M, Moinuddin , Ahmed SA
- KMID: 2252018
- Korean J Hematol.
- 2011 Mar;46(1):41-44.
- doi: 10.5045/kjh.2011.46.1.41
BACKGROUND: The diagnostic criterion for beta thalassemia trait (BTT) is elevated Hb-A2 levels. Iron deficiency anemia (IDA) reduces the synthesis of Hb-A2, resulting in reduced Hb-A2 levels, so patients with... -
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- Epidural anesthesia for laparoscopic cholecystectomy in a patient with sickle cell anemia, beta thalassemia, and Crohn's disease: A case report
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Bas SS, Ozlu O
- KMID: 1767176
- Korean J Anesthesiol.
- 2012 Oct;63(4):357-359.
- doi: 10.4097/kjae.2012.63.4.357
A 37-year-old woman diagnosed with sickle cell anemia (SCA), beta (+) thalassemia, Crohn's disease, and liver dysfunction was scheduled for laparoscopic cholecystectomy (LC) due to acute cholecystitis with gall bladder.... -
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- Detection of alpha-thalassemia-1 Southeast Asian and Thai Type Deletions and beta-thalassemia 3.5-kb Deletion by Single-tube Multiplex Real-time PCR with SYBR Green1 and High-resolution Melting Analysis
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Pornprasert S, Wiengkum T, Srithep S, Chainoi I, Singboottra P, Wongwiwatthananukit S
- KMID: 1735843
- Korean J Lab Med.
- 2011 Jul;31(3):138-142.
- doi: 10.3343/kjlm.2011.31.3.138
BACKGROUND: Prevention and control of thalassemia requires simple, rapid, and accurate screening tests for carrier couples who are at risk of conceiving fetuses with severe thalassemia. METHODS: Single-tube multiplex real-time PCR... -
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- Efficacy and safety of combined oral iron chelation therapy with deferasirox and deferiprone in a patient with beta-thalassemia major and persistent iron overload
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Alavi S, Sadeghi E, Ashenagar
- KMID: 2172829
- Blood Res.
- 2014 Mar;49(1):72-73.
- doi: 10.5045/br.2014.49.1.72
No abstract available. -
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- Clinical Characteristics of Pediatric Thalassemia in Korea: A Single Institute Experience
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Hong CR, Kang HJ, Lee JW, Kim H, Kim NH, Park KD, Park JD, Seong MW, Park SS, Shin HY, Ahn HS
- KMID: 1777663
- J Korean Med Sci.
- 2013 Nov;28(11):1645-1649.
- doi: 10.3346/jkms.2013.28.11.1645
Few literatures have elaborated on the clinical characteristics of children with thalassemia from low-prevalence areas. A retrospective analysis was conducted on children genetically confirmed with thalassemia at Seoul National University... -
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- A Familial Case of beta-Thalassemia Minor due to a Point Mutation (G-->A) at Position 1 in the Second Intervening Sequence
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Choi JH, Lee KH, Kim ST, Choi YM, Park SS, Cho HI
- KMID: 2143389
- Korean J Hematol.
- 1997 Aug;32(2):306-311.
The thalassemias are congenital disorders in which globin chains are present in decreased amount or absent. Beta-thalassemia, a quite common disorder in Central Africa, the Middle East, and Southeast Asia,... -
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