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Congenital Agammaglobulinemia of Bruton Type

Ko KW, Chi JG

  • KMID: 1699394
  • J Korean Pediatr Soc.
  • 1982 Oct;25(10):1082-1087.
No abstract available.
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X-linked agammaglobulinemia

Kim DS, Yoon MY, Lee HS

  • KMID: 1684929
  • Korean J Clin Pathol.
  • 1991 Nov;11(3):545-548.
No abstract available.
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A Case of X-linked Agammaglobulinemia with Delayed Growth

Kim MJ, Kim HY, Lee MD, Kim HS, Shin YG, Chung CH, Shin KC

  • KMID: 2331145
  • J Korean Soc Endocrinol.
  • 1999 Mar;14(1):153-159.
In 1980, the clinical syndrome of X-linked agammaglobulinemia and isolated growth hormone defieiency (XLA/IGHD) was first described by Fleisher. We report here 25-year old man with isolated growth hormone deficiency...
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50 Years Ago in Journal of Academy of Pediatrics: Agammaglobulinemia

Kim DS

No abstract available.
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A Case of Gastric Adenocarcinoma in a Patient with X-linked Agammaglobulinemia

Ok CS, Lee JH, Noh JW, Sohn SY, Chang BS, Ku BH, Koh WJ, Sung CO

  • KMID: 1494770
  • Korean J Gastrointest Endosc.
  • 2010 Jan;40(1):27-30.
X-linked agammaglobulinemia is a common type of primary immunodeficiency disorder that's caused by mutation of the BTK gene. The absence of B lymphocytes and plasma cells causes recurrent infections. Patients...
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A Case of Rheumatoid Arthritis in a Patient with Bruton-Type Agammaglobulinemia

Park DJ, Lee SJ, Kim TJ, Park YW, Bae E, Kang ES, Lee SS

Bruton-type agammaglobulinemia is primary hypogammaglobulinemia followed by severe recurrent infection, including bacterial otitis media, bronchitis, pneumonia, and meningitis. Septic arthritis is a main musculoskeletal disorder that can occur in association...
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Agammaglobulinemia in a 8-year-old boy with recurrent pneumococcal infection and his elder brother

Chung SH, Ahn YJ, Kim SY, Cho BS, Kim SD

Patients with primary immunodeficiencies often have symptoms of their disease for months or years before diagnosis and treatment. This is partly because these disorders are relatively uncommon and the infections...
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A Case of Congenital Agammaglobulinemia

Kim SY, Kim JH, Kang JH, Lee JS, Shim SI

  • KMID: 2208374
  • J Korean Pediatr Soc.
  • 1995 Jan;38(1):99-103.
Congenital agammaglobulinemia was described first among all human immunodeficiencies, and characterized by defect of B lymphocyte maturation and severe panhypogammaglobulinemia. These patients frequently acquire infections with high-grade extracellular pyogenic pyogenic...
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Hepatocellular Carcinoma Following Vertical Transmission of Hepatitis B Virus in a Child with X-linked Agammaglobulinemia

Oh JG, Kim BJ, Kook H, Woo YJ, Choi YY, Ma JS, Hwang TJ, Seo JJ

  • KMID: 2275126
  • Korean J Pediatr Gastroenterol Nutr.
  • 2000 Mar;3(1):105-109.
X-linked agammaglobulinemia (XLA) is a primary inherited B-cell immunodeficiency. The prevalence of neoplastic disease in patients with XLA is approximatedly 0.7%. The most frequent tumor is lymphoreticular malignancy. We report...
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A Case of Agammaglobulinemia Detected by ABO Discrepancy in a 13-year-old Girl

Park TS, Oh SH, Choi JC, Kim HH, Park JH, Lee EY, Son HC

  • KMID: 2082778
  • Korean J Lab Med.
  • 2002 Oct;22(5):364-366.
We report a case of agammaglobulinemia detected by ABO discrepancy in a 13-year-old girl. At first, she visited Pusan National University Hospital complaining of joint swelling and pain. For trans-fusion,...
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A Case of X-Linked Agammaglobulinemia Associated with Severe Neutropenia

Lee KY, Lee DK, Park JE, Lee JH, Lee MI

  • KMID: 2051393
  • Pediatr Allergy Respir Dis.
  • 2002 Dec;12(4):328-333.
X-linked agammaglobulinemia(XLA) is characterized by markedly reduced number of B lymphocytes, panhypogammaglobulinemia, recurrent bacterial infections in the first few years of life because of genetic defect for Bruton's tyrosine kinase...
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A Case of Fabry's Disease with Congenital Agammaglobulinemia

Lee KY, Jeon SY, Hong JW, Kim SE, Song KH, Kim YH, Kim KH

Fabry's disease is an X-linked lysosomal storage disorder caused by abnormalities in the alpha-galactosidase A (GLA) gene, which leads to a GLA deficiency and to the intracellular deposition of globotriaosylceramide...
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A Case of X-linked Agammaglobulinemia

Jang SH, Kho WJ, Kim CH, Chung KH, Lee JH, Chung HS, Han SK

  • KMID: 2251566
  • Korean J Med.
  • 1997 Sep;53(3):426-430.
X-linked agammaglobulinemia is attributed to the genetic defect for Bruton's tyrosine kinase at Xq22 region and the developmental arrest of pre-B lymphocytes. The characteristics of the disease are as follows;...
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A Case of X-Linked Agammaglobulinemia with Btk Gene Intron 2 Mutation

Chung MJ, Jung JY, Son JY, Ku CR, Park BH, Byun MK, Moon JA, Kim YS, Kim SK, Chang J, Kim SK, Shin DM, Park MS

  • KMID: 2319075
  • Tuberc Respir Dis.
  • 2008 Sep;65(3):207-211.
X-linked agammaglobulinemia is the most common type of primary immunodeficiency disorder. Mutation ofthe cytoplasmic tyrosine kinase gene, Btk (Bruton's tyrosine kinase), is known to be the etiology of X-linked agammaglobulinemia....
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A Case of Rectal Cancer in a Patient with X-linked Agammagloubulinemia

Jeon BJ, Kim SW, Ko KS, Kim SH, Kim IH, Lee SO, Lee ST, Kim DG

  • KMID: 2304731
  • Korean J Gastrointest Endosc.
  • 2010 Dec;41(6):360-363.
X-linked agammaglobulinemia (XLA) is a primary immunodeficiency disorder caused by germline mutation of the Bruton tyrosine kinase (BTK) gene. Most of the patients diagnosed X-LA suffer from recurrent infections of...
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Pyoderma Gangrenosum in a Patient with X-Linked Agammaglobulinemia

Tan Q, Ren FL, Wang H

X-linked agammaglobulinemia (XLA) is a primary immunodeficiency disorder caused by germline mutations of B-cell tyrosine kinase (BTK) gene. It is characterized by decreased serum immunoglobulins levels and circulating mature B...
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A Case of X-lined Agammaglobulinemia Presenting Recurrent Respiratory Infections

  • KMID: 2090215
  • Korean J Asthma Allergy Clin Immunol.
  • 2011 Mar;31(1):67-71.
X-linked agammaglobulinemia (XLA) is a primary immunodeficiency disease caused by Bruton's tyrosine kinase (Btk) gene mutation, resulting in the absence or low number of mature B cells, reduced levels of...
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Pneumocystis jiroveci Pneumonia in a 5-month-old Boy with Agammaglobulinemia: A Case Report

Chung BH, Nam HK, Rhie YJ, Lee KC, Choung JT, Lim CH, Yoo Y

Pneumocystis jiroveci (P. jiroveci) pneumonia is known as a common opportunistic infection in patients with impaired immunity. Underlying disease or conditions related to the development of P. jiroveci pneumonia include...
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X-linked Agammaglobulinemia Associated with Bronchiectasis: A Case Report

Yu CM, Koh WJ, Kim KC, Lee BH, Hwang JH, Kang EH, Suh GY, Chung MP, Kim H, Kwon OJ, Ki CS, Kim JW

Bronchiectasis is defined as an abnormal, irreversible dilatation of the bronchi, which may result from a number of possible causes, and the recognition of these causes may lead to a...
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A case of X-linked agammaglobulinemia with deletion of introns 15-18 of Btk gene mediated by Alu-Alu recombination

Lee HJ, Ko JS, Kwon SS, Yoo JH, Min JK

  • KMID: 2252751
  • Korean J Med.
  • 2003 Nov;65(Suppl 3):S798-S804.
X-linked agammaglobulinemia (XLA) is characterized by early onset of recurrent bacterial infection, markedly reduced levels of all major classes of immunoglobulins in the serum and few mature B cells in...
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