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Volumn 46, Issue 2, 2014, Pages 101-103

Historical perspectives in the diagnosis and treatment of primary immune deficiencies

Author keywords

Gene mutations; Newborn screening; Primary immune deficiency; Severe combined immunodeficiency

Indexed keywords

ARTICLE; BONE MARROW TRANSPLANTATION; GENE MUTATION; GENETIC DISORDER; HUMAN; IMMUNE DEFICIENCY; LABORATORY TEST; NEWBORN SCREENING; QUALITY OF LIFE; RECURRENT INFECTION; SEVERE COMBINED IMMUNODEFICIENCY; SKIN MANIFESTATION; SURVIVAL;

EID: 84896549201     PISSN: 10800549     EISSN: 15590267     Source Type: Journal    
DOI: 10.1007/s12016-013-8384-9     Document Type: Article
Times cited : (8)

References (12)
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  • 3
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  • 4
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    • A phenotypic approach for IUIS PID classification and diagnosis: Guidelines for clinicians at the bedside
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  • 5
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    • Population prevalence of diagnosed primary immunodeficiency diseases in the United States
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    • Boyle, J.M.1    Buckley, R.H.2
  • 6
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    • Laboratory technology for the population-based screening for severe combined immunodeficiency in neonates: The winner is T cell receptor excision circles
    • Puck J (2012) Laboratory technology for the population-based screening for severe combined immunodeficiency in neonates: the winner is T cell receptor excision circles. J Allergy Clin Immunol 129:607-616
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  • 7
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  • 8
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  • 11
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.