YU Jia-Lin,ZHAO Xiao-Dong,GUO Yang-Yang et al. Suggestions for diagnosis of primary immunodifficiency disease in infants less than 3 months of age[J]. CJCP, 2017, 19(1): 22-26.
Picard C, Al-Herz W, Bousfiha A, et al. Primary immunodeficiency diseases:an update on the classification from the International Union of Immunological Societies Expert Committee for primary immunodeficiency[J]. J Clin Immunol, 2015, 35(8):696-726.
[4]
Bousfiha AA, Jeddane L, El Hafidi N, et al. First report on the Moroccan registry of primary immunodeficiencies:15 years of experience (1998-2012)[J]. J Clin Immunol, 2014, 34(4):459-468.
[5]
Cooper MA, Pommering TL, Korányi K. Primary immunodeficiencies[J]. Am Fam Physician, 2003, 68(10):2001-2008.
[6]
Carneiro-Sampaio M, Jacob CM, Leone CR. A proposal of warning signs for primary immunodeficiencies in the first year of life[J]. Pediatr Allergy Immunol, 2011, 22(3):345-346.
Roxo-Junior P, Silva J, Andrea M. A family history of serious complications due to BCG vaccination is a tool for the early diagnosis of severe primary immunodeficiency[J]. Ital J Pediatr, 2013, 39:54.
Chase NM, Verbsky JW, Routes JM. Newborn screening for T-cell deficiency[J]. Curr Opin Allergy Clin Immunol, 2010, 10(6):521-525.
[14]
Chase NM, Verbsky JW, Routes JM. Newborn screening for SCID:three years of experience[J]. Ann N Y Acad Sci, 2011, 1238:99-105.
[15]
Hammarström L. Primary immunodeficiencies screening:neonatal screening for T/B cell disorders-a triplex PCR method for quantitation of TRECs and KRECs in newborns[J]. Clin Exp Immunol, 178(Suppl):14-15.
