Combined newborn screening for familial hemophagocytic lymphohistiocytosis and severe T- and B-cell immunodeficiencies

Journal of Allergy and Clinical Immunology

Volumn 134, Issue 1, 2014, Pages

  Borte, Stephan ^a,b,c   Meeths, Marie ^a   Liebscher, Ines ^b   Krist, Kerstin ^b   Nordenskjöld, Magnus ^a   Hammarström, Lennart ^a   Von Döbeln, Ulrika ^a   Henter, Jan Inge ^a   Bryceson, Yenan T ^a,d  

^a KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^b UNIVERSITY OF LEIPZIG   (Germany)

^c Klinikum St Georg   (Germany)

^d UNIVERSITY OF BERGEN   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

B LYMPHOCYTE; DISEASE SEVERITY; GENE; GENETIC SCREENING; GENOTYPE; HEMOPHAGOCYTIC SYNDROME; HETEROZYGOTE; HUMAN; LETTER; MULTIPLEX POLYMERASE CHAIN REACTION; NEWBORN; NEWBORN SCREENING; PRIORITY JOURNAL; SEVERE COMBINED IMMUNODEFICIENCY; T LYMPHOCYTE; UNC13D GENE; X LINKED AGAMMAGLOBULINEMIA; CHROMOSOME INVERSION; DRIED BLOOD SPOT TESTING; EARLY DIAGNOSIS; GENETICS; IMMUNOLOGIC DEFICIENCY SYNDROMES; IMMUNOLOGY; LYMPHOHISTIOCYTOSIS, HEMOPHAGOCYTIC; PATHOLOGY; PROCEDURES;

MEMBRANE PROTEIN; UNC13D PROTEIN, HUMAN;

B-LYMPHOCYTES; DRIED BLOOD SPOT TESTING; EARLY DIAGNOSIS; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; INFANT, NEWBORN; LYMPHOHISTIOCYTOSIS, HEMOPHAGOCYTIC; MEMBRANE PROTEINS; NEONATAL SCREENING; SEQUENCE INVERSION; T-LYMPHOCYTES;

EID: 84903731039     PISSN: 00916749     EISSN: 10976825     Source Type: Journal    
DOI: 10.1016/j.jaci.2014.04.026     Document Type: Article

References (15)

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