PHENOTYPIC HETEROGENEITY IN X-LINKED INFANTILE AGAMMAGLOBULINEMIA WITH INVITRO MONOCYTE SUPPRESSION OF IMMUNOGLOBULIN-SYNTHESIS

被引：8
|
作者：
KRANTMAN, HJ
SAXON, A
STEVENS, RH
STIEHM, ER
机构：
[1] UNIV CALIF LOS ANGELES, SCH MED, DEPT MED, LOS ANGELES, CA 90024 USA
[2] UNIV CALIF LOS ANGELES, SCH MED, DEPT MICROBIOL, LOS ANGELES, CA 90024 USA
[3] UNIV CALIF LOS ANGELES, CTR INTERDISCIPLINARY RES IMMUNOL DIS, LOS ANGELES, CA 90024 USA
来源：
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY | 1981年 / 20卷 / 02期
关键词：
D O I：
10.1016/0090-1229(81)90175-6
中图分类号：
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号：
100102 ;
摘要：
引用
收藏
页码：170 / 178
页数：9
相关论文
共 50 条
  • [21] HETEROGENEITY IN THE MAP DISTANCE BETWEEN X-LINKED AGAMMAGLOBULINEMIA AND A MAP OF 9 RFLP LOCI
    OTT, J
    MENSINK, EJBM
    THOMPSON, A
    SCHOT, JDL
    SCHUURMAN, RKB
    HUMAN GENETICS, 1986, 74 (03) : 280 - 283
  • [22] IMBALANCE IN T-CELL SUBSETS OF 5 CHILDREN WITH CONGENITAL AGAMMAGLOBULINEMIA AND ITS EFFECT ON INVITRO IMMUNOGLOBULIN-SYNTHESIS
    DEMARTINO, M
    ROSSI, ME
    PRATESI, F
    VIERUCCI, A
    BOLLETTINO DELL ISTITUTO SIEROTERAPICO MILANESE, 1983, 62 (03): : 273 - 280
  • [23] A rare progressive neurodegenerative syndrome in a patient with X-linked agammaglobulinemia on chronic IV immunoglobulin therapy
    Barcelon, E. A.
    Domingo, A. R.
    Lukban, M. B.
    MOVEMENT DISORDERS, 2014, 29 : S488 - S489
  • [24] IMMUNOGLOBULIN VARIABLE HEAVY-CHAIN CDNA SEQUENCE FROM A PATIENT WITH X-LINKED AGAMMAGLOBULINEMIA
    MORTARI, F
    OCHS, HD
    WEDGWOOD, RJP
    SCHROEDER, HW
    NUCLEIC ACIDS RESEARCH, 1991, 19 (03) : 673 - 673
  • [25] GENETIC-HETEROGENEITY IN X-LINKED AGAMMAGLOBULINEMIA COMPLICATES CARRIER DETECTION AND PRENATAL-DIAGNOSIS
    MENSINK, EJBM
    THOMPSON, A
    SCHOT, JDL
    KRAAKMAN, MEM
    SANDKUYL, LA
    SCHUURMAN, RKB
    CLINICAL GENETICS, 1987, 31 (02) : 91 - 96
  • [26] X-linked Agammaglobulinemia in Community-acquired Pneumonia Cases Revealed by Immunoglobulin Level Screening at Hospital Admission
    Vancikova, Z.
    Freiberger, T.
    Vach, W.
    Trojanek, M.
    Rizzi, M.
    Janda, A.
    KLINISCHE PADIATRIE, 2013, 225 (06): : 339 - 342
  • [27] Primary Subcutaneous Immunoglobulin (IGSC) Therapy Without Prior Intravenous Treatment in an Infant with X-Linked Agammaglobulinemia (XLA)
    Wasserman, Richard L.
    JOURNAL OF CLINICAL IMMUNOLOGY, 2014, 34 (03) : 376 - 377
  • [28] The phenotypic spectrum of X-linked, infantile onset ALG13-related developmental and epileptic encephalopathy
    Datta, Alexandre N.
    Bahi-Buisson, Nadia
    Bienvenu, Thierry
    Buerki, Sarah E.
    Gardiner, Fiona
    Cross, J. Helen
    Heron, Benedicte
    Kaminska, Anna
    Korff, Christian M.
    Lepine, Anne
    Lesca, Gaetan
    McTague, Amy
    Mefford, Heather C.
    Mignot, Cyrill
    Milh, Matthieu
    Piton, Amelie
    Pressler, Ronit M.
    Ruf, Susanne
    Sadleir, Lynette G.
    de Saint Martin, Anne
    Van Gassen, Koen
    Verbeek, Nienke E.
    Ville, Dorothee
    Villeneuve, Nathalie
    Zacher, Pia
    Scheffer, Ingrid E.
    Lemke, Johannes R.
    EPILEPSIA, 2021, 62 (02) : 325 - 334
  • [29] Enteroviral meningoencephalitis in X-linked agammaglobulinemia: Intensive immunoglobulin therapy and sequential viral detection in cerebrospinal fluid by polymerase chain reaction
    Quartier, P
    Foray, S
    Casanova, JL
    Hau-Rainsard, I
    Blanche, S
    Fischer, A
    PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2000, 19 (11) : 1106 - 1108
  • [30] The lack of BTK does not impair monocytes and polymorphonuclear cells functions in X-linked agammaglobulinemia under treatment with intravenous immunoglobulin replacement
    Cavaliere, Filomena Monica
    Prezzo, Alessandro
    Bilotta, Caterina
    Iacobini, Metello
    Quinti, Isabella
    PLOS ONE, 2017, 12 (04):
12345