Inherited perforin and fas mutations in a patient with autoimmune lymphoproliferative syndrome and lymphoma.

被引：0
|
作者：
Clementi, R
Dagna, L
Dianzani, U
Dupre, L
Dianzani, I
Ciceri, F
Maccario, R
Locatelli, F
Danesino, C
Ferrarini, M
Bregni, M
机构：
[1] Policlin San Matteo, IRCCS, I-27100 Pavia, Italy
[2] Sci Inst H San Raffaele, TIGET, Milan, Italy
[3] Univ Eastern Piedmont, Novara, Italy
来源：
BLOOD | 2004年 / 104卷 / 11期
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
1379
引用
收藏
页码：387A / 387A
页数：1
相关论文
共 50 条
  • [21] Autoimmune lymphoproliferative syndrome (ALPS) due to Fas-ligand mutations.
    Bi, L
    Zheng, L
    Dale, JK
    Atkinson, TP
    Puck, JM
    Lenardo, MJ
    Straus, SE
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 626 - 626
  • [22] Autoimmune lymphoproliferative syndrome (ALPS) in a patient with a new germline Fas gene mutation
    Del-Rey, Manuel J.
    Manzanares, Javier
    Bosque, Alberto
    Aguilo, Juan I.
    Gomez-Rial, Jose
    Roldan, Ernesto
    Serrano, Antonio
    Anel, Alberto
    Paz-Artal, Estela
    Allende, Luis M.
    IMMUNOBIOLOGY, 2007, 212 (02) : 73 - 83
  • [23] Using biomarkers to predict the presence of FAS mutations in patients with features of the autoimmune lymphoproliferative syndrome
    Caminha, Iusta
    Fleisher, Thomas A.
    Hornung, Ronald L.
    Dale, Janet K.
    Niemela, Julie E.
    Price, Susan
    Davis, Joie
    Perkins, Katie
    Dowdell, Kennichi C.
    Brown, Margaret R.
    Rao, V. Koneti
    Oliveira, Joao Bosco
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2010, 125 (04) : 946 - 949
  • [24] Next Generation Sequencing for Detecting Somatic FAS Mutations in Patients With Autoimmune Lymphoproliferative Syndrome
    Lopez-Nevado, Marta
    Docampo-Cordeiro, Jorge
    Ramos, Jose T.
    Rodriguez-Pena, Rebeca
    Gil-Lopez, Celia
    Sanchez-Ramon, Silvia
    Gil-Herrera, Juana
    Diaz-Madronero, Maria J.
    Delgado-Martin, Maria A.
    Morales-Perez, Pablo
    Paz-Artal, Estela
    Magerus, Aude
    Rieux-Laucat, Frederic
    Allende, Luis M.
    FRONTIERS IN IMMUNOLOGY, 2021, 12
  • [25] Missense mutations in the Fas gene resulting in autoimmune lymphoproliferative syndrome: A molecular and immunological analysis
    Bettinardi, A
    Brugnoni, D
    QuirosRoldan, E
    Malagoli, A
    LaGrutta, S
    Correra, A
    Notarangelo, LD
    BLOOD, 1997, 89 (03) : 902 - 909
  • [26] Autoimmune lymphoproliferative syndrome caused by homozygous FAS mutations with normal or residual protein expression
    Agrebi, Nourhen
    Ben-Mansour, Lamia Sfaihi
    Medhaffar, Moez
    Hadiji, Sondes
    Fedhila, Faten
    Ben-Ali, Meriem
    Mekki, Najla
    Hachicha, Mongia
    Barsaoui, Sihem
    Barbouche, Mohamed-Ridha
    Ben-Mustapha, Imen
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2017, 140 (01) : 298 - +
  • [27] Fas gene mutations in the Canale-Smith syndrome, an inherited lymphoproliferative disorder associated with autoimmunity
    Drappa, J
    Vaishnaw, AK
    Sullivan, KE
    Chu, JL
    Elkon, KB
    NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (22): : 1643 - 1649
  • [28] Identification of FAS gene mutation in a patient with nodular lymphocyte predominance Hodgkin's lymphoma and autoimmune lymphoproliferative syndrome.
    Poppema, S
    Van den Berg, A
    BLOOD, 2000, 96 (11) : 727A - 727A
  • [29] The Autoimmune Lymphoproliferative Syndrome with Defective FAS or FAS-Ligand Functions
    Frédéric Rieux-Laucat
    Aude Magérus-Chatinet
    Bénédicte Neven
    Journal of Clinical Immunology, 2018, 38 : 558 - 568
  • [30] The Autoimmune Lymphoproliferative Syndrome with Defective FAS or FAS-Ligand Functions
    Rieux-Laucat, Frederic
    Magerus-Chatinet, Aude
    Neven, Benedicte
    JOURNAL OF CLINICAL IMMUNOLOGY, 2018, 38 (05) : 558 - 568
12345