Clinical and immunological study of a French cohort of AD-HIES patients with STAT3 deficiency

被引：0
|
作者：
Picard, C. [1 ]
Chandesris, M. O. [2 ]
De Beaucoudrey, L. [1 ]
Puel, A. [1 ]
Mahlaoui, N. [3 ]
Durandy, A. [2 ]
Suarez, F. [2 ]
Hermine, O. [2 ]
Lortholary, O. [2 ]
Fischer, A. [2 ]
Casanova, J. L. [1 ]
机构：
[1] Fac Med Necker Enfants Malad, GHMI U550, Paris, France
[2] Hop Necker Enfants Malad, Paris, France
[3] CEREDIH, Necker Hosp, Paris, France
来源：
CLINICAL AND EXPERIMENTAL IMMUNOLOGY | 2008年 / 154卷
关键词：
D O I：
暂无
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：155 / 155
页数：1
相关论文
共 50 条
  • [21] Clinical Variability of STAT3 GOF Amongst a Single-Family Cohort
    Yeager, Jamie
    Paris, Kenneth
    Wisner, Elizabeth
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2022, 149 (02) : AB23 - AB23
  • [22] Stat3 as a Therapeutic Target for the Treatment of Psoriasis: A Clinical Feasibility Study with STA-21, a Stat3 Inhibitor
    Miyoshi, Ken
    Takaishi, Mikiro
    Nakajima, Kimiko
    Ikeda, Mitsunori
    Kanda, Takashi
    Tarutani, Masahito
    Iiyama, Tatsuo
    Asao, Naoki
    DiGiovanni, John
    Sano, Shigetoshi
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2011, 131 (01) : 108 - 117
  • [23] VARIABLE CLINICAL PHENOTYPE IN A KINDRED WITH STAT3 DEFICIENCY/HYPER-IGE SYNDROME
    Boyd, A. W.
    Atkinson, T.
    Schroeder, H.
    Cajacob, A.
    ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 2012, 109 (05) : A31 - A31
  • [24] Autosomal Dominant STAT3 Deficiency and Hyper-IgE Syndrome Molecular, Cellular, and Clinical Features From a French National Survey
    Chandesris, Marie-Olivia
    Melki, Isabelle
    Natividad, Angels
    Puel, Anne
    Fieschi, Claire
    Yun, Ling
    Thumerelle, Caroline
    Oksenhendler, Eric
    Boutboul, David
    Thomas, Caroline
    Hoarau, Cyrille
    Lebranchu, Yvon
    Stephan, Jean-Louis
    Cazorla, Celine
    Aladjidi, Nathalie
    Micheau, Marguerite
    Tron, Francois
    Baruchel, Andre
    Barlogis, Vincent
    Palenzuela, Gilles
    Mathey, Catherine
    Dominique, Stephane
    Body, Gerard
    Munzer, Martine
    Fouyssac, Fanny
    Jaussaud, Rolland
    Bader-Meunier, Brigitte
    Mahlaoui, Nizar
    Blanche, Stephane
    Debre, Marianne
    Le Bourgeois, Muriel
    Gandemer, Virginie
    Lambert, Nathalie
    Grandin, Virginie
    Ndaga, Stephanie
    Jacques, Corinne
    Harre, Chantal
    Forveille, Monique
    Alyanakian, Marie-Alexandra
    Durandy, Anne
    Bodemer, Christine
    Suarez, Felipe
    Hermine, Olivier
    Lortholary, Olivier
    Casanova, Jean-Laurent
    Fischer, Alain
    Picard, Capucine
    MEDICINE, 2012, 91 (04) : E1 - E19
  • [25] Genetic, Immunological, and Clinical Features of 32 Patients with Autosomal Recessive STAT1 Deficiency
    Le Voyer, Tom
    Sakata, Sonoko
    Tsumura, Miyuki
    Khan, Taushif
    Esteve-Sole, Ana
    Al-Saud, Bandar K.
    Gungor, Hatice Eke
    Taur, Prasad
    Jeanne-Julien, Valentine
    Christiansen, Mette
    Koehler, Lisa-Maria
    ElGhazali, Gehad Eltayeb
    Rosain, Jeremie
    Nishimura, Shiho
    Sakura, Fumiaki
    Bouaziz, Matthieu
    Oleaga-Quintas, Carmen
    Nieto-Patlan, Alejandro
    Deya-Martinez, Angela
    Torun, Yasemin Altuner
    Neehus, Anna-Lena
    Roynard, Manon
    Bozdemir, Sefika Elmas
    Al Kaabi, Nawal
    Al Hassani, Moza
    Mersiyanova, Irina
    Rozenberg, Flore
    Speckmann, Carsten
    Hainmann, Ina
    Hauck, Fabian
    Alzahrani, Mohammed Hamdan
    Alhajjar, Sami Hussain
    Al-Muhsen, Saleh
    Cole, Theresa
    Fuleihan, Ramsay
    Arkwright, Peter D.
    Badolato, Raffaele
    Alsina, Laia
    Abel, Laurent
    Desai, Mukesh
    Al-Mousa, Hamoud
    Shcherbina, Anna
    Marr, Nico
    Boisson-Dupuis, Stephanie
    Casanova, Jean-Laurent
    Okada, Satoshi
    Bustamante, Jacinta
    JOURNAL OF IMMUNOLOGY, 2021, 207 (01): : 133 - 152
  • [26] NK Cell Deficiency In Job Syndrome Patients With Dominant Negative STAT3 Mutations
    Phatarpekar, Prasad V.
    Mace, Emily M.
    Orange, Jordan S.
    Freeman, Alexandra F.
    Holland, Steven M.
    Lee, Dean A.
    BLOOD, 2013, 122 (21)
  • [27] Clinical, immunological, and genetic description of a Mexican cohort of patients with DOCK8 deficiency
    Liquidano-Perez, Eduardo
    Maza-Ramos, Gibert
    Arias, Bethy Alexandra Perez
    Reyes, Saul Oswaldo Lugo
    Arevalo, Tania Barragan
    Solorzano-Morales, Sara Alejandra
    Montoya, Edna Venegas
    Staines-Boone, Aide Tamara
    Cotaya, Rogelio Guzman
    Okada, Satoshi
    Picard, Capucine
    Patin, Etienne
    Ramirez-Uribe, Nideshda
    Bustamante-Ogando, Juan Carlos
    Scheffler-Mendoza, Selma Cecilia
    Yamazaki-Nakashimada, Marco Antonio
    Saez-de-Ocariz, Marimar
    Padilla, Sara Elva Espinosa
    Gonzalez-Serrano, Maria Edith
    PEDIATRIC ALLERGY AND IMMUNOLOGY, 2024, 35 (02)
  • [28] Cerebral Vascular Abnormalities in Signal Transducer and Activator of Transcription 3 (STAT3) Deficiency: a Neuropathological Study
    Gray, Francoise
    Chandesris, Marie-Olivia
    Picard, Capucine
    Taleb, Soraya
    Kim-Thanh Ong
    Azarine, Arshid
    Fischer, Alain
    JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2012, 71 (06): : 561 - 561
  • [29] Clinical study of the French cohort of Gaucher disease patients
    Stirnemann, J
    REVUE DE MEDECINE INTERNE, 2006, 27 : S18 - S21
  • [30] Prognostic and clinical significance of STAT3 and MMP9 in patients with gastric cancer: a meta-analysis of a Chinese cohort
    Chen, Jing
    Liu, Xiaoxia
    Jiao, Haiyan
    Peng, Liang
    Huo, Zhenghao
    Yang, Wenjun
    Shen, Qin
    Li, Tao
    Liu, Qilun
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, 2015, 8 (01): : 546 - +
12345