A Cohort Study on Deficiency of ADA2 from China (English)
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In:
Journal of Clinical Immunology
;
43
, 4
; 835-845
;
2023
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ISSN:
- Article (Journal) / Electronic Resource
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Title:A Cohort Study on Deficiency of ADA2 from China
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Contributors:Li, Guo-min ( author ) / Han, Xu ( author ) / Wu, Ye ( author ) / Wang, Wei ( author ) / Tang, Hong-xia ( author ) / Lu, Mei-ping ( author ) / Tang, Xue-mei ( author ) / Lin, Yi ( author ) / Deng, Fan ( author ) / Yang, Jun ( author )
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Published in:Journal of Clinical Immunology ; 43, 4 ; 835-845
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Publisher:
- New search for: Springer US
- New search for: Springer Science + Business Media B.V
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Place of publication:Dordrecht [u.a.]
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Publication date:2023
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ISSN:
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ZDBID:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
- New search for: 44.45 / 44.45$jImmunologie
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Keywords:
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Classification:
BKL: 44.45 Immunologie / 44.45$jImmunologie -
Source:
Table of contents – Volume 43, Issue 4
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 671
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Foreword to the English Translation of Kostmann’s MemoirsCasanova, Jean-Laurent / Hammarström, Lennart et al. | 2023
- 675
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“The Regimental Pediatrician”: Forewords and BackgroundKostmann, Rolf et al. | 2023
- 680
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COVID-19 and Mixed Cryoglobulinemia Syndrome: Long-Term Survey Study on the Prevalence and Outcome, Vaccine Safety, and ImmunogenicityGragnani, Laura / Visentini, Marcella / Lorini, Serena / Santini, Stefano Angelo / Lauletta, Gianfranco / Mazzaro, Cesare / Urraro, Teresa / Quartuccio, Luca / Cacciapaglia, Fabio / Ruscitti, Piero et al. | 2023
- 692
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Pathogenic DDOST Variant Is Associated with Humoral Immune DeficiencySitek, Andrea / Ligezka, Anna / Budhraja, Rohit / Morava, Eva / Chiarella, Sergio E. et al. | 2023
- 695
-
Severe Periodontitis in Adults with Chronic Granulomatous DiseaseBeltrán-Bustamante, Jorge / Ogando, Juan Carlos Bustamante / De la Teja Ángeles, Eduardo / Blancas Galicia, Lizbeth et al. | 2023
- 699
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STING-Associated Vasculopathy with Onset in infancy (SAVI) Presenting as Massive Intra Alveolar HemorrhageLadoux, Clara / Pasquet, Marlène / Crow, Yanick J. / Frémond, Marie Louise / Roditis, Léa et al. | 2023
- 703
-
Compound Heterozygous Mutations in PRKCD Associated with Early-Onset Lupus and Severe and Invasive Infections in SiblingsRoderick, Marion R. / Jefferson, Lucy / Renton, William / Belot, Alexandre et al. | 2023
- 706
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Clinical Non-penetrance Associated with Biallelic Mutations in the RNase H2 ComplexCrow, Yanick J. et al. | 2023
- 709
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Autosomal Recessive Inflammatory Skin Disease Caused by a Novel Biallelic Loss-of-Function Variant in CARD11Nguyen, Amie / Lu, Henry Y. / Turvey, Stuart E. / Snow, Andrew L. et al. | 2023
- 714
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Inborn Errors of Immunity in the Republic of Moldova: Advances and HopeSciuca, Svetlana / Tomacinschii, Cristina / Selevestru, Rodica / Sacara, Victoria / Maródi, László et al. | 2023
- 717
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Distinct Lymphocyte Immunophenotyping and Quantitative Anti-Interferon Gamma Autoantibodies in Taiwanese HIV-Negative Patients with Non-Tuberculous Mycobacterial InfectionsLee, Wen-I. / Fang, Yao-Fan / Huang, Jing-Long / You, Huey-Ling / Hsieh, Meng-Ying / Huang, Wan-Ting / Liang, Chi-Jou / Kang, Chen-Chen / Wu, Ting-Shu et al. | 2023
- 728
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Mendelian Susceptibility to Mycobacterial Disease (MSMD): Clinical, Immunological, and Genetic Features of 22 Patients from 15 Moroccan KindredsErrami, Abderrahmane / Baghdadi, Jamila El / Ailal, Fatima / Benhsaien, Ibtihal / Bakkouri, Jalila El / Jeddane, Leila / Rada, Noureddine / Benajiba, Noufissa / Mokhantar, Khaoula / Ouazahrou, Kaoutar et al. | 2023
- 741
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A Novel Deletion in FERMT3 Causes LAD-III in a Turkish FamilyKöker, Nezihe / Deveci, İhsan / van Leeuwen, Karin / Akbayram, Sinan / Roos, Dirk / Kuijpers, Taco W. / Köker, Mustafa Yavuz et al. | 2023
- 747
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Initial manifestations in Patients with Inborn Errors of Immunity Based on Onset Age: a Study from a Nationwide Survey in JapanKido, Takahiro / Hosaka, Sho / Imagawa, Kazuo / Fukushima, Hiroko / Morio, Tomohiro / Nonoyama, Shigeaki / Takada, Hidetoshi et al. | 2023
- 756
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Clinical and Genetic Characteristics of BCG Disease in Chinese Children: a Retrospective StudyZeng, Yuyuan / Ying, Wenjing / Wang, Wenjie / Hou, Jia / Liu, Luyao / Sun, Bijun / Hui, Xiaoying / Gu, Yu / Song, Xiaoyu / Wang, Xiaochuan et al. | 2023
- 769
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The Association of Serum Immunoglobulins with Risk of Cardiovascular Disease and Mortality: the Rotterdam StudyKhan, Samer R. / Dalm, Virgil A. S. H. / Ikram, M. Kamran / Peeters, Robin P. / van Hagen, P. Martin / Kavousi, Maryam / Chaker, Layal et al. | 2023
- 780
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Thalidomide as an Effective Treatment in Sideroblastic Anemia, Immunodeficiency, Periodic Fevers, and Developmental Delay (SIFD)Li, Yan / Deng, Mengyue / Han, Tongxin / Mo, Wenxiu / Mao, Huawei et al. | 2023
- 794
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Immunologic, Molecular, and Clinical Profile of Patients with Chromosome 22q11.2 DuplicationsBhattarai, Dharmagat / McGinn, Daniel E. / Crowley, T. Blaine / Giunta, Victoria / Gaiser, Kimberly / Zackai, Elaine H. / Emanuel, Beverly S. / Heimall, Jennifer / Jyonouchi, Soma / Lee, Juhee et al. | 2023
- 808
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Type I Interferonopathy due to a Homozygous Loss-of-Inhibitory Function Mutation in STAT2Zhu, Gaofeng / Badonyi, Mihaly / Franklin, Lina / Seabra, Luis / Rice, Gillian I. / Deleuze, Jean-François / El-Chehadeh, Salima / Anheim, Mathieu / de Saint-Martin, Anne / Pellegrini, Sandra et al. | 2023
- 819
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The Autoimmune Manifestations in Patients with Genetic Defects in the B Cell Development and Differentiation StagesAzizi, Gholamreza / Hesari, Mina Fattah / Sharifinejad, Niusha / Fayyaz, Farimah / Chavoshzadeh, Zahra / Mahdaviani, Seyed Alireza / Alan, Mahnaz Seifi / Jamee, Mahnaz / Tavakol, Marzieh / Sadri, Homa et al. | 2023
- 835
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A Cohort Study on Deficiency of ADA2 from ChinaLi, Guo-min / Han, Xu / Wu, Ye / Wang, Wei / Tang, Hong-xia / Lu, Mei-ping / Tang, Xue-mei / Lin, Yi / Deng, Fan / Yang, Jun et al. | 2023
- 846
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Correction to: De Novo Somatic Mosaicism of CYBB Caused by Intronic LINE‑1 Element Insertion Resulting in Chronic Granulomatous DiseaseYu, Lang / Li, Wenhui / Lv, Ge / Sun, Gan / Yang, Lu / Chen, Junjie / Zhou, Lina / Ding, Yuan / Zhang, Zhiyong / Tang, Xuemei et al. | 2023