The Ever-Increasing Array of Novel Inborn Errors of Immunity: an Interim Update by the IUIS Committee (English)
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In:
Journal of Clinical Immunology
;
41
, 3
; 666-679
;
2021
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ISSN:
- Article (Journal) / Electronic Resource
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Title:The Ever-Increasing Array of Novel Inborn Errors of Immunity: an Interim Update by the IUIS Committee
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Contributors:Tangye, Stuart G. ( author ) / Al-Herz, Waleed ( author ) / Bousfiha, Aziz ( author ) / Cunningham-Rundles, Charlotte ( author ) / Franco, Jose Luis ( author ) / Holland, Steven M ( author ) / Klein, Christoph ( author ) / Morio, Tomohiro ( author ) / Oksenhendler, Eric ( author ) / Picard, Capucine ( author )
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Published in:Journal of Clinical Immunology ; 41, 3 ; 666-679
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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:2021
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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$jImmunologie
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BKL: 44.45 Immunologie / 44.45$jImmunologie -
Source:
Table of contents – Volume 41, Issue 3
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.
- 501
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STING-Mediated Lung Inflammation and BeyondFrémond, Marie-Louise / Crow, Yanick J. et al. | 2021
- 515
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SARS-CoV-2-Induced ARDS Associates with MDSC Expansion, Lymphocyte Dysfunction, and Arginine ShortageReizine, Florian / Lesouhaitier, Mathieu / Gregoire, Murielle / Pinceaux, Kieran / Gacouin, Arnaud / Maamar, Adel / Painvin, Benoit / Camus, Christophe / Le Tulzo, Yves / Tattevin, Pierre et al. | 2021
- 526
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Distinctive Features of Kawasaki Disease Following SARS-CoV-2 Infection: a Controlled Study in Paris, FranceToubiana, Julie / Cohen, Jérémie F. / Brice, Joséphine / Poirault, Clément / Bajolle, Fanny / Curtis, William / Moulin, Florence / Matczak, Soraya / Leruez, Marianne / Casanova, Jean-Laurent et al. | 2021
- 536
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Plasma Exchange to Rescue Patients with Autoantibodies Against Type I Interferons and Life-Threatening COVID-19 Pneumoniade Prost, Nicolas / Bastard, Paul / Arrestier, Romain / Fourati, Slim / Mahévas, Mathieu / Burrel, Sonia / Dorgham, Karim / Gorochov, Guy / Tandjaoui-Lambiotte, Yacine / Azzaoui, Iname et al. | 2021
- 545
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Central Nervous System Histoplasma-Associated Post-infectious Inflammatory Response Syndrome (Histo-PIIRS)Dean, Owen / Anjum, Seher / Hess, Bryan / Hammoud, Dima A. / Athas, Deena / Wheat, Joseph / Williamson, Peter R. et al. | 2021
- 552
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Liver Abscess in Chronic Granulomatous Disease—Two Decades of Experience from a Tertiary Care Centre in North-West IndiaPilania, Rakesh Kumar / Rawat, Amit / Vignesh, Pandiarajan / Guleria, Sandesh / Jindal, Ankur Kumar / Das, Gargi / Suri, Deepti / Gupta, Anju / Gupta, Kirti / Chan, Koon-Wing et al. | 2021
- 565
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Serum Sp17 Autoantibody Serves as a Potential Specific Biomarker in Patients with SAPHO SyndromeYou, Hongqin / Dang, Guanglei / Lu, Bichao / Zhang, Siya / Li, Chen / Wang, Lun / Hu, Yu / Chen, Hui / Zhang, Jianmin / He, Wei et al. | 2021
- 576
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An Unusual Pattern of Premature Cervical Spine Degeneration in STAT3-LOFMitchell, Amelia L. / Urban, Amanda K. / Freeman, Alexandra F. / Hammoud, Dima A. et al. | 2021
- 585
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Use of Complementary and Alternative Medicine in Patients with Primary Immunodeficiency: a Multicentric Analysis of 101 PatientsHarasim, Anna S. / Krone, Manuel / Tony, Hans-Peter / Gawlik, Micha / Witte, Torsten / Joos, Stefanie / Gernert, Michael / Schmalzing, Marc / Morbach, Henner / Schwaneck, Eva C. et al. | 2021
- 595
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Newborn Screening for Severe Combined Immunodeficiency: 10-Year Experience at a Single Referral Center (2009–2018)Thorsen, Julia / Kolbert, Kayla / Joshi, Avni / Baker, Mei / Seroogy, Christine M. et al. | 2021
- 603
-
Differential Expression of Interferon-Alpha Protein Provides Clues to Tissue Specificity Across Type I InterferonopathiesLodi, Lorenzo / Melki, Isabelle / Bondet, Vincent / Seabra, Luis / Rice, Gillian I. / Carter, Edwin / Lepelley, Alice / Martin-Niclós, Maria José / Al Adba, Buthaina / Bader-Meunier, Brigitte et al. | 2021
- 610
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Characterization of Infants with Idiopathic Transient and Persistent T Cell Lymphopenia Identified by Newborn Screening—a Single-Center Experience in New York StateJongco, Artemio M. / Sporter, Robert / Hon, Elise / Elshaigi, Omer / Zhang, Shouling / Daian, Foysal / Bae, Emily / Innamorato, Amanda / Capo, Catherine / Navetta-Modrov, Brianne et al. | 2021
- 621
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TREC Screening for WHIM SyndromeEvans, Martin Oman / Petersen, Maureen M. / Khojah, Amer / Jyonouchi, Soma C. / Edwardson, George S. / Khan, Yasmin West / Connelly, James Albert / Morris, David / Majumdar, Shamik / McDermott, David H. et al. | 2021
- 629
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Correction to: TREC Screening for WHIM SyndromeOman Evans, Martin / Petersen, Maureen M. / Khojah, Amer / Jyonouchi, Soma C. / Edwardson, George S. / Khan, Yasmin West / Connelly, James Albert / Morris, David / Majumdar, Shamik / McDermott, David H. et al. | 2021
- 631
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Clinical and Immunological Features of 96 Moroccan Children with SCID Phenotype: Two Decades’ ExperienceBenhsaien, Ibtihal / Ailal, Fatima / El Bakkouri, Jalila / Jeddane, Leïla / Ouair, Hind / Admou, Brahim / Bouskraoui, Mohamed / Hbibi, Mohamed / Hida, Mustapha / Amenzoui, Naïma et al. | 2021
- 639
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Inherited GATA2 Deficiency Is Dominant by Haploinsufficiency and Displays Incomplete Clinical PenetranceOleaga-Quintas, Carmen / de Oliveira-Júnior, Edgar Borges / Rosain, Jérémie / Rapaport, Franck / Deswarte, Caroline / Guérin, Antoine / Sajjath, Sairaj Munavar / Zhou, Yu Jerry / Marot, Stéphane / Lozano, Claire et al. | 2021
- 658
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Biomarkers for Early Diagnosis of Hemophagocytic Lymphohistiocytosis in Critically Ill PatientsDebaugnies, France / Mahadeb, Bhavna / Nagant, Carole / Meuleman, Nathalie / De Bels, David / Wolff, Fleur / Gottignies, Philippe / Salaroli, Adriano / Borde, Patricia / Voué, Michel et al. | 2021
- 666
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The Ever-Increasing Array of Novel Inborn Errors of Immunity: an Interim Update by the IUIS CommitteeTangye, Stuart G. / Al-Herz, Waleed / Bousfiha, Aziz / Cunningham-Rundles, Charlotte / Franco, Jose Luis / Holland, Steven M / Klein, Christoph / Morio, Tomohiro / Oksenhendler, Eric / Picard, Capucine et al. | 2021
- 680
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Uncontrolled Epstein-Barr Virus as an Atypical Presentation of Deficiency in ADA2 (DADA2)Brooks, Joel P. / Rice, Andrew J. / Ji, Weizhen / Lanahan, Stephen M. / Konstantino, Monica / Dara, Jasmeen / Hershfield, Michael S. / Cruickshank, Amy / Dokmeci, Elif / Lakhani, Saquib et al. | 2021
- 684
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Successful Hematopoietic Stem Cell Transplantation for Autosomal Recessive STAT1 Complete DeficiencyKarakawa, Shuhei / Shimomura, Maiko / Sakata, Sonoko / Matsubayashi, Tadashi / Okada, Satoshi et al. | 2021
- 688
-
Benralizumab in Severe and Refractory PDGFRA-Negative Hypereosinophilic SyndromeAlen Coutinho, Iolanda / Regateiro, Frederico S. / Loureiro, Carlos / Todo-Bom, Ana et al. | 2021
- 691
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Chronic Disseminated Gonococcal Infection in a Japanese Man with Novel C5 Gene MutationIkeuchi, Kazuhiko / Okamoto, Koh / Inoue, Norimitsu / Okugawa, Shu / Moriya, Kyoji et al. | 2021
- 694
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Soluble Interleukin-2 Receptor Is a Promising Serum Biomarker for Granulomatous Disease in Common Variable Immune Deficiencyvan Stigt, Astrid C. / Dalm, Virgil A. S. H. / Nagtzaam, Nicole M. A. / van Rijswijk, Damian A. / Barendregt, Barbara H. / van Hagen, P. Martin / IJspeert, Hanna / Dik, Willem A. et al. | 2021
- 698
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Pediatric Demodicosis Associated with Gain-of-Function Variant in STAT1 Presenting as Rosacea-Type RashBaghad, Bouchra / El Fatoiki, Fatima Zahra / Benhsaien, Ibtihal / Bousfiha, Ahmed Aziz / Puel, Anne / Migaud, Mélanie / Chiheb, Soumiya / Ailal, Fatima et al. | 2021
- 701
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Novel IL36RN Mutation Identified in Pediatric-Onset Generalized Pustular Psoriasis Causes IL36 Antagonist DegradationLi, Hongmei / Liao, Dan / Meng, Shasha / Liu, Jingru / Li, Songyang / Ni, Sili / Xu, Yunfei / Zhao, Yong / Zhou, Weihui et al. | 2021
- 705
-
Inflammatory Pseudotumor of Liver and Budd-Chiari Syndrome: a Tale During 10 Years of Follow-up in a Child with Severe Congenital NeutropeniaSugumar, Kiruthiga / Ramamoorthy, Jaikumar Govindaswamy / Anantharaj, Avinash / Baalakumar, Nirmalkumar / Sankar, Pradeep Kumar et al. | 2021
- 709
-
Clinical and Immunological Analyses of Ten Patients with MIRAGE SyndromeMitsui-Sekinaka, Kanako / Narumi, Satoshi / Sekinaka, Yujin / Uematsu, Kenji / Yoshida, Yusuke / Amano, Naoko / Shima, Hirohito / Hasegawa, Tomonobu / Nonoyama, Shigeaki et al. | 2021