arrow
返回
K

Klaus Warnatz

Albert-Ludwigs-University of Freiburg

75H指数
394论文数
2.4W被引数
收录论文 192
发表时间
ABACHAI - Safety and efficacy of abatacept (s.c.) in patients with CTLA4 insufficiency or LRBA deficiency, a phase II clinical trialABACHAI - 阿巴西特(皮下注射)在CTLA4缺乏或LRBA缺陷患者中的安全性与有效性,一项II期临床试验
err2026-09-19
err0
errOAAI
errMáté Krausz; Georgios Sogkas; Annette Uhlmann; Gabriele Ihorst; Sigune Goldacker; Torsten Witte; Manuel Feißt; Laia Alsina; Ingunn Dybedal; Mike Recher; Klaus Warnatz; Bodo Grimbacher
err分享
err收藏
Recombination junctions from antibody isotype switching classify immune and DNA repair dysfunction抗体类别转换产生的重组连接点可区分免疫功能和DNA修复功能障碍
err2025-12-19
err0
errOAAI
errClara Vázquez García; Benedikt Obermayer; Baerbel Keller; Mikhail Lebedin; Christoph Ratswohl; Hassan Abolhassani; Antonia Busse; Michela Di Virgilio; Stephan Mathas; Dorothee Speiser; Dieter Beule; Qiang Pan-Hammarström; Klaus Warnatz; Kathrin de la Rosa
err分享
err收藏
Do CVID patients on SCIG have more autoimmune (thrombo)cytopenic events than CVID patients on IVIG?SCIG治疗的CVID患者是否比IVIG治疗的CVID患者有更多的自身免疫性(血栓)血小板减少事件?
err2025-11-27
err0
errOAAI
errNadezhda Camacho-Ordonez; Aleksandra Hirsch; Luiza Campos; Sigune Goldacker; Siobhan O. Burns; Fernando Moreira; Klaus Warnatz; Bodo Grimbacher
err分享
err收藏
Epidemiology and Management of Malignancies in Patients with Inborn Errors of Immunity - An ESID Registry Study of 19,959 Patients免疫缺陷病患者恶性肿瘤的流行病学与管理——一项基于ESID注册库的19,959例患者研究
err2025-11-14
err0
errOAAI
errDelfien J.A. Bogaert; Christina H. Wolfsberger; Andishe Attarbaschi; Jonathan Gathmann; Klaus Warnatz; Gabriele Mueller; Anna Mukhina; Stephan Rusch; Gerhard Kindle; Joris M. van Montfrans; Markus G. Seidel
err分享
err收藏
Compound heterozygous NFKB1 missense variants in cis associated with immunodeficiency顺式复合杂合NFKB1错义变异与免疫缺陷相关
err2025-11-05
err0
errOAAI
errManfred Fliegauf; Kelly Nitschke; Pavla Mrovecova; Sara Posadas-Cantera; Nadezhda Camacho-Ordonez; Klaus Warnatz; Baerbel Keller; Bodo Grimbacher
err分享
err收藏
Case Report: Late-onset primary hemophagocytic lymphohistiocytosis leading to the diagnosis of Griscelli syndrome type 2 in a young woman with phenotypically inapparent partial albinism病例报告:一例年轻女性因迟发性原发性噬血细胞性淋巴组织细胞增多症,继而导致Griscelli综合征2型的诊断,该患者具有表型不明显的部分白化病。
err2025-08-07
err0
errOAAI
errJohanna Rausch†; Stephanie Herold†; Simone Liebhäuser; Yagmur Bülbül; Edite Antunes Ferreira; Till Wenz; Kevin Jan Legscha; Matthias Bros; Florian Butsch; Oliver Kriege; Klaus Warnatz; Miriam Groß; Kai Lehmberg; Helena Clara Lichtenfeld; Paul La Rosée; Markus Philipp Radsak; Matthias Theobald; Hakim Echchannaoui‡; Markus Munder‡
err分享
err收藏
Clinical and Molecular Characteristics of X-linked Agammaglobulinemia Patients 55 Years or OlderX-连锁无丙种球蛋白血症患者55岁及以上人群的临床及分子特征
err2025-06-24
err0
PREAI
errAaron T. Chin; Hans D. Ochs; Roger Kobayashi; Hassan Abolhassani; Hana Alachkar; Sara Barmettler; Helen Baxendale; Kristina Boiling; Jason Catanzaro; Ignastius Chua; Tanya Coulter; Charlotte Cunningham-Rundles; Suzanne E. Elcombe; Alain Fischer; Bodo Grimbacher; Sudhir Gupta; Richard Herriot; Archana Herwadkar; Kohsuke Imai; Shota Inoue; Charles Kirkpatrick; Alan P. Knutsen; Dinakantha Kumararatne; Edward Lea; Ming-Wei Lin; Jiri Litzman; Nizar Mahlaoui; Kunihiko Moriya; Shigeaki Nonoyama; Smita Patel; Elena Perez; Isabella Quinti; Robert W. Hostoffer; Simon Rothenfusser; Ravishankar Sargur; Adrian Shields; Georgios Sogkas; Dan Suan; Tyng Tan; Moira Thomas; Klaus Warnatz; Elizabeth M. Younger; Caroline Y. Kuo
err分享
err收藏
BENTA disease or CARD11 gain-of-function? A novel variant with atypical features and a literature reviewBENTA 病或 CARD11 获得性功能?一种具有非典型特征的 novel variant 及文献综述
err2025-05-28
err0
PREAI
errBaldini, Letizia; Keller, Baerbel; Dewitte, Lisa; Passarelli, Chiara; Ginevrino, Monia; Carli, Diana; Montin, Davide; Bossuyt, Xavier; Warnatz, Klaus; Licciardi, Francesco
err分享
err收藏
CD21low B cells reveal a unique glycosylation pattern with hypersialylation and hyperfucosylation
err2025-02-12
err0
errOAAI
errFelixberger, Peter Tobias; Andrieux, Geoffroy; Maul-Pavicic, Andrea; Goldacker, Sigune; Harder, Ina; Gutenberger, Sylvia; Landry, Jonathan J. M.; Benes, Vladimir; Jakob, Till Fabian; Boerries, Melanie; Nitschke, Lars; Voll, Reinhard Edmund; Warnatz, Klaus; Keller, Baerbel
err分享
err收藏
Curation of gene-disease relationships in primary antibody deficiencies using the ClinGen validation framework使用ClinGen验证框架对原发性抗体缺陷症的基因-疾病关系进行整理
err2025-01-01
err0
PREAI
errNieto-Patlan, Alejandro; Ross, Justyne; Mohan, Shruthi; Paczosa, Michelle K.; Soliman, Rasha; Sarmento, Olga; Aliu, Ermal; Thiyagarajan, Lavvina; Chandra, Anita; Picard, Capucine; Warnatz, Klaus; Jolles, Stephen; Lesmana, Harry; Maglione, Paul J.; Platt, Craig D.; Sediva, Anna; Sullivan, Kathleen E.; Zhang, Kejian; Raval, Forum; Tangye, Stuart G.; Abraham, Roshini S.
err分享
err收藏
COVID-19 progression and convalescence in common variable immunodeficiency patients show dysregulated adaptive immune responses and persistent type I interferon and inflammasome activation
err2024-11-28
err0
errOAAI
errRodriguez-Ubreva, Javier; Calafell-Segura, Josep; Calvillo, Celia L.; Keller, Baerbel; Ciudad, Laura; Handfield, Louis-Francois; de la Calle-fabregat, Carlos; Godoy-Tena, Gerard; Andres-Leon, Eduardo; Hoo, Regina; Porter, Tarryn; Prigmore, Elena; Hofmann, Maike; Decker, Annegrit; Martin, Javier; Vento-Tormo, Roser; Warnatz, Klaus; Ballestar, Esteban
err分享
err收藏
IL-7-dependent and -independent lineages of IL-7R-dependent human T cells
err2024-10-01
err0
errOAAI
errArango-Franco, Carlos A.; Ogishi, Masato; Unger, Susanne; Delmonte, Ottavia M.; Orrego, Julio Cesar; Yatim, Ahmad; Velasquez-Lopera, Margarita M.; Zea-Vera, Andres F.; Bohlen, Jonathan; Chbihi, Marwa; Fayand, Antoine; Sanchez, Juan Pablo; Rojas, Julian; Seeleuthner, Yoann; Le Voyer, Tom; Philippot, Quentin; Payne, Kathryn J.; Gervais, Adrian; Erazo-Borras, Lucia, V; Correa-Londono, Luis A.; Cederholm, Axel; Gallon-Duque, Alejandro; Goncalves, Pedro; Doisne, Jean-Marc; Horev, Liran; Charmeteau-de Muylder, Benedicte; Alvarez, Jesus A.; Arboleda, Diana M.; Perez-Zapata, Lizet; Vasquez-Echeverri, Estefania; Moncada-Velez, Marcela; Lopez, Juan A.; Caicedo, Yolanda; Palterer, Boaz; Patino, Pablo J.; Montoya, Carlos J.; Chaldebas, Matthieu; Zhang, Peng; Nguyen, Tina; Ma, Cindy S.; Jeljeli, Mohamed; Alzate, Juan F.; Cabarcas, Felipe; Khan, Taushif; Rinchai, Darawan; Pretet, Jean-Luc; Boisson, Bertrand; Marr, Nico; Ibrahim, Ruba; Molho-Pessach, Vered; Boisson-Dupuis, Stephanie; Kiritsi, Dimitra; Barata, Joao T.; Landegren, Nils; Neven, Benedicte; Abe, Laurent; Lisco, Andrea; Beziat, Vivien; Jouanguy, Emmanuelle; Bustamante, Jacinta; Di Santo, James P.; Tangye, Stuart G.; Notarangelo, Luigi D.; Cheynier, Remi; Natsuga, Ken; Arias, Andres A.; Franco, Jose Luis; Warnatz, Klaus; Casanova, Jean-Laurent; Puel, Anne
err分享
err收藏
Current Practices and Considerations in Lung Biopsy for Suspected Granulomatous-Lymphocytic Interstitial Lung Disease: A Clinician Survey
err2024-07-22
err0
errOAAI
errBintalib, Heba M.; Davidsen, Jesper Romhild; van de Ven, Annick A. J. M.; Goddard, Sarah; Burns, Siobhan O.; Warnatz, Klaus; Hurst, John R.
err分享
err收藏
A novel transmembrane CXCR4 variant that expands the WHIM genotype-phenotype paradigm
err2024-07-12
err2
errOAAI
errZmajkovicova, Katarina; Pawar, Sumit; Sharapova, Svetlana O.; Geier, Christoph B.; Wiest, Ivana; Nguyen, Chi; Monticelli, Halenya; Maier-Munsa, Sabine; Chen, Kelly; Sleasman, John W.; Aleshkevich, Svetlana; Polyakova, Ekaterina; Sakovich, Inga; Warnatz, Klaus; Grimbacher, Bodo; Proietti, Michele; Sondheimer, Neal; Ujhazi, Boglarka; Gordon, Sumai; Ellison, Maryssa; Yilmaz, Melis; Walter, Jolan E.; Badarau, Adriana; Taveras, Arthur G.; Neff, Jadee L.; Bledsoe, Jacob R.; Tarrant, Teresa K.
err分享
err收藏
Non-apoptotic FAS signaling controls mTOR activation and extrafollicular maturation in human B cells非凋亡FAS信号控制人b细胞中的mTOR激活和滤泡外成熟
err2024-01-12
err1
PREAI
errStaniek, Julian; Kalina, Tomas; Andrieux, Geoffroy; Boerries, Melanie; Janowska, Iga; Fuentes, Manuel; Diez, Paula; Bakardjieva, Marina; Stancikova, Jitka; Raabe, Jan; Neumann, Julika; Schwenk, Sabine; Arpesella, Leonardo; Stuchly, Jan; Benes, Vladimir; Garcia Valiente, Rodrigo; Fernandez Garcia, Jonatan; Carsetti, Rita; Piano Mortari, Eva; Catala, Albert; de la Calle, Oscar; Sogkas, Georgios; Neven, Benedicte; Rieux-Laucat, Frederic; Magerus, Aude; Neth, Olaf; Olbrich, Peter; Voll, Reinhard E.; Alsina, Laia; Allende, Luis M.; Gonzalez-Granado, Luis I.; Boehler, Chiara; Thiel, Jens; Venhoff, Nils; Lorenzetti, Raquel; Warnatz, Klaus; Unger, Susanne; Seidl, Maximilian; Mielenz, Dirk; Schneider, Pascal; Ehl, Stephan; Rensing-Ehl, Anne; Smulski, Cristian Roberto; Rizzi, Marta
err分享
err收藏
err分享
err收藏
Abnormal biomarkers predict complex FAS or FADD defects missed by exome sequencing
err2024-01-01
err0
PREAI
errRensing-Ehl, Anne; Lorenz, Myriam Ricarda; Fueurohrer, Marita; Willenbacher, Wolfgang; Willenbacher, Ella; Sopper, Sieghart; Abinun, Mario; Maccari, Maria Elena; Koeuronig, Christoph; Haegele, Pauline; Fuchs, Sebastian; Castro, Carla; Kury, Patrick; Pelle, Olivier; Klemann, Christian; Heeg, Maximilian; Thalhammer, Julian; Wegehaupt, Oliver; Fischer, Marco; Goldacker, Sigune; Schulte, Bjoeurorn; Biskup, Saskia; Chatelain, Philippe; Schuster, Volker; Warnatz, Klaus; Grimbacher, Bodo; Meinhardt, Andrea; Holzinger, Dirk; Oommen, Prasad Thomas; Hinze, Tanja; Hebart, Holger; Seeger, Karlheinz; Lehmberg, Kai; Leahy, Timothy Ronan; Claviez, Alexander; Vieth, Simon; Schilling, Freimut H.; Fuchs, Ilka; Gross, Miriam; Rieux-Laucat, Frederic; Magerus, Aude; Speckmann, Carsten; Schwarz, Klaus; Ehl, Stephan
err分享
err收藏
Combined Immunodeficiency Caused by a Novel Nonsense Mutation in LCK
err2023-12-19
err2
errOAAI
errKeller, Baerbel; Kfir-Erenfeld, Shlomit; Matusewicz, Paul; Hartl, Frederike; Lev, Atar; Lee, Yu Nee; Simon, Amos J.; Stauber, Tali; Elpeleg, Orly; Somech, Raz; Stepensky, Polina; Minguet, Susana; Schraven, Burkhart; Warnatz, Klaus
err分享
err收藏
Diagnostic testing for GLILD in Common Variable Immunodeficiency: A Systematic Review
err2023-10-27
err0
PREAI
errBintalib, Heba M.; Van De Ven, Annick A. J. M.; Jacob, Joseph; Davidsen, Jesper R.; Fevanga, Borre; Hanitsch, Leif G.; Routes, John; Malphettes, Marion; Van Montfrans, Joris; Maglioned, Paul J.; Milito, Cinzia; Warnatz, Klaus; Hurst, John R.
err分享
err收藏