Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Annette Uhlmann"'
Autor:
Máté Krausz, Annette Uhlmann, Ina Caroline Rump, Gabriele Ihorst, Sigune Goldacker, Georgios Sogkas, Sara Posadas-Cantera, Reinhold Schmidt, Manuel Feißt, Laia Alsina, Ingunn Dybedal, Mike Recher, Klaus Warnatz, Bodo Grimbacher
Publikováno v:
Contemporary Clinical Trials Communications, Vol 30, Iss , Pp 101008- (2022)
Background: Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) insufficiency and lipopolysaccharide-responsive and beige-like anchor protein (LRBA) deficiency are both complex immune dysregulation syndromes with an underlying regulatory T cell dysf
Externí odkaz:
https://doaj.org/article/5c6b30705b4d40c9b81827a7ec4b87dd
Autor:
Jennifer J. Meerburg, Ieneke J. C. Hartmann, Sigune Goldacker, Ulrich Baumann, Annette Uhlmann, Eleni-Rosalina Andrinopoulou, Mariette P. C. Kemner v/d Corput, Klaus Warnatz, Harm A. W. M. Tiddens
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
BackgroundGranulomatous lymphocytic interstitial lung disease (GLILD) is present in about 20% of patients with common variable immunodeficiency disorders (CVID). GLILD is characterized by nodules, reticulation, and ground-glass opacities on CT scans.
Externí odkaz:
https://doaj.org/article/c9b07c5758fa443e906c2e583c7e4943
Autor:
Björn C. Frye, Ina Caroline Rump, Annette Uhlmann, Fabian Schubach, Gabriele Ihorst, Bodo Grimbacher, Gernot Zissel, Joachim Müller Quernheim
Publikováno v:
Contemporary Clinical Trials Communications, Vol 19, Iss , Pp 100575- (2020)
Introduction: Sarcoidosis is a granulomatous systemic disease that becomes chronic in approximately one third of affected patients resulting in quality of life and functional impairment. Immunosuppressive drugs other than steroids represent alternati
Externí odkaz:
https://doaj.org/article/7ed5d97fa1ba4e21bbba1dec526a405e
Autor:
Maria Elena Maccari, Hassan Abolhassani, Asghar Aghamohammadi, Alessandro Aiuti, Olga Aleinikova, Catherine Bangs, Safa Baris, Federica Barzaghi, Helen Baxendale, Matthew Buckland, Siobhan O. Burns, Caterina Cancrini, Andrew Cant, Pascal Cathébras, Marina Cavazzana, Anita Chandra, Francesca Conti, Tanya Coulter, Lisa A. Devlin, J. David M. Edgar, Saul Faust, Alain Fischer, Marina Garcia Prat, Lennart Hammarström, Maximilian Heeg, Stephen Jolles, Elif Karakoc-Aydiner, Gerhard Kindle, Ayca Kiykim, Dinakantha Kumararatne, Bodo Grimbacher, Hilary Longhurst, Nizar Mahlaoui, Tomas Milota, Fernando Moreira, Despina Moshous, Anna Mukhina, Olaf Neth, Benedicte Neven, Alexandra Nieters, Peter Olbrich, Ahmet Ozen, Jana Pachlopnik Schmid, Capucine Picard, Seraina Prader, William Rae, Janine Reichenbach, Stephan Rusch, Sinisa Savic, Alessia Scarselli, Raphael Scheible, Anna Sediva, Svetlana O. Sharapova, Anna Shcherbina, Mary Slatter, Pere Soler-Palacin, Aurelie Stanislas, Felipe Suarez, Francesca Tucci, Annette Uhlmann, Joris van Montfrans, Klaus Warnatz, Anthony Peter Williams, Phil Wood, Sven Kracker, Alison Mary Condliffe, Stephan Ehl
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Activated phosphoinositide 3-kinase (PI3K) δ Syndrome (APDS), caused by autosomal dominant mutations in PIK3CD (APDS1) or PIK3R1 (APDS2), is a heterogeneous primary immunodeficiency. While initial cohort-descriptions summarized the spectrum of clini
Externí odkaz:
https://doaj.org/article/7b79ae50f1434e608124d8f52a176ab0
Autor:
Bas Smits, Sigune Goldacker, Suranjith Seneviratne, Marion Malphettes, Hilary Longhurst, Omar E. Mohamed, Carla Witt-Rautenberg, Lucy Leeman, Eva Schwaneck, Isabelle Raymond, Kilifa Meghit, Annette Uhlmann, Christine Winterhalter, Joris van Montfrans, Marion Klima, Sarita Workman, Claire Fieschi, Lorena Lorenzo, Sonja Boyle, Shamin Onyango-Odera, Suzanne Price, Marc Schmalzing, Valerie Aurillac, Antje Prasse, Ieneke Hartmann, Jennifer J. Meerburg, Mariette Kemner-van de Corput, Harm Tiddens, Bodo Grimbacher, Peter Kelleher, Smita Y. Patel, Anne-Sophie Korganow, Jean-Francois Viallard, Hans-Peter Tony, Claire Bethune, Hendrik Schulze-Koops, Torsten Witte, Aarnoud Huissoon, Helen Baxendale, Sofia Grigoriadou, Eric Oksenhendler, Siobhan O. Burns, Klaus Warnatz
Publikováno v:
Journal of Allergy and Clinical Immunology. Mosby Inc.
Background: Granulomatous and lymphocytic interstitial lung disease (gl-ILD) is a major cause of morbidity and mortality among patients with common variable immunodeficiency. Corticosteroids are recommended as first-line treatment for gl-ILD, but evi
Autor:
Annette Uhlmann, Gernot Zissel, BC Frye, Fabian Schubach, Joachim Müller Quernheim, Bodo Grimbacher, Ina Caroline Rump, Gabriele Ihorst
Publikováno v:
Contemporary Clinical Trials Communications
Contemporary Clinical Trials Communications, Vol 19, Iss, Pp 100575-(2020)
Contemporary Clinical Trials Communications, Vol 19, Iss, Pp 100575-(2020)
Introduction Sarcoidosis is a granulomatous systemic disease that becomes chronic in approximately one third of affected patients resulting in quality of life and functional impairment. Immunosuppressive drugs other than steroids represent alternativ
Publikováno v:
LymphoSign Journal. 2:91-106
This is a prospective outcome study of patients with profound combined immunodeficiency (P-CID) (study number DRKS00000497). Combined immunodeficiencies (CID) are a heterogeneous group of inherited immune disorders with impaired T-cell development an
Autor:
Despina Moshous, Manfred Hoenig, Alain Fischer, Mónica Martínez-Gallo, Sebastian Fuchs, Caterina Cancrini, Thomas Vraetz, Sujal Ghosh, Ansgar Schulz, Christine Winterhalter, Nikolaus Rieber, Andrew R. Gennery, Annette Uhlmann, Luis M. Allende, Andrew J. Cant, Kimberly Gilmour, Fabian Hauck, Alessia Scarselli, Brigitte Strahm, Tadej Avcin, Klaus Schwarz, Luigi D. Notarangelo, Tim Niehues, Carsten Speckmann, Alessandro Aiuti, Capucine Picard, H. Bobby Gaspar, Michael H. Albert, Klaus Warnatz, Pere Soler-Palacín, Polina Stepensky, Luis Ignacio Gonzalez-Granado, Stephan Ehl, Silvia Di Cesare, Sam Doerken, Andrea Finocchi, Bénédicte Neven, Sophie Hambleton, Waleed Al-Herz, Ruy Perez-Becker, Markus G. Seidel, Austen Worth
Publikováno v:
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Background Absent T-cell immunity resulting in life-threatening infections provides a clear rationale for hematopoetic stem cell transplantation (HSCT) in patients with severe combined immunodeficiency (SCID). Combined immunodeficiencies (CIDs) and "
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1db8f0f84572820e12d3a2b4e64dfecd
http://hdl.handle.net/2108/234359
http://hdl.handle.net/2108/234359
Autor:
Friedrich Lottspeich, Annette Uhlmann, Jürgen Ebel, Britta Möllers, Judith Fliegmann, Harald Meimberg, Christian Lindermayr
Publikováno v:
European Journal of Biochemistry. 269:1304-1315
4-Coumarate:CoA ligase (4CL) is involved in the formation of coenzyme A thioesters of hydroxycinnamic acids that are central substrates for subsequent condensation, reduction, and transfer reactions in the biosynthesis of plant phenylpropanoids. Prev
Publikováno v:
Klinische Monatsblätter für Augenheilkunde. 208:243-245
BACKGROUND Magnesium seeding of haemangiomas is a form of treatment already successfully used in 1900. PATIENT We report about a male infant with a haemangioma of the left temporal region, underlid and orbit. Maximum depth at the time of indication f