Zobrazeno 1 - 10
of 538
pro vyhledávání: '"Ansgar Schulz"'
Autor:
Lusine V. Navasardyan, Ingrid Furlan, Stephanie Brandt, Ansgar Schulz, Martin Wabitsch, Christian Denzer
Publikováno v:
Italian Journal of Pediatrics, Vol 49, Iss 1, Pp 1-10 (2023)
Abstract Background Shwachman-Diamond syndrome (SDS) is a rare congenital disorder caused by mutations in the SBDS gene and characterized by exocrine pancreatic deficiency, hematologic dysfunction, and skeletal growth failure. Although the hematologi
Externí odkaz:
https://doaj.org/article/0496082a937d46b28f99ccc85aad6737
Publikováno v:
EJC Paediatric Oncology, Vol 2, Iss , Pp 100082- (2023)
Externí odkaz:
https://doaj.org/article/c14e431259d849e992254a01d04aeed7
Autor:
Alina Stadermann, Markus Haar, Armin Riecke, Thomas Mayer, Christian Neumann, Arthur Bauer, Ansgar Schulz, Kumar Nagarathinam, Niklas Gebauer, Svea Böhm, Miriam Groß, Michael Grunert, Matthias Müller, Hanno Witte
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 5, p 2762 (2024)
Hemophagocytic lymphohistiocytosis (HLH) is a rare but in most cases life-threatening immune-mediated disease of the hematopoietic system frequently associated with hematologic neoplasms. Here, we report on a case in which we detected a novel constel
Externí odkaz:
https://doaj.org/article/febba51f98dc4947abe10b0796c1861b
Autor:
Amadeus T Heinz, Friso G.J. Calkoen, Alexander Derbich, Lea Miltner, Christian Seitz, Michaela Doering, Christiane Braun, Daniel Atar, Michael Schumm, Florian Heubach, Anne-Marie Arendt, Ansgar Schulz, Friedhelm R Schuster, Roland Meisel, Brigitte Strahm, Juergen Finke, Beatrice Heineking, Susanne Stetter, Gerda Silling, Daniel Stachel, Bernd Gruhn, Klaus-Michael Debatin, Juergen Foell, Johannes H Schulte, Wilhelm Woessmann, Christine Mauz-Körholz, Johanna Tischer, Tobias Feuchtinger, Rupert Handgretinger, Peter Lang
Publikováno v:
Haematologica, Vol 108, Iss 8 (2023)
Therapy-resistant viral reactivations contribute significantly to mortality after hematopoietic stem cell transplantation. Adoptive cellular therapy with virus-specific T cells (VST) has shown efficacy in various single-center trials. However, the sc
Externí odkaz:
https://doaj.org/article/6ada467cb16540358957b223184585b6
Autor:
Médiha Khamassi Khbou, Rihab Romdhane, Faten Bouaicha Zaafouri, Mohsen Bouajila, Limam Sassi, Sofia K. Appelberg, Ansgar Schulz, Ali Mirazimi, Martin H. Groschup, Mourad Rekik, M'hammed Benzarti, Mohamed Gharbi
Publikováno v:
Veterinary Medicine and Science, Vol 7, Iss 6, Pp 2323-2329 (2021)
Abstract Crimean–Congo haemorrhagic fever (CCHF) is an emerging tick‐borne disease causing severe and fatal haemorrhagic syndrome in humans. Hyalomma spp. ticks are the primary vectors and sheep are important CCHF virus (CCHFV)‐amplifying hosts
Externí odkaz:
https://doaj.org/article/e421add740134be1a24596e5e95d1024
Autor:
Cora M. Holicki, Felicitas Bergmann, Franziska Stoek, Ansgar Schulz, Martin H. Groschup, Ute Ziegler, Balal Sadeghi
Publikováno v:
Frontiers in Microbiology, Vol 13 (2022)
Usutu virus (USUV) is a mosquito-borne zoonotic virus and one of the causes of flavivirus encephalitis in birds and occasionally in humans. USUV rapidly disperses in a susceptible host and vector environment, as is the case in South and Central Europ
Externí odkaz:
https://doaj.org/article/010f13c7e0934e8aa16d298e4f5f67b1
Autor:
Ilana Moscatelli, Elena Almarza, Axel Schambach, David Ricks, Ansgar Schulz, Christopher D. Herzog, Kim Henriksen, Maria Askmyr, Jonathan D. Schwartz, Johan Richter
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 20, Iss , Pp 389-397 (2021)
Infantile malignant osteopetrosis is a devastating disorder of early childhood that is frequently fatal and for which there are only limited therapeutic options. Gene therapy utilizing autologous hematopoietic stem and progenitor cells represents a p
Externí odkaz:
https://doaj.org/article/c0603ecb4f8d4f5388fd9fa854ead6c3
Autor:
Franziska Stoek, Yahya Barry, Aliou Ba, Ansgar Schulz, Melanie Rissmann, Claudia Wylezich, Balal Sadeghi, Abdellahi Diambar Beyit, Albert Eisenbarth, Fatimetou Bounene N'diaye, Mohamed Lemine Haki, Baba Abdellahi Doumbia, Mohamed Baba Gueya, Mohamed Yahya Bah, Martin Eiden, Martin H Groschup
Publikováno v:
PLoS Neglected Tropical Diseases, Vol 16, Iss 4, p e0010203 (2022)
In Mauritania, several mosquito-borne viruses have been reported that can cause devastating diseases in animals and humans. However, monitoring data on their occurrence and local distribution are limited. Rift Valley fever virus (RVFV) is an arthropo
Externí odkaz:
https://doaj.org/article/9d7381302f714b46aa40015ac336b182
Autor:
Julia Zinngrebe, Barbara Moepps, Thomas Monecke, Peter Gierschik, Ferdinand Schlichtig, Thomas F E Barth, Gudrun Strauß, Elena Boldrin, Carsten Posovszky, Ansgar Schulz, Ortraud Beringer, Eva Rieser, Eva‐Maria Jacobsen, Myriam Ricarda Lorenz, Klaus Schwarz, Ulrich Pannicke, Henning Walczak, Dierk Niessing, Catharina Schuetz, Pamela Fischer‐Posovszky, Klaus‐Michael Debatin
Publikováno v:
EMBO Molecular Medicine, Vol 14, Iss 3, Pp n/a-n/a (2022)
Abstract Autoinflammatory diseases are a heterogenous group of disorders defined by fever and systemic inflammation suggesting involvement of genes regulating innate immune responses. Patients with homozygous loss‐of‐function variants in the OTU
Externí odkaz:
https://doaj.org/article/83cf35280c7b412da8856b8b0ae57fcf
Autor:
Katharina Hahn, Liart Pollmann, Juliette Nowak, Ariane Hai Ha Nguyen, Kathrin Haake, Anna-Lena Neehus, Syed F. Hassnain Waqas, Frank Pessler, Ulrich Baumann, Miriam Hetzel, Jean-Laurent Casanova, Ansgar Schulz, Jacinta Bustamante, Mania Ackermann, Nico Lachmann
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 17, Iss , Pp 785-795 (2020)
Autosomal recessive (AR) complete interferon-γ receptor 1 (IFN-γR1) deficiency, also known as one genetic etiology of Mendelian susceptibility to mycobacterial disease (MSMD), is a life-threatening congenital disease leading to premature death. Aff
Externí odkaz:
https://doaj.org/article/402b38c898664b7e8e2c466f01b1aa11