Zobrazeno 1 - 10
of 218
pro vyhledávání: '"Gabriele, Escherich"'
Autor:
Hannah Schmidt, Katja Baust, Gabriele Calaminus, Lisa Hohls, Katharina Tetzner, Nicole Griech, Henrike Haugke, Hannah Baltus, Susanne Elsner, Alexander Katalinic, Hera Becker, Chirine Cytera, Judith Gebauer, Ann-Kristin Kock-Schoppenhauer, Anke Neumann, Christian Denzer, Michael M. Schündeln, Jörg Faber, Conny Sattler, Michael C. Frühwald, Anja Borgmann-Staudt, Anke Barnbrock, Markus Metzler, Gabriele Escherich, Inke R. König, Ingo Menrath, Thorsten Langer
Publikováno v:
Trials, Vol 25, Iss 1, Pp 1-10 (2024)
Abstract Background In Germany, around 2.250 children and adolescents are diagnosed with cancer each year. Despite generally positive long-term survival rates, many patients must cope with late effects of the disease and its treatment. This highlight
Externí odkaz:
https://doaj.org/article/9caaafbb762e4b0ab9b08bf6df3dc1f9
Autor:
Susan Farmand, Susanne Eva Aydin, Katharina Wustrau, Svea Böhm, Francis Ayuk, Gabriele Escherich, Julia Skokowa, Ingo Müller, Kai Lehmberg
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
BackgroundHomozygous or compound heterozygous mutations in JAGN1 cause severe congenital neutropenia. JAGN1-mutant patients present with severe early-onset bacterial infections and most have been described as low-responders to recombinant granulocyte
Externí odkaz:
https://doaj.org/article/570edd02dd8c41a4876c19e4f4056a8f
Autor:
Valentino Conter, Maria Grazia Valsecchi, Paola De Lorenzo, Virginie Gandemer, Mats Heyman, Vaskar Saha, Paulina Diaz, Chi-Kong Li, Andishe Attarbaschi, Gabriele Escherich, Jan Stary, Martin Schrappe, Rob Pieters, Gunnar Cario, Andrea Biondi
Publikováno v:
Haematologica, Vol 999, Iss 1 (2024)
Not available.
Externí odkaz:
https://doaj.org/article/f949751deeea4e34bb67721d54d9a8aa
Autor:
Ming Tang, Željko Antić, Pedram Fardzadeh, Stefan Pietzsch, Charlotte Schröder, Adrian Eberhardt, Alena van Bömmel, Gabriele Escherich, Winfried Hofmann, Martin A. Horstmann, Thomas Illig, J. Matt McCrary, Jana Lentes, Markus Metzler, Wolfgang Nejdl, Brigitte Schlegelberger, Martin Schrappe, Martin Zimmermann, Karolina Miarka-Walczyk, Agata Patsorczak, Gunnar Cario, Bernhard Y. Renard, Martin Stanulla, Anke Katharina Bergmann
Publikováno v:
EBioMedicine, Vol 104, Iss , Pp 105171- (2024)
Summary: Background: The increasing volume and intricacy of sequencing data, along with other clinical and diagnostic data, like drug responses and measurable residual disease, creates challenges for efficient clinical comprehension and interpretatio
Externí odkaz:
https://doaj.org/article/73ab5d4f744341ce91b017ca5e0c00a9
Autor:
Naomi Michels, Femke M. Hormann, Aurélie Boeree, Edwin Sonneveld, Anthony V. Moorman, Gabriele Escherich, Rosemary Sutton, H. Berna Beverloo, Rob Pieters, C. Michel Zwaan, Monique L. den Boer, Judith M. Boer
Publikováno v:
EJC Paediatric Oncology, Vol 3, Iss , Pp 100140- (2024)
Background: Chromosome 21 is affected in ∼60% of paediatric B-cell precursor acute lymphoblastic leukaemia (BCP-ALL) patients and includes somatic and constitutional gains, intrachromosomal amplification of chromosome 21 (iAMP21), and the transloca
Externí odkaz:
https://doaj.org/article/ecb1e835fb504ce692dbd72007e10a05
Autor:
Jana Winzig, Laura Inhestern, Désirée Sigmund, Verena Paul, Lesley‐Ann Hail, Stefan Rutkowski, Gabriele Escherich, Corinna Bergelt
Publikováno v:
Cancer Medicine, Vol 13, Iss 10, Pp n/a-n/a (2024)
Abstract Purpose In Germany, children diagnosed with cancer survive their initial disease in more than 80%, and the majority will become long‐term survivors. Around the age of 18, survivors are transferred to adult healthcare. The transition can be
Externí odkaz:
https://doaj.org/article/fd38c7e7e773429fa30818454628a0a8
Autor:
Laura Inhestern, Mona L. Nasse, Konstantin A. Krauth, Daniela Kandels, Stefan Rutkowski, Gabriele Escherich, Corinna Bergelt
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
ObjectiveTo describe the situation of childhood cancer survivors and their parents before and one year after a family-oriented rehabilitation program (FOR) and to identify factors influencing reintegration.MethodsWe included parents of children diagn
Externí odkaz:
https://doaj.org/article/b84409cb885a4335881573963d83c16c
Autor:
Inge van Outersterp, Vincent H.J. van der Velden, Patricia G. Hoogeveen, Goda E. Vaitkevičienė, Edwin Sonneveld, Gijs van Haaften, Roland P. Kuiper, Udo zur Stadt, Gabriele Escherich, Judith M. Boer, Monique L. den Boer
Publikováno v:
HemaSphere, Vol 7, Iss 10, p e967 (2023)
Externí odkaz:
https://doaj.org/article/ef1fe8fac5a545b3a961b76a6c0583e7
Autor:
Mireia Ramos‐Muntada, Juan L. Trincado, Joan Blanco, Clara Bueno, Virginia C. Rodríguez‐Cortez, Alex Bataller, Belén López‐Millán, Claire Schwab, Margarita Ortega, Pablo Velasco, Maria L. Blanco, Josep Nomdedeu, Manuel Ramírez‐Orellana, Alfredo Minguela, Jose L. Fuster, Esther Cuatrecasas, Mireia Camós, Paola Ballerini, Gabriele Escherich, Judith Boer, Monique DenBoer, Jesús M. Hernández‐Rivas, Maria J. Calasanz, Giovanni Cazzaniga, Christine J. Harrison, Pablo Menéndez, Oscar Molina
Publikováno v:
Molecular Oncology, Vol 16, Iss 16, Pp 2899-2919 (2022)
B‐cell acute lymphoblastic leukemia (B‐ALL) is the commonest childhood cancer. High hyperdiploidy (HHD) identifies the most frequent cytogenetic subgroup in childhood B‐ALL. Although hyperdiploidy represents an important prognostic factor in ch
Externí odkaz:
https://doaj.org/article/c4efc3858e8a4dd59893e2d44eb72c0d
Autor:
Anna Østergaard, Amir Enshaei, Rob Pieters, Ajay Vora, Martin A. Horstmann, Gabriele Escherich, Bertil Johansson, Mats Heyman, Kjeld Schmiegelow, Peter M. Hoogerbrugge, Monique L. den Boer, Roland P. Kuiper, Anthony V. Moorman, Judith M. Boer, Frank N. van Leeuwen
Publikováno v:
HemaSphere, Vol 7, Iss 5, p e875 (2023)
IKZF1 deletions are an established prognostic factor in childhood acute lymphoblastic leukemia (ALL). However, their relevance in patients with good risk genetics, namely ETV6::RUNX1 and high hyperdiploid (HeH), ALL remains unclear. We assessed the p
Externí odkaz:
https://doaj.org/article/5645c5c18f97430d84ab7aaaba94a6bf