Case Report: Successful Long-Term Management of a Low-Birth Weight Preterm Infant With Compound Heterozygous Protein C Deficiency With Subcutaneous Protein C Concentrate Up to Adolescence

Autor: Johannes Pöschl, Wolfgang Behnisch, Bernd Beedgen, Navina Kuss

Publikováno v: Frontiers in Pediatrics, Vol 9 (2021)

Homozygous/compound heterozygous forms of congenital protein C deficiency are often associated with severe antenatal and postnatal thrombotic or hemorrhagic complications. Protein C deficiency frequently leads to severe adverse outcomes like blindnes

Externí odkaz: https://doaj.org/article/09b155b463424a6cb9a5738c4fa47ed1

LPS- and LTA-Induced Expression of IL-6 and TNF-α in Neonatal and Adult Blood: Role of MAPKs and NF-κB

Autor: Lutz Koch, David Frommhold, Kirsten Buschmann, Navina Kuss, Johannes Poeschl, Peter Ruef

Publikováno v: Mediators of Inflammation, Vol 2014 (2014)

As nuclear factor kappa B (NF-κB) and mitogen-activated protein kinases (MAPKs) seem to be critical mediators in the inflammatory response, we studied the effects of lipopolysaccharide (LPS) and lipoteichoic acid (LTA) on (a) the activation of NF-κ

Externí odkaz: https://doaj.org/article/f8f93b0e9a6c41639593124464f9adf9

Intervallentbindung bei Drillingsgraviditäten

Autor: M. Elsässer, Sarah F. Jauch, Herbert Fluhr, Navina Kuss, Christof Sohn

Publikováno v: Geburtshilfe und Frauenheilkunde. 79:339-343

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::15c601fd10eaa1e7c50eea041e5348fc
https://doi.org/10.1055/a-0808-9540

L-Arginine Modulates Neonatal Leukocyte Recruitment in a Gestational Age-Dependent Manner

Autor: Nicole Theissig, Simon Alexander Kranig, Raphaela Fitterer, David Frommhold, Hannes Hudalla, Navina Kuss, Trim Lajqi, Johannes Pöschl, Maylis Braun

Publikováno v: Journal of Clinical Medicine
Volume 9
Issue 9
Journal of Clinical Medicine, Vol 9, Iss 2772, p 2772 (2020)

(1) Background: L-arginine is a complex modulator of immune functions, and its levels are known to decrease under septic conditions. L-arginine may suppress leukocyte recruitment in vivo
however, little is known about the gestational age-specifi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c36762766f1699ad1087a142f3ba697
http://europepmc.org/articles/PMC7563285

Mutations in sphingosine-1-phosphate lyase cause nephrosis with ichthyosis and adrenal insufficiency

Autor: Jacek Majewski, A. Madrid, Babak Oskouian, Yves Sznajer, Julie Désir, Julie Patat, York Pei, Megan A. Cooper, Weizhen Tan, Elisabet Ars, Monica Furlano, Anne-Sophie Truant, Alain Schmitt, Rainer Wilcken, Won-Il Choi, Navina Kuss, Carolin E. Sadowski, Corinne Antignac, Jillian S. Parboosingh, Vilain Catheline, Marcia C. Willing, Christelle Arrondel, Jia Rao, Vikas R. Dharnidharka, Johanna Magdalena Schmidt, Nicola A.M. Wright, Thomas Giese, Martin Zenker, Brigitte Adams, Franz Schaefer, Richard P. Lifton, Noelle Lachaussée, Merlin Airik, Ingolf Franke, Klaus Schwarz, Julie D. Saba, David Schapiro, Guido Capitani, Seema Hashmi, Howard Riezman, Ronald Biemann, Johann Greil, Vladimir Girik, Anne M Connolly, Shazia Ashraf, Nuria Lloberas, Julian P. Midgley, Denny Schanze, Svjetlana Lovric, Matias Simons, Friedhelm Hildebrandt, Sara Gonçalves, Vincent Vuiblet, Heon Yung Gee, Eugen Widmeier, Tilman Jobst-Schwan, Francois P. Bernier, A. Micheil Innes, Olivier Gribouval, Olivia Boyer, Jung H. Suh, Ryan E. Lamont, Honnappa Srinivas, Daniela A. Braun, Shirlee Shril

Publikováno v: Journal of Clinical Investigation, Vol. 127, no.3, p. 912-928 (2017)
JOURNAL OF CLINICAL INVESTIGATION
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Instituto de Salud Carlos III (ISCIII)
Dipòsit Digital de la UB
Universidad de Barcelona
Journal of Clinical Investigation, Vol. 127, No 3 (2017) pp. 912-928
Recercat. Dipósit de la Recerca de Catalunya
instname

Steroid-resistant nephrotic syndrome (SRNS) causes 15% of chronic kidney disease cases. A mutation in 1 of over 40 monogenic genes can be detected in approximately 30% of individuals with SRNS whose symptoms manifest before 25 years of age. However,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49e691abe1f6479437ce05e74e30dfd7
https://hdl.handle.net/2078.1/204417