Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Norbert, Teig"'
Autor:
Nancy Keller, Julian Midgley, Ehtesham Khalid, Harry Lesmana, Georgie Mathew, Christine Mincham, Norbert Teig, Zubair Khan, Indu Khosla, Sam Mehr, Tulay Guran, Kathrin Buder, Hong Xu, Khalid Alhasan, Gonul Buyukyilmaz, Nicole Weaver, Julie D. Saba
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-17 (2024)
Abstract Background Sphingosine-1-phosphate lyase insufficiency syndrome (SPLIS) is a recently recognized inborn error of metabolism associated with steroid-resistant nephrotic syndrome as well as adrenal insufficiency and immunological, neurological
Externí odkaz:
https://doaj.org/article/001681b6efb54f18aee01a6b8c1590c9
Autor:
Philipp Gude, Thomas P. Weber, Stefan Dazert, Norbert Teig, Philipp Mathmann, Adrian I. Georgevici, Katrin Neumann
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-12 (2022)
Abstract Background During pediatric general anesthesia (GA) and sedation, clinicians aim to maintain physiological parameters within normal ranges. Accordingly, regional cerebral oxygen saturation (rScO2) should not drop below preintervention baseli
Externí odkaz:
https://doaj.org/article/9ff01ea6a88447d58d7cd150367737c2
Autor:
Angela Nagel, Emmanouela Dimitrakopoulou, Norbert Teig, Peter Kern, Thomas Lücke, Dariusz Michna, Klaus Korn, Philipp Steininger, Khalid Shahada, Katrin Neumann, Klaus Überla
Publikováno v:
PLoS ONE, Vol 15, Iss 1, p e0227143 (2020)
The majority of congenital cytomegalovirus (cCMV) infections are asymptomatic at birth and therefore not diagnosed. Approximately 10-15% of these infants develop late-onset hearing loss and other developmental disorders. Implementation of a universal
Externí odkaz:
https://doaj.org/article/f0b10f295a074cc48c2db7e462e32cfe
Autor:
Cornelius Rau, Lorenz Auer-Hackenberg, Hedwig E. Deubzer, Elisabeth Schwabel, Maria Jaros, Antonia Diederichs, Thomas Lehrnbecher, Mette Holm, Marie-Louise von Linstow, Luise Martin, Sarah Svenja Dinges, Maria Rothensteiner, Meinolf Siepermann, Volker Strenger, Ulrich von Both, Norbert Teig, Folke Brinkmann, Franziska Leeb, Markus Zeitlinger, Robin Kobbe, Florian Götzinger
Publikováno v:
Pediatric Infectious Disease Journal. 42:125-129
Publikováno v:
Burns Open, Vol 1, Iss 2, Pp 74-77 (2017)
Background: Severe burns in pregnant women present an exceedingly challenging situation due to the limitation in therapeutic options including pain management and operative care.Case: We present a 30 years old patient, 38th week of pregnancy, who suf
Externí odkaz:
https://doaj.org/article/cacdcb04e19f4eb28d3b60c0fc8f85b5
Autor:
Heike Corda, Sebastian Kummer, Alena Welters, Norbert Teig, Dirk Klee, Ertan Mayatepek, Thomas Meissner
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-8 (2017)
Abstract Background Treatment of severe diffuse congenital hyperinsulinism (CHI) without sufficient response to diazoxide is complicated by the lack of approved drugs. Therefore, patients are often hospitalized long-term or have to undergo pancreatic
Externí odkaz:
https://doaj.org/article/49e320241c924fe7acaa0b3b020eec50
Autor:
Laura De Rosa, Alessia Secone Seconetti, Giorgio De Santis, Giovanni Pellacani, Tobias Hirsch, Tobias Rothoeft, Norbert Teig, Graziella Pellegrini, Johann W. Bauer, Michele De Luca
Publikováno v:
Cell Reports, Vol 27, Iss 7, Pp 2036-2049.e6 (2019)
Summary: Laminin 332-deficient junctional epidermolysis bullosa (JEB) is a severe genetic skin disease. JEB is marked by epidermal stem cell depletion, the origin of which is unknown. We show that dysregulation of the YAP and TAZ pathway underpins su
Externí odkaz:
https://doaj.org/article/c544bf23565742f0bcd647116e17cb70
Autor:
Norbert Teig
Publikováno v:
Monatsschrift Kinderheilkunde. 170:39-45
Autor:
Heike Olbrich, Gerard W. Dougherty, Heymut Omran, Cordula Koerner-Rettberg, Norbert Teig, Christoph M. Heyer, Mohammed Almannai, Eissa Faqeih, Mark Dzietko, Charlotte Thiels, Ibrahim Al Mogarri, Julia Wallmeier, Wadha Al Otaibi, Diana Bracht, Sandra Cindric, Hessa S. Alsaif, Fowzan S. Alkuraya, Sameena Khan, Aqeela Al-Hashim
Publikováno v:
Am J Hum Genet
Summary TP73 belongs to the TP53 family of transcription factors and has therefore been well studied in cancer research. Studies in mice, however, have revealed non-oncogenic activities related to multiciliogenesis. Utilizing whole-exome sequencing a
Autor:
Wolfgang Göpel, Angela Kribs, Claudia Roll, Christian Wieg, Norbert Teig, Thomas Hoehn, Lars Welzing, Matthias Vochem, Marc Hoppenz, Christoph Bührer, Katrin Mehler, Mechthild Hubert, Joachim Eichhorn, Susanne Schmidtke, Tanja Katrin Rausch, Inke Regina König, Christoph Härtel, Bernd Roth, Egbert Herting
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992)REFERENCES. 111(11)
We explored whether subnormal forced expiratory volume within 1 s (FEVThe multi-centre, randomised Nonintubated Surfactant Application trial enrolled 211 preterm infants born at 23-26 weeks of gestation from 13 level III neonatal intensive care units