Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Karsten Haeffner"'
Autor:
Lidija Ujkic, Karsten Haeffner, Friederike Praus, Martin Pohl, Philippe-Fabian Pohlmann, Malte Kroenig, Alexander Frankenschmidt, Christian Gratzke, Martin Schoenthaler
Publikováno v:
European Urology Open Science, Vol 57, Iss , Pp 106-112 (2023)
Background: Duplex kidneys may be associated with additional pathologies with an indication for surgery. Various surgical approaches have been described. However, little is known about long-term outcomes and quality of life (QoL) for these patients.
Externí odkaz:
https://doaj.org/article/c5245457ebb3421a996ec4e61c6e23d9
Autor:
Kathrin Burgmaier, Samuel Kilian, Klaus Arbeiter, Bahriye Atmis, Anja Büscher, Ute Derichs, Ismail Dursun, Ali Duzova, Loai Akram Eid, Matthias Galiano, Michaela Gessner, Ibrahim Gokce, Karsten Haeffner, Nakysa Hooman, Augustina Jankauskiene, Friederike Körber, Germana Longo, Laura Massella, Djalila Mekahli, Gordana Miloševski-Lomić, Hulya Nalcacioglu, Rina Rus, Rukshana Shroff, Stella Stabouli, Lutz T. Weber, Simone Wygoda, Alev Yilmaz, Katarzyna Zachwieja, Ilona Zagozdzon, Jörg Dötsch, Franz Schaefer, Max Christoph Liebau, The ARegPKD Consortium
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Abstract Autosomal recessive polycystic kidney disease (ARPKD) is characterized by bilateral fibrocystic changes resulting in pronounced kidney enlargement. Impairment of kidney function is highly variable and widely available prognostic markers are
Externí odkaz:
https://doaj.org/article/6626eaeb179242108171c93a0a824388
Autor:
Rebecca D. Burdine, Gyorgy Baktai, Lee Niswander, Richard Reinhardt, Jessica Sullivan-Brown, Heike Olbrich, Heymut Omran, Kathryn V. Anderson, Andrew Pollock, June K. Marthin, Robert Geisler, Judith Horvath, Manfred Fliegauf, Karsten Haeffner, Anita Becker-Heck, Niki T. Loges, Irene E. Zohn, Kim G. Nielsen, Jason C. McSheene, Kari Baker Lenhart, Noriko Okabe
Publikováno v:
Nature Genetics. 43:79-84
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous autosomal recessive disorder characterized by recurrent infections of the respiratory tract associated with the abnormal function of motile cilia. Approximately half of individuals with
Autor:
Nicola Krieghoff, Thomas Frischmuth, J.H. Koch, Karsten Haeffner, Stefan Michelfelder, Lennard L. Bohlender, Juliana Parsons, Todor Tschogonov, Andreas Busch, Ralf Reski, Eva L. Decker, Andreas Schaaf, Paulina Dabrowska-Schlepp
Publikováno v:
Molecular Immunology. 102:209
Autor:
Adrien Frommer, Johanna Raidt, Julia Wallmeier, Christine Edelbusch, June Kehelet Marthin, Kim G. Nielsen, Karsten Haeffner, Yasin Memari, Niki T. Loges, Kerem Eitan, Heymut Omran, Mieke Boon, Sandra Cindric, Claudius Werner, Heike Olbrich, Irael Amirav, David Shoseyov, Martine Jaspers, Charlotte Jahnke, Jörg Große Onnebrink, Rim Hjeij
Publikováno v:
7.4 Paediatric Respiratory Infection and Immunology.
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder caused by several distinct defects in genes responsible for ciliary beating leading to defective mucociliary clearance often associated with randomization of left/righ
Autor:
Kim G. Nielsen, Adrien Frommer, Julia Wallmeier, Martine Jaspers, David Shoseyov, Karsten Haeffner, June K. Marthin, Claudius Werner, Rim Hjeij, Heike Olbrich, Israel Amirav, Heymut Omran, Richard Durbin, Johanna Raidt, Sandra Cindric, Nael Elias, Sascha Sauer, Yasin Memari, Anja Kolb-Kokocinski, Niki T. Loges, Jörg Große-Onnebrink, Christine Edelbusch, Charlotte Jahnke, Eitan Kerem, Mieke Boon
Publikováno v:
American journal of respiratory cell and molecular biology. 53(4)
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder caused by several distinct defects in genes responsible for ciliary beating, leading to defective mucociliary clearance often associated with randomization of left/rig
Publikováno v:
European Journal of Pediatrics. 164:362-365
A 15-year-old healthy girl ingested 38.25 g (0.55 g/kg body weight) of metformin in a suicide attempt. Subsequently she developed lactic acidosis and moderate renal failure. An initial session of haemodialysis was able to treat the acidosis and reduc