Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Konstanze, Hörtnagel"'
Autor:
Maximilian G. W. Witzel, Christian Gebhard, Sören Wenzel, Saskia Kleier, Birgit Eichhorn, Peter Lorenz, Laura von der Heyden, Marius Kuhn, Manuel Luedeke, Miriam Döcker, Jerome Jüngling, Björn Schulte, Konstanze Hörtnagel, Ralf Glaubitz, Sarah Knippenberger, Anna Teubert, Angela Abicht, Teresa M. Neuhann
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
BackgroundEpilepsy is one of the most common and disabling neurological disorders. It is highly prevalent in children with neurodevelopmental delay and syndromic diseases. However, epilepsy can also be the only disease-determining symptom. The exact
Externí odkaz:
https://doaj.org/article/ddb88b4a6eb14a39be8ecc8917e83de0
Autor:
Christian Thomas, Andrea Zühlsdorf, Konstanze Hörtnagel, Lejla Mulahasanovic, Oliver M. Grauer, Philipp Kümpers, Heinz Wiendl, Sven G. Meuth
Publikováno v:
Frontiers in Neurology, Vol 9 (2018)
Autosomal dominant polycystic kidney disease (ADPKD) is a genetic disorder characterized by the presence of renal cysts and specific extrarenal abnormalities. ADPKD is caused by mutations in either PKD1 or PKD2 genes that encode for integral membrane
Externí odkaz:
https://doaj.org/article/e04731d0c73d491ab68b05814a86a46b
Autor:
Tino Wetzig, Konstanze Hörtnagel, Marc Tischkowitz, Mirjana Ziemer, Julia Mentzel, Arno Rütten
Publikováno v:
JDDG: Journal der Deutschen Dermatologischen Gesellschaft. 19:1052-1056
Autor:
Arno Rütten, Konstanze Hörtnagel, Julia Mentzel, Tino Wetzig, Mirjana Ziemer, Marc Tischkowitz
Publikováno v:
Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG. 19(7)
Autor:
Lejla Mulahasanovic, Konstanze Hörtnagel, Anja Schirmacher, Thorsten Hornemann, Arnold von Eckardstein, Saskia Biskup, Bianca Dräger, Saranya Suriyanarayanan, Peter Young, Museer A. Lone, Alaa Othman
Publikováno v:
NeuroMolecular Medicine. 21:182-191
Hereditary sensory and autonomic neuropathy type 1 (HSAN1) is a rare, autosomal dominantly inherited, slowly progressive and length-dependent axonal peripheral neuropathy. HSAN1 is associated with several mutations in serine-palmitoyltransferase (SPT
Autor:
Konstanze Hörtnagel, Amaury Delestienne, Constanza Navarro Moreno, Philippe A. Lysy, Sarah Lechner, Selda Aydin, Véronique Beauloye, Dominique Maiter, Yves Sznajer, Etienne Marbaix
Publikováno v:
Hormone research in paediatrics, Vol. 89, no. 6, p. 423-433 (2018)
Cushing syndrome (CS) is a rare disease in children, frequently associated with subtle or periodic symptoms that may delay its diagnosis. Weight gain and growth failure, the hallmarks of hypercortisolism in pediatrics, may be inconsistent, especially
Autor:
Katja Berndt, Giada Meinel, Konstanze Hörtnagel, Stefan Beissert, Andrea Bauer, Vinzenz Oji, Kerstin Reicherter, Marvin Kuske, Susanne Abraham
Publikováno v:
JDDG: Journal der Deutschen Dermatologischen Gesellschaft. 17:82-84
Autor:
Giada Meinel, Vinzenz Oji, Konstanze Hörtnagel, Stefan Beissert, Marvin Kuske, Kerstin Reicherter, Andrea Bauer, Susanne Abraham, Katja Berndt
Publikováno v:
JDDG: Journal der Deutschen Dermatologischen Gesellschaft. 17:82-84
Autor:
Konstanze Hörtnagel, Saskia Biskup, Bertold Schrank, Harald von Pein, Clemens Sommer, Dorothea Haas
Publikováno v:
Klinische Neurophysiologie. 48:102-106
Autor:
Gerd Kurlemann, Barbara Fiedler, J. Althaus, Konstanze Hörtnagel, Oliver Schwartz, Saskia Biskup, Werner Paulus, K. Heß
Publikováno v:
Neuropediatrics. 48:S1-S45