Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Beate Heinrich"'
Autor:
Sascha Meyer, Jaro Langer, Martin Poryo, Johannes Goaliath Bay, Stefan Wagenpfeil, Beate Heinrich, Holger Nunold, Adam Strzelczyk, Daniel Ebrahimi‐Fakhari
Publikováno v:
Epilepsia Open, Vol 8, Iss 2, Pp 411-424 (2023)
Abstract Objective The aim of this study was to provide seizure etiology, semiology, underlying conditions, and out‐of‐ and in‐hospital diagnostics, treatment, and outcome data on children with out‐of‐ or in‐hospital‐onset status epilep
Externí odkaz:
https://doaj.org/article/9ff624c5dd3b4173ae156f6ddfe7438b
Autor:
Daniel Ebrahimi-Fakhari, Lilian Lisa Mann, Martin Poryo, Norbert Graf, Rüdiger von Kries, Beate Heinrich, Darius Ebrahimi-Fakhari, Marina Flotats-Bastardas, Ludwig Gortner, Michael Zemlin, Sascha Meyer
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-8 (2018)
Abstract Background Tuberous Sclerosis Complex (TSC) is a rare multisystem disorder. In 2012 diagnostic criteria for TSC were revised. However, data on the incidence of TSC are limited. Methods Prospective, national surveillance study in Germany over
Externí odkaz:
https://doaj.org/article/6c50d9a8aa6e4b87ad5e6acec036a639
Autor:
Susanne Nettesheim, Stefan Kölker, Daniela Karall, Johannes Häberle, Roland Posset, Georg F. Hoffmann, Beate Heinrich, Florian Gleich, Sven F. Garbade, On behalf of Arbeitsgemeinschaft für Pädiatrische Stoffwechselstörungen (APS); European registry and network for Intoxication type Metabolic Diseases (E-IMD); Erhebungseinheit für Seltene Pädiatrische Erkrankungen in Deutschland (ESPED); Austrian Metabolic Group; Swiss Paediatric Surveillance Unit (SPSU)
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-8 (2017)
Abstract Background Urea cycle disorders (UCDs) are a group of rare inherited metabolic disorders. Affected individuals often present with hyperammonemic encephalopathy (HE) and have an increased risk of severe neurologic disease and early death. The
Externí odkaz:
https://doaj.org/article/23370ecb154343929b185a6fd1033613
Autor:
Daniel Ebrahimi-Fakhari, Lilian Lisa Mann, Martin Poryo, Norbert Graf, Rüdiger von Kries, Beate Heinrich, Darius Ebrahimi-Fakhari, Marina Flotats-Bastardas, Ludwig Gortner, Michael Zemlin, Sascha Meyer
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-1 (2019)
Externí odkaz:
https://doaj.org/article/7be44a885618431aab8febf573cdb601
Autor:
Lilian, Mann, Daniel, Ebrahimi-Fakhari, Beate, Heinrich, Marina, Flotats-Bastardas, Ludwig, Gortner, Alexander, von Gontard, Justine, Niemcyzk, Martin, Poryo, Sascha, Meyer
Publikováno v:
Wiener medizinische Wochenschrift (1946). 167(11-12)
Tuberous sclerosis complex (TSC) disease is a rare genetic, multi-organ disorder characterized by the occurrence of multiple hamartoma.In cooperation with ESPED, Germany, a prospective, epidemiological study was performed to assess the incidence of n
Publikováno v:
Umweltwissenschaften und Schadstoff-Forschung. 22:686-689
Autor:
H. Meyer, Almut Beate Heinrich
Publikováno v:
Umweltwissenschaften und Schadstoff-Forschung. 22:513-516
s of the lectures will be available in September. The lectures will be posted after the Symposium.
Autor:
Almut Beate Heinrich, Henner Hollert
Publikováno v:
Umweltwissenschaften und Schadstoff-Forschung. 22:495-498
das Editorial der Juniausgabe (Heinrich 2010) befasste sich mit den Grunden, auch englischsprachige Beitrage in die bisher rein deutschsprachige UWSF aufzunehmen. dies geschieht zum einen auf Grund der leserumfrage (Heinrich und Hollert 2009), deren
Autor:
Almut Beate Heinrich
Publikováno v:
The International Journal of Life Cycle Assessment. 15:527-530
Jesper Hedal Kloverpris did his Ph.D. on “Consequential Life Cycle Inventory Modelling of Land Use induced by Crop Consumption”. It was an industrial Ph.D. project in collaboration between DTU Management Engineering at the Technical University of
Autor:
Almut Beate Heinrich
Publikováno v:
Environmental Sciences Europe. 21:580-583