Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Christian, Bosselmann"'
Autor:
Michael Günther, Leonie Schuster, Christian Boßelmann, Holger Lerche, Ulf Ziemann, Katharina Feil, Justus Marquetand
Publikováno v:
Clinical Neurophysiology Practice, Vol 8, Iss , Pp 58-64 (2023)
Objective: Emergency diagnostics, such as acquisition of an electroencephalogram (EEG), are of great diagnostic importance, but there is often a lack of experienced personnel. Wet active electrode sponge-based electroencephalogram (sp-EEG) systems ca
Externí odkaz:
https://doaj.org/article/fa96c44b341642daa2e9fcfd391f09e6
Autor:
Stephan Lauxmann, Lukas Sonnenberg, Nils A. Koch, Christian Bosselmann, Natalie Winter, Niklas Schwarz, Thomas V. Wuttke, Ulrike B. S. Hedrich, Yuanyuan Liu, Holger Lerche, Jan Benda, Josua Kegele
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Introduction: Among genetic paroxysmal movement disorders, variants in ion channel coding genes constitute a major subgroup. Loss-of-function (LOF) variants in KCNA1, the gene coding for KV1.1 channels, are associated with episodic ataxia type 1 (EA1
Externí odkaz:
https://doaj.org/article/20e94abcd4a240c4ab74bc5d56dc90b3
Autor:
Christian Boßelmann, Sven Poli
Publikováno v:
The Ultrasound Journal, Vol 11, Iss 1, Pp 1-4 (2019)
Abstract Background Carotid artery dissection due to extension of aortic dissection (CAEAD) is a severe complication of acute aortic dissection. The risk of ischemic stroke is increased. Early sonographic detection and repeat evaluation are necessary
Externí odkaz:
https://doaj.org/article/bb7b4de3224240eda5723b7a4a904d09
Publikováno v:
Neurological Research and Practice, Vol 1, Iss 1, Pp 1-3 (2019)
Abstract Acute febrile neutrophilic dermatosis (Sweet‘s syndrome) is a dermatological entity, which may be associated with malignancies, drugs, and infections and which is characterized by high fever, elevated neutrophils, and tender erythematous s
Externí odkaz:
https://doaj.org/article/9e24f5f161ae4d73a7b310181773ec86
Autor:
Christian Boßelmann, Jan Zurloh, Maria-Ioanna Stefanou, Vera Stadler, Yvonne Weber, Holger Lerche, Sven Poli, Ulf Ziemann, Annerose Mengel
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
Background: Ten to thirty percent of stroke patients suffer from post-stroke delirium. This leads to a longer hospital stay and increased mortality. Therefore, early detection and treatment are needed. All established delirium screening tools require
Externí odkaz:
https://doaj.org/article/a84d0953e6834a6b9caa072b56920a45
Autor:
Ariadna Pérez Garriga, Stefan Wolking, Jonas Fortmann, Raphael W. Majeed, Christian Stockem, Lukas Niekrenz, Christian Bosselmann, Yvonne Weber, Rainer Röhrig, Myriam Lipprandt
Publikováno v:
Caring is Sharing – Exploiting the Value in Data for Health and Innovation ISBN: 9781643683881
The knowledge transformation process involves the guideline for the diagnosis and therapy of epilepsy to an executable and computable knowledge base that serves as the basis for a decision-support system. We present a transparent knowledge representa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b95e8ae11dec797cdf3faaea9d62c202
https://doi.org/10.3233/shti230218
https://doi.org/10.3233/shti230218
Autor:
Christian Boßelmann, Ingo Borggräfe, Walid Fazeli, Karl-Martin Klein, Gerhard J. Kluger, Karen Müller-Schlüter, Bernd A. Neubauer, Sarah von Spiczak, Celina Steinbeis von Stülpnagel, Yvonne Weber, Johannes R. Lemke, Stefan Wolking, Ilona Krey
Publikováno v:
Clinical Epileptology.
ZusammenfassungDie genetische Diagnostik bei an Epilepsie erkrankten Personen ist inzwischen weit verbreitet und unstrittig sinnhaft geworden. Die Kenntnis einer genetischen Ätiologie kann die Identifikation der Diagnose, genetische Beratung, Therap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::731f01b737a8329da6243db8dcfc46b0
https://doi.org/10.1007/s10309-023-00580-6
https://doi.org/10.1007/s10309-023-00580-6
Autor:
Christian Boßelmann, Holger Lerche
Publikováno v:
Neurologie up2date. :314-322
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9699863ec834541fdad1de4c5510a020
https://doi.org/10.1055/a-1645-6477
https://doi.org/10.1055/a-1645-6477
Autor:
Christian Boßelmann
Publikováno v:
Seizure. 92:230-233
Clinical seizure signs continue to be of central importance to guide diagnosis, classification, treatment and prognosis. Some basic principles guide history-taking and observation in clinical epileptology. The information contained within subjective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3725b3c072450b2dfb65e8c4417b3222
https://doi.org/10.1016/j.seizure.2021.09.019
https://doi.org/10.1016/j.seizure.2021.09.019
Autor:
Allan Bayat, Angel Aledo‐Serrano, Antonio Gil‐Nagel, Christian M. Korff, Ashley Thomas, Christian Boßelmann, Yvonne Weber, Elena Gardella, Allan M Lund, Monique G. M. de Sain‐van der Velden, Rikke S Møller
Publikováno v:
Bayat, A, Aledo-Serrano, A, Gil-Nagel, A, Korff, C M, Thomas, A, Boßelmann, C, Weber, Y, Gardella, E, Lund, AM, de Sain-van der Velden, M G M & Møller, R S 2022, ' Pyridoxine or pyridoxal-5-phosphate treatment for seizures in glycosylphosphatidylinositol deficiency : A cohort study ', Developmental Medicine and Child Neurology, vol. 64, no. 6, pp. 789-798 . https://doi.org/10.1111/dmcn.15142
Aim: To investigate the short-term efficacy and safety of high-dose pyridoxine and pyridoxal 5-phosphate (P5P) in the treatment of inherited glycosylphosphatidylinositol (GPI) deficiency-associated epilepsy. Method: Participants with genetically conf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79f1d9b4836244e67cb44cc0f0bf6661
https://portal.findresearcher.sdu.dk/da/publications/36980c4b-93a9-4520-bd80-320700276d80
https://portal.findresearcher.sdu.dk/da/publications/36980c4b-93a9-4520-bd80-320700276d80