Zobrazeno 1 - 10
of 162
pro vyhledávání: '"A. Spauschus"'
Autor:
Spauschus, Hans O., Henderson, David R., Seeton, Christopher J., Wright, Derryl C., Zietlow, David C., Bramos, Gary D., Abate, William
Publikováno v:
SAE Transactions, 1999 Jan 01. 108, 1615-1621.
Externí odkaz:
https://www.jstor.org/stable/44668038
Autor:
Jeub, Monika, Herbst, Martin, Spauschus, Alexander, Fleischer, Henrik, Klockgether, Thomas, Wuellner, Ullrich, Evert, Bernd O.
Publikováno v:
In Experimental Neurology 2006 201(1):182-192
Publikováno v:
Datenschutz und Datensicherheit - DuD. 40:7-11
Die offentliche Sicherheit zahlt zu den wichtigsten Aufgaben der Innenpolitik. Dazu gehoren der Schutz der Burgerinnen und Burger vor Gewalt, Verbrechen und Terror ebenso wie der Schutz unserer verfassungsmasigen Ordnung. Hierzu gehort auch der Daten
Publikováno v:
PPmP - Psychotherapie · Psychosomatik · Medizinische Psychologie. 63:445-454
This study investigates the association between urbanicity and mental health in the general population. We conducted a representative survey (N = 5,036) measuring depression (PHQ-2), anxiety (GAD-2) as well as life satisfaction (FLZM). Results suppor
Publikováno v:
Suchttherapie. 11:85-88
In order to reach higher rates of abstinence among alkohol dependent patients, the intensity and type of out-patient treatment is important. Inducing alcohol intolerance via disulfiram under controlled conditions can promote abstinence. Initial clini
Autor:
Alexander Spauschus, Ullrich Wuellner, Monika Jeub, Bernd O. Evert, Henrik Fleischer, Thomas Klockgether, Martin Herbst
Publikováno v:
Experimental Neurology. 201:182-192
Spinocerebellar ataxia type 3 (SCA3) is an autosomal dominant inherited neurodegenerative disease caused by the expansion of a polyglutamine repeat within the disease protein, ataxin-3. There is growing evidence that neuronal electrophysiological pro
Publikováno v:
Aktuelle Neurologie; 20240101, Issue: Preprints
Publikováno v:
Aktuelle Neurologie; 20240101, Issue: Preprints
Publikováno v:
The Journal of Physiology. 538:5-23
Mutations of KCNA1, which codes for the K(+) channel subunit hKv1.1, are associated with the human autosomal dominant disease episodic ataxia type 1 (EA1). Five recently described mutations are associated with a broad range of phenotypes: neuromyoton
Autor:
Robert McWilliam, S. Youroukos, L. H. Eunson, A Spauschus, Rocco Liguori, John Stephenson, Ruth Rea, Patrizia Avoni, Dimitri M. Kullmann, C. P. Panayiotopoulos, Michael G. Hanna, Sameer M. Zuberi
Publikováno v:
Annals of Neurology. 48:647-656
Episodic ataxia type 1 (EA1) is an autosomal dominant central nervous system potassium channelopathy characterized by brief attacks of cerebellar ataxia and continuous interictal myokymia. Point mutations in the voltage-gated potassium channel gene K