Siniatchkin, Mikhail ; Groppa S ; Jerosch B ; Muhle, Hiltrud ; Kurth C ; Shepherd AJ ; Siebner H ; Stephani, Ulrich:
Spreading photoparoxysmal EEG response is associated with an abnormal cortical excitability pattern
.
In: Brain 130 (2007), Nr. Pt 1, S. 78-87
Lorenz S ; Taylor KP ; Gehrmann A ; Becker T ; Muhle, Hiltrud ; Gresch M ; Tauer U ; Sander T ; Stephani, Ulrich:
Association of BRD2 polymorphisms with photoparoxysmal response
.
In: Neurosci Lett. 400 (2006), Nr. 1-2, S. 135-9
Lorenz S ; Heils A ; Taylor KP ; Gehrmann A ; Muhle, Hiltrud ; Gresch M ; Becker T ; Tauer U ; Stephani, Ulrich ; Sander T:
Candidate gene analysis of the succinic semialdehyde dehydrogenase gene (ALDH5A1) in patients with idiopathic generalized epilepsy and photosensitivity.
.
In: Neurosci Lett. 397 (2006), Nr. 3, S. 234-9
Baalen, Andreas van ; Muhle, Hiltrud ; Straube, Torsten ; Jansen, Olav ; Stephani, Ulrich:
Nonparalytic polyomyelitis in Lyme borreliosis
.
In: archives of disease in childhood 91 (2006), S. 660
Kearney JA ; Wiste AK ; Stephani, Ulrich ; Trudeau MM ; Siegel A ; RamachandranNair R ; Elterman RD ; Muhle, Hiltrud ; Reinsdorf J ; Shields WD ; Meisler MH ; Escayg A:
Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancy
.
In: Pediatr Neurol. 34 (2006), Nr. 2, S. 116-20
Müller, Markus ; Baier, Gerold ; Galka, Andreas ; Stephani, Ulrich ; Muhle, Hiltrud:
Detection and characterization of changes of the correlation structure in multivariate time series.
.
In: Physical Review 71 (2005), Nr. 046116, S. 1-16
Stichwörter:
Signatur 5/2005
Tauer U ; Lorenz S ; Lenzen KP ; Heils A ; Muhle, Hiltrud ; Gresch M ; Neubauer BA ; Waltz S ; Rudolf G ; Mattheisen M ; Strauch K ; Nurnberg P ; Schmitz B ; Stephani, Ulrich ; Sander T:
Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsy.
.
In: Ann Neurol 57 (2005), Nr. 6, S. 866-73
Santer, René ; Muhle, Hiltrud ; Suormala T ; Baumgartner ER ; Duran M ; Yang X ; Aoki Y ; Suzuki Y ; Stephani, Ulrich:
Partial response to biotin therapy in a patient with holocarboxylase synthetase deficiency: clinical, biochemical, and molecular genetic aspects.
.
In: Mol Genet Metab. 79 (2003), Nr. 3, S. 160-6
Santer, René ; Muhle, Hiltrud ; Suormala T ; Baumgartner ER ; Duran M ; Yang X ; Aoki Y ; Suzuki Y ; Stephani, Ulrich:
Partial response to biotin therapy in a patient with holocarboxylase synthetase deficiency: clinical, biochemical, and molecular genetic aspects.
.
In: Mol Genet Metab. 79 (2003), Nr. 3, S. 160-6
Galka, Andreas ; Stephani, Ulrich ; Muhle, Hiltrud:
Hybrid nonlinear filtering approach to removing anharmonic periodic components from EEG time series.
.
Tokyo : The Institute of statistical Mathematics, 2002
(Research Memorandum Bd. 843).
- 21 Seiten.
Stichwörter:
Signatur : III N 65
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