Steinmann, Elisabeth ; Schmalor, A ; Prehn-Kristensen, Alexander ; Wolff, Stephan ; Galka, Andreas ; Möhring, J ; Gerber, WD ; Petermann, F ; Stephani, Ulrich ; Siniatchkin, Michael:
Developmental changes of neuronal networks associated with strategic social decision-making .
In: Neuropsychologia 65 (2014), S. 37-46
[doi>10.1016/j.neuropsychologia.2013.12.025]

Siniatchkin, Michael ; Glatthaar, N. ; von Müller, G. G. ; Prehn-Kristensen, Alexander ; Wolff, Stephan ; Knöchel, S. ; Steinmann, Elisabeth ; Sotnikova, Anna ; Stephani, Ulrich ; Petermann, F. ; Gerber, W. D.:
Behavioural treatment increases activity in the cognitive neuronal networks in children with attention deficit/hyperactivity disorder. .
In: Brain topography. 25 (2012), Nr. 3, S. 332-344
[doi>10.1007/s10548-012-0221]

van Baalen, Andreas ; Stephani, Ulrich:
Flexible and floating choroid plexus cyst of the third ventricle: an ultrasonographic video documentation .
In: Childs Nerv Syst 23 (2007), Nr. 2, S. 259-61

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

Neubauer BA ; Stefanova I ; Hubner CA ; Neumaier-Probst E ; Bohl J ; Oppermann HC ; Sto H ; Hahn A ; Stephani, Ulrich ; Kohlschutter A ; Gal A:
A new type of leukoencephalopathy with metaphyseal chondrodysplasia maps to Xq25-q27. .
In: Neurology. 67 (2006), Nr. 4, S. 587-91

Siniatchkin, Mikhail ; Groppa S ; Siebner, Hartwig ; Stephani, Ulrich:
A single dose of sulthiame induces a selective increase in resting motor threshold in human motor cortex: A transcranial magnetic stimulation study .
In: Epilepsy Res. (2006),

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

van Baalen, Andreas ; Stephani, Ulrich ; Jansen, Olav:
Confirmation Of Tuberous Sclerosis Complex By High-resolution Ultrasonography .
In: J Child Neurol. 21 (2006), Nr. 9, S. 741-2

Hempelmann A ; Taylor KP ; Heils A ; Lorenz S ; Prud'homme JF ; Nabbout R ; Dulac O ; Rudolf G ; Zara F ; Bianchi A ; Robinson R ; Gardiner RM ; Covanis A ; Lindhout D ; Stephani, Ulrich ; Elger CE ; Weber YG ; Lerche H ; Nurnberg P ; Kron KL ; Scheffer IE ; Mulley JC ; Berkovic SF ; Sander T:
Exploration of the genetic architecture of idiopathic generalized epilepsies .
In: Epilepsia 47 (2006), Nr. 10, S. 1682-90

Ayerdi-Izquierdo A ; Stavrides G ; Selles-Martinez JJ ; Larrea L ; Bovo G ; Munain AL ; Bisulli F ; Marti-Masso JF ; Michelucci R ; Poza JJ ; Tinuper P ; Stephani, Ulrich ; Striano P ; Striano S ; Staub E ; Sarafidou T ; Hinzmann B ; Moschonas N ; Siebert, Reiner ; Deloukas P ; Nobile C ; Perez-Tur J:
Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy. .
In: Epilepsy Res (2006),

van Baalen, Andreas ; Petersen, Birgit ; Stephani, Ulrich:
Infectious mononucleosis and unilateral tongue writhing .
In: Neurology. 66 (2006), Nr. 7, S. 1110
Stichwörter:  Signatur 4/2006

Siniatchkin, Mikhail ; Averkina N ; Andrasik F ; Stephani, Ulrich ; Gerber, Wolf-Dieter:
Neurophysiological reactivity before a migraine attack. .
In: Neurosci Lett. 400 (2006), Nr. 1-2, S. 121-4

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

Heger S ; Kuester RM ; Volk, Ruth Elisabeth ; Stephani, Ulrich ; Sippell, Wolfgang:
Satoyoshi syndrome: a rare multisystemic disorder requiring systemic and symptomatic treatment .
In: Brain Dev 28 (2006), Nr. 5, S. 300-4

Stephani, Ulrich ; Carlsson, Göran:
The Spectrum from BCECTS to LKS: The Rolandic EEG Trait-Impact on Cognition .
In: Epilepsia 47 (2006), Nr. Suppl. 2, S. 67-70

Rau J ; May TW ; Pfäfflin M ; Heubrock D ; Stephani, Ulrich ; Petermann F:
Das Schulungsprogramm FAMOSES und erste Ergebnisse .
In: Patientenschulung von Kindern mit Epilepsie und deren Eltern.
Regensburg : S. Roderer, 2005, S. 189 – 206.

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

Rau J ; May TW ; Pfäfflin M ; Heubrock D ; Stephani, Ulrich ; Petermann F:
Evaluation des Schulungsprogramms FAMOSES .
In: Patientenschulung von Kindern mit Epilepsie und deren Eltern.
Regensburg : S. Roderer, 2005, S. 47 – 77.

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

Möller F ; Ulmer S ; Wolff S ; Stephani, Ulrich ; Jansen, Olav:
Kortikale Reorganisation bei Kindern mit konnataler spastischer Hemiparese - eine funktionelle Magnetresonanztomographie-(fMRT-)Studie .
In: Fortschr Röntgenstr 177 (2005), Nr. 11, S. 1552-1561

Ulmer S ; Moeller F ; Brockmann MA ; Kuhtz-Buschbeck JP ; Stephani, Ulrich ; Jansen, Olav:
Living a normal life with the nondominant hemisphere: magnetic resonance imaging findings and clinical outcome for a patient with left-hemispheric hydranencephaly .
In: Pediatrics. 116 (2005), Nr. 1, S. 242-5

van Baalen, Andreas ; Stephani, Ulrich:
Muscle fibre type grouping in high resolution ultrasound. .
In: Arch Dis Child. 90 (2005), Nr. 11, S. 1189

Siemes H ; Brandl U ; Helmstadter C ; Kurlemann G ; Rating D ; Salke-Kellermann RA ; Stephani, Ulrich ; Uberall M ; Wiemer-Kruel A ; Bergmann L:
Optimierung der Epilepsietherapie von Kindern und Jugendlichen mit Lamotrigin = [Optimizing Epilepsy Therapy in Children and Adolescents with Lamotrigine] .
In: Klinische Pädiatrie 217 (2005), Nr. 4, S. 222-9

Neubauer BA ; Waltz S ; Grothe M ; Hahn A ; Tuxhorn I ; Sander T ; Kurlemann G ; Stephani, Ulrich:
Photosensitivity: genetics and clinical significance .
In: Advances in Neurology 95 (2005), S. 217-26
Stichwörter:  Signatur 13/2005

Ebach K ; Joos H ; Doose, Hermann ; Stephani, Ulrich ; Kurlemann G ; Fiedler B ; Hahn A ; Hauser E ; Hundt K ; Holthausen H ; Müller U ; Neubauer BA:
SCN1A Mutation Analysis in Myoclonic Astatic Epilepsy and Severe Idiopathic Generalized Epilepsy of Infancy with Generalized Tonic-Clonic Seizures .
In: Neuropediatrics 36 (2005), Nr. 3, S. 210-3

Weber YG ; Berger A ; Bebek N ; Maier S ; Karafyllakes S ; Meyer N ; Fukuyama Y ; Halbach A ; Hikel C ; Kurlemann G ; Neubauer B ; Osawa M ; Pust B ; Rating D ; Saito K ; Stephani, Ulrich ; Tauer U ; Lehmann-Horn F ; Jurkat-Rott K ; Lerche H:
Benign Familial Infantile Convulsions: Linkage to Chromosome 16p12-q12 in 14 Families. .
In: Epilepsia. 45 (2004), Nr. 6, S. 601-9

Berger, A. ; Diener, W. ; Korinthenberg, R. ; Krägeloh-Mann, I. ; Stephani, Ulrich ; Neubauer, B ; Todt, H. ; Schächtele, M. ; Rating, D.:
Benigne Partialepilepsie des Kleinkindalters (Watanabe) : Definitionskriterien und genetische Aspekte. .
In: Monatsschrift Kinderheilkunde 152 (2004), Nr. 1, S. 54-61
Stichwörter:  Signatur : 8/2004

Stephani, Ulrich ; Tauer U ; Koeleman B ; Pinto D ; Neubauer BA ; Lindhout D:
Genetics of Photosensitivity (Photoparoxysmal Response): A Review .
In: Epilepsia. 45 (2004), Nr. Sup. 1, S. 19-23

Hahn A ; Fischenbeck, Anke ; Stephani, Ulrich:
Induction of epileptic negative myoclonus by oxcarbazepine in symptomatic epilepsy. .
In: Epileptic Disorders 6 (2004), Nr. 4, S. 271-274

Stephani, Ulrich:
Labor- und Blutspiegelkontrollen bei antiepileptischer Behandlung von Kindern – Notwendigkeit oder Unsinn .
In: Steinlin M ; Kaufmann F ; Fuhrer K ; Strozzi S (Hrsg.) : Aktuelle Neuropädiatrie.
Nürnberg : Novartis Pharma Verlag, 2004, S. 255-259.

Sinzig JK ; Dopfner M ; Pluck J ; Banaschewski T ; Stephani, Ulrich ; Lehmkuhl G ; Rothenberger A ; Arbeitsgruppe Methylphenidat:
Lassen sich hyperkinetische Auffälligkeiten am Nachmittag durch eine Morgengabe von Methylphenidat Retard vermindern? = [Does a morning dose of Methylphenidate Retard reduce hyperkinetic symptoms in the afternoon?] .
In: Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie 32 (2004), Nr. 4, S. 225-233

Michelucci R ; Poza JJ ; Sofia V ; de Feo MR ; Binelli S ; Bisulli F ; Scudellaro E ; Simionati B ; Zimbello R ; D'Orsi G ; Passarelli D ; Avoni P ; Avanzini G ; Tinuper P ; Biondi R ; Valle G ; Mautner VF ; Stephani, Ulrich ; Tassinari CA ; Moschonas NK ; Siebert R ; Lopez de Munain A ; Perez-Tur J ; Nobile C:
Autosomal dominant lateral temporal epilepsy: clinical spectrum, new epitempin mutations, and genetic heterogeneity in seven European families. .
In: Epilepsia. 44 (2003), Nr. 10, S. 1289-97

Brockmann K ; Dechent P ; Meins M ; Haupt M ; Sperner J ; Stephani, Ulrich ; Frahm J ; Hanefeld F:
Cerebral proton magnetic resonance spectroscopy in infantile Alexander disease. .
In: J Neurol. 2003 Mar;250(3):300-6. 250 (2003), Nr. 3, S. 300-6

Gölge, Mukaddes ; Schütz C ; Dreesmann M ; Kuhtz-Buschbeck JP ; Hoppe, Birgit ; Wenzelburger, Roland ; Stephani, Ulrich ; Illert, Michael:
Grip force parameters in precision grip of individuals with myelomeningocele. .
In: Dev Med Child Neurol. 45 (2003), Nr. 4, S. 249-56

Malmgren K ; Flink R ; Guekht AB ; Michelucci R ; Neville B ; Pedersen B ; Pinto F ; Stephani, Ulrich ; Ozkara C ; ILAE Commission of European Affairs, Subcommission on European Guidelines:
ILAE Commission of European Affairs Subcommission on European Guidelines 1998-2001: The provision of epilepsy care across Europe. .
In: Epilepsia 44 (2003), Nr. 5, S. 727-31
Stichwörter:  Signatur 12/2003

Siniatchkin, Mikhail ; Kirsch E ; Arslan S ; Stegemann S ; Gerber WD ; Stephani, Ulrich:
Migraine and asthma in childhood: evidence for specific asymmetric parent-child interactions in migraine and asthma families. .
In: Cephalalgia. 23 (2003), Nr. 8, S. 790-802

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

Humeny A ; Bonk T ; Becker K ; Jafari-Boroujerdi M ; Stephani, Ulrich ; Reuter K ; Becker CM:
A novel recessive hyperekplexia allele GLRA1 (S231R): genotyping by MALDI-TOF mass spectrometry and functional characterisation as a determinant of cellular glycine receptor trafficking. .
In: Eur J Hum Genet. 10 (2002), Nr. 3, S. 188-96

Neubauer BA ; Hahn A ; Stephani, Ulrich ; Doose, Hermann:
Clinical spectrum and genetics of Rolandic epilepsy. .
In: Adv Neurol. 89 (2002), S. 475-9

Ulmer S ; Flemming K, ; Hahn A ; Stephani, Ulrich ; Jansen, Olav:
Detection of acute cytotoxic changes in progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher syndrome) using diffusion-weighted MRI and MR spectroscopy. .
In: J Comput Assist Tomogr. . 26 (2002), Nr. 4, S. 641-6

Flink R ; Pedersen B ; Guekht AB ; Malmgren K ; Michelucci R ; Neville B ; Pinto F ; Stephani, Ulrich ; Ozkara C ; Commission of European Affairs of the International League Against Epilepsy: Subcommission on European Guidelines.:
Guidelines for the use of EEG methodology in the diagnosis of epilepsy. International League Against Epilepsy: commission report. Commission on European Affairs: Subcommission on European Guidelines. .
In: Acta Neurol Scand. 106 (2002), Nr. 1, S. 1-7

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

Meins M ; Brockmann K ; Yadav S ; Haupt M ; Sperner J ; Stephani, Ulrich ; Hanefeld F:
Infantile Alexander disease: a GFAP mutation in monozygotic twins and novel mutations in two other patients. .
In: Neuropediatrics. 33 (2002), Nr. 4, S. 194-8

Gerber WD ; Stephani, Ulrich ; Kirsch E ; Kropp P ; Siniatchkin, Mikhail:
Slow cortical potentials in migraine families are associated with psychosocial factors. .
In: J Psychosom Res. 52 (2002), Nr. 4, S. 215-22

Hahn, A ; Pistohl, J ; Neubauer, BA ; Stephani, Ulrich:
Atypical "benign" partial epilepsy or pseudo-Lennox syndrome. Part I: symptomatology and long-term prognosis. .
In: Neuropediatrics 32 (2001), Nr. 1, S. 1-8

Müller, D ; Ankermann, Tobias ; Stephani, Ulrich ; Kirschstein, M ; Szelestei, T ; Luft, F C ; Willnow, TE:
Holoprosencephaly and low molecular weight proteinuria: the human homologue of murine megalin deficiency. .
In: American journal of kidney diseases 37 (2001), S. 624-628

Waltz, S ; Stephani, Ulrich:
Inheritance of photosensitivity. .
In: Neuropediatrics 31 (2000), Nr. 2, S. 82-5

Siniatchkin M ; Kropp, Peter ; Gerber WD ; Stephani, Ulrich:
Migraine in childhood--are periodically occurring migraine attacks related to dynamic changes of cortical information processing?
In: Neurosci Lett 279 (2000), Nr. 1, S. 1-4

Carlsson, Göran ; Igelbrink-Schulze, N ; Neubauer, BA ; Stephani, Ulrich:
Neuropsychological long-term outcome of rolandic EEG traits. .
In: Epileptic Disord (2000), Nr. Suppl. 1, S. S63-6

Hahn, A ; Claviez, Alexander ; Brinkmann, G. ; Altermatt, HJ ; Schneppenheim, R ; Stephani, Ulrich:
Paraneoplastic cerebellar degeneration in pediatric Hodgkin disease. .
In: Neuropediatrics 31 (2000), Nr. 1, S. 42-44

Hahn, A ; Claviez, Alexander ; Brinkmann, G. ; Altermatt, HJ ; Schneppenheim, R ; Stephani, Ulrich:
Paraneoplastic cerebellar degeneration in pediatric Hodgkin disease. .
In: Neuropediatrics 31 (2000), Nr. 1, S. 42-4

Stephani, Ulrich:
Typical semiology of benign childhood epilepsy with centrotemporal spikes (BCECTS). .
In: Epileptic Disord 2 (2000), Nr. Supp. 1, S. S3-4

Stephani, Ulrich ; Doose, Hermann:
Benign idiopathic partial epilepsy and brain lesion. .
In: Epilepsia 40 (1999), Nr. 3, S. 373-6

Kropp, Peter ; Siniatchkin M ; Stephani, Ulrich ; Gerber WD:
Migraine--evidence for a disturbance of cerebral maturation in man?
In: Neurosci Lett 276 (1999), Nr. 3, S. 181-4

Neubauer, BA ; Fiedler, B ; Himmelein, B ; Kampfer, F ; Lassker, U ; Schwabe, G ; Spanier, I ; Tams, D ; Bretscher, C ; Moldenhauer, Klaus ; Kurlemann, G ; Weise, S ; Tedroff, K ; Eeg-Olofsson, O ; Wadelius, C ; Stephani, Ulrich:
Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14. .
In: Neurology 51 (1998), Nr. 6, S. 1608-12

Müller, D ; Neubauer, B A ; Waltz, S ; Stephani, Ulrich:
Neuroborreliosis and isolated trochlear palsy. .
In: European journal of paediatric neurology 2 (1998), S. 275-276

Neubauer, BA ; Moises, HW ; Lassker, U ; Waltz, S ; Diebold, U ; Stephani, Ulrich:
Benign childhood epilepsy with centrotemporal spikes and electroencephalography trait are not linked to EBN1 and EBN2 of benign neonatal familial convulsions. .
In: Epilepsia 38 (1997), Nr. 7, S. 782-7