Search Results - "STEPHANI, U"

Prospective memory in patients with juvenile myoclonic epilepsy and their healthy siblings by WANDSCHNEIDER, B, KOPP, U. A, KLIEGEL, M, STEPHANI, U, KURLEMANN, G, JANZ, D, SCHMITZ, B

“…Prospective memory (PM) describes the ability to fulfill previously planned intentions and is highly dependent on executive functions. Previous studies have…”
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KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes by NEUBAUER, B. A, WALDEGGER, S, EEG-OLOFSSON, O, MÜLLER, U, SANDER, T, HEINZINGER, J, HAHN, A, KURLEMANN, G, FIEDLER, B, EBERHARD, F, MUHLE, H, STEPHANI, U, GARKISCH, S

“…To explore the involvement of M-type potassium channels KCNQ2, Q3, and Q5 in the pathogenesis of common idiopathic epilepsies. Sequence analysis of the KCNQ2,…”
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Myoclonus-dystonia: significance of large SGCE deletions by Grünewald, A, Djarmati, A, Lohmann-Hedrich, K, Farrell, K, Zeller, J.A, Allert, N, Papengut, F, Petersen, B, Fung, V, Sue, C.M, O'Sullivan, D, Mahant, N, Kupsch, A, Chuang, R.S, Wiegers, K, Pawlack, H, Hagenah, J, Ozelius, L.J, Stephani, U, Schuit, R, Lang, A.E, Volkmann, J, Münchau, A, Klein, C

“…Myoclonus-dystonia (M-D) is an autosomal-dominant movement disorder caused by mutations in SGCE. We investigated the frequency and type of SGCE mutations with…”
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Interictal and postictal performances on dichotic listening test in children with focal epilepsy by Carlsson, G., Wiegand, G., Stephani, U.

“…► Dichotic listening (DL) is an instrument used to determine speech dominance. ► Children with focal epilepsy, left-sided speech dominance and average IQ were…”
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Pädiatrische Epileptologie by Stephani, U.

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Central mechanisms of controlled-release metoprolol in migraine: a double-blind, placebo-controlled study by Siniatchkin, M, Andrasik, F, Kropp, P, Niederberger, U, Strenge, H, Averkina, N, Lindner, V, Stephani, U, Gerber, W-D

“…beta-Blockers are widely used in the prophylaxis of migraine and have been described as very effective drugs in many studies. Some investigators have…”
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Intravenous levetiracetam in clinical practice – Results from an independent registry by Lang, N, Esser, W, Evers, S, Kellinghaus, C, Nguento, A, Schlegel, U, Gaida, B, Gburek-Augustat, J, Altenmüller, D.M, Burghaus, L, Hoffmann, F, Fiedler, B, Bast, T, Rehfeld, T, Happe, S, Seitz, R.J, Boor, R, Stephani, U

“…Abstract Purpose Most common clinical studies with antiepileptic drugs do not reflect medical everyday practice due to their strict in- and exclusion criteria…”
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Evidence for linkage of restless legs syndrome to chromosome 9p : Are there two distinct loci? by LOHMANN-HEDRICH, K, NEUMANN, A, ZIEGLER, A, STEPHANI, U, KLEIN, C, KLEENSANG, A, LOHNAU, T, MUHLE, H, DJARMATI, A, KÖNIG, I. R, PRAMSTALLER, P. P, SCHWINGER, E, KRAMER, P. L

“…Restless legs syndrome (RLS) is a common sensory-motor disorder characterized by paresthesias and an intense urge to move the legs with a considerable familial…”
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Beiträge des Königsteiner Arbeitskreises (für Epileptologie) by Stephani, U.

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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 by FLINK, R, PEDERSEN, B, GUEKHT, A. B, MALMGREN, K, MICHELUCCI, R, NEVILLE, B, PINTO, F, STEPHANI, U, ÖZKARA, C

“…The Commission of European Affairs of the International League Against Epilepsy published 'Appropriate Standards for Epilepsy Care Across Europe' which…”
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Whole-genome linkage scan for epilepsy-related photosensitivity: A mega-analysis by de Kovel, C.G.F, Pinto, D, Tauer, U, Lorenz, S, Muhle, H, Leu, C, Neubauer, B.A, Hempelmann, A, Callenbach, P.M.C, Scheffer, I.E, Berkovic, S.F, Rudolf, G, Striano, P, Siren, A, Baykan, B, Sander, T, Lindhout, D, Trenité, D.G. Kasteleijn-Nolst, Stephani, U, Koeleman, B.P.C

“…Summary Photoparoxysmal response (PPR) is considered to be a risk factor for idiopathic generalised epilepsy (IGE) and it has a strong genetic basis. Two…”
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Centrotemporal spikes in families with rolandic epilepsy : Linkage to chromosome 15q14 by NEUBAUER, B. A, FIEDLER, B, KURLEMANN, G, WEISE, S, TEDROFF, K, EEG-OLOFSSON, O, WADELIUS, C, STEPHANI, U, HIMMELEIN, B, KÄMPFER, F, LÄSSKER, U, SCHWABE, G, SPANIER, I, TAMS, D, BRETSCHER, C, MOLDENHAUER, K

“…To localize a gene predisposing to benign epilepsy of childhood with centrotemporal spikes (BECTS). BECTS, or rolandic epilepsy, is the most prevalent…”
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Typical semiology of benign childhood epilepsy with centrotemporal spikes (BCECTS) by Stephani, U

“…The ILAE (1989) has defined benign childhood epilepsy with centro-temporal spikes (BCECTS) as follows: BCECTS is a syndrome of brief, simple, partial,…”
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M.P.5.07 Serial high-resolution muscle ultrasonography by van Baalen, A, Wiegand, G, Stephani, U

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The Wada test in Austrian, Dutch, German, and Swiss epilepsy centers from 2000 to 2005: a review of 1421 procedures by Haag, A, Knake, S, Hamer, H.M, Boesebeck, F, Freitag, H, Schulz, R, Baum, P, Helmstaedter, C, Wellmer, J, Urbach, H, Hopp, P, Mayer, T, Hufnagel, A, Jokeit, H, Lerche, H, Uttner, I, Meencke, H.-J, Meierkord, H, Pauli, E, Runge, U, Saar, J, Trinka, E, Benke, T, Vulliemoz, S, Wiegand, G, Stephani, U, Wieser, H.G, Rating, D, Werhahn, K, Noachtar, S, Schulze-Bonhage, A, Wagner, K, Alpherts, W.C.J, Boas, W. van Emde, Rosenow, F

“…Abstract Twenty-six Austrian, Dutch, German, and Swiss epilepsy centers were asked to report on use of the Wada test (intracarotid amobarbital procedure, IAP)…”
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Inheritance of photosensitivity by Waltz, S, Stephani, U

“…To investigate the mode of inheritance of the photoparoxysmal response (PPR) and to obtain more information about the influence of photosensitivity on the…”
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Muscle fibre type grouping in high resolution ultrasound by van Baalen, A, Stephani, U

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Benign Idiopathic Partial Epilepsy and Brain Lesion by Stephani, U., Doose, H.

“…A 14‐year‐old girl had severe head trauma from a dog bite at the age of 9 days. This resulted in extensive brain damage, tetraplegia, mental retardation, and…”
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G.P.17.01 Intravenous inotropic treatment of end stage heart failure in neuromuscular disorders by van Baalen, A, Fischer, G, von Spiczak, S, Wiegand, G, Stephani, U

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Atypical "benign" partial epilepsy or pseudo-Lennox syndrome. Part I: symptomatology and long-term prognosis by Hahn, A, Pistohl, J, Neubauer, B A, Stephani, U

“…Atypical benign partial epilepsy (ABPE) or pseudo-Lennox syndrome (PLS) is characterised by generalised minor seizures and focal sharp slow waves and spikes…”
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