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Results:
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Results: 25
Authors:
Muller, D
Ankermann, T
Stephani, U
Kirschstein, M
Szelestei, T
Luft, FC
Willnow, TE
Citation: D. Muller et al., Holoprosencephaly and low molecular weight proteinuria: The human homologue of murine megalin deficiency, AM J KIDNEY, 37(3), 2001, pp. 624-628
Authors:
Hahn, A
Pistohl, J
Neubauer, BA
Stephani, U
Citation: A. Hahn et al., Atypical "benign" partial epilepsy or pseudo-Lennox syndrome. Part I: Symptomatology and long-term prognosis, NEUROPEDIAT, 32(1), 2001, pp. 1-8
Authors:
Doose, H
Hahn, A
Neubauer, BA
Pistohl, J
Stephani, U
Citation: H. Doose et al., Atypical "benign" partial epilepsy of childhood or pseudo-Lennox syndrome.Part II: Family study, NEUROPEDIAT, 32(1), 2001, pp. 9-13
Authors:
Stephani, U
Eeg-Olofsson, O
Citation: U. Stephani et O. Eeg-olofsson, Introduction, EPILEPT DIS, 2, 2000, pp. S1-S2
Authors:
Stephani, U
Citation: U. Stephani, Typical semiology of benign childhood epilepsy with centrotemporal spikes (BCECTS), EPILEPT DIS, 2, 2000, pp. S3-S4
Authors:
Carlsson, G
Igelbrink-Schulze, N
Neubauer, BA
Stephani, U
Citation: G. Carlsson et al., Neuropsychological long-term outcome of rolandic EEG traits, EPILEPT DIS, 2, 2000, pp. S63-S66
Authors:
Stephani, U
Citation: U. Stephani, This volume of Epileptic Disorders is dedicated to Hermann Doose, EPILEPT DIS, 2, 2000, pp. V-V
Authors:
Siniatchkin, M
Hierundar, A
Kropp, P
Kuhnert, R
Gerber, WD
Stephani, U
Citation: M. Siniatchkin et al., Self-regulation of slow cortical potentials in children with migraine: An exploratory study, APPL PSY BI, 25(1), 2000, pp. 13-32
Authors:
Kuhtz-Buschbeck, JP
Dreesmann, M
Golge, M
Stephani, U
Citation: Jp. Kuhtz-buschbeck et al., Prenatal infarction of the left middle cerebral artery: A case report of excellent functional outcome, NEUROREHAB, 15(3), 2000, pp. 167-173
Authors:
Siniatchkin, M
Kirsch, E
Kropp, P
Stephani, U
Gerber, WD
Citation: M. Siniatchkin et al., Slow cortical potentials in migraine families, CEPHALALGIA, 20(10), 2000, pp. 881-892
Authors:
Siniatchkin, M
Kropp, P
Neumann, M
Gerber, WD
Stephani, U
Citation: M. Siniatchkin et al., Intensity dependence of auditory evoked cortical potentials in migraine families, PAIN, 85(1-2), 2000, pp. 247-254
Authors:
Siniatchkin, M
Kropp, P
Gerber, WD
Stephani, U
Citation: M. Siniatchkin et al., Migraine in childhood - are periodically occurring migraine attacks related to dynamic changes of cortical information processing?, NEUROSCI L, 279(1), 2000, pp. 1-4
Authors:
Schmidt, D
Brandl, U
Elger, CE
Kramer, G
Siemes, H
Stephani, U
Aksu, F
Boenigk, HE
Froscher, W
Keimer, R
Kluger, G
Kurlemann, G
Rochel, M
Schmitz, B
Stefan, H
Stodieck, S
Citation: D. Schmidt et al., The current role of vigabatrin (Sabril (R)) in the treatment of epilepsies: Results of a consensus conference, AKT NEUROL, 27(10), 2000, pp. 470-474
Authors:
Hoffmann-Riem, M
Diener, W
Benninger, C
Rating, D
Unnebrink, K
Stephani, U
Ernst, HP
Korinthenberg, R
Citation: M. Hoffmann-riem et al., Nonconvulsive status epilepticus - A possible cause of mental retardation in patients with Lennox-Gastaut syndrome, NEUROPEDIAT, 31(4), 2000, pp. 169-174
Authors:
Waltz, S
Stephani, U
Citation: S. Waltz et U. Stephani, Inheritance of photosensitivity, NEUROPEDIAT, 31(2), 2000, pp. 82-85
Authors:
Hahn, A
Claviez, A
Brinkmann, G
Altermatt, HJ
Schneppenheim, R
Stephani, U
Citation: A. Hahn et al., Paraneoplastic cerebellar degeneration in pediatric Hodgkin disease, NEUROPEDIAT, 31(1), 2000, pp. 42-44
Authors:
Baumgarten-Walczak, A
Reinicke, U
Rabenhorst, A
Stephani, U
Citation: A. Baumgarten-walczak et al., Lamotrigine in treatment of therapy resistant epilepsies of childhood, NERVENHEILK, 18(6), 1999, pp. 304-307
Authors:
Rabenhorst, A
Baumgarten-Walczak, A
Stephani, U
Citation: A. Rabenhorst et al., Unexpected side effects of Tiagabine in five children with therapy resistant epileptic syndromes, NERVENHEILK, 18(6), 1999, pp. 308-310
Authors:
Stephani, U
Diener, W
Ramm, S
Citation: U. Stephani et al., Today's treatment of epilepsy with potassium bromide, NERVENHEILK, 18(6), 1999, pp. 311-316
Authors:
Kropp, P
Kirbach, U
Detlefsen, JO
Siniatchkin, M
Gerber, WD
Stephani, U
Citation: P. Kropp et al., Slow cortical potentials in migraine: a comparison of adults and children, CEPHALALGIA, 19, 1999, pp. 60-64
Authors:
Kropp, P
Siniatchkin, M
Stephani, U
Gerber, WD
Citation: P. Kropp et al., Migraine - evidence for a disturbance of cerebral maturation in man?, NEUROSCI L, 276(3), 1999, pp. 181-184
Authors:
Korner, C
Knauer, R
Stephani, U
Marquardt, T
Lehle, L
von Figura, K
Citation: C. Korner et al., Carbohydrate deficient glycoprotein syndrome type IV: deficiency of dolichyl-P-Man : Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase, EMBO J, 18(23), 1999, pp. 6816-6822
Authors:
Voit, T
Abe, T
Antunes, NL
Aso, K
Beck, M
Becker, LE
Berthet, F
Bourgeois, B
Braddick, O
Cioni, G
Cowan, F
DiFazio, MP
DiMauro, S
Dodge, N
Enders, G
Forsting, N
Frahm, J
Futagi, Y
Gabreels-Festen, A
Gartner, J
Gillessen-Kaesbach, G
Golden, J
Greisen, G
Guichenai, P
Hagberg, B
Heinen, F
Hohlfeld, R
Holmes, GL
Inoue, Y
Iwamoto, H
Jaeken, J
Kaufmann, W
Kimura, H
Kohyama, J
Korinthenberg, R
Kramer, H
Kreth, W
Krivit, W
Logan, W
Lorenz, B
Lou, H
Martin, JJ
Matshushima, Y
Munnich, A
Naidu, S
Neubauer, W
Oguni, H
Oka, E
Osawa, M
Panayiotopoulos, CP
Partridge, T
Raemaekers, V
Rapin, I
Reis, A
Rivkin, M
Roll, C
Rosenbaum, T
Ross, E
Rotteveel, J
Schroder, JM
Seitz, R
Soul, J
Steinlein, O
Stephani, U
Tanaka, J
Taylor, G
Tome, F
Topcu, N
Tuxhorn, I
Urlesberger, B
Wahn, V
Wenk, G
Wilichowski, E
Wraith, JE
Wynshaw-Boris, A
Citation: T. Voit et al., Pediatric neurology on the threshold of a new millenium, NEUROPEDIAT, 30(6), 1999, pp. 277-277
Authors:
Stephani, U
Doose, H
Citation: U. Stephani et H. Doose, Benign idiopathic partial epilepsy and brain lesion, EPILEPSIA, 40(3), 1999, pp. 373-376
Authors:
Neubauer, BA
Fiedler, B
Himmelein, B
Kampfer, F
Lassker, U
Schwabe, G
Spanier, I
Tams, D
Bretscher, C
Moldenhauer, K
Kurlemann, G
Weise, S
Tedroff, K
Eeg-Olofsson, O
Wadelius, C
Stephani, U
Citation: Ba. Neubauer et al., Centrotemporal spikes in families with rolandic epilepsy - Linkage to chromosome 15q14, NEUROLOGY, 51(6), 1998, pp. 1608-1612
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