Neuronal nicotinic acetylcholine receptors: From the genetic analysis to neurological diseases von Steinlein, O.K., Bertrand, D.

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Fluorescent annulated imidazo[4,5- c ]isoquinolines via a GBB-3CR/imidoylation sequence - DNA-interactions in pUC-19 gel electrophoresis mobility shift assay von Stahlberger, M, Steinlein, O, Adam, C R, Rotter, M, Hohmann, J, Nieger, M, Köberle, B, Bräse, S

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Cutaneous melanoma in Birt–Hogg–Dubé syndrome: part of the clinical spectrum? von Sattler, E.C., Ertl‐Wagner, B., Pellegrini, C., Peris, K., Reithmair, M., Schädle, N., Ruzicka, T., Steinlein, O.K.

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Delayed diagnosis of Birt-Hogg-Dubé syndrome due to marked intrafamilial clinical variability: a case report von Sattler, E C, Steinlein, O K

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A Potassium Channel Mutation in Neonatal Human Epilepsy von Biervert, Christian, Schroeder, Björn C., Kubisch, Christian, Berkovic, Samuel F., Propping, Peter, Jentsch, Thomas J., Steinlein, Ortrud K.

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Benign familial neonatal convulsions: Always benign? von Steinlein, O.K, Conrad, C, Weidner, B

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Myokymia and Neonatal Epilepsy Caused by a Mutation in the Voltage Sensor of the KCNQ2 K+Channel von Dedek, Karin, Kunath, Bernhard, Kananura, Colette, Reuner, Ulrike, Jentsch, Thomas J., Steinlein, Ortrud K.

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Upstream open reading frames regulate cannabinoid receptor 1 expression under baseline conditions and during cellular stress von Eggert, M., Pfob, M., Jurinovic, V., Schelling, G., Steinlein, O.K.

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Association of Common Polymorphisms in the Nicotinic Acetylcholine Receptor Alpha4 Subunit Gene with an Electrophysiological Endophenotype in a Large Population-Based Sample von Mobascher, A, Diaz-Lacava, A, Wagner, M, Gallinat, J, Wienker, T F, Drichel, D, Becker, T, Steffens, M, Dahmen, N, Gründer, G, Thürauf, N, Kiefer, F, Kornhuber, J, Toliat, M R, Thiele, H, Nürnberg, P, Steinlein, O, Winterer, G

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Mutated Nicotinic Receptors Responsible for Autosomal Dominant Nocturnal Frontal Lobe Epilepsy are More Sensitive to Carbamazepine von Picard, F., Bertrand, S., Steinlein, O. K., Bertrand, D.

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An Insertion Mutation of the CHRNA4 Gene in a Family With Autosomal Dominant Nocturnal Frontal Lobe Epilepsy von Steinlein, Ortrud K., Magnusson, Andres, Stoodt, Jens, Bertrand, Sonia, Weiland, Sigrid, Berkovic, Samuel F., Nakken, Karl O., Propping, Peter, Bertrand, Daniel

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Properties of neuronal nicotinic acetylcholine receptor mutants from humans suffering from autosomal dominant nocturnal frontal lobe epilepsy von Bertrand, S, Weiland, S, Berkovic, S F, Steinlein, O K, Bertrand, D

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A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions von Lerche, H., Biervert, C., Alekov, A. K., Schleithoff, L., Lindner, M., Klingler, W., Bretschneider, F., Mitrovic, N., Jurkat-Rott, K., Bode, H., Lehmann-Horn, F., Steinlein, O. K.

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Ion channels and epilepsy in man and mouse von Steinlein, Ortrud K, Noebels, Jeffrey L

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Hippocampal malformation as a cause of familial febrile convulsions and subsequent hippocampal sclerosis von FERNANDEZ, G, EFFENBERGER, O, VINZ, B, STEINLEIN, O, ELGER, C. E, DÖHRING, W, HEINZE, H. J

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Compound heterozygosity for three common MEFV mutations in a highly consanguineous family with familial Mediterranean fever von Seidel, H., Steinlein, O. K.

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MUTATIONS OF THE OREXIN SYSTEM, A REGULATOR OF SLEEP AROUSAL, ARE NOT A COMMON CAUSE OF ADNFLE von BOUCHARDY, I, STEINLEIN, O, COMBI, R, FERINI-STRAMBI, L, GAMBARDELLA, A, RUDOLF, G, MORRIS, M. A, PICARD, F

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Independent Occurrence of the CHRNA4 Ser248Phe Mutation in a Norwegian Family with Nocturnal Frontal Lobe Epilepsy von Steinlein, Ortrud K., Stoodt, Jens, Mulley, John, Berkovic, Sam, Scheffer, Ingrid E., Brodtkorb, Eylert

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Expression of nicotinic acetylcholine receptors in Alzheimer’s disease: postmortem investigations and experimental approaches von Wevers, Andrea, Burghaus, Lothar, Moser, Natasha, Witter, Brigitte, Steinlein, Ortrud K, Schütz, Ulrich, Achnitz, Bernd, Krempel, Udo, Nowacki, Sonja, Pilz, Kirsten, Stoodt, Jens, Lindstrom, Jon, De Vos, Rob A.I, Jansen Steur, Ernst N.H, Schröder, Hannsjörg

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A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy von Steinlein, O K, Mulley, J C, Propping, P, Wallace, R H, Phillips, H A, Sutherland, G R, Scheffer, I E, Berkovic, S F

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