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

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

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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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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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Congenital myasthenic syndrome of Brahman cattle in South Africa von Thompson, P. N., Steinlein, O. K., Harper, C. K., Kraner, S., Sieb, J. B., Guthrie, A. J.

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EFNS task force on molecular diagnosis of neurologic disorders Guidelines for the molecular diagnosis of inherited neurologic diseases Second of two parts von Gasser, T, Dichgans, M, Finsterer, J, Hausmanowa-Petrusewicz, I, Jurkat-Rott, K, Klopstock, T, Leguern, E, Lehesjoki, A E, Lehmann-Horn, F, Lynch, T, Morris, H, Rossor, M, Steinlein, O K, Wood, N, Zaremba, J, Zeviani, M, Zoharn, A

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Molecular analysis of a mutation in the S5-H5 linker of the KCNQ2 K+ channel causing neonatal convulsions von Naros, G., Yalcin, O., Maljevic, S., Wuttke, T.V., Dervent, A., Saltik, S., Cokar, O., Aykut-Bingol, C., Agan, K., Caglayan, H., Steinlein, O.K., Lerche, H.

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