AAAAAA
Results: 1-25/30
Authors:
Gasser, T
Dichgans, M
Finsterer, J
Hausmanowa-Petrusewicz, I
Jurkat-Rott, K
Klopstock, T
Leguern, E
Lehesjoki, AE
Lehmann-Horn, F
Lynch, T
Morris, H
Rossor, M
Steinlein, OK
Wood, N
Zaremba, J
Zeviani, M
Zoharn, A
Citation: T. Gasser et al., EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - Second of two parts, EUR J NEUR, 8(5), 2001, pp. 407-424
Authors:
Gasser, T
Dichgans, M
Finsterer, J
Hausmanowa-Petrusewicz, I
Jurkat-Rott, K
Klopstock, T
LeGuern, E
Lehesjoki, AE
Lehmann-Horn, F
Lynch, T
Morris, H
Rossor, M
Steinlein, OK
Wood, N
Zaremba, J
Zeviani, M
Zoharn, A
Citation: T. Gasser et al., EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - First of two parts, EUR J NEUR, 8(4), 2001, pp. 299-314
Authors:
Xiao, JF
Fischer, C
Steinlein, OK
Citation: Jf. Xiao et al., Cloning and mutations analysis of the human potassium channel KCNQ2 gene promoter, NEUROREPORT, 12(17), 2001, pp. 3733-3739
Authors:
Steinlein, OK
Neubauer, BA
Sander, T
Song, LY
Stoodt, J
Mount, DB
Citation: Ok. Steinlein et al., Mutation analysis of the potassium chloride cotransporter KCC3 (SLC12A6) in rolandic and idiopathic generalized epilepsy, EPILEPSY R, 44(2-3), 2001, pp. 191-195
Authors:
Steinlein, OK
Citation: Ok. Steinlein, Genes and mutations in idiopathic epilepsy, AM J MED G, 106(2), 2001, pp. 139-145
Authors:
Dedek, K
Kunath, B
Kananura, C
Reuner, U
Jentsch, TJ
Steinlein, OK
Citation: K. Dedek et al., Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channel, P NAS US, 98(21), 2001, pp. 12272-12277
Authors:
Sieb, JP
Kraner, S
Steinlein, OK
Bufler, J
Citation: Jp. Sieb et al., Congential myasthenic syndromes, KLIN NEUROP, 31(3), 2000, pp. 148-154
Authors:
Kananura, C
Biervert, C
Hechenberger, M
Engels, H
Steinlein, OK
Citation: C. Kananura et al., The new voltage gated potassium channel KCNQ5 and neonatal convulsions, NEUROREPORT, 11(9), 2000, pp. 2063-2067
Authors:
Steinlein, OK
Noebels, JL
Citation: Ok. Steinlein et Jl. Noebels, Ion channels and epilepsy in man and mouse, CUR OP GEN, 10(3), 2000, pp. 286-291
Authors:
Sieb, JP
Kraner, S
Schrank, B
Reitter, B
Goebel, THH
Tzartos, SJ
Steinlein, OK
Citation: Jp. Sieb et al., Severe congenital myasthenic syndrome due to homozygosity of the 1293insG epsilon-acetylcholine receptor subunit mutation, ANN NEUROL, 48(3), 2000, pp. 379-383
Authors:
Sieb, JP
Kraner, S
Rauch, M
Steinlein, OK
Citation: Jp. Sieb et al., Immature end-plates and utrophin deficiency in congenital myasthenic syndrome caused by epsilon-AChR subunit truncating mutations, HUM GENET, 107(2), 2000, pp. 160-164
Authors:
Lee, WL
Biervert, C
Hallmann, K
Tay, A
Dean, JCS
Steinlein, OK
Citation: Wl. Lee et al., A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family, NEUROPEDIAT, 31(1), 2000, pp. 9-12
Authors:
Wevers, A
Burghaus, L
Moser, N
Witter, B
Steinlein, OK
Schutz, U
Achnitz, B
Krempel, U
Nowacki, S
Pilz, K
Stoodt, J
Lindstrom, J
De Vos, RAI
Steur, ENHJ
Schroder, H
Citation: A. Wevers et al., Expression of nicotinic acetylcholine receptors in Alzheimer's disease: postmortem investigations and experimental approaches, BEH BRA RES, 113(1-2), 2000, pp. 207-215
Authors:
Hallmann, K
Durner, M
Sander, T
Steinlein, OK
Citation: K. Hallmann et al., Mutation analysis of the inwardly rectifying K+ channels KCNJ6 (GIRK2) andKCNJ3 (GIRK1) in juvenile myoclonic epilepsy, AM J MED G, 96(1), 2000, pp. 8-11
Authors:
Steinlein, OK
Citation: Ok. Steinlein, Benign familial neonatal convulsions molecular pathology, NERVENARZT, 71(8), 2000, pp. 611-615
Authors:
Steinlein, OK
Citation: Ok. Steinlein, Neuronal nicotinic receptors in human epilepsy, EUR J PHARM, 393(1-3), 2000, pp. 243-247
Authors:
Steinlein, OK
Stoodt, J
Mulley, J
Berkovic, S
Scheffer, IE
Brodtkorb, E
Citation: Ok. Steinlein et al., Independent occurrence of the CHRNA4 Ser248Phe mutation in a Norwegian family with nocturnal frontal lobe epilepsy, EPILEPSIA, 41(5), 2000, pp. 529-535
Authors:
Steinlein, OK
Citation: Ok. Steinlein, Genetic analysis of idiopathic epilepsies: the role of ion channel mutations, CHANNELOPATHIES - COMMON MECHANISMS IN AURA, ARRHYTHMIA AND ALKALOSIS, 2000, pp. 181-197
Authors:
Weavers, A
Witter, B
Moser, N
Burghaus, L
Banerjee, C
Steinlein, OK
Schutz, U
de Vos, RAI
Steur, ENHJ
Lindstrom, J
Schroder, H
Citation: A. Weavers et al., Classical Alzheimer features and cholinergic dysfunction: towards a unifying hypothesis?, ACT NEUR SC, 102, 2000, pp. 42-48
Authors:
Steinlein, OK
Citation: Ok. Steinlein, Strategies to identify genes contributing to epilepsy in man, ACT NEUR SC, 102, 2000, pp. 19-20
Authors:
Steinlein, OK
Stoodt, J
Biervert, C
Janz, D
Sander, T
Citation: Ok. Steinlein et al., The voltage gated potassium channel KCNQ2 and idiopathic generalized epilepsy, NEUROREPORT, 10(6), 1999, pp. 1163-1166
Authors:
Steinlein, OK
Stoodt, J
de Vos, RAI
Steur, ENHJ
Wevers, A
Schutz, U
Schroder, H
Citation: Ok. Steinlein et al., Mutation screening of the CHRNA4 and CHRNB2 nicotinic cholinergic receptorgenes in Alzheimer's disease, NEUROREPORT, 10(14), 1999, pp. 2919-2922
Authors:
Lerche, H
Biervert, C
Alekov, AK
Schleithoff, L
Lindner, M
Klingler, W
Bretschneider, F
Mitrovic, N
Jurkat-Rott, K
Bode, H
Lehmann-Horn, F
Steinlein, OK
Citation: H. Lerche et al., A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions, ANN NEUROL, 46(3), 1999, pp. 305-312
Authors:
Biervert, C
Steinlein, OK
Citation: C. Biervert et Ok. Steinlein, Structural and mutational analysis of KCNQ2, the major gene locus for benign familial neonatal convulsions, HUM GENET, 104(3), 1999, pp. 234-240
Authors:
Steinlein, OK
Citation: Ok. Steinlein, Gene defects in idiopathic epilepsy, REV NEUROL, 155(6-7), 1999, pp. 450-453