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O.K. Steinlein, Germany
24
results:
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english (19)
german (4)
Sorted by: Relevance
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?
1
EFNS task force on molecular diagnosis of neurologic disord..:
Members of the task force on molecular diagnosis of neurologic disorders: T. Gasser, Germany
;
M. Dichgans, Germany
;
J. Finsterer, Austria
;
I. Hausmanowa‐Petrusewicz, Poland
;
K. Jurkat‐Rott, Germany
;
T. Klopstock, Germany
;
E. Leguern, France
;
A.‐E. Lehesjoki, Finland
;
F. Lehmann‐Horn, Germany
;
T. Lynch, UK
;
H. Morris, UK
;
M. Rossor, UK
;
O.K. Steinlein, Germany
;
N. Wood, UK
;
J. Zaremba, Poland
;
M. Zeviani, Italy
;
A. Zoharn, Israel
European Journal of Neurology. 8 (2001) 5 - p. 407-424 , 2001
Link:
https://doi.org/10.1046/..
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2
Tumorassoziierte Genodermatosen:
Frommherz, L. H.
;
Steinlein, O. K.
;
French, L. E.
.
Der Hautarzt. 72 (2021) 4 - p. 288-294 , 2021
Link:
https://doi.org/10.1007/..
?
3
Cutaneous melanoma in Birt-Hogg-Dubé syndrome: part of the ..:
Sattler, E.C.
;
Ertl-Wagner, B.
;
Pellegrini, C.
...
British Journal of Dermatology. 178 (2018) 2 - p. e132-e133 , 2018
Link:
https://doi.org/10.1111/..
?
4
Delayed diagnosis of Birt-Hogg-Dubé syndrome due to marked ..:
Sattler, E. C.
;
Steinlein, O. K.
BMC Medical Genetics. 19 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1186/..
?
5
Upstream open reading frames regulate cannabinoid receptor ..:
Eggert, M.
;
Pfob, M.
;
Jurinovic, V.
..
Molecular and Cellular Endocrinology. 399 (2015) - p. 103-109 , 2015
Link:
https://doi.org/10.1016/..
?
6
Neuronal nicotinic acetylcholine receptors: From the geneti..:
Steinlein, O.K.
;
Bertrand, D.
Biochemical Pharmacology. 76 (2008) 10 - p. 1175-1183 , 2008
Link:
https://doi.org/10.1016/..
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7
Benign familial neonatal convulsions: Always benign?:
Steinlein, O.K.
;
Conrad, C.
;
Weidner, B.
Epilepsy Research. 73 (2007) 3 - p. 245-249 , 2007
Link:
https://doi.org/10.1016/..
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8
Compound heterozygosity for three common MEFV mutations in ..:
Seidel, H.
;
Steinlein, O. K.
European Journal of Pediatrics. 167 (2007) 7 - p. 827-828 , 2007
Link:
https://doi.org/10.1007/..
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9
Molecular analysis of a mutation in the S5-H5 linker of the..:
Naros, G.
;
Yalcin, O.
;
Maljevic, S.
...
Aktuelle Neurologie. 33 (2006) S 1 - p. , 2006
Link:
https://doi.org/10.1055/..
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10
LGI1: a gene involved in epileptogenesis and glioma progres..:
Gu, W.
;
Brodtkorb, E.
;
Piepoli, T.
..
Neurogenetics. 6 (2005) 2 - p. 59-66 , 2005
Link:
https://doi.org/10.1007/..
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11
Diagnose und Therapie der kongenitalen Myastheniesyndrome:
Sieb, J. P.
;
Hans, M.
;
Swandulla, D.
..
Monatsschrift Kinderheilkunde. 153 (2005) 5 - p. 453-462 , 2005
Link:
https://doi.org/10.1007/..
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12
Genetik der idiopathischen Epilepsien:
Steinlein, O. K.
Monatsschrift Kinderheilkunde. 152 (2004) 11 - p. 1211-1216 , 2004
Link:
https://doi.org/10.1007/..
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13
Congenital myasthenic syndrome due to heteroallelic nonsens..:
Kraner, S.
;
Burgunder, J.‐M.
;
Rösler, K. M.
..
European Journal of Neurology. 9 (2002) 6 - p. 694-695 , 2002
Link:
https://doi.org/10.1046/..
?
14
Strategies to identify genes contributing to epilepsy in ma:
Steinlein, O. K.
Acta Neurologica Scandinavica. 102 (2000) - p. 5-52 , 2000
Link:
https://doi.org/10.1034/..
?
15
Severe congenital myasthenic syndrome due to homozygosity o..:
Sieb, J. P.
;
Kraner, S.
;
Schrank, B.
...
Annals of Neurology. 48 (2000) 3 - p. 379-383 , 2000
Link:
https://doi.org/10.1002/..
1-15