E-LIB Suche - Ergebnisse für: O.K. Steinlein, Germany

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/..

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/..

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/..

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/..

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/..

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/..

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/..

12

Genetik der idiopathischen Epilepsien:

Steinlein, O. K.
Monatsschrift Kinderheilkunde. 152 (2004) 11 - p. 1211-1216 , 2004

Link: https://doi.org/10.1007/..

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/..