I agree that this site is using cookies. You can find further informations
here
.
X
Login
My folder (
0
)
Home
About us
Home About us
Our history
Profile
Press & public relations
Friends
The library in figures
Exhibitions
Projects
Training, internships, careers
Films
Services & Information
Home Services & Information
Lending and interlibrary loans
Returns and renewals
Training and library tours
My Account
Library cards
New to the library?
Download Information
Opening hours
Learning spaces
PC, WLAN, copy, scan and print
Catalogs and collections
Home Catalogs and Collections
Rare books and manuscripts
Digital collections
Subject Areas
Our sites
Home Our sites
Central Library
Law Library (Juridicum)
BB Business and Economics (BB11)
BB Physics and Electrical Engineering
TB Engineering and Social Sciences
TB Economics and Nautical Sciences
TB Music
TB Art & Design
TB Bremerhaven
Contact the library
Home Contact the library
Staff Directory
Open access & publishing
Home Open access & publishing
Reference management: Citavi & RefWorks
Publishing documents
Open Access in Bremen
Show Desktop-Version
Toggle navigation
Steinlein, O. K.
137
results:
Search for persons
X
Format
Online (137)
Mediatypes
Articles (Online) (131)
Bookchapter (Online) (2)
OpenAccess-fulltext (4)
Languages
english (119)
german (8)
Sorted by: Relevance
Sorted by: Year
?
1
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/..
?
2
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/..
?
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
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/..
?
5
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/..
?
6
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/..
?
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
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/..
?
9
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/..
?
10
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/..
?
11
Genetik der idiopathischen Epilepsien:
Steinlein, O. K.
Monatsschrift Kinderheilkunde. 152 (2004) 11 - p. 1211-1216 , 2004
Link:
https://doi.org/10.1007/..
?
12
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/..
?
13
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/..
?
14
The new voltage gated potassium channel KCNQ5 and neonatal ..:
Kananura, C
;
Biervert, C
;
Hechenberger, M
..
NeuroReport. 11 (2000) 9 - p. 2063-2067 , 2000
Link:
https://doi.org/10.1097/..
?
15
A reduced K+ current due to a novel mutation in KCNQ2 cause..:
Lerche, H.
;
Biervert, C.
;
Alekov, A. K.
...
Annals of Neurology. 46 (1999) 3 - p. 305-312 , 1999
Link:
https://doi.org/10.1002/..
1-15