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
Auer-Grumbach, M
~ 400
results:
Search for persons
X
Format
Online
Print
Mediatypes
Books
Articles (Online)
OpenAccess-fulltext
more...
Audio (DVD/CD)
Bookchapter (Online)
less...
Languages
german (5)
english (315)
Sorted by: Relevance
Sorted by: Year
?
1
I.06 Late onset forms of inherited neuropathies:
Auer-Grumbach, M.
Neuromuscular Disorders. 32 (2022) - p. S93 , 2022
Link:
https://doi.org/10.1016/..
?
2
Hereditäre Transthyretinamyloidose (ATTRv-Amyloidose): Neue..:
Schilling, M.
;
Auer-Grumbach, M.
;
Baron, R.
...
DGNeurologie. 3 (2020) 5 - p. 369-383 , 2020
Link:
https://doi.org/10.1007/..
?
3
Diabetic neuropathy increases stimulation threshold during ..:
Heschl, S
;
Hallmann, B
;
Zilke, T
...
British Journal of Anaesthesia. 116 (2016) 4 - p. 538-545 , 2016
Link:
https://doi.org/10.1093/..
?
4
P967: Two novel HSJ1 mutations in a cohort of distal heredi..:
Gess, B.
;
Schirmacher, A.
;
Auer-Grumbach, M.
..
Clinical Neurophysiology. 125 (2014) - p. S305 , 2014
Link:
https://doi.org/10.1016/..
?
5
O.10 Mutations in a new dynein/dynactin adaptor gene cause ..:
Oates, E.C.
;
Rosser, A.M.
;
Hafezparast, M.
...
Neuromuscular Disorders. 23 (2013) 9-10 - p. 798 , 2013
Link:
https://doi.org/10.1016/..
?
6
Genetic spectrum of hereditary neuropathies with onset in t..:
Baets, J.
;
Deconinck, T.
;
De Vriendt, E.
...
Brain. 134 (2011) 9 - p. 2664-2676 , 2011
Link:
https://doi.org/10.1093/..
?
7
DominantGDAP1mutations cause predominantly mild CMT phenoty..:
Zimoń, M.
;
Baets, J.
;
Fabrizi, G.M.
...
Neurology. 77 (2011) 6 - p. 540-548 , 2011
Link:
https://doi.org/10.1212/..
?
8
P3.2 Novel mutation of TRPV4 in congenital distal SMA with ..:
Fiorillo, C.
;
Moro, F.
;
Astrea, G.
...
Neuromuscular Disorders. 21 (2011) 9-10 - p. 682 , 2011
Link:
https://doi.org/10.1016/..
?
9
Multi-system neurological disease is common in patients wit..:
Yu-Wai-Man, P.
;
Griffiths, P.G.
;
Gorman, G.S.
...
Brain. 133 (2010) 3 - p. 771-786 , 2010
Link:
https://doi.org/10.1093/..
?
10
SPG15is the second most common cause of hereditary spastic ..:
Goizet, C.
;
Boukhris, A.
;
Maltete, D.
...
Neurology. 73 (2009) 14 - p. 1111-1119 , 2009
Link:
https://doi.org/10.1212/..
?
11
Genes for hereditary sensory and autonomic neuropathies: a ..:
Rotthier, A.
;
Baets, J.
;
Vriendt, E. D.
...
Brain. 132 (2009) 10 - p. 2699-2711 , 2009
Link:
https://doi.org/10.1093/..
?
12
G.P.17.01 A novel slow-skeletal myosin (MYH7) mutation in a..:
Auer-Grumbach, M.
;
John, E.
;
Wallefeld, W.
...
Neuromuscular Disorders. 17 (2007) 9-10 - p. 883-884 , 2007
Link:
https://doi.org/10.1016/..
?
13
Hereditary motor and sensory neuropathy type V or complicat..:
Schöls, L.
;
Schüle, R.
;
Mauko, B.
..
Clinical Neurophysiology. 118 (2007) 4 - p. e90-e91 , 2007
Link:
https://doi.org/10.1016/..
?
14
Relative contribution of mutations in genes for autosomal d..:
Dierick, I.
;
Baets, J.
;
Irobi, J.
...
Brain. 131 (2007) 5 - p. 1217-1227 , 2007
Link:
https://doi.org/10.1093/..
?
15
G.P.5.06 LMNA p.R644C: Pathogenic mutation of low penetranc..:
Auer-Grumbach, M.
;
Fischer, C.
;
Duong, N.
...
Neuromuscular Disorders. 17 (2007) 9-10 - p. 799 , 2007
Link:
https://doi.org/10.1016/..
1-15
Related subjects
Diagnostik
Allgemeines