E-LIB Suche - Ergebnisse für: Auer-Grumbach, M

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

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/..

7

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/..

8

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/..

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

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/..

11

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/..

12

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/..

13

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/..

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.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/..