E-LIB Suche - Ergebnisse für: Rautenstrauss, B

1

Laing distal myopathy with a novel mutation in exon 34 of t..:

Ferbert, A. ; Zibat, A. ; Rautenstrauß, B....
Neuromuscular Disorders. 26 (2016) 9 - p. 598-603 , 2016

Link: https://doi.org/10.1016/..

2

Hallucinations and delusions are frequently reported in ind..:

Martin, J. Peter ; Kümmerle, Annika ; Rautenstrauß, B.
Epilepsy & Behavior. 52 (2015) - p. 222-224 , 2015

Link: https://doi.org/10.1016/..

3

P67 MFN2 mutations cause compensatory mitochondrial DNA pro..:

Sitarz, K.S. ; Yu-Wai-Man, P. ; Pyle, A....
Neuromuscular Disorders. 22 (2012) - p. S25-S26 , 2012

Link: https://doi.org/10.1016/..

4

A novel mutation in CACNA1A associated with hemiplegic migr..:

Freilinger, T. ; Ackl, N. ; Ebert, A....
Journal of the Neurological Sciences. 300 (2011) 1-2 - p. 160-163 , 2011

Link: https://doi.org/10.1016/..

5

A 71‐nucleotide deletion in the periaxin gene in a Romani p..:

Baránková, L. ; Šišková, D. ; Hühne, K....
European Journal of Neurology. 15 (2008) 6 - p. 548-551 , 2008

Link: https://doi.org/10.1111/..

6

G.P.18.01 Giant axonal neuropathy: Phenotype–genotype corre..:

Tazir, M. ; Hühne, K. ; Nouioua, S....
Neuromuscular Disorders. 17 (2007) 9-10 - p. 890 , 2007

Link: https://doi.org/10.1016/..

7

Assoziation eines Neprilysin (NEP) Genpolymorphismus mit de..:

Leis, S ; Hühne, K ; Preller, C...
Aktuelle Neurologie. 32 (2005) S 4 - p. , 2005

Link: https://doi.org/10.1055/..

8

Novel EGR2 mutation R359Q is associated with CMT type 1 and..:

Mikešová, E. ; Hühne, K. ; Rautenstrauss, B....
Neuromuscular Disorders. 15 (2005) 11 - p. 764-767 , 2005

Link: https://doi.org/10.1016/..

9

Hearing loss as the first feature of late-onset axonal CMT ..:

Seeman, P. ; Mazanec, R. ; Huehne, K....
Neurology. 63 (2004) 4 - p. 733-735 , 2004

Link: https://doi.org/10.1212/..

10

A polymorphic locus in the intron 16 of the human angiotens..:

Hühne, K. ; Leis, S. ; Schmelz, M...
European Journal of Pain. 8 (2004) 3 - p. 221-225 , 2004

Link: https://doi.org/10.1016/..

11

Charcot-Marie-Tooth disease and related peripheral neuropat..:

Ekici, A. B. ; Schweitzer, D. ; Park, O....
Neurogenetics. 3 (2000) 1 - p. 49-50 , 2000

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

12

PMP22 Thr118Met is not a clinically relevant CMT1 marker:

Young, P. ; Stögbauer, F. ; Eller, B....
Journal of Neurology. 247 (2000) 9 - p. 696-700 , 2000

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

13

A GLClA Gene Gln368Stop Mutation in a Patient with Normal-T..:

Mardin, Christian Y. ; Velten, I. ; ??zbey, S...
Journal of Glaucoma. 8 (1999) 2 - p. 154 , 1999

Link: https://doi.org/10.1097/..

14

Regional Localization of the Human Epithelial Membrane Prot..:

Liehr, T. ; Kuhlenbäumer, G. ; Wulf, P....
Genomics. 58 (1999) 1 - p. 106-108 , 1999

Link: https://doi.org/10.1006/..

15

Molecular genetics and biology of inherited peripheral neur..:

Nelis, E. ; Timmerman, V. ; De Jonghe, P...
neurogenetics. 2 (1999) 3 - p. 137-148 , 1999

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