Results
|
|
1.
|
|
|
|
2.
|
|
|
|
3.
|
|
|
|
4.
|
Semantic memory and depressive symptoms in patients with subjective cognitive decline, mild cognitive impairment, and Alzheimer's disease. [electronic resource] by
- Lehrner, J
- Coutinho, G
- Mattos, P
- Moser, D
- Pflüger, M
- Gleiss, A
- Auff, E
- Dal-Bianco, P
- Pusswald, G
- Stögmann, E
Producer: 20180423
In:
International psychogeriatrics vol. 29
Availability: No items available.
|
|
|
5.
|
Andreas Rett and benign familial neonatal convulsions revisited. [electronic resource] by
- Zimprich, F
- Ronen, G M
- Stögmann, W
- Baumgartner, C
- Stögmann, E
- Rett, B
- Pappas, C
- Leppert, M
- Singh, N
- Anderson, V E
Producer: 20060926
In:
Neurology vol. 67
Availability: No items available.
|
|
|
6.
|
Increased risk of death associated with the use of proton-pump inhibitors in patients with dementia and controls - a pharmacoepidemiological claims data analysis. [electronic resource] by
- Cetin, H
- Wurm, R
- Reichardt, B
- Tomschik, M
- Silvaieh, S
- Parvizi, T
- König, T
- Erber, A
- Schernhammer, E
- Stamm, T
- Stögmann, E
Producer: 20210625
In:
European journal of neurology vol. 27
Availability: No items available.
|
|
|
7.
|
Hereditary spastic paraplegia caused by compound heterozygous mutations outside the motor domain of the KIF1A gene. [electronic resource] by
- Krenn, M
- Zulehner, G
- Hotzy, C
- Rath, J
- Stogmann, E
- Wagner, M
- Haack, T B
- Strom, T M
- Zimprich, A
- Zimprich, F
Producer: 20170605
In:
European journal of neurology vol. 24
Availability: No items available.
|
|
|
8.
|
Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutations. [electronic resource] by
- Stogmann, E
- Lichtner, P
- Baumgartner, C
- Bonelli, S
- Assem-Hilger, E
- Leutmezer, F
- Schmied, M
- Hotzy, C
- Strom, T M
- Meitinger, T
- Zimprich, F
- Zimprich, A
Producer: 20070108
In:
Neurology vol. 67
Availability: No items available.
|
|
|
9.
|
Genotype-guided diagnostic reassessment after exome sequencing in neuromuscular disorders: experiences with a two-step approach. [electronic resource] by
- Krenn, M
- Tomschik, M
- Rath, J
- Cetin, H
- Grisold, A
- Zulehner, G
- Milenkovic, I
- Stogmann, E
- Zimprich, A
- Strom, T M
- Meitinger, T
- Wagner, M
- Zimprich, F
Producer: 20201223
In:
European journal of neurology vol. 27
Availability: No items available.
|
|
|
10.
|
A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosis. [electronic resource] by
- Stogmann, E
- El Tawil, S
- Wagenstaller, J
- Gaber, A
- Edris, S
- Abdelhady, A
- Assem-Hilger, E
- Leutmezer, F
- Bonelli, S
- Baumgartner, C
- Zimprich, F
- Strom, T M
- Zimprich, A
Producer: 20090713
In:
Neurogenetics vol. 10
Availability: No items available.
|
|
|
11.
|
Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes. [electronic resource] by
- Stogmann, E
- Lichtner, P
- Baumgartner, C
- Schmied, M
- Hotzy, C
- Asmus, F
- Leutmezer, F
- Bonelli, S
- Assem-Hilger, E
- Vass, K
- Hatala, K
- Strom, T M
- Meitinger, T
- Zimprich, F
- Zimprich, A
Producer: 20070912
In:
Neurogenetics vol. 7
Availability: No items available.
|
|
|
12.
|
A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures. [electronic resource] by
- Schlachter, K
- Gruber-Sedlmayr, U
- Stogmann, E
- Lausecker, M
- Hotzy, C
- Balzar, J
- Schuh, E
- Baumgartner, C
- Mueller, J C
- Illig, T
- Wichmann, H E
- Lichtner, P
- Meitinger, T
- Strom, T M
- Zimprich, A
- Zimprich, F
Producer: 20090410
In:
Neurology vol. 72
Availability: No items available.
|