Stogmann E - Search Results

1

Lack of association between a GABA receptor 1 gene polymorphism and temporal lobe epilepsy.

Stogmann E, Zimprich A, Baumgartner C, Gleiss A, Zimprich F. Stogmann E, et al. Epilepsia. 2006 Feb;47(2):437-9. doi: 10.1111/j.1528-1167.2006.00441.x. Epilepsia. 2006. PMID: 16499773 Free article.

2

Real-world performance of plasma p-tau181 in a heterogeneous memory clinic cohort.

Parvizi T, Wurm R, König T, Silvaieh S, Altmann P, Klotz S, Regelsberger G, Traub-Weidinger T, Gelpi E, Stögmann E. Parvizi T, et al. Among authors: stogmann e. Ann Clin Transl Neurol. 2024 Aug;11(8):1988-1998. doi: 10.1002/acn3.52116. Epub 2024 Jul 4. Ann Clin Transl Neurol. 2024. PMID: 38965832 Free PMC article.

3

A functional polymorphism in the prodynorphin gene promotor is associated with temporal lobe epilepsy.

Stögmann E, Zimprich A, Baumgartner C, Aull-Watschinger S, Höllt V, Zimprich F. Stögmann E, et al. Ann Neurol. 2002 Feb;51(2):260-3. doi: 10.1002/ana.10108. Ann Neurol. 2002. PMID: 11835385

4

Association of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsy.

Zimprich F, Sunder-Plassmann R, Stogmann E, Gleiss A, Dal-Bianco A, Zimprich A, Plumer S, Baumgartner C, Mannhalter C. Zimprich F, et al. Among authors: stogmann e. Neurology. 2004 Sep 28;63(6):1087-9. doi: 10.1212/01.wnl.0000141021.42763.f6. Neurology. 2004. PMID: 15452305

5

Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes.

Stogmann E, Lichtner P, Baumgartner C, Schmied M, Hotzy C, Asmus F, Leutmezer F, Bonelli S, Assem-Hilger E, Vass K, Hatala K, Strom TM, Meitinger T, Zimprich F, Zimprich A. Stogmann E, et al. Neurogenetics. 2006 Nov;7(4):265-8. doi: 10.1007/s10048-006-0057-x. Epub 2006 Aug 24. Neurogenetics. 2006. PMID: 16932951

6

Andreas Rett and benign familial neonatal convulsions revisited.

Zimprich F, Ronen GM, Stögmann W, Baumgartner C, Stögmann E, Rett B, Pappas C, Leppert M, Singh N, Anderson VE. Zimprich F, et al. Among authors: stogmann w, stogmann e. Neurology. 2006 Sep 12;67(5):864-6. doi: 10.1212/01.wnl.0000234066.46806.90. Neurology. 2006. PMID: 16966552

7

Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutations.

Stogmann E, Lichtner P, Baumgartner C, Bonelli S, Assem-Hilger E, Leutmezer F, Schmied M, Hotzy C, Strom TM, Meitinger T, Zimprich F, Zimprich A. Stogmann E, et al. Neurology. 2006 Dec 12;67(11):2029-31. doi: 10.1212/01.wnl.0000250254.67042.1b. Neurology. 2006. PMID: 17159113

8

Clinical seizure lateralization in frontal lobe epilepsy.

Bonelli SB, Lurger S, Zimprich F, Stogmann E, Assem-Hilger E, Baumgartner C. Bonelli SB, et al. Among authors: stogmann e. Epilepsia. 2007 Mar;48(3):517-23. doi: 10.1111/j.1528-1167.2006.00943.x. Epilepsia. 2007. PMID: 17346249 Free article.

9

A functional polymorphism in the SCN1A gene is not associated with carbamazepine dosages in Austrian patients with epilepsy.

Zimprich F, Stogmann E, Bonelli S, Baumgartner C, Mueller JC, Meitinger T, Zimprich A, Strom TM. Zimprich F, et al. Among authors: stogmann e. Epilepsia. 2008 Jun;49(6):1108-9. doi: 10.1111/j.1528-1167.2008.01549_4.x. Epilepsia. 2008. PMID: 18554361 Free article. No abstract available.

10

A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosis.

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 TM, Zimprich A. Stogmann E, et al. Neurogenetics. 2009 Feb;10(1):73-7. doi: 10.1007/s10048-008-0153-1. Epub 2008 Oct 11. Neurogenetics. 2009. PMID: 18850119

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