Hereditary spastic paraplegia caused by compound heterozygous mutations outside the motor domain of the KIF1A gene von Krenn, M., Zulehner, G., Hotzy, C., Rath, J., Stogmann, E., Wagner, M., Haack, T. B., Strom, T. M., Zimprich, A., Zimprich, F.

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Genotype‐guided diagnostic reassessment after exome sequencing in neuromuscular disorders: experiences with a two‐step approach von 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.

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Hemoglobin A1c Serum Level Predicts 5-year Mortality in Patients with Cognitive Impairment von Dreier, J., Schernhammer, E., Haslacher, H., Stögmann, E., Lehrner, J.

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The impact of depressive symptoms on health-related quality of life in patients with subjective cognitive decline, mild cognitive impairment, and Alzheimer's disease von Pusswald, G., Moser, D., Pflüger, M., Gleiss, A., Auff, E., Stögmann, E., Dal-Bianco, P., Lehrner, J.

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Semantic memory and depressive symptoms in patients with subjective cognitive decline, mild cognitive impairment, and Alzheimer's disease von Lehrner, J., Coutinho, G., Mattos, P., Moser, D., Pflüger, M., Gleiss, A., Auff, E., Dal-Bianco, P., Pusswald, G., Stögmann, E.

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Association of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsy von ZIMPRICH, F, SUNDER-PLASSMANN, R, STOGMANN, E, GLEISS, A, DAL-BIANCO, A, ZIMPRICH, A, PLUMER, S, BAUMGARTNER, C, MANNHALTER, C

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Homocysteine – A predictor for five year-mortality in patients with subjective cognitive decline, mild cognitive impairment and Alzheimer's dementia von Futschek, Ines Elisabeth, Schernhammer, E., Haslacher, H., Stögmann, E., Lehrner, J.

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A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures von SCHLACHTER, K, GRUBER-SEDLMAYR, U, WICHMANN, H. E, LICHTNER, P, MEITINGER, T, STROM, T. M, ZIMPRICH, A, ZIMPRICH, F, STOGMANN, E, LAUSECKER, M, HOTZY, C, BALZAR, J, SCHUH, E, BAUMGARTNER, C, MUELLER, J. C, ILLIG, T

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Argyrophilic grain disease in individuals younger than 75 years: clinical variability in an under‐recognized limbic tauopathy von Wurm, R., Klotz, S., Rahimi, J., Katzenschlager, R., Lindeck‐Pozza, E., Regelsberger, G., Danics, K., Kapas, I., Bíró, Z. A., Stögmann, E., Gelpi, E., Kovacs, G. G.

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Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutations von STOGMANN, E, LICHTNER, P, ZIMPRICH, F, ZIMPRICH, A, BAUMGARTNER, C, BONELLI, S, ASSEM-HILGER, E, LEUTMEZER, F, SCHMIED, M, HOTZY, C, STROM, T. M, MEITINGER, T

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

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Identification of odors, faces, cities and naming of objects in patients with subjective cognitive decline, mild cognitive impairment and Alzheimer´s disease: a longitudinal study von Tahmasebi, R., Zehetmayer, S., Pusswald, G., Kovacs, G., Stögmann, E., Lehrner, J.

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Long-term Olfactory Functions in Patients with Subjective Cognitive Decline and Mild Cognitive Impairment von Novotny, D., Stögmann, E., Lehrner, J.

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Odor identification testing is inferior compared to neurocognitive testing in predicting conversion to Alzheimer's Disease von Pusswald, G., Ocak, S., Stögmann, E., Lehrner, J.

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Increased risk of death associated with the use of proton‐pump inhibitors in patients with dementia and controls – a pharmacoepidemiological claims data analysis von Cetin, H., Wurm, R., Reichardt, B., Tomschik, M., Silvaieh, S., Parvizi, T., König, T., Erber, A., Schernhammer, E., Stamm, T., Stögmann, E.

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Awareness of Olfactory Dysfunction in Subjective Cognitive Decline, Mild Cognitive Decline, and Alzheimer’s Disease von Tahmasebi, R., Zehetmayer, S., Stögmann, E., Lehrner, Johann

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Depressive symptoms and olfactory function in patients with subjective cognitive decline, mild cognitive impairment and Alzheimer's disease von Bergmann, C., Stögmann, E., Lehrner, J.

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Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes von STOGMANN, E, LICHTNER, P, HATALA, K, STROM, T. M, MEITINGER, T, ZIMPRICH, F, ZIMPRICH, A, BAUMGARTNER, C, SCHMIED, M, HOTZY, C, ASMUS, F, LEUTMEZER, F, BONELLI, S, ASSEM-HILGER, E, VASS, K

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Andreas Rett and benign familial neonatal convulsions revisited von ZIMPRICH, F, RONEN, G. M, STÖGMANN, W, BAUMGARTNER, C, STÖGMANN, E, RETT, B, PAPPAS, C, LEPPERT, M, SINGH, N, ANDERSON, V. E

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Autosomal recessive cortical myoclonic tremor and epilepsy: Association with a mutation in the potassium channel associated gene CNTN2 von Stögmann, E.

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