By Authors

Publications - sorted by Authors

• König T, Stögmann E (2021) Genetics of Alzheimer’s disease Wien Med Wochenschr,

• Wurm R, Stamm T, Reichardt B, Schwarz F, Parvizi T, Silvaieh S, König T, Cetin H, Stögmann E (2020) Prescription patterns of antidementives in a high income country: A pharmacoepidemiologic study Alzheimer's Dement, 6 (1)
• Defrancesco M, Bancher C, Dal-Bianco P, Hinterhuber H, Schmidt R, Struhal W, Ransmayr G, Stögmann E, Marksteiner J (2020) Positionspapier der Österreichische Alzheimer Gesellschaft (ÖAG) Neuropsychiatr,
• Dankl K, Stögmann E, König T, Moritsch S, Hanke S (2020) Multidimensional Design Research for Dementia and Its Methodological Opportunities for Cross-Disciplinary Consortia The Design Journal, 23 (4): 597-619
• Rosas A, Stögmann E, Lehrner J (2020) Individual cognitive changes in subjective cognitive decline, mild cognitive impairment and Alzheimer’s disease using the reliable change index methodology Wien. Klin. Wochenschr.,
• Cetin H, Wurm R, Reichardt B, Tomschik M, Silvaieh S, Parvizi T, König T, Erber A, Schernhammer E, Stamm T, Stögmann E (2020) Increased risk of death associated with the use of proton‐pump inhibitors in patients with dementia and controls – a pharmacoepidemiological claims data analysis Eur J Neurol, 27 (8): 1422-1428
• Krenn M, Wagner M, Hotzy C, Graf E, Weber S, Brunet T, Lorenz-Depiereux B, Kasprian G, Aull-Watschinger S, Pataraia E, Stogmann E, Zimprich A, Strom T, Meitinger T, Zimprich F (2020) Diagnostic exome sequencing in non-acquired focal epilepsies highlights a major role of GATOR1 complex genes J Med Genet, 57 (9): 624-633
• Wurm R, Klotz S, Rahimi J, Katzenschlager R, Lindeck‐Pozza E, Regelsberger G, Danics K, Kapas I, Bíró Z, Stögmann E, Gelpi E, Kovacs G (2020) Argyrophilic grain disease in individuals younger than 75 years: clinical variability in an under‐recognized limbic tauopathy Eur J Neurol, 27 (10): 1856-1866
• Szegedi S, Dal‐Bianco P, Stögmann E, Traub‐Weidinger T, Rainer M, Masching A, Schmidl D, Werkmeister R, Chua J, Schmetterer L, Garhöfer G (2020) Anatomical and functional changes in the retina in patients with Alzheimer’s disease and mild cognitive impairment Acta Ophtalmol, 98 (7)
• Greisenegger E, Llufriu S, Chamorro A, Cervera A, Jimenez-Escrig A, Rappersberger K, Marik W, Greisenegger S, Stögmann E, Kopp T, Strom T, Henes J, Joutel A, Zimprich A (2020) A NOTCH3 homozygous nonsense mutation in familial Sneddon syndrome with pediatric stroke J Neurol,
• Klotz S, König T, Erdler M, Ulram A, Nguyen A, Ströbel T, Zimprich A, Stögmann E, Regelsberger G, Höftberger R, Budka H, Kovacs G, Gelpi E (2020) Co‐incidental C9orf72 expansion mutation‐related frontotemporal lobar degeneration pathology and sporadic Creutzfeldt−Jakob disease Eur J Neurol,
• Kamitaki N, Sekar A, Handsaker R, de Rivera H, Tooley K, Morris D, Taylor K, Whelan C, Tombleson P, Loohuis L, Boehnke M, Kimberly R, Kaufman K, Harley J, Langefeld C, Seidman C, Pato M, Pato C, Ophoff R, Graham R, Criswell L, Vyse T, McCarroll S (2020) Complement genes contribute sex-biased vulnerability in diverse disorders Nature, 582 (7813): 577-581

• Tahmasebi R, Zehetmayer S, Stögmann E, Lehrner J (2019) Awareness of Olfactory Dysfunction in Subjective Cognitive Decline, Mild Cognitive Decline, and Alzheimer’s Disease Chemosens Percept, 13 (1): 59-70

• Tahmasebi R, Zehetmayer S, Pusswald G, Kovacs G, Stögmann E, Lehrner J (2018) 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 Int Psychogeriatr, : 1-13 [Epub ahead of print]

• Lehrner J, Coutinho G, Mattos P, Moser D, Pflüger M, Gleiss A, Auff E, Dal-Bianco P, Pusswald G, Stögmann E (2017) Semantic memory and depressive symptoms in patients with subjective cognitive decline, mild cognitive impairment, and Alzheimer's disease Int Psychogeriatr, 29 (7): 1123-1135
• Rommer P, Zschocke J, Fowler B, Födinger M, Konstantopoulou V, Möslinger D, Stögmann E, Suess E, Baumgartner M, Auff E, Sunder-Plassmann G (2017) Manifestations of neurological symptoms and thromboembolism in adults with MTHFR-deficiency J Neurol Sci, 383: 123-127
• Krenn M, Zulehner G, Hotzy C, Rath J, Stogmann E, Wagner M, Haack T, Strom T, Zimprich A, Zimprich F (2017) Hereditary spastic paraplegia caused by compound heterozygous mutations outside the motor domain of the KIF1A gene Eur J Neurol, 24 (5): 741-747

• Silva M, Moser D, Pflüger M, Pusswald G, Stögmann E, Dal-Bianco P, Auff E, Lehrner J (2016) Self-reported and informant-reported memory functioning and awareness in patients with mild cognitive impairment and Alzheimer´s disease Neuropsychiatr, 30 (2): 103-112
• Pusswald G, Moser D, Pflüger M, Gleiss A, Auff E, Stögmann E, Dal-Bianco P, Lehrner J (2016) The impact of depressive symptoms on health-related quality of life in patients with subjective cognitive decline, mild cognitive impairment, and Alzheimer's disease Int Psychogeriatr, 28 (12): 2045-2054

• Stogmann E, Zimprich A, Zimprich F (2013) Reply: Autosomal recessive epilepsy associated with contactin 2 mutation is different from familial cortical tremor, myoclonus and epilepsy Brain, 136 (10): e254-e254
• Stogmann E, Reinthaler E, ElTawil S, El Etribi M, Hemeda M, El Nahhas N, Gaber A, Fouad A, Edris S, Benet-Pages A, Eck S, Pataraia E, Mei D, Brice A, Lesage S, Guerrini R, Zimprich F, Strom T, Zimprich A (2013) Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2 Brain, 136 (4): 1155-1160

• Hilger E, Reinthaler E, Stogmann E, Hotzy C, Pataraia E, Baumgartner C, Zimprich A, Zimprich F (2012) Lack of association between ABCC2 gene variants and treatment response in epilepsy Pharmacogenomics, 13 (2): 185-190

• Assem-Hilger E, Lanzenberger R, Savli M, Wadsak W, Mitterhauser M, Mien LK, Stögmann E, Baumgartner C, Kletter K, Asenbaum S (2010) Central serotonin 1A receptor binding in temporal lobe epilepsy: a [carbonyl-(11)C]WAY-100635 PET study Epilepsy Behav, 19(3): 467-73
• Assem-Hilger E, Lanzenberger R, Savli M, Wadsak W, Mitterhauser M, Mien L, Stogmann E, Baumgartner C, Kletter K, Asenbaum S (2010) Central serotonin 1A receptor binding in temporal lobe epilepsy: A [carbonyl-11C]WAY-100635 PET study Epilepsy Behav, 19 (3): 467-473

• 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, Zimprich A (2008) A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosis Neurogenetics, 10 (1): 73-77

• Bonelli S, Lurger S, Zimprich F, Stogmann E, Assem-Hilger E, Baumgartner C (2007) Clinical Seizure Lateralization in Frontal Lobe Epilepsy Epilepsia, 48 (3): 517-523

• 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 (2006) Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes Neurogenetics, 7(4): 265-8
• 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 (2006) Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutations. Neurology, 67(11): 2029-31.
• Zimprich F, Ronen G, Stogmann W, Baumgartner C, Stogmann E, Rett B, Pappas C, Leppert M, Singh N, Anderson V (2006) Andreas Rett and benign familial neonatal convulsions revisited Neurology, 67 (5): 864-866
• Stogmann E, Zimprich A, Baumgartner C, Gleiss A, Zimprich F (2006) Lack of association between a GABA receptor 1 gene polymorphism and temporal lobe epilepsy Epilepsia,
• 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 (2006) Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes Neurogenetics,
• 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 (2006) Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutations Neurology,

• Zimprich F, Sunder-Plassmann R, Stogmann E, Gleiss A, Dal-Bianco A, Zimprich A, Plumer S, Baumgartner C, Mannhalter C (2004) Association of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsy Neurology,

• Stögmann E, Zimprich A, Baumgartner C, Aull-Watschinger S, Höllt V, Zimprich F (2002) A functional polymorphism in the prodynorphin gene promotor is associated with temporal lobe epilepsy Ann Neurol,