Sortiert nach PI

Publikationen - sortiert nach Principle Investigator

• 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