Person's Publications

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]

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 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

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,