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1

Semantic memory and depressive symptoms in patients with subjective cognitive decline, mild cognitive impairment, and Alzheimer's disease

Lehrner, J., Coutinho, G., Mattos, P., Moser, D., Pflüger, M., Gleiss, A., Auff, E., Dal-Bianco, P., Pusswald, G., Stögmann, E.

Journal:

International Psychogeriatrics

Year:

2017

Language:

english

File:

PDF, 268 KB

english, 2017

2

A novel mutation in the VCP gene (G157R) in a german family with inclusion-body myopathy with paget disease of bone and frontotemporal dementia

Atbin Djamshidian, Jochen Schaefer, Dietrich Haubenberger, Elisabeth Stogmann, Friedrich Zimprich, Eduard Auff, Alexander Zimprich

Journal:

Year:

2009

Language:

english

File:

PDF, 115 KB

english, 2009

3

Reply: Autosomal recessive epilepsy associated with contactin 2 mutation is different from familial cortical tremor, myoclonus and epilepsy

Stogmann, E., Zimprich, A., Zimprich, F.

Journal:

Year:

2013

Language:

english

File:

PDF, 81 KB

english, 2013

4

Activities of Daily Living and Depressive Symptoms in Patients with Subjective Cognitive Decline, Mild Cognitive Impairment, and Alzheimer’s Disease

Stogmann, Elisabeth, Moser, Doris, Klug, Stefanie, Gleiss, Andreas, Auff, Eduard, Dal-Bianco, Peter, Pusswald, Gisela, Lehrner, Johann

Journal:

Journal of Alzheimer's Disease

Year:

2015

Language:

english

File:

PDF, 223 KB

english, 2015

5

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

Elisabeth Stögmann, Alexander Zimprich, Christoph Baumgartner, Susanne Aull-Watschinger, Volker Höllt, Fritz Zimprich

Journal:

Annals of Neurology

Year:

2002

Language:

english

File:

PDF, 203 KB

english, 2002

6

Reply

Elisabeth Stögmann, Christoph Baumgartner, Fritz Zimprich

Journal:

Annals of Neurology

Year:

2003

Language:

english

File:

PDF, 41 KB

english, 2003

7

Calcium-Phosphor-Stoffwechseluntersuchungen an einem Fall von McCune-Albright-Syndrom mit Phosphatdiabetes

H. M. Grubbauer, W. Stögmann, H. Meßner

Journal:

European Journal of Pediatrics

Year:

1974

File:

PDF, 2.09 MB

1974

8

Fructose-1,6-diphosphatase deficiency: glycerol excretion during fasting test

P. A. Dremsek, M. Sacher, W. Stögmann, R. Gitzelmann, C. Bachmann

Journal:

European Journal of Pediatrics

Year:

1985

Language:

english

File:

PDF, 195 KB

english, 1985

9

Immunodeficiency with lymphoid hyperplasia

I. Mutz, W. Stögmann

Journal:

European Journal of Pediatrics

Year:

1977

Language:

english

File:

PDF, 1.42 MB

english, 1977

10

Immunological studies in childhood scleroderma

W. Stögmann, M. Sandhofer, J. Fritz

Journal:

European Journal of Pediatrics

Year:

1977

Language:

english

File:

PDF, 407 KB

english, 1977

11

Lipoiddermatoarthritis (multizentrische Reticulohistiocytose)

W. Stögmann, H. Kerl, H. Schmidberger

Journal:

European Journal of Pediatrics

Year:

1975

File:

PDF, 2.23 MB

1975

12

Das Pseudolymphomsyndrom

W. Stögmann, W. Müller

Journal:

European Journal of Pediatrics

Year:

1974

Language:

german

File:

PDF, 961 KB

german, 1974

13

Long-term follow up of a new case of hawkinsinuria

W. Lehnert, W. Stögmann, U. Engelke, R. A. Wevers, G. B. van den Berg

Journal:

European Journal of Pediatrics

Year:

1999

Language:

english

File:

PDF, 128 KB

english, 1999

14

Mutations in theCLCN2gene are a rare cause of idiopathic generalized epilepsy syndromes

E. Stogmann, P. Lichtner, C. Baumgartner, M. Schmied, C. Hotzy, F. Asmus, F. Leutmezer, S. Bonelli, E. Assem-Hilger, K. Vass, K. Hatala, T. M. Strom, T. Meitinger, F. Zimprich, A. Zimprich

Journal:

Year:

2006

Language:

english

File:

PDF, 94 KB

english, 2006

15

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

E. Stogmann, S. El Tawil, J. Wagenstaller, A. Gaber, S. Edris, A. Abdelhady, E. Assem-Hilger, F. Leutmezer, S. Bonelli, C. Baumgartner, F. Zimprich, T. M. Strom, A. Zimprich

Journal:

Year:

2009

Language:

english

File:

PDF, 146 KB

english, 2009

16

Lack of Association between a GABAB Receptor 1 Gene Polymorphism and Temporal Lobe Epilepsy

Elisabeth Stogmann, Alexander Zimprich, Christoph Baumgartner, Andreas Gleiss, Fritz Zimprich

Journal:

Year:

2006

Language:

english

File:

PDF, 108 KB

english, 2006

17

Clinical Seizure Lateralization in Frontal Lobe Epilepsy

Silvia Beatrice Bonelli, Stefanie Lurger, Fritz Zimprich, Elisabeth Stogmann, Eva Assem-Hilger, Christoph Baumgartner

Journal:

Year:

2007

Language:

english

File:

PDF, 72 KB

english, 2007

18

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

Fritz Zimprich, Elisabeth Stogmann, Silvia Bonelli, Christoph Baumgartner, Jakob C. Mueller, Thomas Meitinger, Alexander Zimprich, Tim M. Strom

Journal:

Year:

2008

Language:

english

File:

PDF, 1.27 MB

english, 2008

19

Pseudohypoparathyroidism: Disappearance of the resistance to parathyroid extract during treatment with vitamin D

Walter Stögmann, Jan A. Fischer

Journal:

The American Journal of Medicine

Year:

1975

Language:

english

File:

PDF, 510 KB

english, 1975

20

Central serotonin 1A receptor binding in temporal lobe epilepsy: A [carbonyl-11C]WAY-100635 PET study

Eva Assem-Hilger, Rupert Lanzenberger, Markus Savli, Wolfgang Wadsak, Markus Mitterhauser, Leonhard-Key Mien, Elisabeth Stögmann, Christoph Baumgartner, Kurt Kletter, Susanne Asenbaum

Journal:

Epilepsy & Behavior

Year:

2010

Language:

english

File:

PDF, 673 KB

english, 2010

21

The architecture of Norway spruce ectomycorrhizae: three-dimensional models of cortical cells, fungal biomass, and interface for potential nutrient exchange

Bernhard Stögmann, Andreas Marth, Barbara Pernfuß, Reinhold Pöder

Journal:

Year:

2013

Language:

english

File:

PDF, 646 KB

english, 2013

22

Autosomal recessive cortical myoclonic tremor and epilepsy: Association with a mutation in the potassium channel associated gene CNTN2

Journal:

Journal of the Neurological Sciences

Year:

2013

Language:

english

File:

PDF, 67 KB

english, 2013

23

In vitro evaluation of a tumor vaccine based on the xenogenization of tumor cells with tetanus toxoid molecules

Felzmann, T., Buchberger, M., Jechlinger, M., Stögmann, E., Buschle, M., Schmidt, W., Kircheis, R., Wagner, E., Birnstiel, M., Gadner, H.

Journal:

European Journal of Cancer

Year:

1999

Language:

english

File:

PDF, 165 KB

english, 1999

24

A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures

Schlachter, K., Gruber-Sedlmayr, U., Stogmann, E., Lausecker, M., Hotzy, C., Balzar, J., Schuh, E., Baumgartner, C., Mueller, J. C., Illig, T., Wichmann, H. E., Lichtner, P., Meitinger, T., Strom, T.

Journal:

Year:

2009

Language:

english

File:

PDF, 244 KB

english, 2009

25

From Eugenic Euthanasia to Habilitation of ``Disabled'' Children: Andreas Rett's Contribution

Ronen, G. M., Meaney, B., Dan, B., Zimprich, F., Stogmann, W., Neugebauer, W.

Journal:

Journal of Child Neurology

Year:

2009

Language:

english

File:

PDF, 405 KB

english, 2009

26

Lack of association between ABCC2 gene variants and treatment response in epilepsy

Hilger, Eva, Reinthaler, Eva Maria, Stogmann, Elisabeth, Hotzy, Christoph, Pataraia, Ekaterina, Baumgartner, Christoph, Zimprich, Alexander, Zimprich, Fritz

Journal:

Pharmacogenomics

Year:

2012

Language:

english

File:

PDF, 505 KB

english, 2012

27

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.

Journal:

Year:

2004

Language:

english

File:

PDF, 121 KB

english, 2004

28

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, T. M., Meitinger, T., Zimprich, F., Zimprich, A.

Journal:

Year:

2006

Language:

english

File:

PDF, 256 KB

english, 2006

29

Prolactin and thyrotrophin response to thyrotrophin-releasing hormone in growth hormone deficiency.

Frisch, H, Herkner, K, Schober, E, Stogmann, W, Waldhauser, F, Weissel, M

Journal:

Archives of Disease in Childhood

Year:

1982

Language:

english

File:

PDF, 817 KB

english, 1982

30

Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2

Stogmann, E., Reinthaler, E., ElTawil, S., El Etribi, M. A., Hemeda, M., El Nahhas, N., Gaber, A. M., Fouad, A., Edris, S., Benet-Pages, A., Eck, S. H., Pataraia, E., Mei, D., Brice, A., Lesage, S., G

Journal:

Year:

2013

Language:

english

File:

PDF, 179 KB

english, 2013

31

Andreas Rett and benign familial neonatal convulsions revisited

Zimprich, F., Ronen, G. M., Stogmann, W., Baumgartner, C., Stogmann, E., Rett, B., Pappas, C., Leppert, M., Singh, N., Anderson, V. E.

Journal:

Year:

2006

Language:

english

File:

PDF, 272 KB

english, 2006

32

Theophylline for Infants with Abnormal Pneumographic Results. A Randomized Double Blind, Placebo-controlled Trial

Paky, Franz, Donath, Peter, Huebmer, Edith, Stögmann, Walter

Journal:

Klinische Pädiatrie

Year:

1997

Language:

english

File:

PDF, 358 KB

english, 1997

33

Chemische Pneumonitis mit Jodoliposputosis nach Lymphangiographie im Kindesalter

Stögmann, W., Kammerhuber, F., Messner, H.

Journal:

RöFo - Fortschritte auf dem Gebiet der R

Year:

1974

File:

PDF, 398 KB

1974

34

Obstruktive Apnoen bei Frühgeborenen und Säuglingen

Kurz, H., Paky, F., Stögmann, W.

Journal:

Klinische Pädiatrie

Year:

1994

File:

PDF, 358 KB

1994

35

Das röntgenologische Erscheinungsbild des Pseudohypoparathyreoidismus und Pseudo-Pseudohypoparathyreoidismus und seine Pathogenese

Stögmann, W., Oser, W.

Journal:

RöFo - Fortschritte auf dem Gebiet der R

Year:

1974

Language:

german

File:

PDF, 435 KB

german, 1974

36

Sequence analysis of the complete SLITRK1 gene in Austrian patients with Touretteʼs disorder

Zimprich, Alexander, Hatala, Katharina, Riederer, Franz, Stogmann, Elisabeth, Aschauer, Harald N., Stamenkovic, Mara

Journal:

Psychiatric Genetics

Year:

2008

Language:

english

File:

PDF, 56 KB

english, 2008

37

Self-reported and informant-reported memory functioning and awareness in patients with mild cognitive impairment and Alzheimer´s disease

Silva, Martina Rios, Moser, Doris, Pflüger, Melanie, Pusswald, Gisela, Stögmann, Elisabeth, Dal-Bianco, Peter, Auff, Eduard, Lehrner, Johann

Journal:

Neuropsychiatrie

Year:

2016

File:

PDF, 282 KB

2016

38

The impact of depressive symptoms on health-related quality of life in patients with subjective cognitive decline, mild cognitive impairment, and Alzheimer's disease

Pusswald, G., Moser, D., Pflüger, M., Gleiss, A., Auff, E., Stögmann, E., Dal-Bianco, P., Lehrner, J.

Journal:

International Psychogeriatrics

Year:

2016

Language:

english

File:

PDF, 274 KB

english, 2016

39

Hereditary spastic paraplegia caused by compound heterozygous mutations outside the motor domain of the KIF1A gene

Krenn, M., Zulehner, G., Hotzy, C., Rath, J., Stogmann, E., Wagner, M., Haack, T. B., Strom, T. M., Zimprich, A., Zimprich, F.

Journal:

European Journal of Neurology

Year:

2017

Language:

english

File:

PDF, 321 KB

english, 2017

40

Normal values for circulating thyroid hormones (T4, T3, reverse T3), T3 Uptake and Thyrotropin ( before and after TRH ) of Austrian children

Stögmann, W A, Borken-Stein, M, Stöffler, G, Fueger, G

Journal:

Pediatric Research

Year:

1979

Language:

english

File:

PDF, 138 KB

english, 1979

41

Normal Values of Serum Prolactin (PRL) in Children before and during TRH-Stimulation

Stögmann, W A, Frey, E, Herkner, K, Gruber, B, Höller, B, Gleispach, H

Journal:

Pediatric Research

Year:

1981

Language:

english

File:

PDF, 125 KB

english, 1981

42

Manifestations of neurological symptoms and thromboembolism in adults with MTHFR-deficiency

Rommer, Paulus S., Zschocke, Johannes, Fowler, Brian, Födinger, Manuela, Konstantopoulou, Vassiliki, Möslinger, Dorothea, Stögmann, Elisabeth, Suess, Erhard, Baumgartner, Matthias, Auff, Eduard, Sunde

Journal:

Journal of the Neurological Sciences

Year:

2017

Language:

english

File:

PDF, 441 KB

english, 2017

43

Home Monitoring with Event Recording (Vita Guard 1000™) in 35 Infants

Kurz, H, Schafhauser, R, Mittnik, A, Neunteufl, R, Stögmann, W

Journal:

Pediatric Research

Year:

1999

File:

PDF, 70 KB

1999

44

Differences regarding the five-factor personality model in patients with subjective cognitive decline and mild cognitive impairment; Unterschiedliche Ausprägung der Persönlichkeit bei Patienten mit subjektiver kognitiver Beeinträchtigung und leichter kognitiver Beeinträchtigung;

Berger-Sieczkowski, Evelyn, Gruber, Bernadette, Stögmann, Elisabeth, Lehrner, Johann

Journal:

Neuropsychiatrie

Year:

2018

File:

PDF, 570 KB

2018

45

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

Tahmasebi, R., Zehetmayer, S., Pusswald, G., Kovacs, G., Stögmann, E., Lehrner, J.

Journal:

International Psychogeriatrics

Year:

2019

Language:

english

File:

PDF, 487 KB

english, 2019

46

Awareness of Olfactory Dysfunction in Subjective Cognitive Decline, Mild Cognitive Decline, and Alzheimer’s Disease

Tahmasebi, R., Zehetmayer, S., Stögmann, E., Lehrner, Johann

Journal:

Chemosensory Perception

Year:

2019

Language:

english

File:

PDF, 530 KB

english, 2019

47

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

Krenn, Martin, Tomschik, Matthias, Rath, Jakob, Cetin, Hakan, Grisold, Anna, Zulehner, Gudrun, Milenkovic, Ivan, Stogmann, Elisabeth, Zimprich, Alexander, Strom, Tim M., Meitinger, Thomas, Wagner, Mat

Journal:

European Journal of Neurology

Year:

2019

Language:

english

File:

PDF, 460 KB

english, 2019

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