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Works by Regelsberger, G.

Results: 4

1

Danon disease: Case report and detection of new mutation.

Published in:

Journal of Inherited Metabolic Disease, 2009, v. 32, p. 115, doi. 10.1007/s10545-009-1097-9

By:

Regelsberger, G.;
Höftberger, R.;
Pickl, W.;
Zlabinger, G.;
Körmöczi, U.;
Salzer-Muhar, U.;
Luckner, D.;
Bodamer, O.;
Mayr, J.;
Muss, W.;
Budka, H.;
Bernheimer, H.

Publication type:

Article

2

Argyrophilic grain disease in individuals younger than 75 years: clinical variability in an under‐recognized limbic tauopathy.

Published in:

European Journal of Neurology, 2020, v. 27, n. 10, p. 1856, doi. 10.1111/ene.14321

By:

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.

Publication type:

Article

3

Cerebrotendinous xanthomatosis with the c.379 C> T (p. R127 W) mutation in the CYP27A1 gene associated with premature age-associated limbic tauopathy.

Published in:

Neuropathology & Applied Neurobiology, 2014, v. 40, n. 3, p. 345, doi. 10.1111/nan.12058

By:

Kapás, I.;
Katkó, M.;
Harangi, M.;
Paragh, G.;
Balogh, I.;
Kóczi, Z.;
Regelsberger, G.;
Molnár, M. J.;
Kovacs, G. G.

Publication type:

Article

4

Plasma and cerebrospinal fluid tau and neurofilament concentrations in rapidly progressive neurological syndromes: a neuropathology-based cohort.

Published in:

European Journal of Neurology, 2017, v. 24, n. 11, p. 1326, doi. 10.1111/ene.13389

By:

Kovacs, G. G.;
Andreasson, U.;
Liman, V.;
Regelsberger, G.;
Lutz, M. I.;
Danics, K.;
Keller, E.;
Zetterberg, H.;
Blennow, K.

Publication type:

Article