TY  - GEN
AU  - Löscher,W N
AU  - Huemer,M
AU  - Stulnig,T M
AU  - Simschitz,P
AU  - Iglseder,S
AU  - Eggers,C
AU  - Moser,H
AU  - Möslinger,D
AU  - Freilinger,M
AU  - Lagler,F
AU  - Grinzinger,S
AU  - Reichhardt,M
AU  - Bittner,R E
AU  - Schmidt,W M
AU  - Lex,U
AU  - Brunner-Krainz,M
AU  - Quasthoff,S
AU  - Wanschitz,J V
TI  - Pompe disease in Austria: clinical, genetic and epidemiological aspects
SN  - 1432-1459
PY  - 2018///0727
KW  - Adolescent
KW  - Adult
KW  - Age of Onset
KW  - Aged
KW  - Austria
KW  - epidemiology
KW  - Child
KW  - Delayed Diagnosis
KW  - Enzyme Replacement Therapy
KW  - methods
KW  - Female
KW  - Follow-Up Studies
KW  - Glycogen Storage Disease Type II
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - Mutation
KW  - genetics
KW  - Retrospective Studies
KW  - Vital Capacity
KW  - physiology
KW  - alpha-Glucosidases
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1007/s00415-017-8686-6
ER  -