O. Schreiber-Katz

发表

Christophe Béroud, Hanns Lochmüller, Petr Brabec, 2015, Human mutation.

K. Bushby, K. Flanigan, C. Béroud, 2017, Journal of neuromuscular diseases.

S. Petri, O. Abu-Fares, O. Schreiber-Katz, 2019, Nervenheilkunde.

A. Pestronk, A. Blamire, J. Mendell, 2019, Neurology.

H. Otero, A. Pestronk, A. Blamire, 2018, Journal of Neurology, Neurosurgery, and Psychiatry.

S. Petri, A. Ludolph, B. Stolte, 2021, Therapeutic advances in neurological disorders.

M. Walter, P. Reilich, K. Nagels, 2016, Orphanet Journal of Rare Diseases.

S. Krause, M. Walter, P. Reilich, 2019, Neurology.

M. Walter, P. Reilich, Olivia Schreiber-Katz, 2014, Orphanet Journal of Rare Diseases.

G. Valle, S. Kojic, G. Faulkner, 2016, Histochemistry and Cell Biology.

A. Pestronk, A. Blamire, J. Mendell, 2016, Neurology: Genetics.

S. Petri, K. Rostásy, A. Ludolph, 2021, Orphanet Journal of Rare Diseases.

K. Mathews, H. Lochmüller, J. Vissing, 2020, Annals of clinical and translational neurology.

S. Petri, A. Ludolph, T. Meyer, 2021, Annals of clinical and translational neurology.

S. Petri, K. Rostásy, A. Ludolph, 2022, Annals of clinical and translational neurology.

S. Petri, A. Ludolph, C. Kamm, 2022, Annals of clinical and translational neurology.

S. Petri, Olivia Schreiber-Katz, Alma Osmanovic, 2021, Brain sciences.

S. Petri, A. Ludolph, J. Grosskreutz, 2020, Journal of Neurology, Neurosurgery, and Psychiatry.

S. Petri, Olivia Schreiber-Katz, Alma Osmanovic, 2020, Orphanet Journal of Rare Diseases.

S. Petri, W. Bayer, B. Stolte, 2022, Human gene therapy.

Alma Osmanovic, O. Schreiber-Katz, Camilla Wohnrade, 2024, BMC neurology.