Research output per year
Research output per year
Personal profile
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Dive into the research topics where Katja Steinbrücker is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 1 Similar Profiles
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Vaccine safety in children with genetically confirmed mitochondrial disease
de Vreugd, A., Zimmermann, F. A. (First author), Steinbruecker, K. (Co-author), de Vries, M. C., de Boer, L., Janssen, M. C. H., Huemer, M. & Wortmann, S. B. (Last author), Feb 2025, In: IMMUNOLOGY LETTERS . 271, 6 p., 106946.Research output: Contribution to journal › Original Article › peer-review
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Mitochondrial disorder diagnosis and management- what the pediatric neurologist wants to know
Heath, O. (First author), Feichtinger, R. G. (Co-author), Achleitner, M. T. (Co-author), Hofbauer, P., Mayr, D., Merkevicius, K., Spenger, J. (Co-author), Steinbrücker, K. (Co-author), Steindl, C., Tiefenthaler, E., Mayr, J. A. (Co-author) & Wortmann, S. B. (Last author), 15 Dec 2024, (E-pub ahead of print) In: EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY. 54, p. 75-88 14 p.Research output: Contribution to journal › Review article › peer-review
Open Access -
Nicotinamide Riboside for Ataxia Telangiectasia: A Report of an Early Treated Individual.
Steinbrücker, K. (First author), Tiefenthaler, E., Schernthaner, E.-M., Jungwirth, J. & Wortmann, S. (Last author), Feb 2023, In: NEUROPEDIATRICS . 54, 1, p. 78-81 4 p.Research output: Contribution to journal › Original Article › peer-review
4 Citations (Web of Science) -
Treatment of Mitochondrial Phenylalanyl-tRNa-Synthetase Deficiency (FARS2) with Oral Phenylalanine.
Oswald, S. L., Steinbrücker, K. (First author), Achleitner, M. (Co-author), Göschl, E., Bittner, R. E., Schmidt, W. M., Tiefenthaler, E., Hammerl, E. (Co-author), Eisl, A., Mayr, D., Mayr, J. A. (Co-author) & Wortmann, S. (Last author), 2023, In: NEUROPEDIATRICS . 54, 5, p. 351-355Research output: Contribution to journal › Original Article › peer-review
5 Citations (Web of Science) -
A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome.
Feichtinger, R. (First author), Preisel, M., Steinbrücker, K. (Co-author), Brugger, K., Radda, A., Wortmann, S. (Last author) & Mayr, J. A. (Last author), 2022, In: GENES. 13, 12Research output: Contribution to journal › Case report › peer-review
2 Citations (Web of Science)
Activities
- 2 Supervision
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Die Regulation des HIF-Signalweges nach Hypoxie-Ischämie im neonatalen Maushirn
Steinbrücker, K. (Supervisor)
2014Activity: Examination, Supervision or Reviewing of graduation work › Supervision
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Neuroprotektive Effekte durch Hypothermie und Levetiracetam nach Hypoxie-Ischämie im neonatalen MAushirn
Steinbrücker, K. (Supervisor)
2013Activity: Examination, Supervision or Reviewing of graduation work › Supervision