E-LIB Suche - Ergebnisse für: Feichtinger, R.G

1

Molekulare Medizin: Pathobiochemie als Schlüssel zur person..:

Mayr, J. A. ; Feichtinger, R. G. ; Achleitner, M. T....
Monatsschrift Kinderheilkunde. 169 (2021) 9 - p. 828-836 , 2021

Link: https://doi.org/10.1007/..

2

Multidisziplinäre Diagnostik von Entwicklungsstörungen: Gru..:

Wortmann, S. B. ; Preisel, M. ; Feichtinger, R. G....
Monatsschrift Kinderheilkunde. 169 (2021) 9 - p. 815-827 , 2021

Link: https://doi.org/10.1007/..

3

242. Investigation of oxygen surface complexes on carbon by..:

Fischer, F.G. ; Feichtinger, A.R.
Carbon. 20 (1982) 2 - p. 151 , 1982

Link: https://doi.org/10.1016/..

4

Riding the waves from epidemic to endemic: Viral mutations,..:

Grass, D. ; Wrzaczek, S. ; Caulkins, J.P....
Theoretical Population Biology. 156 (2024) - p. 46-65 , 2024

Link: https://doi.org/10.1016/..

5

The hammer and the jab: Are COVID-19 lockdowns and vaccinat..:

Caulkins, J.P. ; Grass, D. ; Feichtinger, G....
European Journal of Operational Research. 311 (2023) 1 - p. 233-250 , 2023

Link: https://doi.org/10.1016/..

6

Genotypic and phenotypic spectrum of infantile liver failur..:

Mozer-Glassberg Y ; Vogel G.F ; Landau Y.E...
Genetics in Medicine. , 2022

Link: https://hdl.handle.net/1..

7

Genotypic and phenotypic spectrum of infantile liver failur..:

Vogel G.F ; Mozer-Glassberg Y ; Landau Y.E...
Genetics in Medicine. , 2022

Link: https://hdl.handle.net/1..

8

Bi-allelic LETM1 variants perturb mitochondrial ion homeost..:

Kaiyrzhanov, R ; Mohammed, S.E.M ; Maroofian, R...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2022.07.007. , 2022

Link: https://push-zb.helmholt..

9

Genotypic and phenotypic spectrum of infantile liver failur..:

Vogel G.F ; Mozer-Glassberg Y ; Landau Y.E...
Genetics in Medicine. , 2022

Link: https://hdl.handle.net/1..

10

Molekulare Medizin: Pathobiochemie als Schlüssel zur person..:

Mayr, J. A ; Feichtinger, R. G ; Achleitner, M. T...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8320310/. , 2021

Link: http://www.ncbi.nlm.nih...

11

Neutropenia and intellectual disability are hallmarks of bi..:

Wortmann, S.B ; Zietkiewicz, S ; Guerrero-Castillo, S...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41436-021-01194-x. , 2021

Link: https://push-zb.helmholt..

12

Mutations in HID1 cause syndromic infantile encephalopathy ..:

Schänzer, A ; Achleitner, M ; Trümbach, D...
info:eu-repo/semantics/altIdentifier/doi/10.1002/ana.26127. , 2021

Link: https://push-zb.helmholt..

13

Characterising a homozygous two-exon deletion in UQCRH : Co..:

Vidali, S ; Gerlini, R ; Thompson, K...
info:eu-repo/semantics/altIdentifier/doi/10.15252/emmm.202114397. , 2021

Link: https://push-zb.helmholt..

14

From old to new - Repurposing drugs to target mitochondrial..:

Aminzadeh-Gohari, S ; Weber, D.D ; Vidali, S...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.semcdb.2019.05.025. , 2020

Link: https://push-zb.helmholt..

15

Bi-allelic UQCRFS1 variants are associated with mitochondri..:

Gusic, M ; Schottmann, G ; Feichtinger, R.G...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2019.12.005. , 2020

Link: https://push-zb.helmholt..