E-LIB Suche - Ergebnisse für: Brunner-Krainz, Michaela

1

Ketogenic Diet Treatment of Defects in the Mitochondrial Ma..:

Bölsterli, Bigna K. ; Boltshauser, Eugen ; Palmieri, Luigi...
Nutrients. 14 (2022) 17 - p. 3605 , 2022

Link: https://doi.org/10.3390/..

2

Efficacy and safety of empagliflozin in glycogen storage di..:

Grünert, Sarah C. ; Derks, Terry G.J. ; Adrian, Katarina...
Genetics in Medicine. 24 (2022) 8 - p. 1781-1788 , 2022

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

3

Project "Backtoclinic I": An overview on the state of care ..:

Beghini, Marianna ; Resch, Felix J. ; Möslinger, Dorothea...
Molecular Genetics and Metabolism. 133 (2021) 3 - p. 257-260 , 2021

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

4

A retrospective study on disease management in children and..:

Herle, Marion ; Brunner-Krainz, Michaela ; Karall, Daniela...
Orphanet Journal of Rare Diseases. 16 (2021) 1 - p. , 2021

Link: https://doi.org/10.1186/..

5

The genotypic and phenotypic spectrum of MTO1 deficiency:

O'Byrne, James J. ; Tarailo-Graovac, Maja ; Ghani, Aisha...
Molecular Genetics and Metabolism. 123 (2018) 1 - p. 28-42 , 2018

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

6

Clinical-Pathological Conference Series from the Medical Un..:

Fabian, Elisabeth ; Schiller, Dietmar ; Toplak, Hermann...
Wiener klinische Wochenschrift. 130 (2017) 3-4 - p. 151-160 , 2017

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

7

Combined Respiratory Chain Deficiency and UQCC2 Mutations i..:

Feichtinger, René G. ; Brunner-Krainz, Michaela ; Alhaddad, Bader...
Oxidative Medicine and Cellular Longevity. 2017 (2017) - p. 1-11 , 2017

Link: https://doi.org/10.1155/..

8

Clinical outcome, biochemical and therapeutic follow-up in ..:

Karall, Daniela ; Brunner-Krainz, Michaela ; Kogelnig, Katharina...
Orphanet Journal of Rare Diseases. 10 (2015) 1 - p. , 2015

Link: https://doi.org/10.1186/..

9

Mutation screen reveals novel variants and expands the phen..:

Strickland, Alleene V. ; Schabhüttl, Maria ; Offenbacher, Hans...
Journal of Neurology. 262 (2015) 9 - p. 2124-2134 , 2015

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

10

Cross-sectional study of 168 patients with hepatorenal tyro..:

Mayorandan, Sebene ; Meyer, Uta ; Gokcay, Gülden...
Orphanet Journal of Rare Diseases. 9 (2014) 1 - p. , 2014

Link: https://doi.org/10.1186/..

11

Propionic acidemia: clinical course and outcome in 55 pedia..:

Grünert, Sarah C ; Müllerleile, Stephanie ; De Silva, Linda...
Orphanet Journal of Rare Diseases. 8 (2013) 1 - p. , 2013

Link: https://doi.org/10.1186/..

12

Ketogenic Diet Treatment of Defects in the Mitochondrial Ma..:

Bölsterli, Bigna, K ; Boltshauser, Eugen ; Palmieri, Luigi...
info:eu-repo/semantics/altIdentifier/doi/10.3390/nu14173605. , 2022

Link: https://hal.science/hal-..

13

Ketogenic Diet Treatment of Defects in the Mitochondrial Ma..:

Bölsterli, Bigna, K ; Boltshauser, Eugen ; Palmieri, Luigi...
info:eu-repo/semantics/altIdentifier/doi/10.3390/nu14173605. , 2022

Link: https://hal.science/hal-..

14

Efficacy and safety of empagliflozin in glycogen storage di..:

Grünert, Sarah C ; Derks, Terry G J ; Adrian, Katarina...
https://research.rug.nl/en/publications/25cc5998-0f5d-469d-ac05-2eca9bb979ee. , 2022

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

15

Ketogenic Diet Treatment of Defects in the Mitochondrial Ma..:

Bölsterli, Bigna K ; Boltshauser, Eugen ; Palmieri, Luigi...
3605. , 2022

Link: https://nbn-resolving.or..