E-LIB Suche - Ergebnisse für: Brunner-Krainz, M.

1

Epileptic phenotypes, electroclinical features and clinical..:

Haberlandt, E. ; Ensslen, M. ; Gruber-Sedlmayr, U....
European Journal of Paediatric Neurology. 21 (2017) 3 - p. 457-464 , 2017

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

2

Pompe disease in Austria: clinical, genetic and epidemiolog..:

Löscher, W. N. ; Huemer, M. ; Stulnig, T. M....
Journal of Neurology. 265 (2017) 1 - p. 159-164 , 2017

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

3

Konsensus zur Ernährung in der pädiatrischen Palliativmediz..:

Jones, R. ; Behrens, R. ; Dilch, A....
Monatsschrift Kinderheilkunde. 163 (2015) 9 - p. 928-933 , 2015

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

4

Leitlinien zur Ernährung in der pädiatrischen Palliativmedi..:

Jones, R. ; Behrens, R. ; Brunner-Krainz, M....
Pädiatrie & Pädologie. 50 (2015) S1 - p. 4-24 , 2015

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

5

Persisting myelin oligodendrocyte glycoprotein antibodies i..:

Rostásy, K ; Mader, S ; Hennes, EM...
Multiple Sclerosis Journal. 19 (2012) 8 - p. 1052-1059 , 2012

Link: https://doi.org/10.1177/..

6

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

Grünert, S.C ; Derks, TGJ ; Adrian, K...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.gim.2022.04.001. , 2022

Link: https://serval.unil.ch/n..

7

A generic emergency protocol for patients with inborn error..:

Rossi, A ; Hoogeveen, IJ ; Lubout, CMA...
https://discovery.ucl.ac.uk/id/eprint/10149887/1/J%20of%20Inher%20Metab%20Disea%20-%202021%20-%20Rossi%20-%20A%20generic%20emergency%20protocol%20for%20patients%20with%20inborn%20errors%20of%20metabolism%20causing.pdf. , 2021

Link: https://discovery.ucl.ac..

8

Combined respiratory chain deficiency and UQCC2 mutations i..:

Feichtinger, R.G ; Brunner-Krainz, M ; Alhaddad, B...
info:eu-repo/semantics/altIdentifier/doi/10.1155/2017/7202589. , 2017

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

9

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

Grünert, S.C ; Müllerleile, S ; De Silva, L...
info:eu-repo/semantics/altIdentifier/doi/10.1186/1750-1172-8-6. , 2013

Link: https://serval.unil.ch/n..

10

Epilepsie als Leitsymptom angeborener Stoffwechselstörungen:

Plecko B ; Brunner-Krainz M ; Gruber-Sedlmayr U.
http://www.kup.at/kup/pdf/5525.pdf. , 2005

Link: http://www.kup.at/kup/pd..

11

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/..

12

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/..

13

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/..

14

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-..

15

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..