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Daniela Karall

Showing results (31-40 of 129) with videos related to

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Journal of Pediatric Endocrinology & Metabolism : JPEM|September 10, 2021
Nitisinone treatment during two pregnancies and breastfeeding in a woman with tyrosinemia type 1 - a case reportThomas Zöggeler, Gabriele Ramoser, Alexander Höller, et al.
Italian Journal of Pediatrics|August 27, 2021
Dietary treatment of congenital chylothorax with skimmed breast milkMichaela Höck, Alexander Höller, Marlene Hammerl, et al.
Cardiovascular and Interventional Radiology|October 24, 2013
Stereotactic radiofrequency ablation for liver tumors in inherited metabolic disordersDaniela Karall, Sabine Scholl-Bürgi, Gerlig Widmann, et al.
Frontiers in Immunology|April 11, 2022
Immunological Memory and Affinity Maturation After Vaccination in Patients With Propionic AcidemiaManuela Zlamy, Thomas Zöggeler, Magdalena Bachmann, et al.
JIMD Reports|March 26, 2025
Treatment of an Opposing Metabolic Situation: GLUT1-Deficiency Syndrome and Type 1 DiabetesAnna K Schoenlaub, Alexander Hoeller, Sabine Hofer, et al.
Orphanet Journal of Rare Diseases|January 15, 2021
Long-term experience with triheptanoin in 12 Austrian patients with long-chain fatty acid oxidation disordersThomas Zöggeler, Katharina Stock, Monika Jörg-Streller, et al.
Pediatric Emergency Care|July 16, 2021
The Manchester Triage System in a Pediatric Emergency Department of an Austrian University Hospital: A Retrospective Analysis of Urgency LevelsNikolas Beck, Miriam Michel, Elisabeth Binder, et al.
Muscle & Nerve|June 27, 2015
A novel therapeutic approach for LPIN1 mutation-associated rhabdomyolysis--The Austrian experienceKarin Pichler, Sabine Scholl-Buergi, Robert Birnbacher, et al.
Epilepsia|December 12, 2007
Adiponectin and visfatin concentrations in children treated with valproic acidMarkus Rauchenzauner, Edda Haberlandt, Sabine Scholl-Bürgi, et al.
Orphanet Journal of Rare Diseases|November 16, 2014
Three new cases of late-onset cblC defect and review of the literature illustrating when to consider inborn errors of metabolism beyond infancyMartina Huemer, Sabine Scholl-Bürgi, Karine Hadaya, et al.
Pageof 13

Showing results (31-40 of 129) with videos related to

Sort By:
Pageof 13
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 10, 2021
Nitisinone treatment during two pregnancies and breastfeeding in a woman with tyrosinemia type 1 - a case reportThomas Zöggeler, Gabriele Ramoser, Alexander Höller, et al.
Italian Journal of Pediatrics|August 27, 2021
Dietary treatment of congenital chylothorax with skimmed breast milkMichaela Höck, Alexander Höller, Marlene Hammerl, et al.
Cardiovascular and Interventional Radiology|October 24, 2013
Stereotactic radiofrequency ablation for liver tumors in inherited metabolic disordersDaniela Karall, Sabine Scholl-Bürgi, Gerlig Widmann, et al.
Frontiers in Immunology|April 11, 2022
Immunological Memory and Affinity Maturation After Vaccination in Patients With Propionic AcidemiaManuela Zlamy, Thomas Zöggeler, Magdalena Bachmann, et al.
JIMD Reports|March 26, 2025
Treatment of an Opposing Metabolic Situation: GLUT1-Deficiency Syndrome and Type 1 DiabetesAnna K Schoenlaub, Alexander Hoeller, Sabine Hofer, et al.
Orphanet Journal of Rare Diseases|January 15, 2021
Long-term experience with triheptanoin in 12 Austrian patients with long-chain fatty acid oxidation disordersThomas Zöggeler, Katharina Stock, Monika Jörg-Streller, et al.
Pediatric Emergency Care|July 16, 2021
The Manchester Triage System in a Pediatric Emergency Department of an Austrian University Hospital: A Retrospective Analysis of Urgency LevelsNikolas Beck, Miriam Michel, Elisabeth Binder, et al.
Muscle & Nerve|June 27, 2015
A novel therapeutic approach for LPIN1 mutation-associated rhabdomyolysis--The Austrian experienceKarin Pichler, Sabine Scholl-Buergi, Robert Birnbacher, et al.
Epilepsia|December 12, 2007
Adiponectin and visfatin concentrations in children treated with valproic acidMarkus Rauchenzauner, Edda Haberlandt, Sabine Scholl-Bürgi, et al.
Orphanet Journal of Rare Diseases|November 16, 2014
Three new cases of late-onset cblC defect and review of the literature illustrating when to consider inborn errors of metabolism beyond infancyMartina Huemer, Sabine Scholl-Bürgi, Karine Hadaya, et al.
Pageof 13