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Spenger, Johannes
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1

Empagliflozin for treating neutropenia and neutrophil dysfu..:

Grünert, Sarah C. ; Gautschi, Matthias ; Baker, Joshua...
Molecular Genetics and Metabolism.  142 (2024)  2 - p. 108486 , 2024
Link: https://doi.org/10.1016/..
 
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2

Poor adherence during adolescence is a risk factor for beco..:

Beghini, Marianna ; Pichler, Maximilian ; Tinnefeld, Fiona Carolina...
Molecular Genetics and Metabolism Reports.  39 (2024)  - p. 101087 , 2024
Link: https://doi.org/10.1016/..
 
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3

PPA1 Deficiency Causes a Deranged Galactose Metabolism Reco..:

Achleitner, Melanie T. ; Jans, Judith J. M. ; Ebner, Laura...
Metabolites.  13 (2023)  11 - p. 1141 , 2023
Link: https://doi.org/10.3390/..
 
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4

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/..
 
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5

The clinical and molecular landscape of congenital myasthen..:

Krenn, Martin ; Sener, Merve ; Rath, Jakob...
Journal of Neurology.  270 (2022)  2 - p. 909-916 , 2022
Link: https://doi.org/10.1007/..
 
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6

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/..
 
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7

Congenital disorders of glycosylation with defective fucosy..:

Hüllen, Andreas ; Falkenstein, Kristina ; Weigel, Corina...
Journal of Inherited Metabolic Disease.  44 (2021)  6 - p. 1441-1452 , 2021
Link: https://doi.org/10.1002/..
 
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8

Glutaric Aciduria Type I Missed by Newborn Screening: Repor..:

Spenger, Johannes ; Maier, Esther ; Wechselberger, Katharina...
International Journal of Neonatal Screening.  7 (2021)  2 - p. 32 , 2021
Link: https://doi.org/10.3390/..
 
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9

100 years of inherited metabolic disorders in Austria—A nat..:

Ramoser, Gabriele ; Caferri, Federica ; Radlinger, Bernhard...
Journal of Inherited Metabolic Disease.  45 (2021)  2 - p. 144-156 , 2021
Link: https://doi.org/10.1002/..
 
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10

Long-term experience with triheptanoin in 12 Austrian patie..:

Zöggeler, Thomas ; Stock, Katharina ; Jörg-Streller, Monika...
Orphanet Journal of Rare Diseases.  16 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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11

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/..
 
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12

Correction: Spenger et al. Glutaric Aciduria Type I Missed ..:

Spenger, Johannes ; Maier, Esther M. ; Wechselberger, Katharina...
International Journal of Neonatal Screening.  8 (2021)  1 - p. 2 , 2021
Link: https://doi.org/10.3390/..
 
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13

Elevated Homocysteine after Elevated Propionylcarnitine or ..:

Rozmarič, Tomaž ; Mitulović, Goran ; Konstantopoulou, Vassiliki...
Diagnostics.  10 (2020)  9 - p. 626 , 2020
Link: https://doi.org/10.3390/..
 
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14

Next-Generation-Sequenzierung – Next-Generation-Qualität in..:

Wortmann, Saskia B. ; Spenger, Johannes ; Preisel, Martin...
Pädiatrie & Pädologie.  53 (2018)  6 - p. 278-283 , 2018
Link: https://doi.org/10.1007/..
 
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15

Multiple Leberherde und Eosinophilie – ein Fallbericht eine..:

Trifina, Eva ; Spenger, Johannes ; Zandieh, Shahin...
Wiener Medizinische Wochenschrift.  161 (2011)  17-18 - p. 448-454 , 2011
Link: https://doi.org/10.1007/..
 
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