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Results of search for 'au:"Endmann, Matthias"'
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Authors
Endmann, Matthias
Haftel, Lior
Hofmann, Thomas
Rust, Stephan
Rutsch, Frank
Rühe, Lars
Sass, Jörn Oliver
Schwade, Jan-Niclas
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Topics
Acidosis
Coenzyme A-Transferases
DNA Mutational Analysis
Female
Glucose
Humans
Infant
Mutation
Phenylketonurias
Sodium Bicarbonate
complications
deficiency
therapeutic use
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English
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1.
Extrapontine Myelinolysis following Extreme Hypernatremia and Hyperosmolarity.
[electronic resource]
by
Schwade, Jan-Niclas
Haftel, Lior
Rühe, Lars
Endmann, Matthias
Publication details:
Case reports in pediatrics
2019
In:
Case reports in pediatrics
vol. 2019
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2.
When one disease is not enough: succinyl-CoA: 3-oxoacid coenzyme A transferase (SCOT) deficiency due to a novel mutation in OXCT1 in an infant with known phenylketonuria.
[electronic resource]
by
Schwade, Jan-Niclas
Endmann, Matthias
Hofmann, Thomas
Rust, Stephan
Sass, Jörn Oliver
Rutsch, Frank
Producer:
20180530
In:
Journal of pediatric endocrinology & metabolism : JPEM
vol. 30
Online resources:
Available from publisher's website
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No items available.
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