Facetten
Zugriff
Einrichtung
Medientyp
- Text 6
Karte
Erscheinungsjahr
Autor/in
- Grünert, Sarah C
- Lindner, Martin 4
- Thimm, Eva 3
- Freisinger, Peter 2
- Gleich, Florian 2
- alle zeigen
Sprache
- Englisch 6
6 Einträge gefunden
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Long-term anthropometric development of individuals with inherited metabolic diseases identified by newborn screening
- Mütze, Ulrike
- Garbade, Sven F
- Gleich, Florian
- Lindner, Martin
- Freisinger, Peter
- Hennermann, Julia B
- Thimm, Eva
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The spectrum of peripheral neuropathy in disorders of the mitochondrial trifunctional protein
- Grünert, Sarah C
- Eckenweiler, Matthias
- Haas, Dorothea
- Lindner, Martin
- Tsiakas, Konstantinos
- Santer, René
- Tucci, Sara
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Newborn screening and disease variants predict neurological outcome in isovaleric aciduria
- Mütze, Ulrike
- Henze, Lucy
- Gleich, Florian
- Lindner, Martin
- Grünert, Sarah C
- Spiekerkoetter, Ute
- Santer, René
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Newborn screening, a disease-changing intervention for glutaric aciduria type 1
- Boy, Nikolas
- Mengler, Katharina
- Thimm, Eva
- Schiergens, Katharina A
- Marquardt, Thorsten
- Weinhold, Natalie
- Marquardt, Iris
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Cross-sectional observational study of 208 patients with non-classical urea cycle disorders
- Rüegger, Corinne M
- Lindner, Martin
- Ballhausen, Diana
- Baumgartner, Matthias R
- Beblo, Skadi
- Das, Anibh
- Gautschi, Matthias
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3-methylcrotonyl-CoA carboxylase deficiency: clinical, biochemical, enzymatic and molecular studies in 88 individuals.
- Grünert, Sarah C
- Stucki, Martin
- Morscher, Raphael J
- Suormala, Terttu
- Bürer, Celine
- Burda, Patricie
- Christensen, Ernst