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Clinical and biochemical footprints of inherited metabolic diseases: III. psychiatric presentations by Horvath, Gabriela Ana (Author) , Stowe, Robert M. (Author) , Ferreira, Carlos R. (Author) , Blau, Nenad (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Extended diagnosis of purine and pyrimidine disorders from urine: LC MS/MS assay development and clinical validation by Monostori, Péter (Author) , Klinke, Glynis (Author) , Garbade, Sven (Author) , Hoffmann, Georg F. (Author) , Langhans, Claus-Dieter (Author) , Haas, Dorothea (Author) , Okun, Jürgen G. (Author) ,

• Verlag, Volltext
• Verlag, Volltext

6-Pyruvoyltetrahydropterin synthase deficiency: review and report of 28 Arab subjects by Almannai, Mohammed (Author) , Blau, Nenad (Author) ,

• Verlag, Volltext

Clinical and biochemical footprints of inherited metabolic diseases: I. Movement disorders by Ferreira Lopez, Carlos R (Author) , Hoffmann, Georg F. (Author) , Blau, Nenad (Author) ,

• Verlag, Volltext
• Verlag

Multifactorial modulation of susceptibility to l-lysine in an animal model of glutaric aciduria type I by Sauer, Sven (Author) , Opp, Silvana (Author) , Komatsuzaki, Shoko (Author) , Burgard, Peter (Author) , Okun, Jürgen G. (Author) , Kölker, Stefan (Author) ,

• Verlag, kostenfrei, Volltext
• Verlag, kostenfrei, Volltext