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The PKU Book: Phenylketonuria and Other Hyperphenylalaninemias
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The PKU Book: Phenylketonuria and Other Hyperphenylalaninemias
Early diagnosis and treatment with a low-Phe diet has enabled an almost normal life for the majority of PKU subject. Pharmacological treatment with BH4 (sapropterin) and enzyme substitution therapy with Phe ammonia lyase (PAL) provide alternative treatment options for some PKU subjects.
| Media | Books Hardcover Book (Book with hard spine and cover) |
| To be released | July 20, 2026 |
| ISBN13 | 9783032266897 |
| Publishers | Springer Nature Switzerland AG |
| Pages | 534 |
| Dimensions | 150 × 220 × 20 mm · 831 g (Weight (estimated)) |
| Editor | Blau, Nenad |
| Editor | MacDonald, Anita |
| Editor | Van Spronsen, Francjan |
| Editor | Vockley, Jerry |
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