Characterization of changes in the tyrosine pathway by 24-h profiling during nitisinone treatment in alkaptonuria

Author:

Ranganath L.R.,Milan A.M.,Hughes A.T.,Davison A.S.,Khedr M.,Norman B.P.,Bou-Gharios G.,Gallagher J.A.,Gornall M.,Jackson R.,Imrich R.,Rovensky J.,Rudebeck M.,Olsson B.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference29 articles.

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2. Natural history of alkaptonuria;Phornphutkul;N. Engl. J. Med.,2002

3. A 3-year randomized therapeutic trial of nitisinone in alkaptonuria;Introne;Mol. Genet. Metab.,2011

4. Nitisinone arrests ochronosis and decreases rate of progression of alkaptonuria: evaluation of the effect of nitisinone in the United Kingdom National Alkaptonuria Centre;Ranganath;Mol. Genet. Metab.,2018

5. First treatment for rare metabolic disorder alkaptonuria. https://www.ema.europa.eu/en/news/first-treatment-raremetabolic-disorder-alkaptonuria. Accessed December 1, 2021.

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