Sapropterin dihydrochloride for the treatment of hyperphenylalaninemias-Reference-Cited by-同舟云学术

Sapropterin dihydrochloride for the treatment of hyperphenylalaninemias

Published:2013-05-27 Issue:9 Volume:9 Page:1207-1218
ISSN:1742-5255
Container-title:Expert Opinion on Drug Metabolism & Toxicology
language:en
Short-container-title:Expert Opinion on Drug Metabolism & Toxicology

Author:

Blau Nenad¹²³

Affiliation:

1. University Children's Hospital, Division of Inborn Metabolic Diseases, Department of General Pediatrics, Im Neuenheimer Feld 430, 69120 Heidelberg, Germany ;

2. University Children's Hospital, Division of Metabolism, Zürich, Switzerland

3. Zürich Center for Integrative Human Physiology (ZIHP), Zürich, Switzerland

Publisher

Informa Healthcare

Subject

Pharmacology,Toxicology,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1517/17425255.2013.804064

Reference65 articles.

1. Tetrahydrobiopterin: biochemistry and pathophysiology

2. Phenylketonuria

3. National Institutes of Health Consensus Development Conference Statement: Phenylketonuria: Screening and Management, October 16–18, 2000

4. Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency

5. High frequency of tetrahydrobiopterin-responsiveness among hyperphenylalaninemias: a study of 1919 patients observed from 1988 to 2002

Cited by 50 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Pre-analytic decrease of phenylalanine in plasma of patients with phenylketonuria treated with pegvaliase;Molecular Genetics and Metabolism Reports;2024-09

2. Longitudinal Dietary Intake Data in Patients with Phenylketonuria from Europe: The Impact of Age and Phenylketonuria Severity;Nutrients;2024-08-31

3. Adverse events of pegvaliase in the treatment of phenylketonuria: A pharmacovigilance study based on the FAERS database;2024-07-23

4. The Role of Pharmacogenomics in Rare Diseases;Drug Safety;2024-03-14

5. Tetrahydrobiopterin (BH₄) treatment stabilizes tyrosine hydroxylase: Rescue of tyrosine hydroxylase deficiency phenotypes in human neurons and in a knock‐in mouse model;Journal of Inherited Metabolic Disease;2024-01-09