|1.||Yang, Wen-Chao: 2 articles (03/2015 - 10/2014)|
|2.||Xu, Yu-Ling: 2 articles (03/2015 - 10/2014)|
|3.||Yang, Guang-Fu: 2 articles (03/2015 - 10/2014)|
|4.||Lin, Hong-Yan: 2 articles (03/2015 - 10/2014)|
|5.||Diaz Napal, Georgina Natalia: 1 article (10/2015)|
|6.||Chiari, María Eugenia: 1 article (10/2015)|
|7.||Joray, Mariana Belén: 1 article (10/2015)|
|8.||Palacios, Sara María: 1 article (10/2015)|
|9.||Tosoni, Leonardo: 1 article (10/2015)|
|10.||Vera, Domingo Mariano A: 1 article (10/2015)|
|1.||Peripheral Nervous System Diseases (PNS Diseases)
06/01/1972 - "Hereditary tyrosinemia: metabolic studies in a patient with partial p-hydroxyphenylpyruvate hydroxylase activity."
06/01/2009 - "Tyrosinemia type III (OMIM 276710) is an autosomal recessive disorder caused by the deficiency of 4-hydroxyphenylpyruvate dioxygenase (4-HPD). "
01/01/2009 - "4-hydroxyphenylpyruvate dioxygenase activity in liver was normal, which is atypical for tyrosinemia type I. A novel mutation was found in the FAH gene: c.103G>A (Ala35Thr). "
06/01/2000 - "Mutations in the 4-hydroxyphenylpyruvate dioxygenase gene (HPD) in patients with tyrosinemia type III."
02/01/1972 - "p-hydroxyphenylpyruvate hydroxylase activity in fine-needle aspiration liver biopsies in hereditary tyrosinemia."
|3.||Inborn Genetic Diseases (Disease, Hereditary)
10/01/2015 - "In mammals, this enzyme is the molecular target of drugs used for the treatment of metabolic disorders associated with defects in the tyrosine catabolism, mainly the fatal hereditary disease tyrosinemia type 1. This study evaluated the inhibitory effect of 91 extracts on 4-hydroxyphenylpyruvate dioxygenase from mostly native plants from central Argentina. "
06/01/2005 - "Nitisinone, an inhibitor of the enzyme 4-hydroxyphenylpyruvate dioxygenase, can drastically reduce urinary excretion of HGA in individuals with alkaptonuria. "
10/01/2014 - "4-Hydroxyphenylpyruvate dioxygenase (HPPD), converting 4-hydroxyphenylpyruvate acid to homogentisate, is an important target for treating type I tyrosinemia and alkaptonuria due to its significant role in tyrosine catabolism. "
|2.||Tyrosinemia type 1
|3.||Tyrosine Transaminase (Tyrosine Aminotransferase)
|8.||Procollagen-Proline Dioxygenase (Prolyl Hydroxylase)