Literature DB >> 9323575

Partial epilepsy in a girl with a symptom-free sister: first two Finnish patients with dihydropyrimidine dehydrogenase deficiency.

I Holopainen1, K Pulkki, O J Heinonen, K Näntö-Salonen, L Haataja, J Greter, E Holme, A B van Kuilenburg, P Vreken, A H van Gennip.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1997        PMID： 9323575     DOI： 10.1023/a:1005399131620

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


× No keyword cloud information.
  2 in total

1.  Dihydropyrimidine dehydrogenase pharmacogenetics in Caucasian subjects.

Authors:  S A Ridge; J Sludden; O Brown; L Robertson; X Wei; A Sapone; P M Fernandez-Salguero; F J Gonzalez; P Vreken; A B van Kuilenburg; A H van Gennip; H L McLeod
Journal:  Br J Clin Pharmacol       Date:  1998-08       Impact factor: 4.335

2.  Head imaging abnormalities in dihydropyrimidine dehydrogenase deficiency.

Authors:  G M Enns; A J Barkovich; A B P van Kuilenburg; M Manning; T Sanger; D R Witt; A H van Gennip
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.