Literature DB >> 1527998

Transient 5-oxoprolinuria in a very low-birthweight infant.

A Goto1, A Ishida, R Goto, K Hayasaka, K Nanao, A Yamashita, S Yamaguchi, G Takada.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1992        PMID： 1527998     DOI： 10.1007/bf01799646

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


× No keyword cloud information.
  2 in total

1.  5-oxoprolinuria due to hereditary 5-oxoprolinase deficiency in two brothers--a new inborn error of the gamma-glutamyl cycle.

Authors:  A Larsson; B Mattsson; E A Wauters; J D van Gool; M Duran; S K Wadman
Journal:  Acta Paediatr Scand       Date:  1981

2.  Glutathione synthetase deficiency, an inborn error of metabolism involving the gamma-glutamyl cycle in patients with 5-oxoprolinuria (pyroglutamic aciduria).

Authors:  V P Wellner; R Sekura; A Meister; A Larsson
Journal:  Proc Natl Acad Sci U S A       Date:  1974-06       Impact factor: 11.205
  2 in total
  2 in total

1.  Massive 5-oxoprolinuria with normal 5-oxoprolinase and glutathione synthetase activities.

Authors:  E Riudor; J A Arranz; R Alvarez; K Carlsson; M del Toro; F Salmerón; F Piñol; E Ristoff; M Sentis; A Larsson
Journal:  J Inherit Metab Dis       Date:  2001-06       Impact factor: 4.982

Review 2.  Inborn errors in the metabolism of glutathione.

Authors:  Ellinor Ristoff; Agne Larsson
Journal:  Orphanet J Rare Dis       Date:  2007-03-30       Impact factor: 4.123
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.