Literature DB >> 3930869

L-carnitine and glycine therapy in isovaleric acidaemia.

R A Chalmers, C de Sousa, B M Tracey, T E Stacey, C Weaver, D Bradley.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1985        PMID： 3930869     DOI： 10.1007/bf01811499

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


× No keyword cloud information.
  6 in total

1.  Organic aciduria associated with isovaleric acidemia.

Authors:  S J Wysocki; N P French; A Grauaug
Journal:  Clin Chem       Date:  1983-05       Impact factor: 8.327

2.  Therapeutic effects of glycine in isovaleric acidemia.

Authors:  I Krieger; K Tanaka
Journal:  Pediatr Res       Date:  1976-01       Impact factor: 3.756

3.  Glycine therapy in isovaleric acidemia.

Authors:  M Yudkoff; R M Cohn; R Puschak; R Rothman; S Segal
Journal:  J Pediatr       Date:  1978-05       Impact factor: 4.406

4.  Complementation studies of isovaleric acidemia and glutaric aciduria type II using cultured skin fibroblasts.

Authors:  B Dubiel; C Dabrowski; R Wetts; K Tanaka
Journal:  J Clin Invest       Date:  1983-11       Impact factor: 14.808

5.  Metabolic response to carnitine in methylmalonic aciduria. An effective strategy for elimination of propionyl groups.

Authors:  C R Roe; C L Hoppel; T E Stacey; R A Chalmers; B M Tracey; D S Millington
Journal:  Arch Dis Child       Date:  1983-11       Impact factor: 3.791

6.  New metabolites in isovaleric acidemia.

Authors:  R J Truscott; D Malegan; E McCairns; D Burke; L Hick; P Sims; B Halpern; K Tanaka; L Sweetman; W L Nyhan; J Hammond; C Bumack; E A Haan; D M Danks
Journal:  Clin Chim Acta       Date:  1981-03-05       Impact factor: 3.786
  6 in total
  6 in total

1.  Glycine and L-carnitine therapy in 3-methylcrotonyl-CoA carboxylase deficiency.

Authors:  S L Rutledge; G T Berry; C A Stanley; J L van Hove; D Millington
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

2.  Dietary practices in isovaleric acidemia: A European survey.

Authors:  A Pinto; A Daly; S Evans; M F Almeida; M Assoun; A Belanger-Quintana; S Bernabei; S Bollhalder; D Cassiman; H Champion; H Chan; J Dalmau; F de Boer; C de Laet; A de Meyer; A Desloovere; A Dianin; M Dixon; K Dokoupil; S Dubois; F Eyskens; A Faria; I Fasan; E Favre; F Feillet; A Fekete; G Gallo; C Gingell; J Gribben; K Kaalund-Hansen; N Horst; C Jankowski; R Janssen-Regelink; I Jones; C Jouault; G E Kahrs; I L Kok; A Kowalik; C Laguerre; S Le Verge; R Lilje; C Maddalon; D Mayr; U Meyer; A Micciche; M Robert; J C Rocha; H Rogozinski; C Rohde; K Ross; I Saruggia; A Schlune; K Singleton; E Sjoqvist; L H Stolen; A Terry; C Timmer; L Tomlinson; A Tooke; K Vande Kerckhove; E van Dam; T van den Hurk; L van der Ploeg; M van Driessche; M van Rijn; A van Teeffelen-Heithoff; A van Wegberg; C Vasconcelos; H Vestergaard; I Vitoria; D Webster; F J White; L White; H Zweers; A MacDonald
Journal:  Mol Genet Metab Rep       Date:  2017-02-27

Review 3.  Hyperammonaemia in classic organic acidaemias: a review of the literature and two case histories.

Authors:  Johannes Häberle; Anupam Chakrapani; Nicholas Ah Mew; Nicola Longo
Journal:  Orphanet J Rare Dis       Date:  2018-12-06       Impact factor: 4.123

Review 4.  Drug treatment of inborn errors of metabolism: a systematic review.

Authors:  Majid Alfadhel; Khalid Al-Thihli; Hiba Moubayed; Wafaa Eyaid; Majed Al-Jeraisy
Journal:  Arch Dis Child       Date:  2013-03-26       Impact factor: 3.791

Review 5.  Single amino acid supplementation in aminoacidopathies: a systematic review.

Authors:  Danique van Vliet; Terry G J Derks; Margreet van Rijn; Martijn J de Groot; Anita MacDonald; M Rebecca Heiner-Fokkema; Francjan J van Spronsen
Journal:  Orphanet J Rare Dis       Date:  2014-01-13       Impact factor: 4.123

6.  Disorders of branched chain amino acid metabolism.

Authors:  I Manoli; C P Venditti
Journal:  Transl Sci Rare Dis       Date:  2016-11-07
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.