Literature DB >> 8127066

3-Hydroxy-3-methylglutaryl-CoA lyase deficiency: absence of clinical symptoms due to a self-imposed dietary fat and protein restriction.

H D Bakker1, R J Wanders, R B Schutgens, N G Abeling, A H van Gennip.   

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Year:  1993        PMID： 8127066     DOI： 10.1007/bf00711535

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


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  2 in total

1.  The contribution of protein catabolism to metabolic decompensation in 3-hydroxy-3-methylglutaric aciduria.

Authors:  G N Thompson; R A Chalmers; D Halliday
Journal:  Eur J Pediatr       Date:  1990-02       Impact factor: 3.183

2.  3-Hydroxy-3-methylglutaryl coenzyme A lyase deficiency. Follow-up of first described case.

Authors:  R Shilkin; G Wilson; E Owles
Journal:  Acta Paediatr Scand       Date:  1981-03
  2 in total
  1 in total

1.  3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease - many faces.

Authors:  Sarah C Grünert; Jörn Oliver Sass
Journal:  Orphanet J Rare Dis       Date:  2020-02-14       Impact factor: 4.123
  1 in total

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