Literature DB >> 6103410

Fatty-acid-responsive alopecia in multiple carboxylase deficiency.

A Munnich, J M Saudubray, F X Coude, C Charpentier, J H Saurat, J Frezal.   

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Year:  1980        PMID: 6103410     DOI: 10.1016/s0140-6736(80)91518-4

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


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  11 in total

Review 1.  The biotin-dependent carboxylase deficiencies.

Authors:  B Wolf; G L Feldman
Journal:  Am J Hum Genet       Date:  1982-09       Impact factor: 11.025

2.  International Symposium on Inborn Errors of Metabolism in Humans, 2-5 September 1980, Interlaken, Switzerland. Work in progress.

Authors: 
Journal:  J Inherit Metab Dis       Date:  1981       Impact factor: 4.982

3.  Lipid metabolism in biotin-responsive multiple carboxylase deficiency.

Authors:  M C Gonzalez-Rios; S C Whitney; M L Williams; P M Elias; S Packman
Journal:  J Inherit Metab Dis       Date:  1985       Impact factor: 4.982

4.  An overview of inborn errors of complex lipid biosynthesis and remodelling.

Authors:  Foudil Lamari; Fanny Mochel; Jean-Marie Saudubray
Journal:  J Inherit Metab Dis       Date:  2014-09-20       Impact factor: 4.982

5.  Abnormal fatty acid composition of biotin-responsive multiple carboxylase deficiency fibroblasts.

Authors:  S Packman; S C Whitney; M Fitch; S E Fleming
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

6.  Biotin dependent multiple carboxylase deficiency presenting as a congenital lactic acidosis.

Authors:  A Munnich; J M Saudubray; A Cotisson; F X Coudĕ; H Ogier; C Charpentier; C Marsac; G Carrĕ; M Bourgeay-Causse; J Frĕzal
Journal:  Eur J Pediatr       Date:  1981-10       Impact factor: 3.183

7.  Organic aciduria in neonatal multiple carboxylase deficiency.

Authors:  L Sweetman; W L Nyhan; N A Sakati; A Ohlsson; M S Mange; R B Boychuk; R Kaye
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

8.  Acetyl CoA carboxylase in cultured fibroblasts: differential biotin dependence in the two types of biotin-responsive multiple carboxylase deficiency.

Authors:  S Packman; N Caswell; M C Gonzalez-Rios; T Kadlecek; H Cann; D Rassin; C McKay
Journal:  Am J Hum Genet       Date:  1984-01       Impact factor: 11.025

9.  Mutant holocarboxylase synthetase: evidence for the enzyme defect in early infantile biotin-responsive multiple carboxylase deficiency.

Authors:  B J Burri; L Sweetman; W L Nyhan
Journal:  J Clin Invest       Date:  1981-12       Impact factor: 14.808

10.  Evidence for a defect of holocarboxylase synthetase activity in cultured lymphoblasts from a patient with biotin-responsive multiple carboxylase deficiency.

Authors:  M E Saunders; W G Sherwood; M Duthie; L Surh; R A Gravel
Journal:  Am J Hum Genet       Date:  1982-07       Impact factor: 11.025

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