Literature DB >> 6790844

Two forms of biotin-responsive multiple carboxylase deficiency.

L Sweetman.   

Abstract

Biotin-responsive multiple carboxylase deficiencies are classified into early and late forms. The early form showed higher urinary excretion of 3-hydroxyisovalerate and 3-hydroxypropionate than the late form and was associated with normal plasma biotin concentrations. It is proposed that holocarboxylase synthetase and intestinal biotin absorption are defective in the early and late forms respectively.

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Year:  1981        PMID: 6790844     DOI: 10.1007/BF02263587

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


  7 in total

1.  A new assay method for biotin in blood, serum, urine, and tissues.

Authors:  H BAKER; O FRANK; V B MATOVITCH; I PASHER; S AARONSON; S H HUTNER; H SOBOTKA
Journal:  Anal Biochem       Date:  1962-01       Impact factor: 3.365

2.  Biotin-responsive beta-methylcrotonylglycinuria.

Authors:  D Gompertz; G H Draffan; J L Watts; D Hull
Journal:  Lancet       Date:  1971-07-03       Impact factor: 79.321

3.  Biotin-response organicaciduria. Multiple carboxylase defects and complementation studies with propionicacidemia in cultured fibroblasts.

Authors:  M Saunders; L Sweetman; B Robinson; K Roth; R Cohn; R A Gravel
Journal:  J Clin Invest       Date:  1979-12       Impact factor: 14.808

4.  Beta-methylcrotonic aciduria associated with lactic acidosis.

Authors:  K Roth; R Cohn; J Yandrasitz; G Preti; P Dodd; S Segal
Journal:  J Pediatr       Date:  1976-02       Impact factor: 4.406

5.  Multiple biotin-dependent carboxylase deficiencies associated with defects in T-cell and B-cell immunity.

Authors:  M J Cowan; D W Wara; S Packman; A J Ammann; M Yoshino; L Sweetman; W Nyhan
Journal:  Lancet       Date:  1979-07-21       Impact factor: 79.321

6.  Abnormal metabolites of isoleucine in a patient with propionyl-CoA carboxylase deficiency.

Authors:  L Sweetman; W Weyler; W L Nyhan; C de Céspedes; A R Loria; Y Estrada
Journal:  Biomed Mass Spectrom       Date:  1978-03

7.  Deficiency of propionyl-Co A carboxylase and methylcrotonyl-Co A carboxylase in a patient with methylcrotonylglycinuria.

Authors:  W Weyler; L Sweetman; D C Maggio; W L Nyhan
Journal:  Clin Chim Acta       Date:  1977-05-02       Impact factor: 3.786

  7 in total
  11 in total

1.  The development and organization of newborn screening programs in Turkey.

Authors:  Başak Tezel; Dilek Dilli; Hilal Bolat; Hatice Sahman; Sema Ozbaş; Deniz Acıcan; Mustafa Ertek; Mehmet Rıfat Köse; Uğur Dilmen
Journal:  J Clin Lab Anal       Date:  2013-12-27       Impact factor: 2.352

Review 2.  Holocarboxylase synthetase deficiency: 9-year follow-up of a patient on chronic biotin therapy and a review of the literature.

Authors:  A J Michalski; G T Berry; S Segal
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

Review 3.  Biotinidase deficiency: a novel vitamin recycling defect.

Authors:  B Wolf; R E Grier; J R Secor McVoy; G S Heard
Journal:  J Inherit Metab Dis       Date:  1985       Impact factor: 4.982

Review 4.  The biotin-dependent carboxylase deficiencies.

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

Review 5.  Enzyme studies in biotin-responsive disorders.

Authors:  K Bartlett; H K Ghneim; H J Stirk; H Wastell
Journal:  J Inherit Metab Dis       Date:  1985       Impact factor: 4.982

6.  Pyruvate carboxylase deficiency.

Authors:  K Bartlett; H K Ghneim; J H Stirk; G Dale; K G Alberti
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

7.  Intestinal absorption and renal excretion of biotin in patients with biotinidase deficiency.

Authors:  T Suormala; H Wick; J P Bonjour; E R Baumgartner
Journal:  Eur J Pediatr       Date:  1985-05       Impact factor: 3.183

8.  Heterogeneity of holocarboxylase synthetase in patients with biotin-responsive multiple carboxylase deficiency.

Authors:  B J Burri; L Sweetman; W L Nyhan
Journal:  Am J Hum Genet       Date:  1985-03       Impact factor: 11.025

9.  Biotin-responsive multiple carboxylase deficiency in an 8-year-old boy with normal serum biotinidase and fibroblast holocarboxylase-synthetase activities.

Authors:  E Holme; C E Jacobson; B Kristiansson
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

10.  Neuropathology of biotinidase deficiency.

Authors:  M Honavar; I Janota; B G Neville; R A Chalmers
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

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