Literature DB >> 3930844

Thiamine-responsive inborn errors of metabolism.

M Duran, S K Wadman.   

Abstract

Three different inherited disorders are known in which thiamine may exert a beneficial effect: maple syrup urine disease (MSUD), lactic acidaemia and the syndrome of megaloblastic anaemia with sensorineural deafness and diabetes mellitus. The amounts of thiamine which were used for long-term treatment varied from 20 to 2400 mg day-1. Additional treatment, such as the reduction of dietary branched chain amino acids in MSUD, could not be omitted in some cases. It has been shown that the vitamin improves the stability of the branched chain ketoacid decarboxylase, although some weeks may be needed to observe the in vivo effect of treatment. A prolonged trial with high doses of thiamine should always be given.

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Year:  1985        PMID: 3930844     DOI: 10.1007/bf01800663

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


  20 in total

1.  Maple syrup disease; isolation and identification of organic acids in the urine.

Authors:  J H MENKES
Journal:  Pediatrics       Date:  1959-02       Impact factor: 7.124

2.  Thiamine-responsive megaloblastic anemia.

Authors:  F S Porter; L E Rogers; J B Sidbury
Journal:  J Pediatr       Date:  1969-04       Impact factor: 4.406

Review 3.  The role of thiamin in maple syrup urine disease.

Authors:  L J Elsas; D J Danner
Journal:  Ann N Y Acad Sci       Date:  1982       Impact factor: 5.691

Review 4.  Clinical chemistry of thiamin.

Authors:  R E Davis; G C Icke
Journal:  Adv Clin Chem       Date:  1983       Impact factor: 5.394

5.  In vivo and in vitro response of human branched chain alpha-ketoacid dehydrogenase to thiamine and thiamine pyrophosphate.

Authors:  D J Danner; F B Wheeler; S K Lemmon; L J Elsas
Journal:  Pediatr Res       Date:  1978-03       Impact factor: 3.756

6.  Thiamin-responsive maple-syrup-urine disease: decreased affinity of the mutant branched-chain alpha-keto acid dehydrogenase for alpha-ketoisovalerate and thiamin pyrophosphate.

Authors:  D T Chuang; L S Ku; R P Cox
Journal:  Proc Natl Acad Sci U S A       Date:  1982-05       Impact factor: 11.205

7.  Effects of thiamine in a patient with a variant form of branched-chian ketoaciduria.

Authors:  M Duran; A G Tielens; S K Wadman; J C Stigter; W J Kleijer
Journal:  Acta Paediatr Scand       Date:  1978-05

8.  [Intermittent maple syrup urine disease in a 12-year-old boy: clinical aspects, diagnosis and treatment].

Authors:  G Fritsch; U Langenbeck; U Wendel; W Lehnert; W Palm; W Steger
Journal:  Klin Padiatr       Date:  1983 Sep-Oct       Impact factor: 1.349

9.  Thiamine triphosphate deficiency in subacute necrotizing encephalomyelopathy.

Authors:  J R Cooper; Y Itokawa; J H Pincus
Journal:  Science       Date:  1969-04-04       Impact factor: 47.728

10.  Thiamine dependency in a patient with congenital lacticacidaemia due to pyruvate dehydrogenase deficiency.

Authors:  H Wick; K Schweizer; R Baumgartner
Journal:  Agents Actions       Date:  1977-09
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  5 in total

1.  Vitamin-responsive pyruvate dehydrogenase deficiency in a young girl with external ophthalmoplegia, myopathy and lactic acidosis.

Authors:  H R Scholte; H F Busch; I E Luyt-Houwen
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

Review 2.  Maple syrup urine disease 1954 to 1993.

Authors:  F Peinemann; D J Danner
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

3.  Mitochondrial Disease.

Authors:  Roser Pons; Darryl C. De Vivo
Journal:  Curr Treat Options Neurol       Date:  2001-05       Impact factor: 3.598

Review 4.  Animal models of maple syrup urine disease.

Authors:  K J Skvorak
Journal:  J Inherit Metab Dis       Date:  2009-03-09       Impact factor: 4.982

Review 5.  The biochemical basis of mitochondrial diseases.

Authors:  H R Scholte
Journal:  J Bioenerg Biomembr       Date:  1988-04       Impact factor: 2.945

  5 in total

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