Literature DB >> 5452306

Clinical and biochemical-genetic aspects of intermittent branched-chain ketoaciduria. Report of two Scandinavian families.

H W Goedde, U Langenbeck, D Brackertz, W Keller, T Rokkones, S Halvorsen, R Kiil, B Merton.   

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Year:  1970        PMID: 5452306     DOI: 10.1111/j.1651-2227.1970.tb15519.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN: 0001-656X


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  6 in total

Review 1.  Food intolerance in humans.

Authors:  R H Herman; L Hagler
Journal:  West J Med       Date:  1979-02

2.  Maple syrup urine disease variant: report on an infant.

Authors:  P Koepp; C Rybak; H W Rüdiger; U Wendel
Journal:  Z Kinderheilkd       Date:  1974-02-11

Review 3.  [Genetic aspects of metabolic disorders].

Authors:  W Fuhrmann
Journal:  Klin Wochenschr       Date:  1971-05

4.  Evaluation of a heterozygote test for maple syrup urine disease in leucocytes and cultured fibroblasts.

Authors:  U Langenbeck; H W Rüdiger; M Schulze-Schencking; W Keller; D Brackertz; H W Goedde
Journal:  Humangenetik       Date:  1971

5.  Maple syrup urine disease: treatment of the acutely ill newborn.

Authors:  G Hammersen; L Wille; H Schmidt; P Lutz; H Bickel
Journal:  Eur J Pediatr       Date:  1978-10-12       Impact factor: 3.183

6.  Glucose and alanine metabolism in children with maple syrup urine disease.

Authors:  M W Haymond; E Ben-Galim; K E Strobel
Journal:  J Clin Invest       Date:  1978-08       Impact factor: 14.808

  6 in total

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