Literature DB >> 3099081

A new type of hyperlysinaemia due to a transport defect of lysine into mitochondria.

K Oyanagi, T Aoyama, A Tsuchiyama, T Nakao, N Uetsuji, K Wagatsuma, S Tsugawa.   

Abstract

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Year:  1986        PMID： 3099081     DOI： 10.1007/bf01799673

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


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  8 in total

1.  HYPERLYSINEMIA.

Authors:  N C WOODY
Journal:  Am J Dis Child       Date:  1964-11

2.  Lysine-ketoglutarate reductase in human tissues.

Authors:  J Hutzler; J Dancis
Journal:  Biochim Biophys Acta       Date:  1975-01-23

3.  Multiple enzyme defects in familial hyperlysinemia.

Authors:  J Dancis; J Hutzler; N C Woody; R P Cox
Journal:  Pediatr Res       Date:  1976-07       Impact factor: 3.756

4.  Enzyme studies in a patient with saccharopinuria: a defect of lysine metabolism.

Authors:  F C Fellows; N A Carson
Journal:  Pediatr Res       Date:  1974-01       Impact factor: 3.756

5.  Hyperlysinaemia. Harmless inborn error of metabolism?

Authors:  H H van Gelderen; H L Teijema
Journal:  Arch Dis Child       Date:  1973-11       Impact factor: 3.791

6.  Saccharopinuria.

Authors:  O Simell; J K Visakorpi; M Donner
Journal:  Arch Dis Child       Date:  1972-02       Impact factor: 3.791

7.  Hyperlysinemia associated with retardation.

Authors:  H Ghadimi; V I Binnington; P Pecora
Journal:  N Engl J Med       Date:  1965-09-30       Impact factor: 91.245

8.  Familial hyperlysinemia: enzyme studies, diagnostic methods, comments on terminology.

Authors:  J Dancis; J Hutzler; R P Cox
Journal:  Am J Hum Genet       Date:  1979-05       Impact factor: 11.025
  8 in total
  1 in total

Review 1.  The biochemical basis of mitochondrial diseases.

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

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