Literature DB >> 16754714

Mutation in the ATP7A gene may not be responsible for hypocupraemia in copper deficiency myelopathy.

N Kumar1, J B Gross.   

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Year:  2006        PMID: 16754714      PMCID: PMC2563737          DOI: 10.1136/pgmj.2005.043505

Source DB:  PubMed          Journal:  Postgrad Med J        ISSN: 0032-5473            Impact factor:   2.401


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  7 in total

1.  Menkes' kinky hair disease: further definition of the defect in copper transport.

Authors:  D M Danks; E Cartwright; B J Stevens; R R Townley
Journal:  Science       Date:  1973-03-16       Impact factor: 47.728

Review 2.  Metabolic and molecular bases of Menkes disease and occipital horn syndrome.

Authors:  S G Kaler
Journal:  Pediatr Dev Pathol       Date:  1998 Jan-Feb

3.  Acquired hypocupremia after gastric surgery.

Authors:  Neeraj Kumar; J Eric Ahlskog; John B Gross
Journal:  Clin Gastroenterol Hepatol       Date:  2004-12       Impact factor: 11.382

Review 4.  The molecular basis of copper-transport diseases.

Authors:  J F Mercer
Journal:  Trends Mol Med       Date:  2001-02       Impact factor: 11.951

Review 5.  Copper deficiency myelopathy produces a clinical picture like subacute combined degeneration.

Authors:  Neeraj Kumar; John B Gross; J Eric Ahlskog
Journal:  Neurology       Date:  2004-07-13       Impact factor: 9.910

Review 6.  Intracellular copper transport in mammals.

Authors:  Joseph R Prohaska; Anna A Gybina
Journal:  J Nutr       Date:  2004-05       Impact factor: 4.798

7.  Copper deficiency myelopathy.

Authors:  Neeraj Kumar; Brian Crum; Ronald C Petersen; Steven A Vernino; J Eric Ahlskog
Journal:  Arch Neurol       Date:  2004-05
  7 in total
  2 in total

Review 1.  Copper deficiency myelopathy.

Authors:  Stephan R Jaiser; Gavin P Winston
Journal:  J Neurol       Date:  2010-03-16       Impact factor: 4.849

2.  Dietary Trace Minerals.

Authors:  Elad Tako
Journal:  Nutrients       Date:  2019-11-19       Impact factor: 5.717

  2 in total

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