Literature DB >> 2512440

A method for the diagnosis of glycogen storage disease type Ib using polymorphonuclear leukocytes.

N Bashan1, R Potashnik, M Phillip, Y S Shin, S W Moses.   

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Year:  1989        PMID: 2512440     DOI: 10.1007/bf03335418

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


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  6 in total

1.  Glucose-6-phosphatase of the liver in glycogen storage disease.

Authors:  G T CORI; C F CORI
Journal:  J Biol Chem       Date:  1952-12       Impact factor: 5.157

2.  Type Ib glycogen storage disease is caused by a defect in the glucose-6-phosphate translocase of the microsomal glucose-6-phosphatase system.

Authors:  A J Lange; W J Arion; A L Beaudet
Journal:  J Biol Chem       Date:  1980-09-25       Impact factor: 5.157

3.  Impaired carbohydrate metabolism of polymorphonuclear leukocytes in glycogen storage disease Ib.

Authors:  N Bashan; Y Hagai; R Potashnik; S W Moses
Journal:  J Clin Invest       Date:  1988-05       Impact factor: 14.808

4.  Glycogen storage disease type 1b: genetic disorder involving the transport system of intracellular membrane.

Authors:  K Narisawa; Y Igarashi; K Tada
Journal:  Enzyme       Date:  1987

Review 5.  Glycogen storage disease type Ib.

Authors:  J Schaub; K Heyne
Journal:  Eur J Pediatr       Date:  1983-09       Impact factor: 3.183

6.  Type Ic, a novel glycogenosis. Underlying mechanism.

Authors:  R C Nordlie; K A Sukalski; J M Muñoz; J J Baldwin
Journal:  J Biol Chem       Date:  1983-08-25       Impact factor: 5.157

  6 in total
  1 in total

1.  Postnatal regression of glucose transport in a patient with glycogen storage disease type 1b.

Authors:  J Levy; M T Abu-Ras; T Berenstein; R Potashnik; I Meisner; S W Moses; N Bashan
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

  1 in total

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