Literature DB >> 4738991

Fine structure of the spleen and liver in glucosephosphate isomerase (GPI) deficiency hereditary nonspherocytic hemolytic anemia. Selective reticulocyte destruction as a mechanism of hemolysis.

N Matsumoto, T Ishihara, E Oda, S Miwa, K Nakashima.   

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Year:  1973        PMID： 4738991

Source DB:  PubMed          Journal:  Nihon Ketsueki Gakkai Zasshi        ISSN： 0001-5806


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  3 in total

1.  Glucosephosphate isomerase deficiency, a new variant in a Dutch family. Case report.

Authors:  J J Rotteveel; G A de Vaan; G E Staal; J P van Biervliet; E D Schretlen
Journal:  Eur J Pediatr       Date:  1977-04-26       Impact factor: 3.183

Review 2.  Inherited glucosephosphate isomerase deficiency. A review of known variants and some aspects of the pathomechanism of the deficiency.

Authors:  H Arnold
Journal:  Blut       Date:  1979-12

Review 3.  [Enzyme deficiencies in glycolysis and nucleotide metabolism of red blood cells in nonspherocytic hemolytic anemia (author's transl)].

Authors:  H D Waller; H C Benöhr
Journal:  Klin Wochenschr       Date:  1976-09-01
  3 in total

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