Literature DB >> 12029011

Leukocyte phosphomannomutase activity in diagnosis of congenital disorder of glycosylation Ia.

Anne Barnier1, Thierry Dupré, Maryvonne Cuer, Sandrine Vuillaumier-Barrot, Geneviève Durand, Nathalie Seta.   

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Year:  2002        PMID： 12029011

Source DB:  PubMed          Journal:  Clin Chem        ISSN： 0009-9147            Impact factor:   8.327


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  2 in total

1.  Congenital disorders of glycosylation type I: a rare but new cause of hyperechoic kidneys in infants and children due to early microcystic changes.

Authors:  Lucie Hertz-Pannier; Michele Déchaux; Martine Sinico; Sophie Emond; Valerie Cormier-Daire; Jean-Marie Saudubray; Francis Brunelle; Patrick Niaudet; Nathalie Seta; Pascale de Lonlay
Journal:  Pediatr Radiol       Date:  2005-11-22

2.  Leukocyte Phosphomannomutase and Phosphomannose Isomerase Activity in an Indian Cohort.

Authors:  Mihika B Dave; Alpa J Dherai; Vrajesh P Udani; Tester F Ashavaid
Journal:  Indian J Clin Biochem       Date:  2020-11-17
  2 in total

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