Showing 1 - 2 results of 2 for search 'Sevasti Maragkou', query time: 0.02s Refine Results
  1. 1
    Dent-2 disease with a Bartter-like phenotype caused by the Asp631Glu mutation in the OCRL gene

    Dent-2 disease with a Bartter-like phenotype caused by the Asp631Glu mutation in the OCRL gene by Eleni Drosataki, Sevasti Maragkou, Kleio Dermitzaki, Ioanna Stavrakaki, Dimitra Lygerou, Helen Latsoudis, Christos Pleros, Ioannis Petrakis, Ioannis Zaganas, Kostas Stylianou

    Published 2022-05-01
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  2. 2
    The p.Pro482Ala Variant in the CNNM2 Gene Causes Severe Hypomagnesemia Amenable to Treatment with Spironolactone

    The p.Pro482Ala Variant in the CNNM2 Gene Causes Severe Hypomagnesemia Amenable to Treatment with Spironolactone by Ioannis Petrakis, Eleni Drosataki, Ioanna Stavrakaki, Kleio Dermitzaki, Dimitra Lygerou, Myrto Konidaki, Christos Pleros, Nikolaos Kroustalakis, Sevasti Maragkou, Ariadni Androvitsanea, Ioannis Stylianou, Ioannis Zaganas, Kostas Stylianou

    Published 2022-06-01
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