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  1. 1
    A mutation in mannose‐phosphate‐dolichol utilization defect 1 reveals clinical symptoms of congenital disorders of glycosylation type I and dystroglycanopathy

    A mutation in mannose‐phosphate‐dolichol utilization defect 1 reveals clinical symptoms of congenital disorders of glycosylation type I and dystroglycanopathy by Walinka vanTol, Angel Ashikov, Eckhard Korsch, Nurulamin Abu Bakar, Michèl A. Willemsen, Christian Thiel, Dirk J. Lefeber

    Published 2019-11-01
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    Article
  2. 2
    An expanded clinical spectrum of hypoinsulinaemic hypoketotic hypoglycaemia

    An expanded clinical spectrum of hypoinsulinaemic hypoketotic hypoglycaemia by Alena Welters, Sarah M Leiter, Nadine Bachmann, Carsten Bergmann, Henrike Hoermann, Eckhard Korsch, Thomas Meissner, Felicity Payne, Rachel Williams, Khalid Hussain, Robert K. Semple, Sebastian Kummer

    Published 2023-11-01
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    Article

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