Dima Kayal
2PUBLICATIONS
0CO-AUTHORS
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Publications (2)
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|Aug 01, 2024
Unveiling atypical diagnoses: when whole-genome analysis performed for refractory infantile hypomagnesemia reveals primary hyperoxaluria.Dima Kayal, Enzo Vedrine, Claire Goursaud
|Jan 23, 2024
Nephrocalcinosis can disappear in infants receiving early lumasiran therapy.Dima Kayal, Anne-Laure Sellier-Leclerc, Cécile Acquaviva-Bourdain
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