Neonatal hypocalcemic seizures in offspring of a mother with familial hypocalciuric hypercalcemia type 1 (FHH1)

Slični predmeti

• Cinacalcet rectifies hypercalcemia in a patient with familial hypocalciuric hypercalcemia type 2 (FHH2) caused by a germline loss‐of‐function Gα11 mutation
  od: Gorvin, C, i dr.
  Izdano: (2017)
• A G-protein subunit-α11 loss-of-function mutation, Thr54Met, causes familial hypocalciuric hypercalcemia type 2 (FHH2)
  od: Gorvin, C, i dr.
  Izdano: (2016)
• Familial hypocalciuric hypercalcemia type 1 and autosomal-dominant hypocalcemia type 1: prevalence in a large healthcare population
  od: Dershem, R, i dr.
  Izdano: (2020)
• Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3
  od: Nesbit, M, i dr.
  Izdano: (2013)
• Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3.
  od: Nesbit, M, i dr.
  Izdano: (2013)