Calcium-sensing receptor mutations in familial hypocalciuric hypercalcaemia with recurrent pancreatitis.

Podobne zapisy

• Recurrent pancreatitis in a patient with familial hypocalciuric hypercalcaemia treated successfully with cinacalcet.
  od: Gunganah, K, i wsp.
  Wydane: (2014)
• Linkage studies in a kindred from Oklahoma, with familial benign (hypocalciuric) hypercalcaemia (FBH) and developmental elevations in serum parathyroid hormone levels, indicate a third locus for FBH.
  od: Trump, D, i wsp.
  Wydane: (1995)
• Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism.
  od: Pearce, S, i wsp.
  Wydane: (1995)
• ASSOCIATION OF DE-NOVO MUTATIONS IN THE CALCIUM-SENSING RECEPTOR GENE WITH SPORADIC NEONATAL SEVERE HYPERPARATHYROIDISM
  od: Pearce, S, i wsp.
  Wydane: (1995)
• Comparison of human chromosome 19q13 and syntenic region on mouse chromosome 7 reveals absence, in man, of 11.6 Mb containing four mouse calcium-sensing receptor-related sequences: relevance to familial benign hypocalciuric hypercalcaemia type 3.
  od: Hannan, F, i wsp.
  Wydane: (2010)