Neonatal severe hyperparathyroidism: further clinical and molecular delineation-Reference-Cited by-同舟云学术

Neonatal severe hyperparathyroidism: further clinical and molecular delineation

Published:2010-10-23 Issue:5 Volume:170 Page:625-631
ISSN:0340-6199
Container-title:European Journal of Pediatrics
language:en
Short-container-title:Eur J Pediatr

Author:

Al-Khalaf Fawziya A.,Ismail Adel,Soliman Ashraf T.,Cole David E. C.,Ben-Omran Tawfeg

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00431-010-1335-z.pdf

Reference36 articles.

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2. Bambach CP, Reeve TS (1978) Parathyroid identification by methylene blue infusion. Aust N Z J Surg 48(3):314–317

3. Brown EM (2010) Clinical utility of calcimimetics targeting the extracellular calcium-sensing receptor (CaSR). Biochem Pharmacol 80:297–307

4. Cole DE, Forsythe CR, Dooley JM, Grantmyre EB, Salisbury SR (1997) Primary neonatal hyperparathyroidism: a devastating neurodevelopmental disorder if left untreated. J Craniofac Genet Dev Biol 10:205–214

5. Cole DE, Janicic N, Salisbury SR, Hendy GN (1997) Neonatal severe hyperparathyroidism, secondary hyperparathyroidism, and familial hypocalciuric hypercalcemia: multiple different phenotypes associated with an inactivating Alu insertion mutation of the calcium-sensing receptor gene. Am J Med Genet 71:202–210

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