Simultaneous diagnosis of primary adrenal insufficiency and Type 1 diabetes mellitus von Espenschied, Tahlia, Lawford, Robyn, Zacharin, Margaret, Gray, Lawrence EK

Volltext

Primary amoebic meningoencephalitis in North Queensland: the paediatric experience von Nicholls, Claire L, Parsonson, Fiona, Gray, Lawrence EK, Heyer, Adele, Donohue, Steven, Wiseman, Greg, Norton, Robert

Volltext

Congenital adrenal hyperplasia (CAH) or Wolff-Parkinson-White (WPW): The difficulties of diagnosing a shocked neonate von Gray, Lawrence EK, Vuillermin, Peter

Volltext

ASCIA-P37: FAMILY HISTORY OF ALLERGIC DISEASE IS ASSOCIATED WITH ADVERSE INFANT RESPIRATORY HEALTH AND INCREASED HEALTHCARE UTILISATION: FINDINGS FROM THE BARWON INFANT STUDY von Gray, Lawrence EK, Lin, Tiffany, O'Hely, Martin, Vuillermin, Peter, Investigator Group, the BIS

Volltext

Simultaneous diagnosis of primary adrenal insufficiency and Type 1 diabetes mellitus von Espenschied, Tahlia, Lawford, Robyn, Zacharin, Margaret, Gray, Lawrence Ek

Volltext

Use of denaturing gradient gel blots to screen for point mutations in the factor VIII gene von Laprise, Shari L., Mak, Elsa K., Killoran, Katherine A., Layman, Lawrence C., Gray, Mark R.

Volltext