J. Warner

发表

Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications

B. Teh, J. Prins, J. Cardinal, 2004, Journal of Medical Genetics.

Can one point-of-care glucose meter be used for all pediatric and adult hospital patients? Evaluation of three meters, including recently modified test strips.

Joyce Y. Wu, D. McLeod, J. Warner, 2011, Diabetes technology & therapeutics.

Intravenous zoledronate improves bone density in adults with cystic fibrosis (CF)

T. Kotsimbos, I. Chapman, P. Ebeling, 2009, Clinical endocrinology.

High incidence of macrotroponin I with a high-sensitivity troponin I assay

J. Warner, G. Marshall, 2016, Clinical chemistry and laboratory medicine.

Breakpoint determination of X;autosome balanced translocations in four patients with premature ovarian failure

Y. Fukushima, N. Matsumoto, F. Hirahara, 2011, Journal of Human Genetics.

LC-MS/MS method for the quantitation of metabolites of eight commonly-used synthetic cannabinoids in human urine--an Australian perspective.

J. Warner, A. D. de Jager, M. Henman, 2012, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Familial isolated hyperparathyroidism is linked to a 1.7 Mb region on chromosome 2p13.3–14

B. Teh, D. Nyholt, J. Cardinal, 2005, Journal of Medical Genetics.

Genotyping FOXG 1 Mutations in Patients with Clinical Evidence of the FOXG 1 Syndrome

M. Williams, J. Warner, D. Pratt, 2013 .

Genotyping FOXG1 Mutations in Patients with Clinical Evidence of the FOXG1 Syndrome

J. Warner, M. Williams, D. Pratt, 2012, Molecular Syndromology.

A report of a national mutation testing service for the MEN1 gene: clinical presentations and implications for mutation testing

T. Dwight, N. Hayward, B. Teh, 2005, Journal of Medical Genetics.

C-Reactive Protein as a Prognostic Marker After Lacunar Stroke: Levels of Inflammatory Markers in the Treatment of Stroke Study

Mark D. Johnson, David C. Anderson, P. Karanjia, 2014, Stroke.

implications for mutation testing gene : clinical presentations and MEN 1 for the A report of a national mutation testing service and

T. Dwight, N. Hayward, B. Teh, 2004 .

Symptomatic Hypocalcemia Secondary to Rifampicin-induced Hypovitaminosis D.

M. Harris, J. Warner, C. Nourse, 2016, The Pediatric infectious disease journal.

Antibody-mediated interferences affecting cardiac troponin assays: recommendations from the IFCC Committee on Clinical Applications of Cardiac Biomarkers

A. Jaffe, P. Collinson, B. Lindahl, 2023, Clinical chemistry and laboratory medicine.

Macrotroponin Probably Contributes to a Difference in Patient Stratification in Suspected Acute Coronary Syndromes.

L. Lam, J. Warner, 2021, Journal of the American College of Cardiology.

Total bilirubin assay differences may cause inconsistent treatment decisions in neonatal hyperbilirubinaemia

D. Macey, J. Warner, Graham R D Jones, 2022, Clinical chemistry and laboratory medicine.