J. Cardinal

发表

Elevated plasma S100B levels in high altitude hypobaric hypoxia do not correlate with acute mountain sickness

S. Rose, C. Winter, T. Whyte, 2014, Neurological research.

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

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

Fasting gut hormone levels change with modest weight loss in obese adolescents

R. Ware, J. Cardinal, H. Truby, 2015, Pediatric obesity.

Effects of atorvastatin on NGAL and cystatin C in chronic kidney disease: a post hoc analysis of the LORD trial.

J. Coombes, J. Cardinal, R. Fassett, 2012, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas.

C. Larsson, B. Teh, J. Cardinal, 1996, The Journal of clinical endocrinology and metabolism.

Novel susceptibility gene for late-onset NIDDM is localized to human chromosome 12q.

D. Duffy, B. Wainwright, J. Cardinal, 1998, Diabetes.

Differential Metabolite Accumulation May Be the Cause of Strain Differences in Sensitivity to Streptozotocin-Induced β Cell Death in Inbred Mice.

J. Cardinal, D. Allan, D. Cameron, 1998, Endocrinology.

Biological and diurnal variation in glucocorticoid sensitivity detected with a sensitive in vitro dexamethasone suppression of cytokine production assay.

J. Cardinal, J. Ungerer, C. Pretorius, 2010, The Journal of clinical endocrinology and metabolism.

Increased Susceptibility to Streptozotocin-Induced β-Cell Apoptosis and Delayed Autoimmune Diabetes in Alkylpurine- DNA-N-Glycosylase-Deficient Mice

G. Margison, J. Cardinal, A. Yates, 2001, Molecular and Cellular Biology.

Insulin autoimmune syndrome in a child with type 1 diabetes: Clinical, immunological, and biochemical correlations.

J. Cardinal, T. Huynh, I. Hughes, 2016, Pathology.

Identification of MEN1 gene mutations in families with MEN 1 and related disorders

N. Hayward, B. Teh, J. Cardinal, 2000, British Journal of Cancer.

Glucocorticoid Sensitivity Is Highly Variable in Critically Ill Patients With Septic Shock and Is Associated With Disease Severity*

A. Blumenthal, J. Cardinal, J. Ungerer, 2016, Critical care medicine.

Genetic mapping of the multiple endocrine neoplasia type 1 locus at 11q13

C. Larsson, N. Hayward, B. Teh, 1995, Journal of internal medicine.

DMP1-CDG (CDG1e) with Significant Gastrointestinal Manifestations; Phenotype and Genotype Expansion.

J. Cardinal, F. Connor, D. Coman, 2016, JIMD reports.

Re-exposure to the hypobaric hypoxic brain injury of high altitude: plasma S100B levels and the possible effect of acclimatisation on blood–brain barrier dysfunction

C. Winter, T. Whyte, J. Cardinal, 2016, Neurological Sciences.

Poly(ADP-ribose)polymerase activation determines strain sensitivity to streptozotocin-induced beta cell death in inbred mice.

J. Cardinal, D. Allan, D. Cameron, 1999, Journal of molecular endocrinology.

Behçet Disease-Like Symptoms with a Novel COPA Mutation

J. Cardinal, D. Coman, J. Hatch, 2020 .

Rapid mutation screening for HRPT2 and MEN1 mutations associated with familial and sporadic primary hyperparathyroidism.

D. Marsh, A. Richardson, J. Cardinal, 2006, The Journal of molecular diagnostics : JMD.

COXPD9 an Evolving Multisystem Disease; Congenital Lactic Acidosis, Sensorineural Hearing Loss, Hypertrophic Cardiomyopathy, Cirrhosis and Interstitial Nephritis.

J. Cardinal, B. Lewis, R. Justo, 2017, JIMD reports.

Congenital Glaucoma: a Novel Ocular Manifestation of Hajdu-Cheney Syndrome

G. Gole, J. Cardinal, D. Coman, 2018, Case reports in genetics.

Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism.

C. Larsson, N. Hayward, B. Teh, 1998, The Journal of clinical endocrinology and metabolism.

J. Cardinal, D. Coman, L. Swan, 2018, Clinics and practice.

A deletion in chromosome 6q is associated with human abdominal aortic aneurysm.

J. Golledge, P. Walker, E. Biros, 2014, Clinical science.

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.

Predictive diagnosis of multiple endocrine neoplasia (MEN 1) in four Australian kindreds.

N. Hayward, B. Teh, S. Grimmond, 1996, Australian and New Zealand journal of medicine.

microRNA profiling in patients with abdominal aortic aneurysms: the significance of miR-155.

J. Golledge, P. Walker, E. Biros, 2014, Clinical science.

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.

Resistance training improves metainflammation and body composition in obese adolescents

N. Byrne, A. Hills, J. Cardinal, 2015, International Journal of Pediatric Endocrinology.

Blood–brain barrier dysfunction following traumatic brain injury: correlation of Ktrans (DCE-MRI) and SUVR (99mTc-DTPA SPECT) but not serum S100B

S. Rose, C. Winter, T. Whyte, 2015, Neurological research.

Autosomal dominant hypocalcemia: a novel activating mutation (E604K) in the cysteine-rich domain of the calcium-sensing receptor.

A. Conigrave, J. Prins, J. Cardinal, 2003, The Journal of clinical endocrinology and metabolism.

Abnormal NF-κB Function Characterizes Human Type 1 Diabetes Dendritic Cells and Monocytes1

Z. Mollah, J. Prins, J. Cardinal, 2008, The Journal of Immunology.

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 .

Relation of reduced preclinical left ventricular diastolic function and cardiac remodeling in overweight youth to insulin resistance and inflammation.

K. Kostner, N. Byrne, A. Hills, 2015, The American journal of cardiology.

Mitochondrial Trifunctional Protein Deficiency: Severe Cardiomyopathy and Cardiac Transplantation.

J. Cardinal, R. Justo, R. Weintraub, 2017, JIMD reports.

Abnormal NF-kappa B function characterizes human type 1 diabetes dendritic cells and monocytes.

Z. Mollah, J. Prins, J. Cardinal, 2008, Journal of immunology.

Squalene Synthase Deficiency: Clinical, Biochemical, and Molecular Characterization of a Defect in Cholesterol Biosynthesis.

L. Vissers, H. Waterham, J. Christodoulou, 2018, American journal of human genetics.

Tread carefully: A functional variant in the human NADPH oxidase 4 (NOX4) is not disease causing.

J. Christodoulou, J. Cardinal, W. Gold, 2018, Molecular genetics and metabolism.

Acute Mountain Sickness Following Incremental Trekking to High Altitude: Correlation With Plasma Vascular Endothelial Growth Factor Levels and the Possible Effects of Dexamethasone and Acclimatization Following Re-exposure

C. Winter, V. Vegh, J. Cardinal, 2021, Frontiers in Physiology.

A Randomized Controlled Trial of Two Different Macronutrient Profiles on Weight, Body Composition and Metabolic Parameters in Obese Adolescents Seeking Weight Loss

R. Ware, J. Cardinal, H. Truby, 2016, PloS one.

Differential metabolite accumulation may be the cause of strain differences in sensitivity to streptozotocin-induced beta cell death in inbred mice.

J. Cardinal, D. Allan, D. Cameron, 1998, Endocrinology.

Susceptibility to insulin resistance in indigenous Australians may be down stream of resistin.

R. Ware, J. Cardinal, L. Marks, 2008 .

Effect of atorvastatin on the biomarkers NGAL and Cystain C in chronic kidney disease: A post-hoc analysis of the LORD Trial

J. Coombes, J. Cardinal, R. Fassett, 2010 .