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Connective Tissue Growth Factor Induces Extracellular Matrix in Asthmatic Airway Smooth Muscle

American journal of respiratory and critical care medicine, 2006-01, Vol.173 (1), p.32-41

2006

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Causes of death in young Australians with type 1 diabetes: a review of coronial postmortem examinations

Medical journal of Australia, 2008-06, Vol.188 (12), p.699-702

2008

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Position statement of the Australian Diabetes Society: individualisation of glycated haemoglobin targets for adults with diabetes mellitus

Medical journal of Australia, 2009-09, Vol.191 (6), p.339-344

2009

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Hypoglycaemia following a mixed meal in eating disorder patients

Postgraduate medical journal, 2011-06, Vol.87 (1028), p.405-409

2011

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Genetic testing for familial cancer. Consequences of RET proto-oncogene mutation analysis in multiple endocrine neoplasia, type 2

Archives of surgery (Chicago. 1960), 1997-09, Vol.132 (9), p.1022

1997

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Mutations in Multidomain Protein MEGF8 Identify a Carpenter Syndrome Subtype Associated with Defective Lateralization

American journal of human genetics, 2012-11, Vol.91 (5), p.897-905

2012

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Hearing loss in a mouse model of Muenke syndrome

Human molecular genetics, 2009-01, Vol.18 (1), p.43-50

2009

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Genomic Screening of Fibroblast Growth-Factor Receptor 2 Reveals a Wide Spectrum of Mutations in Patients with Syndromic Craniosynostosis

American journal of human genetics, 2002-02, Vol.70 (2), p.472-486

2002

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Medication Safety: an audit of medication discrepancies in transferring type 2 diabetes mellitus (T2DM) patients from Australian primary care to tertiary ambulatory care

International journal for quality in health care, 2014-08, Vol.26 (4), p.397-403

2014

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De Novo Alu-Element Insertions in FGFR2 Identify a Distinct Pathological Basis for Apert Syndrome

American journal of human genetics, 1999-02, Vol.64 (2), p.446-461

1999

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Expanding the phenotype of craniofrontonasal syndrome: two unrelated boys with EFNB1 mutations and congenital diaphragmatic hernia

European journal of human genetics : EJHG, 2006-07, Vol.14 (7), p.884-887

2006

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Lung Fluid Immunoglobulin from HIV-Infected Subjects Has Impaired Opsonic Function against Pneumococci

Clinical infectious diseases, 2007-06, Vol.44 (12), p.1632-1638

2007

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Vitamin D supplementation and bone mineral density in early postmenopausal women

The American journal of clinical nutrition, 2003-05, Vol.77 (5), p.1324-1329

2003

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Pulmonary Immunoglobulin Responses to Streptococcus pneumoniae Are Altered but Not Reduced in Human Immunodeficiency Virus–Infected Malawian Adults

The Journal of infectious diseases, 2003-09, Vol.188 (5), p.666-670

2003

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A Comprehensive Screen for TWIST Mutations in Patients with Craniosynostosis Identifies a New Microdeletion Syndrome of Chromosome Band 7p21.1

American journal of human genetics, 1998-11, Vol.63 (5), p.1282-1293

1998

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A cryptic t(5;11)(q35;p15.5) in 2 children with acute myeloid leukemia with apparently normal karyotypes, identified by a multiplex fluorescence in situ hybridization telomere assay

Blood, 2002-04, Vol.99 (7), p.2526-2531

2002

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Genotype-Phenotype Correlation for Nucleotide Substitutions in the IgII-IgIII Linker of FGFR2

Human molecular genetics, 1997-01, Vol.6 (1), p.137-143

1997

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Artificial neural networks distinguish among subtypes of neoplastic colorectal lesions

Gastroenterology (New York, N.Y. 1943), 2002-03, Vol.122 (3), p.606-613

2002

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Discrepancies in categorizing rheumatoid arthritis patients by DAS-28(ESR) and DAS-28(CRP): can they be reduced?

Rheumatology (Oxford, England), 2010-08, Vol.49 (8), p.1521-1529

2010

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Persistently moderate DAS-28 is not benign: loss of function occurs in early RA despite step-up DMARD therapy

Rheumatology (Oxford, England), 2010-10, Vol.49 (10), p.1894-1899

2010

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Connective Tissue Growth Factor Induces Extracellular Matrix in Asthmatic Airway Smooth Muscle

Causes of death in young Australians with type 1 diabetes: a review of coronial postmortem examinations

Position statement of the Australian Diabetes Society: individualisation of glycated haemoglobin targets for adults with diabetes mellitus

Hypoglycaemia following a mixed meal in eating disorder patients

Genetic testing for familial cancer. Consequences of RET proto-oncogene mutation analysis in multiple endocrine neoplasia, type 2

Mutations in Multidomain Protein MEGF8 Identify a Carpenter Syndrome Subtype Associated with Defective Lateralization

Hearing loss in a mouse model of Muenke syndrome

Genomic Screening of Fibroblast Growth-Factor Receptor 2 Reveals a Wide Spectrum of Mutations in Patients with Syndromic Craniosynostosis

Medication Safety: an audit of medication discrepancies in transferring type 2 diabetes mellitus (T2DM) patients from Australian primary care to tertiary ambulatory care

De Novo Alu-Element Insertions in FGFR2 Identify a Distinct Pathological Basis for Apert Syndrome

Expanding the phenotype of craniofrontonasal syndrome: two unrelated boys with EFNB1 mutations and congenital diaphragmatic hernia

Lung Fluid Immunoglobulin from HIV-Infected Subjects Has Impaired Opsonic Function against Pneumococci

Vitamin D supplementation and bone mineral density in early postmenopausal women

Pulmonary Immunoglobulin Responses to Streptococcus pneumoniae Are Altered but Not Reduced in Human Immunodeficiency Virus–Infected Malawian Adults

A Comprehensive Screen for TWIST Mutations in Patients with Craniosynostosis Identifies a New Microdeletion Syndrome of Chromosome Band 7p21.1

A cryptic t(5;11)(q35;p15.5) in 2 children with acute myeloid leukemia with apparently normal karyotypes, identified by a multiplex fluorescence in situ hybridization telomere assay

Genotype-Phenotype Correlation for Nucleotide Substitutions in the IgII-IgIII Linker of FGFR2

Artificial neural networks distinguish among subtypes of neoplastic colorectal lesions

Discrepancies in categorizing rheumatoid arthritis patients by DAS-28(ESR) and DAS-28(CRP): can they be reduced?

Persistently moderate DAS-28 is not benign: loss of function occurs in early RA despite step-up DMARD therapy

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