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Bilineal Disease and Trans-Heterozygotes in Autosomal Dominant Polycystic Kidney Disease

American journal of human genetics, 2001-02, Vol.68 (2), p.355-363

2001

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Mutations of PKD1 in ADPKD2 cysts suggest a pathogenic effect of trans -heterozygous mutations

Nature genetics, 2000-06, Vol.25 (2), p.143-144

2000

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The Canadian STOP-PAIN Project: The Burden of Chronic Pain—Does Sex Really Matter?

The Clinical journal of pain, 2014-05, Vol.30 (5), p.443-452

2014

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Advance Prediction of Early Death in Patients Starting Maintenance Dialysis

American journal of kidney diseases, 1994-06, Vol.23 (6), p.836-845

1994

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Association of TNF-α polymorphisms in Crohn disease

Human immunology, 2005, Vol.66 (1), p.56-59

2005

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A Fifth Locus for Bardet-Biedl Syndrome Maps to Chromosome 2q31

American journal of human genetics, 1999-03, Vol.64 (3), p.900-904

1999

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Familial risk of preeclampsia in Newfoundland: A population-based study

Journal of the American Society of Nephrology, 2002-07, Vol.13 (7), p.1901-1906

2002

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The importance of renal impairment in the natural history of bardet-biedl syndrome

American journal of kidney diseases, 1996-06, Vol.27 (6), p.776-783

1996

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Contrast nephropathy in patients with impaired renal function: High versus low osmolar media

Kidney international, 1992-05, Vol.41 (5), p.1274-1279

1992

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Association of SEEK1 polymorphisms in Crohn's disease

Human immunology, 2004-07, Vol.65 (7), p.706-709

2004

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Differences in hormonal and renal vascular responses between normotensive patients with autosomal dominant polycystic kidney disease and unaffected family members

Kidney international, 1994-10, Vol.46 (4), p.1118-1123

1994

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A Founder Effect in the Newfoundland Population Reduces the Bardet-Biedl Syndrome I ( BBS1 ) Interval to 1 cM

American journal of human genetics, 1999-12, Vol.65 (6), p.1680-1687

1999

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Genetic Heterogeneity of Bardet–Biedl Syndrome in a Distinct Canadian Population: Evidence for a Fifth Locus

Genomics (San Diego, Calif.), 1999-01, Vol.55 (1), p.2-9

1999

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A spectrum of mutations in the polycystic kidney disease-2 (PKD2) gene from eight Canadian kindreds

Journal of the American Society of Nephrology, 1998-10, Vol.9 (10), p.1853-1860

1998

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Nonionic low-osmolality versus ionic high-osmolality contrast material for intravenous use in patients perceived to be at high risk: randomized trial

Radiology, 1992-04, Vol.183 (1), p.105-110

1992

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Increased MDR1 P‐glycoprotein expression in methotrexate resistance: Comment on the article by Yudoh et al

Arthritis and rheumatism, 2000-07, Vol.43 (7), p.1661-1662

2000

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Canadian Bardet-Biedl syndrome family reduces the critical region of BBS3 (3p) and presents with a variable phenotype

American journal of medical genetics, 1998-08, Vol.78 (5), p.461-467

1998

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Bilineal Disease and Trans-Heterozygotes in Autosomal Dominant Polycystic Kidney Disease

Mutations of PKD1 in ADPKD2 cysts suggest a pathogenic effect of trans -heterozygous mutations

The Canadian STOP-PAIN Project: The Burden of Chronic Pain—Does Sex Really Matter?

Advance Prediction of Early Death in Patients Starting Maintenance Dialysis

Association of TNF-α polymorphisms in Crohn disease

A Fifth Locus for Bardet-Biedl Syndrome Maps to Chromosome 2q31

Familial risk of preeclampsia in Newfoundland: A population-based study

The importance of renal impairment in the natural history of bardet-biedl syndrome

Contrast nephropathy in patients with impaired renal function: High versus low osmolar media

Association of SEEK1 polymorphisms in Crohn's disease

Differences in hormonal and renal vascular responses between normotensive patients with autosomal dominant polycystic kidney disease and unaffected family members

A Founder Effect in the Newfoundland Population Reduces the Bardet-Biedl Syndrome I ( BBS1 ) Interval to 1 cM

Genetic Heterogeneity of Bardet–Biedl Syndrome in a Distinct Canadian Population: Evidence for a Fifth Locus

A spectrum of mutations in the polycystic kidney disease-2 (PKD2) gene from eight Canadian kindreds

Nonionic low-osmolality versus ionic high-osmolality contrast material for intravenous use in patients perceived to be at high risk: randomized trial

Increased MDR1 P‐glycoprotein expression in methotrexate resistance: Comment on the article by Yudoh et al

Canadian Bardet-Biedl syndrome family reduces the critical region of BBS3 (3p) and presents with a variable phenotype

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