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Diagnosis and management of pancreatic exocrine insufficiency (PEI) in primary care: consensus guidance of a Canadian expert panel

Current medical research and opinion, 2018-01, Vol.34 (1), p.25-33

2018

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Pathogenesis of malnutrition in cystic fibrosis, and its treatment

Clinical Nutrition, 2000-12, Vol.19 (6), p.387-394

2000

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Do common in silico tools predict the clinical consequences of amino-acid substitutions in the CFTR gene?

Clinical genetics, 2010-05, Vol.77 (5), p.464-473

2010

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Outcomes of patients with cystic fibrosis undergoing lung transplantation with and without cystic fibrosis-associated liver cirrhosis

Clinical transplantation, 2012-01, Vol.26 (1), p.34-41

2012

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Simultaneous liver–pancreas transplantation for cystic fibrosis-related liver disease: A multicenter experience

Journal of cystic fibrosis, 2014-07, Vol.13 (4), p.471-477

2014

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Molecular consequences of cystic fibrosis transmembrane regulator (CFTR) gene mutations in the exocrine pancreas

Gut, 2003-08, Vol.52 (8), p.1159-1164

2003

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Shwachman syndrome: Phenotypic manifestations of sibling sets and isolated cases in a large patient cohort are similar

The Journal of pediatrics, 1999-07, Vol.135 (1), p.81-88

1999

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High-Dose Pancreatic-Enzyme Supplements and Fibrosing Colonopathy in Children with Cystic Fibrosis

The New England journal of medicine, 1997-05, Vol.336 (18), p.1283-1289

1997

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Sweat gland bioelectrics differ in cystic fibrosis: a new concept for potential diagnosis and assessment of CFTR function in cystic fibrosis

Thorax, 2009-11, Vol.64 (11), p.932-938

2009

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Shwachman syndrome: Exocrine pancreatic dysfunction and variable phenotypic expression

Gastroenterology (New York, N.Y. 1943), 1996-12, Vol.111 (6), p.1593-1602

1996

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Cystic fibrosis modifier genes related to Pseudomonas aeruginosa infection

Genes and immunity, 2011-07, Vol.12 (5), p.370-377

2011

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Skeletal phenotype in patients with Shwachman-Diamond syndrome and mutations in SBDS

Clinical genetics, 2004-02, Vol.65 (2), p.101-112

2004

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Pancreatitis and Mutations of the Cystic Fibrosis Gene

The New England journal of medicine, 1998-09, Vol.339 (10), p.687-688

Durie, Peter R

1998

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Patterns of GI disease in adulthood associated with mutations in the CFTR gene

Gut, 2007-08, Vol.56 (8), p.1153-1163

2007

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Inconclusive diagnosis of cystic fibrosis after newborn screening

Pediatrics (Evanston), 2015-06, Vol.135 (6), p.e1377-e1385

2015

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Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutations

The Journal of pediatrics, 1995-11, Vol.127 (5), p.705-710

1995

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Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13

Nature genetics, 1999-06, Vol.22 (2), p.128-129

1999

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Understanding the population structure of North American patients with cystic fibrosis

Clinical genetics, 2011-02, Vol.79 (2), p.136-146

2011

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188 DO CHILDREN WITH END STAGE CF-RELATED LIVER DISEASE BENEFIT FROM COMBINED LIVER-PANCREAS TRANSPLANT?

Journal of hepatology, 2012-04, Vol.56, p.S81-S81

2012

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Does the Macroduct ® collection system reliably define sweat chloride concentration in subjects with intermediate results?

Clinical biochemistry, 2009-08, Vol.42 (12), p.1260-1264

2009

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WS1.2 Rate of decline in serum trypsinogen as a validation for the PIP score

Journal of cystic fibrosis, 2012-06, Vol.11, p.S1-S1

2012

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Draft consensus guidelines for diagnosis and treatment of Shwachman-Diamond syndrome

Annals of the New York Academy of Sciences, 2011-12, Vol.1242 (1), p.40-55

2011

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PANCREATIC ASPECTS OF CYSTIC FIBROSIS AND OTHER INHERITED CAUSES OF PANCREATIC DYSFUNCTION

The Medical clinics of North America, 2000-05, Vol.84 (3), p.609-620

Durie, Peter R.

2000

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Segregation Analysis in Shwachman-Diamond Syndrome: Evidence for Recessive Inheritance

American journal of human genetics, 2000-04, Vol.66 (4), p.1413-1416

2000

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WS14.6 Beta-adrenergic sweat secretion rate as accurate biomarker for CFTR function

Journal of cystic fibrosis, 2012-06, Vol.11, p.S32-S32

2012

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Diagnosis and management of pancreatic exocrine insufficiency (PEI) in primary care: consensus guidance of a Canadian expert panel

Pathogenesis of malnutrition in cystic fibrosis, and its treatment

Do common in silico tools predict the clinical consequences of amino-acid substitutions in the CFTR gene?

Outcomes of patients with cystic fibrosis undergoing lung transplantation with and without cystic fibrosis-associated liver cirrhosis

Simultaneous liver–pancreas transplantation for cystic fibrosis-related liver disease: A multicenter experience

Molecular consequences of cystic fibrosis transmembrane regulator (CFTR) gene mutations in the exocrine pancreas

Shwachman syndrome: Phenotypic manifestations of sibling sets and isolated cases in a large patient cohort are similar

High-Dose Pancreatic-Enzyme Supplements and Fibrosing Colonopathy in Children with Cystic Fibrosis

Sweat gland bioelectrics differ in cystic fibrosis: a new concept for potential diagnosis and assessment of CFTR function in cystic fibrosis

Shwachman syndrome: Exocrine pancreatic dysfunction and variable phenotypic expression

Cystic fibrosis modifier genes related to Pseudomonas aeruginosa infection

Skeletal phenotype in patients with Shwachman-Diamond syndrome and mutations in SBDS

Pancreatitis and Mutations of the Cystic Fibrosis Gene

Patterns of GI disease in adulthood associated with mutations in the CFTR gene

Inconclusive diagnosis of cystic fibrosis after newborn screening

Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutations

Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13

Understanding the population structure of North American patients with cystic fibrosis

188 DO CHILDREN WITH END STAGE CF-RELATED LIVER DISEASE BENEFIT FROM COMBINED LIVER-PANCREAS TRANSPLANT?

Does the Macroduct ® collection system reliably define sweat chloride concentration in subjects with intermediate results?

WS1.2 Rate of decline in serum trypsinogen as a validation for the PIP score

Draft consensus guidelines for diagnosis and treatment of Shwachman-Diamond syndrome

PANCREATIC ASPECTS OF CYSTIC FIBROSIS AND OTHER INHERITED CAUSES OF PANCREATIC DYSFUNCTION

Segregation Analysis in Shwachman-Diamond Syndrome: Evidence for Recessive Inheritance

WS14.6 Beta-adrenergic sweat secretion rate as accurate biomarker for CFTR function

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