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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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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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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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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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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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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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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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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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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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Uncertainty in the diagnosis of cystic fibrosis: Possible role of in vivo nasal potential difference measurements

The Journal of pediatrics, 1998-04, Vol.132 (4), p.596-599

1998

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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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Vitamin K and the management of patients with cystic fibrosis

Canadian Medical Association journal, 1994-10, Vol.151 (7), p.933

Durie, P. R

1994

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Management of fibrosing pancreatitis in children presenting with obstructive jaundice

Gut, 1998-11, Vol.43 (5), p.715-720

1998

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Longitudinal evaluation of serum trypsinogen measurement in pancreatic-insufficient and pancreatic-sufficient patients with cystic fibrosis

The Journal of pediatrics, 1995-09, Vol.127 (3), p.408-413

1995

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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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Challenges in the dietary treatment of cystic fibrosis related diabetes mellitus

Clinical Nutrition, 2000-04, Vol.19 (2), p.87-93

2000

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Nutritional management of cystic fibrosis

Annual review of nutrition, 1993-01, Vol.13 (1), p.111-136

1993

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Inconclusive diagnosis of cystic fibrosis after newborn screening

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

2015

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Dietary intakes of young children with cystic fibrosis: Is there a difference?

Journal of pediatric gastroenterology and nutrition, 1996-04, Vol.22 (3), p.254-258

1996

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Shwachman-Diamond Syndrome with Exocrine Pancreatic Dysfunction and Bone Marrow Failure Maps to the Centromeric Region of Chromosome 7

American journal of human genetics, 2001-04, Vol.68 (4), p.1048-1054

2001

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The cystic fibrosis gene and resting energy expenditure

The Journal of pediatrics, 1991-12, Vol.119 (6), p.913-916

1991

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Microvillus Inclusion Disease: An Inherited Defect of Brush-Border Assembly and Differentiation

The New England journal of medicine, 1989-03, Vol.320 (10), p.646-651

1989

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Analysis of Cystic Fibrosis Gener Product (CFTR) Function in Patients with Pancreas Divisum and Recurrent Acute Pancreatitis

The American journal of gastroenterology, 2004-08, Vol.99 (8), p.1557-1562

2004

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Guidelines for Diagnosis of Cystic Fibrosis in Newborns through Older Adults: Cystic Fibrosis Foundation Consensus Report

The Journal of pediatrics, 2008-08, Vol.153 (2), p.S4-S14

2008

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Pathogenesis of malnutrition in cystic fibrosis, and its treatment

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

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

Shwachman syndrome: Exocrine pancreatic dysfunction and variable phenotypic expression

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

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

Pancreatitis and Mutations of the Cystic Fibrosis Gene

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

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

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

Uncertainty in the diagnosis of cystic fibrosis: Possible role of in vivo nasal potential difference measurements

Cystic fibrosis modifier genes related to Pseudomonas aeruginosa infection

Vitamin K and the management of patients with cystic fibrosis

Management of fibrosing pancreatitis in children presenting with obstructive jaundice

Longitudinal evaluation of serum trypsinogen measurement in pancreatic-insufficient and pancreatic-sufficient patients with cystic fibrosis

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

Challenges in the dietary treatment of cystic fibrosis related diabetes mellitus

Nutritional management of cystic fibrosis

Inconclusive diagnosis of cystic fibrosis after newborn screening

Dietary intakes of young children with cystic fibrosis: Is there a difference?

Shwachman-Diamond Syndrome with Exocrine Pancreatic Dysfunction and Bone Marrow Failure Maps to the Centromeric Region of Chromosome 7

The cystic fibrosis gene and resting energy expenditure

Microvillus Inclusion Disease: An Inherited Defect of Brush-Border Assembly and Differentiation

Analysis of Cystic Fibrosis Gener Product (CFTR) Function in Patients with Pancreas Divisum and Recurrent Acute Pancreatitis

Guidelines for Diagnosis of Cystic Fibrosis in Newborns through Older Adults: Cystic Fibrosis Foundation Consensus Report

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