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Presence of cystic fibrosis-related diabetes mellitus is tightly linked to poor lung function in patients with cystic fibrosis: Data from the European Epidemiologic Registry of Cystic Fibrosis

Pediatric pulmonology, 2001-11, Vol.32 (5), p.343-350

2001

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Does Optimal Egg Size Vary with Demographic Stage Because of a Physiological Constraint?

Functional ecology, 2004-08, Vol.18 (4), p.522-529

2004

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Allergic bronchopulmonary aspergillosis in cystic fibrosis. A European epidemiological study

The European respiratory journal, 2000-09, Vol.16 (3), p.464-471

2000

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Factors associated with poor pulmonary function: cross-sectional analysis of data from the ERCF

The European respiratory journal, 2001-08, Vol.18 (2), p.298-305

2001

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Diversity of the basic defect of homozygous CFTR mutation genotypes in humans

Journal of medical genetics, 2008-01, Vol.45 (1), p.47-54

2008

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European Epidemiologic Registry of Cystic Fibrosis (ERCF): Comparison of major disease manifestations between patients with different classes of mutations

Pediatric pulmonology, 2001-01, Vol.31 (1), p.1-12

2001

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Dornase alfa in the treatment of cystic fibrosis in Europe: A report from the Epidemiologic Registry of Cystic Fibrosis

Pediatric pulmonology, 2003-11, Vol.36 (5), p.427-432

2003

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Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy

The Journal of clinical investigation, 1998-04, Vol.101 (7), p.1414-1420

1998

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Adenovirus infection in cystic fibrosis patients : implications for the use of adenoviral vectors for gene transfer

Infection, 1996, Vol.24 (1), p.5-8

1996

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Allergic bronchopulmonary aspergillosis in cystic fibrosis

The European respiratory journal, 2001-05, Vol.17 (5), p.1052-1053

2001

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Age and season impact resource allocation to eggs and nesting behavior in the painted turtle

Physiological and biochemical zoology, 2005-11, Vol.78 (6), p.996-1004

2005

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Oral mannose therapy persistently corrects the severe clinical symptoms and biochemical abnormalities of phosphomannose isomerase deficiency

Acta Paediatrica, 2002-10, Vol.91 (10), p.1065-1072

2002

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Mycoserological study of the treatment of paediatric cystic fibrosis patients with Saccharomyces boulardii (Saccharomyces cerevisiae Hansen CBS 5926)

Mycoses, 1995-03, Vol.38 (3-4), p.119-123

1995

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Geographic distribution and origin of CFTR mutations in Germany

Human genetics, 1996-06, Vol.97 (6), p.727-731

1996

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Correlation of IgE antibody titer to Aspergillus fumigatus with decreased lung function in cystic fibrosis

Pediatric pulmonology, 1990, Vol.8 (1), p.12-15

1990

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Enzyme-substitution therapy with the yeast Saccharomyces cerevisiae in congenital sucrase-isomaltase deficiency

The New England journal of medicine, 1987-05, Vol.316 (21), p.1306-1309

1987

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Genetic determination of diabetes mellitus in patients with cystic fibrosis

The Journal of pediatrics, 1995, Vol.127 (3), p.441-443

1995

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Biliary atresia: which factors predict the success of a Kasai operation? An analysis of 36 patients

European journal of medical research, 2000-03, Vol.5 (3), p.110-114

2000

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EARLY ALLOGRAFT REJECTION IN CHILDREN AFTER LIVER TRANSPLANTATION IS ASSOCIATED WITH PERIPHERAL AND GRAFT EOSINOPHILIA

Journal of pediatric gastroenterology and nutrition, 1999-05, Vol.28 (5), p.582-582

1999

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Zystische Fibrose und Zöliakie : Zwei Fallbeschreibungen

Monatsschrift Kinderheilkunde, 1990, Vol.138 (9), p.623-626

1990

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A reliable screening test for childhood celiac disease: fluorescent immunosorbent test for gliadin antibodies. A prospective multicenter study

The Journal of pediatrics, 1983-05, Vol.102 (5), p.655-660

1983

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Allergic bronchopulmonary aspergillosis in cystic fibrosis. A European epidemiological study. Epidemiologic Registry of Cystic Fibrosis

The European respiratory journal, 2000-09, Vol.16 (3), p.464-471

2000

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Calcium metabolism and cystic fibrosis: mitochondrial abnormalities suggest a modification of the mitochondrial membrane

Pediatric research, 1984-07, Vol.18 (7), p.594-599

1984

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Renal function and renotropic effects of secretin in cystic fibrosis

European journal of medical research, 1997-10, Vol.2 (10), p.431-436

1997

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Cow's milk protein sensitive enteropathy

Klinische Pädiatrie, 1982-11, Vol.194 (6), p.375-380

Harms, H K

1982

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Presence of cystic fibrosis-related diabetes mellitus is tightly linked to poor lung function in patients with cystic fibrosis: Data from the European Epidemiologic Registry of Cystic Fibrosis

Does Optimal Egg Size Vary with Demographic Stage Because of a Physiological Constraint?

Allergic bronchopulmonary aspergillosis in cystic fibrosis. A European epidemiological study

Factors associated with poor pulmonary function: cross-sectional analysis of data from the ERCF

Diversity of the basic defect of homozygous CFTR mutation genotypes in humans

European Epidemiologic Registry of Cystic Fibrosis (ERCF): Comparison of major disease manifestations between patients with different classes of mutations

Dornase alfa in the treatment of cystic fibrosis in Europe: A report from the Epidemiologic Registry of Cystic Fibrosis

Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy

Adenovirus infection in cystic fibrosis patients : implications for the use of adenoviral vectors for gene transfer

Allergic bronchopulmonary aspergillosis in cystic fibrosis

Age and season impact resource allocation to eggs and nesting behavior in the painted turtle

Oral mannose therapy persistently corrects the severe clinical symptoms and biochemical abnormalities of phosphomannose isomerase deficiency

Mycoserological study of the treatment of paediatric cystic fibrosis patients with Saccharomyces boulardii (Saccharomyces cerevisiae Hansen CBS 5926)

Geographic distribution and origin of CFTR mutations in Germany

Correlation of IgE antibody titer to Aspergillus fumigatus with decreased lung function in cystic fibrosis

Enzyme-substitution therapy with the yeast Saccharomyces cerevisiae in congenital sucrase-isomaltase deficiency

Genetic determination of diabetes mellitus in patients with cystic fibrosis

Biliary atresia: which factors predict the success of a Kasai operation? An analysis of 36 patients

EARLY ALLOGRAFT REJECTION IN CHILDREN AFTER LIVER TRANSPLANTATION IS ASSOCIATED WITH PERIPHERAL AND GRAFT EOSINOPHILIA

Zystische Fibrose und Zöliakie : Zwei Fallbeschreibungen

A reliable screening test for childhood celiac disease: fluorescent immunosorbent test for gliadin antibodies. A prospective multicenter study

Allergic bronchopulmonary aspergillosis in cystic fibrosis. A European epidemiological study. Epidemiologic Registry of Cystic Fibrosis

Calcium metabolism and cystic fibrosis: mitochondrial abnormalities suggest a modification of the mitochondrial membrane

Renal function and renotropic effects of secretin in cystic fibrosis

Cow's milk protein sensitive enteropathy

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