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The complex relationships between cystic fibrosis and congenital bilateral absence of the vas deferens: clinical, electrophysiological and genetic data

Human reproduction (Oxford), 1999-02, Vol.14 (2), p.371-374

1999

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Cystic-fibrosis-like disease unrelated to the cystic fibrosis transmembrane conductance regulator

Human genetics, 1998-05, Vol.102 (5), p.582-586

1998

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Ion transport abnormalities in rectal suction biopsies from children with cystic fibrosis

Gastroenterology (New York, N.Y. 1943), 1991-08, Vol.101 (2), p.398-403

1991

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Residual chloride secretion in intestinal tissue of ΔF508 homozygous twins and siblings with cystic fibrosis

Gastroenterology (New York, N.Y. 1943), 2000-07, Vol.119 (1), p.32-40

2000

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Diagnosis of cystic fibrosis

Netherlands journal of medicine, 1995-06, Vol.46 (6), p.271

Veeze, H J

1995

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Cystic fibrosis: genetics and intestinal secretion

Netherlands journal of medicine, 1992-10, Vol.41 (3-4), p.115

Veeze, H J

1992

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Identification of the L927P and ΔL1260 mutations in the CFTR gene

Human molecular genetics, 1994-07, Vol.3 (7), p.1199-1200

1994

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New Insights into the Pathogenesis of Cystic Fibrosis

Scandinavian journal of gastroenterology, 1990, Vol.25 (S178), p.17-25

1990

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The CLCA gene locus as a modulator of the gastrointestinal basic defect in cystic fibrosis

Human genetics, 2004-11, Vol.115 (6), p.483-491

2004

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In vivo electrophysiologic evaluation of intestinal grafts in dogs

Transplantation proceedings, 1990-12, Vol.22 (6), p.2449-2450

1990

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The mutation delta F508 on Dutch cystic fibrosis chromosomes: frequency and relation to patients age at diagnosis

Human genetics, 1990-09, Vol.85 (4), p.407-408

1990

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Anticipated Costs of Hospitalization for Respiratory Syncytial Virus Infection in Young Children at Risk

The Pediatric infectious disease journal, 2004-06, Vol.23 (6), p.523-529

2004

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Residual chloride secretion in intestinal tissue of deltaF508 homozygous twins and siblings with cystic fibrosis. The European CF Twin and Sibling Study Consortium

Gastroenterology (New York, N.Y. 1943), 2000-07, Vol.119 (1), p.32-40

2000

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PIN21 HOSPITALISATION COSTS FOR YOUNG CHILDREN WITH RESPIRATORY SYNCYTIAL VIRUS INFECTION

Value in health, 2002-11, Vol.5 (6), p.569-570

2002

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The SWEET Project 10-Year Benchmarking in 19 Countries Worldwide Is Associated with Improved HbA1c and Increased Use of Diabetes Technology in Youth with Type 1 Diabetes

Diabetes technology & therapeutics, 2021-07, Vol.23 (7), p.491

2021

Volltextzugriff (PDF)

Overweight children with type 1 diabetes have a more favourable lipid profile than overweight non-diabetic children

European journal of pediatrics, 2012-03, Vol.171 (3), p.493-498

2012

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The role of radiotherapy in the treatment of bile duct carcinoma

International journal of radiation oncology, biology, physics, 1990, Vol.18 (1), p.63-67

1990

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44 CLINICAL USE OF ACID STEATOCRIT

Journal of pediatric gastroenterology and nutrition, 1995-05, Vol.20 (4), p.456

1995

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44 CLINICAL USE OF ACID STEATOCRIT

Journal of pediatric gastroenterology and nutrition, 1995-05, Vol.20 (4), p.456-456

1995

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The complex relationships between cystic fibrosis and congenital bilateral absence of the vas deferens: clinical, electrophysiological and genetic data

Cystic-fibrosis-like disease unrelated to the cystic fibrosis transmembrane conductance regulator

Ion transport abnormalities in rectal suction biopsies from children with cystic fibrosis

Residual chloride secretion in intestinal tissue of ΔF508 homozygous twins and siblings with cystic fibrosis

Diagnosis of cystic fibrosis

Cystic fibrosis: genetics and intestinal secretion

Identification of the L927P and ΔL1260 mutations in the CFTR gene

New Insights into the Pathogenesis of Cystic Fibrosis

The CLCA gene locus as a modulator of the gastrointestinal basic defect in cystic fibrosis

In vivo electrophysiologic evaluation of intestinal grafts in dogs

The mutation delta F508 on Dutch cystic fibrosis chromosomes: frequency and relation to patients age at diagnosis

Anticipated Costs of Hospitalization for Respiratory Syncytial Virus Infection in Young Children at Risk

Residual chloride secretion in intestinal tissue of deltaF508 homozygous twins and siblings with cystic fibrosis. The European CF Twin and Sibling Study Consortium

PIN21 HOSPITALISATION COSTS FOR YOUNG CHILDREN WITH RESPIRATORY SYNCYTIAL VIRUS INFECTION

The SWEET Project 10-Year Benchmarking in 19 Countries Worldwide Is Associated with Improved HbA1c and Increased Use of Diabetes Technology in Youth with Type 1 Diabetes

Overweight children with type 1 diabetes have a more favourable lipid profile than overweight non-diabetic children

The role of radiotherapy in the treatment of bile duct carcinoma

44 CLINICAL USE OF ACID STEATOCRIT

44 CLINICAL USE OF ACID STEATOCRIT

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