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Routine use of continuous glucose monitoring in 10 501 people with diabetes mellitus

Diabetic medicine, 2015-12, Vol.32 (12), p.1568-1574

2015

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De virtuele diabeteskliniek in een stroomversnelling?

Nederlands Tijdschrift voor Diabetolog, 2020-01, Vol.18 (2), p.16-26

2020

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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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Clinical presentation of exclusive cystic fibrosis lung disease

Thorax, 1999-03, Vol.54 (3), p.278-281

1999

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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.271-274

Veeze, H J

1995

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Genetic correlates of early accelerated infant growth associated with juvenile-onset type 1 diabetes

Pediatric diabetes, 2012-05, Vol.13 (3), p.266-271

2012

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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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Zes vragen over zorgvernieuwing in diabeteszorg: het value-based healthcare-model in de praktijk

Nederlands Tijdschrift voor Diabetolog, 2017, Vol.15 (2), p.36-42

2017

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Passive immunisation against respiratory syncytial virus: a cost-effectiveness analysis

Archives of disease in childhood, 2010-07, Vol.95 (7), p.493-498

2010

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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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Value of in vivo electrophysiological measurements to evaluate canine small bowel autotransplants

Gut, 1991-11, Vol.32 (11), p.1329-1335

1991

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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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Decreased excitability of the distal motor nerve of young patients with type 1 diabetes mellitus: Subclinical peripheral neuropathy

Pediatric diabetes, 2013-11, Vol.14 (7), p.519-525

2013

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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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Terapia antigenica con GAD65 nel diabete mellito di tipo 1 di recente diagnosi

L'Endocrinologo, 2012-04, Vol.13 (2), p.89-90

2012

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From gene to disease; from defective chloride ion transport to cystic fibrosis

Nederlands tijdschrift voor geneeskunde, 2001-04, Vol.145 (14), p.686

2001

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Complicatieregistratie in de kindergeneeskundige praktijk

Tijdschrift voor kindergeneeskunde, 2006-06, Vol.74 (3), p.128-136

2006

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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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CHLORIDE SECRETION PATTERNS IN RECTAL EPITHELIUM OF CYSTIC FIBROSIS (CF) PATIENTS AND ITS RELATION TO THE δ F508 MUTATION

Pediatric research, 1990-05, Vol.27 (5), p.532-532

1990

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ROLE OF A NOVEL GTP-SENSITIVE APICAL CHLORIDE CHANNEL IN CHOLERATOXIN- AND CYCLIC AMP-PROVOKED INTESTINAL CI' SECRETION AND ITS RELEVANCE IN CYSTIC FIBROSIS

Pediatric research, 1990-05, Vol.27 (5), p.538-538

1990

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1152-P: Achieving Diabetic Management Targets in People with Type 1 Diabetes

Diabetes (New York, N.Y.), 2022-06, Vol.71 (Supplement_1)

2022

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Routine use of continuous glucose monitoring in 10 501 people with diabetes mellitus

De virtuele diabeteskliniek in een stroomversnelling?

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

Clinical presentation of exclusive cystic fibrosis lung disease

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

Diagnosis of cystic fibrosis

Genetic correlates of early accelerated infant growth associated with juvenile-onset type 1 diabetes

Cystic fibrosis: genetics and intestinal secretion

Zes vragen over zorgvernieuwing in diabeteszorg: het value-based healthcare-model in de praktijk

Passive immunisation against respiratory syncytial virus: a cost-effectiveness analysis

Identification of the L927P and ΔL1260 mutations in the CFTR gene

Value of in vivo electrophysiological measurements to evaluate canine small bowel autotransplants

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

Decreased excitability of the distal motor nerve of young patients with type 1 diabetes mellitus: Subclinical peripheral neuropathy

Anticipated costs of hospitalization for respiratory syncytial virus infection in young children at risk

Terapia antigenica con GAD65 nel diabete mellito di tipo 1 di recente diagnosi

From gene to disease; from defective chloride ion transport to cystic fibrosis

Complicatieregistratie in de kindergeneeskundige praktijk

PIN21 HOSPITALISATION COSTS FOR YOUNG CHILDREN WITH RESPIRATORY SYNCYTIAL VIRUS INFECTION

CHLORIDE SECRETION PATTERNS IN RECTAL EPITHELIUM OF CYSTIC FIBROSIS (CF) PATIENTS AND ITS RELATION TO THE δ F508 MUTATION

ROLE OF A NOVEL GTP-SENSITIVE APICAL CHLORIDE CHANNEL IN CHOLERATOXIN- AND CYCLIC AMP-PROVOKED INTESTINAL CI' SECRETION AND ITS RELEVANCE IN CYSTIC FIBROSIS

1152-P: Achieving Diabetic Management Targets in People with Type 1 Diabetes

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