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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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Seasonality at the clinical onset of type 1 diabetes—Lessons from the SWEET database

Pediatric diabetes, 2016-10, Vol.17, p.32-37

2016

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Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblings

The Journal of clinical investigation, 2001-12, Vol.108 (11), p.1705-1715

2001

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Revisiting infant growth prior to childhood onset type 1 diabetes

Clinical endocrinology (Oxford), 2010-05, Vol.72 (5), p.620-624

2010

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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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De virtuele diabeteskliniek in een stroomversnelling?

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

2020

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A Cystic Fibrosis Mutation Associated with Mild Lung Disease

The New England journal of medicine, 1995-07, Vol.333 (2), p.95-99

1995

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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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Determinants of mild clinical symptoms in cystic fibrosis patients : residual chloride secretion measured in rectal biopsies in relation to the genotype

The Journal of clinical investigation, 1994-02, Vol.93 (2), p.461-466

1994

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Decreased excitability of the distal motor nerve of young patients with type 1 diabetes mellitus

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

2013

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Clinical use of acid steatocrit

Acta Paediatrica, 1997-05, Vol.86 (5), p.466-469

1997

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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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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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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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Heterogeneity in the systems of pediatric diabetes care across the European Union

Pediatric diabetes, 2012-09, Vol.13 (s16), p.5-14

2012

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

Seasonality at the clinical onset of type 1 diabetes—Lessons from the SWEET database

Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblings

Revisiting infant growth prior to childhood onset type 1 diabetes

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

De virtuele diabeteskliniek in een stroomversnelling?

A Cystic Fibrosis Mutation Associated with Mild Lung Disease

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

Determinants of mild clinical symptoms in cystic fibrosis patients : residual chloride secretion measured in rectal biopsies in relation to the genotype

Decreased excitability of the distal motor nerve of young patients with type 1 diabetes mellitus

Clinical use of acid steatocrit

Clinical presentation of exclusive cystic fibrosis lung disease

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

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

Heterogeneity in the systems of pediatric diabetes care across the European Union

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

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