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Leo A.H. Monnens
Title:
PhD
Email:
Organization:
University Hospital Nijmegen
Department:
Dept. of Pediatrics
Address:
P.O. Box 9101
Nijmegen 6500 HB,
Netherlands
23 Articles
23 Articles
Clinical Presentation and Follow-Up of 30 Patients with Congenital Nephrogenic Diabetes Insipidus
New Mutations in the AQP2 Gene in Nephrogenic Diabetes Insipidus Resulting in Functional but Misrouted Water Channels
Physiology and Pathophysiology of Aquaporins
Cognitive and Psychosocial Functioning of Patients with Congenital Nephrogenic Diabetes Insipidus
Aquaporins: From Physiology to Nephrogenic Diabetes Insipidus
Normal Fibrinolytic Responses to 1-Desamino-8-D-Arginine Vasopressin in Patients with Nephrogenic Diabetes Insipidus Caused by Mutations in the Aquaporin 2 Gene
Effects of Arginine Vasopressin and 1-Desamino-8-D Arginine Vasopressin on Forearm Vasculature of Healthy Subjects and Patients with a V2 Receptor Defect
Clinical Phenotype of Nephrogenic Diabetes Insipidus in Females Heterozygous for a Vasopressin Type 2 Receptor Mutation
Patients with Autosomal Nephrogenic Diabetes Insipidus Homozygous for Mutations in the Aquaporin 2 Water-Channel Gene
Inheritance of Mutations in the V2 Receptor Gene in Thirteen Families with Nephrogenic Diabetes Insipidus
Requirement of Human Renal Water Channel Aquaporin-2 for Vasopressin-Dependent Concentration of Urine
Nephrogenic Diabetes Insipidus: Identification of the Genetic Defect
Mutations in the Vasopressin Type 2 Receptor Gene (AVPR2) Associated with Nephrogenic Diabetes Insipidus
Nephrogenic Diabetes Insipidus: Clinical Symptoms, Pathogenesis, Genetics and Treatment
Colocalization of the Gene for Nephrogenic Diabetes Insipidus (DIR) and the Vasopressin Type 2 Receptor Gene (AVPR2) in the Xq28 Region
Evidence for Intact V1-vasopressin Receptors in Congenital Nephrogenic Diabetes Insipidus
A Variant of Nephrogenic Diabetes Insipidus: V
2
Receptor Abnormality Restricted to the Kidney
Amiloride-Hydrochlorothiazide Versus Indomethacin-Hydrochlorothiazide in the Treatment of Nephrogenic Diabetes Insipidus
Fibrinolytic Responses to 1-desamino-8-D-arginine-vasopressin in Patients with Congenital Nephrogenic Diabetes Insipidus
Three-point Linkage Analysis using Multiple DNA Polymorphic Markers in Families with X-linked Nephrogenic Diabetes Insipidus
Linkage Analyses in Families with Nephrogenic Diabetes Insipidus
Nephrogenic Diabetes Insipidus: Close Linkage with Markers from the Distal Long Arm of the Human X Chromosome
Linkage of X-linked Nephrogenic Diabetes Insipidus with DXS52, a Polymorphic DNA Marker
1 Conference Proceeding
1 Conference Proceeding
Nephrogenic Diabetes Insipidus in a Palestine Sibship
23 Articles
23 Articles