H. K. A. Visser

A NEW HEREDITARY DEFECT IN THE BIOSYNTHESIS OF ALDOSTERONE: URINARY C21-CORTICOSTEROID PATTERN IN THREE RELATED PATIENTS WITH A SALT-LOSING SYNDROME, SUGGESTING AN 18-OXIDATION DEFECT

H. K. A. Visser, W. S. Cost · European Journal of Endocrinology · 1964 · 97 citations

Adrenal Gland, Urology, Salt-losing Syndrome +13

EVIDENCE FOR DEFICIENT 20α-CHOLESTEROL-HYDROXYLASE ACTIVITY IN ADRENAL TISSUE OF A PATIENT WITH LIPOID ADRENAL HYPERPLASIA

H.J. Degenhart, H. K. A. Visser, Hanneke Boon · European Journal of Endocrinology · 1972 · 89 citations

Abstract Enzyme Preparations, Adrenal Gland, Normal Controls +9

Vitamin D Metabolism in Breast-Fed Infants and their Mothers

Theo Hoogenboezem, H.J. Degenhart, Sabine M.P.F. de Muinck Keizer‐Schrama et al. · Pediatric Research · 1989 · 70 citations · Full text

Nutrition, Lactation, Vitamin D Metabolism +11

Failure of lymphocyte-membrane HLA-A and -B expression in two siblings with combined immunodeficiency

Ruud K. B. Schuurman, J. J. van Rood, Jaak M. Vossen et al. · Clinical Immunology and Immunopathology · 1979 · 66 citations

Primary Immunodeficiency, Histocompatibility, Autoimmune Disease +15

ALDOSTERONE- AND CORTISOL SECRETION RATES IN INFANTS AND CHILDREN WITH CONGENITAL ADRENAL HYPERPLASIA SUGGESTING DIFFERENT 21-HYDROXYLATION DEFECTS IN »SALT-LOSERS« AND »NON SALT-LOSERS«

H.J. Degenhart, H. K. A. Visser, Rineke Wilmink et al. · European Journal of Endocrinology · 1965 · 42 citations

Human Growth, Education, Abstract Aldosterone- +18