H. Landau

Vitamin D-dependent rickets types I and II. Diagnosis and response to therapy.

J. Silver, M. Friedlaender, D. Rubinger, 1985, Israel journal of medical sciences.

Clinical variability of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency.

J. Sack, A. Rösler, T. Cohen, 1983, Hormone research.

Male pseudohermaphroditism due to 17 beta-hydroxysteroid dehydrogenase deficiency: gender reassignment in early infancy.

A. Rösler, G. Kohn, D. Gross, 1986, Acta endocrinologica.

Clinical Variability of Congenital Adrenal Hyperplasia Due to 11 β-Hydroxylase Deficiency

J. Sack, A. Rösler, T. Cohen, 1983 .

Amniotic fluid 3,3',5'-triiodothyronine in the detection of congenital hypothyroidism.

J. Sack, H. Frucht, D. Hochner-Celnikier, 1980, The Journal of clinical endocrinology and metabolism.

No linkage between HLA and congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency.

J. Sack, M. New, B. Dupont, 1979, The New England journal of medicine.

Detection of albumin binding abnormalities in sera of patients with familial dysalbuminaemic hyperthyroxinaemia using isoelectric focusing.

R. Reifen, I. Flechner, G. Aranoff, 1992, Endocrine research.