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Publications by J Dissing

HLA and Hormonal Studies in Families of Patients With 21-Hydroxylase Deficiency - Cryptic Patients?

Pediatric Research

English

Related publications

21-Hydroxylase Deficiency Families With HLA Identical Affected and Unaffected Sibs.

Journal of Medical Genetics

English

Analysis of Steroid 21-Hydroxylase Gene in Five Unrelated Japanese Patients With 21-Hydroxylase Deficiency

Endocrinologia Japonica

English

HLA Class I-, Complement C4- And 21-Hydroxylase Probes in the Genetic Analysis of 21-Hydroxylase Deficiency

Clinical Chemistry and Laboratory Medicine

Clinical Biochemistry

English

Clinical Course of Patients With Nonclassical 21-Hydroxylase Deficiency (21-Ohd) Diagnosed in Infancy and Childhood

Endocrine Journal

English

Genetic Analysis of Two Japanese Patients With Non-Classical 21-Hydroxylase Deficiency

Internal Medicine

Internal Medicine

English

Tetrahydrobiopterin Responsiveness of Patients With Phenylalanine Hydroxylase Deficiency

Jornal de Pediatria

English

Genotype-Phenotype Correlation in 1,507 Families With Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

English

Molecular Pathology of 21-Hydroxylase Deficiency

Pediatric Research

English

Cathepsin a Deficiency in Galactosialidosis: Studies of Patients and Carriers in 16 Families

Pediatric Research

English