ABSENT AND DEFECTIVE IODOTYROSINE DEIODINATION IN A FAMILY SOME OF WHOSE MEMBERS ARE GOITROUS CRETINS
- 23 January 1965
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 285 (7378), 183-185
- https://doi.org/10.1016/s0140-6736(65)90971-2
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- THE SYNDROME OF CONGENITAL HYPOTHYROIDISM WITH DEFECTIVE DEHALOGENATION OF IODOTYROSINES. FURTHER OBSERVATIONS AND A DISCUSSION OF THE PATHOPHYSIOLOGYJournal of Clinical Endocrinology & Metabolism, 1960
- Goitre and Cretinism Due to the Production of an Abnormal Iodinated Thyroid CompoundScottish Medical Journal, 1960
- SPORADIC GOITROUS CRETINISMThe Lancet, 1959
- Impaired Dehalogenase Activity as a Cause of Goitre with Malignant ChangesScottish Medical Journal, 1959
- CONGENITAL DEFECTS IN THE BIOSYNTHESIS OF THYROID HORMONEPediatrics, 1958
- SPORADIC NON-ENDEMIC GOITROUS CRETINISM: IDENTIFICATION AND SIGNIFICANCE OF MONOIODOTYROSINE AND DIIODOTYROSINE IN SERUM AND URINEThe Lancet, 1956
- THE METABOLISM OF IODOTYROSINES. II THE METABOLISM OF MONO- AND DI-IODOTYROSINE II CERTAIN PATIENTS WITH FAMILIAL GOITER*Journal of Clinical Endocrinology & Metabolism, 1956
- SPORADIC NON-ENDEMIC GOITROUS CRETINISM: HEREDITARY TRANSMISSIONThe Lancet, 1956
- THE OCCURRENCE OF MONO- AND DI-IODOTYROSINE IN THE BLOOD OF A PATIENT WITH CONGENITAL GOITER*Journal of Clinical Endocrinology & Metabolism, 1955
- RADIOACTIVE-IODINE STUDIES IN NON-ENDEMIC GOITROUS CRETINISMThe Lancet, 1953