The Constitutional Factor in Thyroid Disease [Abridged]

Overview

Journal Proc R Soc Med

Specialty General Medicine

Date 2009 Dec 9

PMID 19994079

Citations 6

Authors

J B Stanbury

Affiliations

Soon will be listed here.

Citing Articles

ANNOTATIONS.

Br Med J. 2010; 1(5272):167-8.

PMID: 20789322 PMC: 1957364.

Heredity in common diseases. A retrospective survey of twins in a hospital population.

G Marshall A, HUTCHINSON E, HONISETT J Br Med J. 1962; 1(5270):1-6.

PMID: 14470235 PMC: 1959281. DOI: 10.1136/bmj.1.5270.1.

ENDEMIC GOITRE IN GREECE: FAMILY STUDIES.

HADJIDAKIS S, Koutras D, Daikos G J Med Genet. 1964; 1(2):82-7.

PMID: 14234110 PMC: 1012752. DOI: 10.1136/jmg.1.2.82.

TERMINAL HYPERKALEMIA.

Chandra R Indian J Pediatr. 1963; 30:304-5.

PMID: 14058300 DOI: 10.1007/BF02802468.

Hereditary thyroid dysgenesis. Report of a case with masked symptoms.

BOWMAN K, Gould M Calif Med. 1963; 98:37-9.

PMID: 14014648 PMC: 1575565.

References

FLOYD Jr J, BEIERWALTES W, DODSON V, CARR Jr E . Defective iodination of tyrosine a cause of nodular goiter?. J Clin Endocrinol Metab. 1960; 20:881-8. DOI: 10.1210/jcem-20-6-881. View

HADDAD H, SIDBURY Jr J . Defect of the iodinating system in congenital goitrous cretinism: report of a case with biochemical studies. J Clin Endocrinol Metab. 1959; 19:1446-57. DOI: 10.1210/jcem-19-11-1446. View

Stanbury J, HEDGE A . A study of a family of goitrous cretins. J Clin Endocrinol Metab. 1950; 10(11):1471-84. DOI: 10.1210/jcem-10-11-1471. View

TROTTER W . The association of deafness with thyroid dysfunction. Br Med Bull. 1960; 16:92-8. DOI: 10.1093/oxfordjournals.bmb.a069828. View

Stanbury J, Meijer J, KASSENAAR A . The metabolism of iodotyrosines. II. The metabolism of mono- and diiodotyrosine in certain patients with familial goiter. J Clin Endocrinol Metab. 1956; 16(7):848-68. DOI: 10.1210/jcem-16-7-848. View