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3. Iodine metabolism in endemic goitre in countries of the Middle East. II. Dyshormonogenetic goitre: a study of 46 cases. Abdel-Wahab MF; Ibrahim MS; Khalifa S; Megahed YM Radiobiol Radiother (Berl); 1967; 8(4):463-70. PubMed ID: 5603951 [No Abstract] [Full Text] [Related]
4. Abnormal metabolism of thiourea-S 35 in Pendred's syndrome. Ibrahim MS; Abdel-Wahab MF; Megahed YM Endokrinologie; 1966 Dec; 50(5):286-90. PubMed ID: 5991064 [No Abstract] [Full Text] [Related]
5. [Thyroid hormonosynthesis disorders due to iodotyrosine-dehalogenase deficiency. Value of the D.I.T. test for the detection of heterozygotes]. Rochiccioli P; Dutau G Arch Fr Pediatr; 1974 Jan; 31(1):25-36. PubMed ID: 4135480 [No Abstract] [Full Text] [Related]
6. Endemic goiter with hypothyroidism in three generations. Stanbury JB; Fierro-Benitez R; Estrella E; Milutinovic PS; Tellez MU; Refetoff S J Clin Endocrinol Metab; 1969 Dec; 29(12):1596-600. PubMed ID: 5347689 [No Abstract] [Full Text] [Related]
7. [A study of 2 congenital hypothyroid goiters in siblings: identification of a genetic abnormality in thyroid hormonogenesis marked by the absence of thyroglobulin and by the iodination of unsuitable proteins rich in iodohistidine and deficient in thyroxine]. Savoie JC; Massin JP; Sizonenko PC; Job JC Ann Endocrinol (Paris); 1973; 34(5):539-48. PubMed ID: 4136284 [No Abstract] [Full Text] [Related]
8. Iodine kinetics in organification defect. Negri M; De Luca F; Cramarossa L; Benedetti GA Folia Endocrinol; 1967 Apr; 20(2):205-13. PubMed ID: 4169478 [No Abstract] [Full Text] [Related]
10. [Study of a family with goiter caused by an iodine organification defect]. Limbert E; Botelho L; Sobrinho L Arq Patol; 1972 Aug; 44(2):139-46. PubMed ID: 4641690 [No Abstract] [Full Text] [Related]
12. Relationship between the serum thyrotropin level, the prevalence of goiter and the pattern of iodine metabolism in Idjwi Island. Delange F; Hershman JM; Ermans AM J Clin Endocrinol Metab; 1971 Aug; 33(2):261-8. PubMed ID: 4105239 [No Abstract] [Full Text] [Related]
13. [Clinical and chromosomal studies in a congenital hypothyroidism caused by thyroxin synthesis disorders and middle ear hearing disorders (Pendred- or goiter-deafness syndrome)]. Kitlak W; Gebert P Arch Kinderheilkd; 1968; 177(2):170-83. PubMed ID: 5723894 [No Abstract] [Full Text] [Related]
14. Biochemical and clinical studies in familial goitre caused by an iodotyrosine deiodinase defect. Niall HD; Wellby ML; Hetzel BS; Hudson B; Chenoweth RA Australas Ann Med; 1968 May; 17(2):89-95. PubMed ID: 4299848 [No Abstract] [Full Text] [Related]
15. [Congenital hypothyroidism with goiter caused by altered structure of thyroid iodoproteins]. Tangheroni W; Cao A Folia Endocrinol; 1967 Jun; 20(3):261-75. PubMed ID: 5630798 [No Abstract] [Full Text] [Related]
16. [Physiological significance of iodotyrosine-deiodinases]. Voss C; Hartmann N Z Gesamte Inn Med; 1972 Mar; 27(5):193-7. PubMed ID: 4558910 [No Abstract] [Full Text] [Related]
17. Defective iodide organification in "cryptothyroidism". Smith JD; Cagas CR; Seely JR; Neeman J J Okla State Med Assoc; 1970 May; 63(5):195-9. PubMed ID: 5511591 [No Abstract] [Full Text] [Related]
18. [Pendred's syndrome: a clinical and biochemical study of abnormal thyroid hormone synthesis associated with congenital deaf-mutism]. de Medeiros-Netto GA; Nicolau W; Cintra AB Rev Paul Med; 1969 Feb; 74(2):53-74. PubMed ID: 4190511 [No Abstract] [Full Text] [Related]
19. Familial isolated thyrotropin deficiency with cretinism. Miyai K; Azukizawa M; Kumahara Y N Engl J Med; 1971 Nov; 285(19):1043-8. PubMed ID: 4106196 [No Abstract] [Full Text] [Related]
20. [Radioiodine diagnosis of hypothyroidism in childhood]. Struwe FE; Kempe H Monatsschr Kinderheilkd (1902); 1970 Jun; 118(6):217-20. PubMed ID: 5523639 [No Abstract] [Full Text] [Related] [Next] [New Search]