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22. [Thyroidin in the treatment of nodular nontoxic goiter]. Kukharskaia EP Probl Endokrinol (Mosk); 1970; 16(1):15-9. PubMed ID: 5437224 [No Abstract] [Full Text] [Related]
23. Two novel mutations in the thyroid peroxidase gene with goitrous hypothyroidism. Tajima T; Tsubaki J; Fujieda K Endocr J; 2005 Oct; 52(5):643-5. PubMed ID: 16284446 [TBL] [Abstract][Full Text] [Related]
24. [Papillary carcinoma arising from dyshormonogenetic goiter]. Kallel R; Mnif Hachicha L; Mnif M; Hammami B; Ayadi L; Bahri I; Ghorbel A; Abid M; Makni S; Boudawara T Ann Endocrinol (Paris); 2009 Dec; 70(6):485-8. PubMed ID: 19880092 [TBL] [Abstract][Full Text] [Related]
25. Further studies on the recovery of thyroid function in non-endemic goitrous cretinism. ZONDEK H; LESZYNSKY HE; ZONDEK GW; STEIN JA; GUTTMANN S Br Med J; 1961 Jan; 1(5219):97-9. PubMed ID: 13788788 [No Abstract] [Full Text] [Related]
26. Endemic goiter and endemic cretinism in the Andean region. Fierro-Benítez R; Penafiel W; De Groot LJ; Ramirez I N Engl J Med; 1969 Feb; 280(6):296-302. PubMed ID: 5762371 [No Abstract] [Full Text] [Related]
27. Goitrous cretinism with chromosomal aberration and defect in thyroglobulin synthesis. Lizarralde G; Jones B; Seal US; Jones JE J Clin Endocrinol Metab; 1966 Nov; 26(11):1227-31. PubMed ID: 4162599 [No Abstract] [Full Text] [Related]
29. MANAGEMENT OF HYPOTHYROIDISM DURING INFANCY AND CHILDHOOD. FISHER DA Mod Treat; 1964 Jan; 1():128-45. PubMed ID: 14161707 [No Abstract] [Full Text] [Related]
31. Pseudodominant inheritance of goitrous congenital hypothyroidism caused by TPO mutations: molecular and in silico studies. Deladoëy J; Pfarr N; Vuissoz JM; Parma J; Vassart G; Biesterfeld S; Pohlenz J; Van Vliet G J Clin Endocrinol Metab; 2008 Feb; 93(2):627-33. PubMed ID: 18029453 [TBL] [Abstract][Full Text] [Related]
32. Five cases of absence of iodide concentrating mechanism. Toyoshima K; Matsumoto Y; Nishida M; Yabuuchi H Acta Endocrinol (Copenh); 1977 Mar; 84(3):527-37. PubMed ID: 576528 [TBL] [Abstract][Full Text] [Related]
33. Fetal Goitrous Hypothyroidism and Polyhydramnios in a Patient with Compound Heterozygous DUOXA2 Mutations. Tanase-Nakao K; Miyata I; Terauchi A; Saito M; Wada S; Hasegawa T; Narumi S Horm Res Paediatr; 2018; 90(2):132-137. PubMed ID: 30110704 [TBL] [Abstract][Full Text] [Related]
34. ABSENT AND DEFECTIVE IODOTYROSINE DEIODINATION IN A FAMILY SOME OF WHOSE MEMBERS ARE GOITROUS CRETINS. MURRAY P; THOMSON JA; MCGIRR EM; WALLACE TJ; MACDONALD EM; MACCABE HJ Lancet; 1965 Jan; 1(7378):183-5. PubMed ID: 14238044 [No Abstract] [Full Text] [Related]
35. [Contribution to the study of the Pendred syndrome (association of goiter, deaf-mutism and cretinism)]. Zechini F; Felici A Ann Ital Chir; 1966; 42(11):1000-13. PubMed ID: 5999250 [No Abstract] [Full Text] [Related]
36. [Congenital hypothyroidism in lingual thyroid]. Eber O; Wascher H Wien Z Inn Med; 1965 Jul; 46(7):280-5. PubMed ID: 5835578 [No Abstract] [Full Text] [Related]
37. 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]
38. Transient impairment of thyroid function in newborn from an area of endemic goiter. Sava L; Delange F; Belfiore A; Purrello F; Vigneri R J Clin Endocrinol Metab; 1984 Jul; 59(1):90-5. PubMed ID: 6725528 [TBL] [Abstract][Full Text] [Related]