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25. Familial thyroxine-binding globulin deficiency associated with hyperthyroidism. Tojo K; Miura Y; Mori Y; Yano M; Tanaka H; Hosoya T; Sakai O Intern Med; 1995 May; 34(5):413-7. PubMed ID: 7647413 [TBL] [Abstract][Full Text] [Related]
26. Inherited X chromosome linked thyroxine-binding globulin (TBG) deficiency in a homozygous female. Bigazzi M; Ronga R; Olivotti AL; Scarselli G; Refetoff S J Endocrinol Invest; 1980; 3(4):349-52. PubMed ID: 6162876 [TBL] [Abstract][Full Text] [Related]
27. Graves' disease and thyroxine-binding globulin deficiency. Dall'Aglio E; Robuschi G; Minelli R; Guerra M; Bentivoglio M; Roti E Arch Intern Med; 1988 Jun; 148(6):1445-6. PubMed ID: 3132126 [TBL] [Abstract][Full Text] [Related]
28. Two novel mutations in the gene encoding thyroxine-binding globulin (TBG) as a cause of complete TBG deficiency in Taiwan. Su CC; Wu YC; Chiu CY; Won JG; Jap TS Clin Endocrinol (Oxf); 2003 Apr; 58(4):409-14. PubMed ID: 12641622 [TBL] [Abstract][Full Text] [Related]
29. [Partial thyroxine binding globulin deficiency in test tube infants: report of cases and literature review]. Fang YL; Wang CL; Liang L Zhonghua Er Ke Za Zhi; 2016 Jun; 54(6):428-32. PubMed ID: 27256229 [TBL] [Abstract][Full Text] [Related]
31. Sequence of a variant thyroxine-binding globulin (TBG) in a family with partial TBG deficiency in Japanese (TBG-PDJ). Miura Y; Mori Y; Yamamori I; Tani Y; Murata Y; Yoshimoto M; Kinoshita E; Matsumoto T; Oiso Y; Seo H Endocr J; 1993 Feb; 40(1):127-32. PubMed ID: 7951486 [TBL] [Abstract][Full Text] [Related]
32. TBG deficiency: description of two novel mutations associated with complete TBG deficiency and review of the literature. Mannavola D; Vannucchi G; Fugazzola L; Cirello V; Campi I; Radetti G; Persani L; Refetoff S; Beck-Peccoz P J Mol Med (Berl); 2006 Oct; 84(10):864-71. PubMed ID: 16947003 [TBL] [Abstract][Full Text] [Related]
33. Gene screening in Japanese families with complete deficiency of thyroxine-binding globulin demonstrates that a nucleotide deletion at codon 352 may be a race specific mutation. Takeda K; Iyota K; Mori Y; Tamura Y; Suehiro T; Kubo Y; Refetoff S; Hashimoto K Clin Endocrinol (Oxf); 1994 Feb; 40(2):221-6. PubMed ID: 8137521 [TBL] [Abstract][Full Text] [Related]
34. A novel mutation (del 1711 G) in the TBG gene as a cause of complete TBG deficiency. Lacka K; Nizankowska T; Ogrodowicz A; Lacki JK Thyroid; 2007 Nov; 17(11):1143-6. PubMed ID: 17887925 [TBL] [Abstract][Full Text] [Related]
35. Gene amplification as a cause of inherited thyroxine-binding globulin excess in two Japanese families. Mori Y; Miura Y; Takeuchi H; Igarashi Y; Sugiura J; Saito H; Oiso Y J Clin Endocrinol Metab; 1995 Dec; 80(12):3758-62. PubMed ID: 8530630 [TBL] [Abstract][Full Text] [Related]
36. Sequencing of the variant thyroxine-binding globulin (TBG)-Quebec reveals two nucleotide substitutions. Bertenshaw R; Takeda K; Refetoff S Am J Hum Genet; 1991 Apr; 48(4):741-4. PubMed ID: 1901689 [TBL] [Abstract][Full Text] [Related]
37. [Inborn defect of thyroxine binding globulin (TBG) diagnosed during screening for congenital hypothyroidism]. Hníková O; Kracmar P Cesk Pediatr; 1983 Jul; 38(7):416-8. PubMed ID: 6413079 [No Abstract] [Full Text] [Related]
38. Familial thyroxine-binding globulin deficiency in association with non-toxic goitre. Bratusch-Marrain P; Haydl H; Waldhäusl W; Dudczak R; Graninger W Acta Endocrinol (Copenh); 1979 May; 91(1):70-6. PubMed ID: 110022 [TBL] [Abstract][Full Text] [Related]
40. Nucleotide deletion resulting in frameshift as a possible cause of complete thyroxine-binding globulin deficiency in six Japanese families. Yamamori I; Mori Y; Seo H; Hirooka Y; Imamura S; Miura Y; Matsui N; Oiso Y J Clin Endocrinol Metab; 1991 Aug; 73(2):262-7. PubMed ID: 1906892 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]