90 related articles for article (PubMed ID: 1811097)
21. [DNA diagnosis in endocrinological disease--pituitary disease].
Tatsumi K; Miyai K
Rinsho Byori; 1991 Oct; 39(10):1065-71. PubMed ID: 1762181
[TBL] [Abstract][Full Text] [Related]
22. An identical neo-mutation in the thyroid hormone receptor beta gene (A317T) in 2 unrelated Thai families with resistance to thyroid hormone.
Sunthornthepvarakul T; Jaruratanasirikul S; Likitmaskul S; Angsusingha K; Ngowngarmratana S
J Med Assoc Thai; 2000 Feb; 83(2):139-45. PubMed ID: 10710882
[TBL] [Abstract][Full Text] [Related]
23. Comparison between TRH-stimulated TSH and basal TSH measurement by a commercial immunoradiometric assay in the management of thyroid disease.
De Rosa G; Testa A; Giacomini D; Carrozza C; Maussier ML; Valenza V; D'Errico GF
Q J Nucl Med; 1996 Jun; 40(2):182-7. PubMed ID: 8909104
[TBL] [Abstract][Full Text] [Related]
24. Clinical experience with sensitive thyrotropin measurements: diagnostic and therapeutic implications.
Bayer MF; Kriss JP; McDougall IR
J Nucl Med; 1985 Nov; 26(11):1248-56. PubMed ID: 3840528
[TBL] [Abstract][Full Text] [Related]
25. Thyroid-stimulating hormone (TSH) deficiency caused by a single base substitution in the CAGYC region of the beta-subunit.
Hayashizaki Y; Hiraoka Y; Endo Y; Miyai K; Matsubara K
EMBO J; 1989 Aug; 8(8):2291-6. PubMed ID: 2792087
[TBL] [Abstract][Full Text] [Related]
26. Congenital secondary hypothyroidism caused by exon skipping due to a homozygous donor splice site mutation in the TSHbeta-subunit gene.
Pohlenz J; Dumitrescu A; Aumann U; Koch G; Melchior R; Prawitt D; Refetoff S
J Clin Endocrinol Metab; 2002 Jan; 87(1):336-9. PubMed ID: 11788671
[TBL] [Abstract][Full Text] [Related]
27. Two novel mutations of the TSH-beta subunit gene underlying congenital central hypothyroidism undetectable in neonatal TSH screening.
Baquedano MS; Ciaccio M; Dujovne N; Herzovich V; Longueira Y; Warman DM; Rivarola MA; Belgorosky A
J Clin Endocrinol Metab; 2010 Sep; 95(9):E98-103. PubMed ID: 20534762
[TBL] [Abstract][Full Text] [Related]
28. Familial hypothyroidism caused by a nonsense mutation in the thyroid-stimulating hormone beta-subunit gene.
Dacou-Voutetakis C; Feltquate DM; Drakopoulou M; Kourides IA; Dracopoli NC
Am J Hum Genet; 1990 May; 46(5):988-93. PubMed ID: 1971148
[TBL] [Abstract][Full Text] [Related]
29. Serum free thyrotropin subunit in congenital isolated thyrotropin deficiency.
Miyai K; Endo Y; Iijima Y; Kabutomori O; Hayashizaki Y
Endocrinol Jpn; 1988 Jun; 35(3):517-21. PubMed ID: 2461855
[TBL] [Abstract][Full Text] [Related]
30. Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: phenotypic variability and founder effect.
Borck G; Topaloglu AK; Korsch E; Martiné U; Wildhardt G; Onenli-Mungan N; Yuksel B; Aumann U; Koch G; Ozer G; Pfäffle R; Scherberg NH; Refetoff S; Pohlenz J
J Clin Endocrinol Metab; 2004 Aug; 89(8):4136-41. PubMed ID: 15292359
[TBL] [Abstract][Full Text] [Related]
31. A circulating, biologically inactive thyrotropin caused by a mutation in the beta subunit gene.
Medeiros-Neto G; Herodotou DT; Rajan S; Kommareddi S; de Lacerda L; Sandrini R; Boguszewski MC; Hollenberg AN; Radovick S; Wondisford FE
J Clin Invest; 1996 Mar; 97(5):1250-6. PubMed ID: 8636437
[TBL] [Abstract][Full Text] [Related]
32. Thyroid ultrasonography in congenital isolated thyroid stimulating hormone deficiency.
Wakamoto H; Miyazaki M; Tatsumi K; Amino N
Arch Dis Child; 1995 May; 72(5):439-40. PubMed ID: 7618914
[TBL] [Abstract][Full Text] [Related]
33. Central Congenital Hypothyroidism Caused by a Novel Mutation, C47W, in the Cysteine Knot Region of TSHβ.
Ebrhim RS; Bruellman RJ; Watanabe Y; Creech MK; Abdullah MA; Dumitrescu AM; Refetoff S; Weiss RE
Horm Res Paediatr; 2019; 92(6):390-394. PubMed ID: 31914441
[TBL] [Abstract][Full Text] [Related]
34. [Congenital central hypothyroidism due to the mutations of the thyrotropin-releasing hormone receptor gene].
Yamada M; Mori M
Nihon Rinsho; 2002 Feb; 60(2):277-83. PubMed ID: 11857914
[TBL] [Abstract][Full Text] [Related]
35. Deoxyribonucleic acid analyses of five families with familial inherited thyroid stimulating hormone deficiency.
Hayashizaki Y; Hiraoka Y; Tatsumi K; Hashimoto T; Furuyama J; Miyai K; Nishijo K; Matsuura M; Kohno H; Labbe A
J Clin Endocrinol Metab; 1990 Oct; 71(4):792-6. PubMed ID: 2401711
[TBL] [Abstract][Full Text] [Related]
36. [Isolated thyroid stimulating hormone deficiency].
Monden T; Kasai K; Mori M
Nihon Rinsho; 2006 May; Suppl 1():70-2. PubMed ID: 16776096
[No Abstract] [Full Text] [Related]
37. Severe congenital hypothyroidism due to a homozygous mutation of the betaTSH gene.
Biebermann H; Liesenkötter KP; Emeis M; Oblanden M; Grüters A
Pediatr Res; 1999 Aug; 46(2):170-3. PubMed ID: 10447110
[TBL] [Abstract][Full Text] [Related]
38. Genetic basis of congenital hypothyroidism: abnormalities in the TSHbeta gene, the PIT1 gene, and the NIS gene.
Tatsumi K; Miyai K; Amino N
Clin Chem Lab Med; 1998 Aug; 36(8):659-62. PubMed ID: 9806481
[TBL] [Abstract][Full Text] [Related]
39. Congenital central hypothyroidism due to homozygous thyrotropin beta 313 Delta T mutation is caused by a Founder effect.
Brumm H; Pfeufer A; Biebermann H; Schnabel D; Deiss D; Grüters A
J Clin Endocrinol Metab; 2002 Oct; 87(10):4811-6. PubMed ID: 12364478
[TBL] [Abstract][Full Text] [Related]
40. Novel TSHbeta subunit gene mutation causing congenital central hypothyroidism in a newborn male.
Morales AE; Shi JD; Wang CY; She JX; Muir A
J Pediatr Endocrinol Metab; 2004 Mar; 17(3):355-9. PubMed ID: 15112912
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
