Treatment of congenital thyroid dysfunction: Achievements and challenges.
Krude H, Kühnen P, Biebermann H.
Best Pract Res Clin Endocrinol Metab. 2015 Jun;29(3):399-413. doi: 10.1016/j.beem.2015.04.004. Epub 2015 Apr 26.
A Japanese patient of congenital hypothyroidism with cerebellar atrophy.
Tajima T, Fujiwara F, Sudo A, Saito S, Fujieda K.
Endocr J. 2007 Dec;54(6):941-4. doi: 10.1507/endocrj.k07-105. Epub 2007 Nov 14.
Etiopathogenesis of canine hypothyroidism.
Kemppainen RJ, Clark TP.
Vet Clin North Am Small Anim Pract. 1994 May;24(3):467-76. doi: 10.1016/s0195-5616(94)50052-4.
Endemic cretinism: toward a unifying hypothesis.
Boyages SC, Halpern JP.
Thyroid. 1993 Spring;3(1):59-69. doi: 10.1089/thy.1993.3.59.
Thyroid involvement in Chanarin-Dorfman syndrome in adults in the largest series of patients carrying the same founder mutation in ABHD5 gene.
Louhichi N, Bahloul E, Marrakchi S, Othman HB, Triki C, Aloulou K, Trabelsi L, Mahfouth N, Ayadi-Mnif Z, Keskes L, Fakhfakh F, Turki H.
Orphanet J Rare Dis. 2019 May 22;14(1):112. doi: 10.1186/s13023-019-1095-4.
Male congenital hypothyroid Pax8-/- mice are infertile despite adequate treatment with thyroid hormone.
Wistuba J, Mittag J, Luetjens CM, Cooper TG, Yeung CH, Nieschlag E, Bauer K.
J Endocrinol. 2007 Jan;192(1):99-109. doi: 10.1677/JOE-06-0054.
Congenital goiter with areas of signet ring cell differentiation in a juvenile giraffe: a very rare entity.
Wang J, Ding Y, Sulijid J, Zhao L, Lu S, Wang X, Liu Y.
BMC Vet Res. 2020 Oct 31;16(1):414. doi: 10.1186/s12917-020-02637-4.
A comparative study of neurological and myxedematous endemic cretinism in western China.
Boyages SC, Halpern JP, Maberly GF, Eastman CJ, Morris J, Collins J, Jupp JJ, Jin CE, Wang ZH, You CY.
J Clin Endocrinol Metab. 1988 Dec;67(6):1262-71. doi: 10.1210/jcem-67-6-1262.
Blocking type immunoglobulins in patients with nongoitrous primary hypothyroidism in area of iodine deficiency.
Tang T, Wang YG, Tsuboi K, Irie M, Ma T, Ingbar SH.
Endocrinol Jpn. 1991 Dec;38(6):661-5. doi: 10.1507/endocrj1954.38.661.
A homozygous Y443C variant in the RNPC3 is associated with severe syndromic congenital hypopituitarism and diffuse brain atrophy.
Bezen D, Kutlu O, Mouilleron S, Rizzoti K, Dattani M, Guran T, Yeşil G.
Am J Med Genet A. 2022 Sep;188(9):2701-2706. doi: 10.1002/ajmg.a.62888. Epub 2022 Jul 6.
