Vono J

References (5)

Title : Congenital goiter with hypothyroidism caused by a 5' splice site mutation in the thyroglobulin gene - Targovnik_2001_Thyroid_11_685
Author(s) : Targovnik HM , Rivolta CM , Mendive FM , Moya CM , Vono J , Medeiros-Neto G
Ref : Thyroid , 11 :685 , 2001
Abstract :
PubMedSearch : Targovnik_2001_Thyroid_11_685
PubMedID: 11484898
Gene_locus related to this paper: human-TG

Title : Evidence for the segregation of three different mutated alleles of the thyroglobulin gene in a Brazilian family with congenital goiter and hypothyroidism - Targovnik_1998_Thyroid_8_291
Author(s) : Targovnik HM , Frechtel GD , Mendive FM , Vono J , Cochaux P , Vassart G , Medeiros-Neto G
Ref : Thyroid , 8 :291 , 1998
Abstract :
PubMedSearch : Targovnik_1998_Thyroid_8_291
PubMedID: 9588493

Title : Congenital hypothyroid goiter with deficient thyroglobulin. Identification of an endoplasmic reticulum storage disease with induction of molecular chaperones - Medeiros-Neto_1996_J.Clin.Invest_98_2838
Author(s) : Medeiros-Neto G , Kim PS , Yoo SE , Vono J , Targovnik HM , Camargo R , Hossain SA , Arvan P
Ref : J Clinical Investigation , 98 :2838 , 1996
Abstract :
PubMedSearch : Medeiros-Neto_1996_J.Clin.Invest_98_2838
PubMedID: 8981932

Title : The effect of oral administration of iodine to patients with goiter and hypothyroidism due to defective synthesis of thyroglobulin - Vono_1996_Thyroid_6_11
Author(s) : Vono J , Lima N , Knobel M , Medeiros-Neto G
Ref : Thyroid , 6 :11 , 1996
Abstract :
PubMedSearch : Vono_1996_Thyroid_6_11
PubMedID: 8777378

Title : A 138-nucleotide deletion in the thyroglobulin ribonucleic acid messenger in a congenital goiter with defective thyroglobulin synthesis - Targovnik_1995_J.Clin.Endocrinol.Metab_80_3356
Author(s) : Targovnik HM , Vono J , Billerbeck AE , Cerrone GE , Varela V , Mendive F , Wajchenberg BL , Medeiros-Neto G
Ref : J Clinical Endocrinology Metab , 80 :3356 , 1995
Abstract :
PubMedSearch : Targovnik_1995_J.Clin.Endocrinol.Metab_80_3356
PubMedID: 7593451
Gene_locus related to this paper: human-TG