Rute Alexandra da Costa Tomaz
AuthID: R-000-XH9
1
TITLE: Identification of a novel germline FOXE1 variant in patients with familial non-medullary thyroid carcinoma (FNMTC) Full Text
AUTHORS: Joana S Pereira; Joana Gomes da Silva; Rute Alexandra Tomaz; Antonio Evaristo Pinto; Maria Joao Bugalho; Valeriano Leite; Branca Maria Cavaco;
PUBLISHED: 2015, SOURCE: ENDOCRINE, VOLUME: 49, ISSUE: 1
AUTHORS: Joana S Pereira; Joana Gomes da Silva; Rute Alexandra Tomaz; Antonio Evaristo Pinto; Maria Joao Bugalho; Valeriano Leite; Branca Maria Cavaco;
PUBLISHED: 2015, SOURCE: ENDOCRINE, VOLUME: 49, ISSUE: 1
2
TITLE: FOXE1 polymorphisms are associated with familial and sporadic nonmedullary thyroid cancer susceptibility Full Text
AUTHORS: Rute A Tomaz; Ines Sousa; Joana G Silva; Catarina Santos; Manuel R Teixeira ; Valeriano Leite ; Branca M Cavaco ;
PUBLISHED: 2012, SOURCE: CLINICAL ENDOCRINOLOGY, VOLUME: 77, ISSUE: 6
AUTHORS: Rute A Tomaz; Ines Sousa; Joana G Silva; Catarina Santos; Manuel R Teixeira ; Valeriano Leite ; Branca M Cavaco ;
PUBLISHED: 2012, SOURCE: CLINICAL ENDOCRINOLOGY, VOLUME: 77, ISSUE: 6
3
TITLE: Identification of the first germline HRPT2 whole-gene deletion in a patient with primary hyperparathyroidism. Germline HRPT2 whole-gene deletion Full Text
AUTHORS: Rita Domingues; Rute Alexandra Tomaz; Carmo Martins ; Carla Nunes; Maria Joao Bugalho ; Branca Maria Cavaco ;
PUBLISHED: 2012, SOURCE: CLINICAL ENDOCRINOLOGY, VOLUME: 76, ISSUE: 1
AUTHORS: Rita Domingues; Rute Alexandra Tomaz; Carmo Martins ; Carla Nunes; Maria Joao Bugalho ; Branca Maria Cavaco ;
PUBLISHED: 2012, SOURCE: CLINICAL ENDOCRINOLOGY, VOLUME: 76, ISSUE: 1
4
TITLE: Differential Methylation as a Cause of Allele Dropout at the Imprinted GNAS Locus
AUTHORS: Rute A Tomaz; Branca M Cavaco ; Valeriano Leite ;
PUBLISHED: 2010, SOURCE: GENETIC TESTING AND MOLECULAR BIOMARKERS, VOLUME: 14, ISSUE: 4
AUTHORS: Rute A Tomaz; Branca M Cavaco ; Valeriano Leite ;
PUBLISHED: 2010, SOURCE: GENETIC TESTING AND MOLECULAR BIOMARKERS, VOLUME: 14, ISSUE: 4
5
TITLE: Clinical and genetic characterization of Portuguese patients with pseudohypoparathyroidism type Ib Full Text
AUTHORS: Branca Maria Cavaco ; Rute Alexandra Tomaz; Fernando Fonseca; Mario Rui Mascarenhas ; Valeriano Leite ; Luis G Goncalves Sobrinho;
PUBLISHED: 2010, SOURCE: ENDOCRINE, VOLUME: 37, ISSUE: 3
AUTHORS: Branca Maria Cavaco ; Rute Alexandra Tomaz; Fernando Fonseca; Mario Rui Mascarenhas ; Valeriano Leite ; Luis G Goncalves Sobrinho;
PUBLISHED: 2010, SOURCE: ENDOCRINE, VOLUME: 37, ISSUE: 3
