Showing results (191-200 of 1,403) with videos related to
Sort By:
Pageof 141
Arquivos Brasileiros De Endocrinologia E Metabologia|December 17, 2008
Fatal outcome of a young woman with papillary thyroid carcinoma and graves' disease: possible implication of "cross-signalling" mechanismGraciela A de Cross, Horacio Suarez, Fabián Pitoia, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|January 27, 2009
Absence of mutations in Pax6 gene in three cases of morning glory syndrome associated with isolated growth hormone deficiencyGil Guerra-Junior, Angela Maria Spinola-Castro, Adriana A Siviero-Miachon, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|January 27, 2009
Atypical generalized lipoatrophy and severe insulin resistance due to a heterozygous LMNA p.T10I mutationPatricia B Mory, Felipe Crispim, Teresa Kasamatsu, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|January 27, 2009
[Novel nonsense mutation (p.Y113X) in the human growth hormone receptor gene in a Brazilian patient with Laron syndrome]Erik Trovão Diniz, Alexander A L Jorge, Ivo J P Arnhold, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|January 27, 2009
Apparent mineralocorticoid excess syndrome in a Brazilian boy caused by the homozygous missense mutation p.R186C in the HSD11B2 geneFernanda Borchers Coeli, Lúcio Fábio Caldas Ferraz, Sofia H V de Lemos-Marini, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|January 27, 2009
Seven-year follow-up of a juvenile female with papillary thyroid carcinoma with poor outcome, BRAF mutation and loss of expression of iodine-metabolizing genesGisele Oler, Claudia D Nakabashi, Rosa Paula M Biscolla, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|January 27, 2009
Combined 17 alpha-hydroxylase/17,20-lyase deficiency due to a homozygous 25 BP duplication (NT 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon predicted by molecular modelingRegina M Martin, Paulo S L Oliveira, Elaine M F Costa, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|January 27, 2009
HNF1alpha mutations are present in half of clinically defined MODY patients in South-Brazilian individualsJorge de Faria Maraschin, Caroline Kannengiesser, Nádia Murussi, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|January 27, 2009
Unusual occurrence of intestinal pseudo obstruction in a patient with maternally inherited diabetes and deafness (MIDD) and favorable outcome with coenzyme Q10Carla S Bergamin, Luiz Clemente Rolim, Sergio A Dib, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|January 27, 2009
Heterozygosis for CYP21A2 mutation considered as 21-hydroxylase deficiency in neonatal screeningFernanda Caroline Soardi, Sofia Helena V Lemos-Marini, Fernanda Borchers Coeli, et al.Pageof 141