Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Paloma Cabanas Rodriguez"'
Autor:
Teresa Rego, Ana Fernández-Marmiesse, Helder Simoes, Rebeca Saborido Fiaño, Francisco Sousa-Santos, Angel Carracedo, Jesus Barreiro Conde, Lidia Castro-Feijoo, Paloma Cabanas Rodriguez
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
Archives of Endocrinology and Metabolism, Vol 62, Iss 5, Pp 560-565
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
Archives of Endocrinology and Metabolism, Vol 62, Iss 5, Pp 560-565
Congenital hyperinsulinism (CHI) is a heterogenous disease caused by insulin secretion regulatory defects, being ABCC8/KCNJ11 the most commonly affected genes. Therapeutic options include diazoxide, somatostatin analogues and surgery, which is curati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38e868f4a9b774806243ac99f9907a10
Autor:
Francisco Sousa Santos, Lidia Castro-Feijoo, Teresa Rego, Francisco Barros Angueira, Paloma Cabanas Rodriguez, Manuel Castro-Gago, Carmen Gomez Lado, Jesus Barreiro Conde
Publikováno v:
HORMONES. 16
Monocarboxylate transporter 8 (MCT8) is an active and specific thyroid hormone transporter into neurons. MCT8 mutations cause an X-linked condition known as Allan-Herndon-Dudley syndrome and are characterized by impaired psychomotor development and t
Autor:
Jesus Barreiro Conde, Teresa Rego, Paloma Cabanas Rodriguez, Francisco Sousa Santos, Ana Fernández-Marmiesse, Rebeca Saborido Fiaño, Helder Simoes, Angel Carracedo, Lidia Castro-Feijoo
Publikováno v:
Endocrine Abstracts.
Autor:
Francisco Sousa-Santos, Helder Simões, Lidia Castro-Feijóo, Paloma Cabanas Rodríguez, Ana Fernández-Marmiesse, Rebeca Saborido Fiaño, Teresa Rego, Ángel Carracedo, Jesús Barreiro Conde
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 62, Iss 5, Pp 560-565
SUMMARY Congenital hyperinsulinism (CHI) is a heterogenous disease caused by insulin secretion regulatory defects, being ABCC8/KCNJ11 the most commonly affected genes. Therapeutic options include diazoxide, somatostatin analogues and surgery, which i
Externí odkaz:
https://doaj.org/article/5f848febb63447a59a29afe718a2628b