Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Leonardo Abdala Giacomini"'
Autor:
Andrei Fernandes Joaquim, Enrico Ghizoni, Helder Tedeschi, Eduardo Baldon Pereira, Leonardo Abdala Giacomini
Publikováno v:
Einstein (São Paulo), Vol 11, Iss 2, Pp 247-255
OBJECTIVE: The spine is the most common location for bone metastases. Since cure is not possible, local control and relief of symptoms is the basis for treatment, which is grounded on the use of conventional radiotherapy. Recently, spinal radiosurger
Externí odkaz:
https://doaj.org/article/002101dc003d4009bc4f5c5d0d1d489d
Autor:
Leonardo Abdala Giacomini
Publikováno v:
Biblioteca Digital de Teses e Dissertações da Universidade Estadual de Campinas (UNICAMP)
Universidade Estadual de Campinas (UNICAMP)
instacron:UNICAMP
Universidade Estadual de Campinas (UNICAMP)
instacron:UNICAMP
Orientadores: Enrico Ghizoni, Andrei Fernandes Joaquim Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas Resumo: Introdução: A epilepsia do lobo temporal é o tipo mais comum de epilepsia focal em adolescentes e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::764e7ab4fe500674fea3423a74c29657
Autor:
Lawrence C. Layman, Lucilia Domingues Casulari da Motta, Luciana Ansaneli Naves, Luiz Augusto Casulari, Leonardo Abdala Giacomini, Paula P. Nascimento, Adriana Lofrano-Porto
Publikováno v:
Fertility and Sterility. 90:1169-1174
Objective To quantify gonadal steroid responses to different gonadotropin regimens. Design Transversal clinical study. Setting Academic medical center. Patient(s) A 41-year-old woman and her 37-year-old brother with isolated FSH deficiency due to a h
Autor:
Adriana Lofrano-Porto, Ana Claudia Latronico, Gustavo Barcelos Barra, Luiz Augusto Casulari, Paula P. Nascimento, Leonardo Abdala Giacomini, Francisco de Assis Rocha Neves
Publikováno v:
New England Journal of Medicine. 357:897-904
Selective luteinizing hormone deficiency due to mutations in the luteinizing hormone beta-subunit gene (LHB) is a rare cause of hypogonadism. We describe the clinical features of a consanguineous family in which three siblings, two men and one woman,
Autor:
C. Spilioti, Adrian Daly, Jean François Vanbellinghen, Leonardo Abdala Giacomini, Luciana Ansaneli Naves, Rousielysson O. Nunes, Marie Lise Jaffrain-Rea, João Willy Corrêa Rosa, Vincent Bours, Albino Verçosa de Magalhães, Albert Beckers, Monalisa F. Azevedo, Luiz Augusto Casulari, Paula P. Nascimento
Background: Germline aryl hydrocarbon receptor-interacting protein (AIP) mutations occur in 15% of familial isolated pituitary adenoma (FIPA) cases. To date, studies have focused on the identification of such mutations in large international cohorts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6d67893f2e763c95fe4387d3373b2e8
http://hdl.handle.net/11697/11836
http://hdl.handle.net/11697/11836