Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Rita, Jenuso"'
Autor:
Maurizio de Martino, Chiara Azzari, Eleonora Gambineri, Stefano Stagi, Roberto Salti, Rita Jenuso, Elisabetta Lapi, Maurizio Genuardi, Francesco Chiarelli, Gloria Colarusso, Camilla Conti
Publikováno v:
Clinical Endocrinology. 72:839-844
Summary Introduction Monoallelic microdeletion of chromosome 22q11 (22q11DS) is considered to be the commonest human microdeletion syndrome. Abnormalities of thyroid function are sporadically reported in this syndrome, but very few studies have speci
Autor:
Stefano, Stagi, Elisabetta, Lapi, Eleonora, Gambineri, Roberto, Salti, Maurizio, Genuardi, Gloria, Colarusso, Camilla, Conti, Rita, Jenuso, Francesco, Chiarelli, Chiara, Azzari, Maurizio, de Martino
Publikováno v:
Clinical endocrinology. 72(6)
Monoallelic microdeletion of chromosome 22q11 (22q11DS) is considered to be the commonest human microdeletion syndrome. Abnormalities of thyroid function are sporadically reported in this syndrome, but very few studies have specifically assessed this
Autor:
Roberto Salti, Elisabetta Lapi, Stefania Losi, Rita Jenuso, Anna Neri, Stefano Stagi, G. Bindi, Francesco Chiarelli
Publikováno v:
Clinical endocrinology. 63(4)
Summary Objective To evaluate the prevalence of abnormalities of thyroid function and morphology in a cohort of patients with Williams syndrome (WS). Methods Serum concentrations of free-T3, free-T4, TSH, thyroperoxidase antibodies (TPOA) and thyrogl
Publikováno v:
RoFo : Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin. 145(1)