9 results on '"Marinho, Cindi G."'
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2. Reduced fibroblast growth factor 21 and β-Klotho secretion in untreated congenital isolated GH deficiency
3. Cerebral vasoreactivity, a surrogate marker of cerebrovascular disease, is not impaired in subjects with lifetime, untreated, congenital isolated GH deficiency
4. Occurrence of neoplasms in individuals with congenital, severe GH deficiency from the Itabaianinha kindred
5. Sweat and vitamin D status in congenital, lifetime, untreated GH deficiency
6. Hypothalamic abnormalities: Growth failure due to defects of the GHRH receptor
7. Circulating microRNA profile in humans and mice with congenital GH deficiency
8. Enteroendocrine Connections in Congenital Isolated GH Deficiency Due to a GHRH Receptor Gene Mutation
9. Portuguese version of the Literacy Independent Cognitive Assessment (LICA) instrument in the evaluation of individuals aged 50 years or older with Itabaianinha syndrome.
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