Browsing by Author de Lemos-Marini, SHV
Showing results 1 to 6 of 6
Preview | Issue Date | Title | Author(s) | Advisor | Type |
| 2007 | Spontaneous final height in Turner's syndrome in Brazil | de Lemos-Marini, SHV; Morcillo, AM; Matias Baptista, MT; Guerra, G; Maciel-Guerra, AT | - | Artigo de periódico |
| 2011 | Growth hormone effect on body composition in Turner syndrome | Baldin, AD; Fabbri, T; Siviero-Miachon, AA; Spinola-Castro, AM; de Lemos-Marini, SHV; Baptista, MTM; D'Souza-Li, LFR; Maciel-Guerra, AT; Guerra, G | - | Artigo de periódico |
| 2009 | Impairment in Anthropometric Parameters and Body Composition in Females with Classical 21-Hydroxylase Deficiency | Goncalves, EM; de Lemos-Marini, SHV; de Mello, MP; Baptista, MTM; D'Souza-Li, LFR; Baldin, AD; Carvalho, WRG; Farias, ES; Guerra, G | - | Artigo de periódico |
| 2009 | Turner's Syndrome and Subclinical Autoimmune Thyroid Disease: A Two-Year Follow-up Study | Medeiros, CCM; de Lemos-Marini, SHV; Bricola, M; Camargo, EE; Santos, AO; Magna, LA; Guerra, G; Baptista, MTM; Maciel-Guerra, AT | - | Artigo de periódico |
| 2012 | Turner syndrome and metabolic derangements: Another example of fetal programming | Baldin, AD; Siviero-Miachon, AA; Fabbri, T; de Lemos-Marini, SHV; Spinola-Castro, AM; Baptista, MTM; D'Souza-Li, LFR; Morcillo, AM; Maciel-Guerra, AT; Guerra, G | - | Artigo de periódico |
| 2010 | Nobel deletion alleles carrying CYP21A1P/A2 chimeric genes in Brazilian patients with 21-hydroxylase deficiency | Coeli, FB; Soardi, FC; Bernardi, RD; de Araujo, M; Paulino, LC; Lau, IF; Petroli, RJ; de Lemos-Marini, SHV; Baptista, MTM; Guerra, G; de-Mello, MP | - | Artigo de periódico |