Mory PB - Search Results

1

A new method for body fat evaluation, body adiposity index, is useful in women with familial partial lipodystrophy.

Godoy-Matos AF, Moreira RO, Valerio CM, Mory PB, Moises RS. Godoy-Matos AF, et al. Among authors: mory pb. Obesity (Silver Spring). 2012 Feb;20(2):440-3. doi: 10.1038/oby.2011.343. Epub 2011 Nov 17. Obesity (Silver Spring). 2012. PMID: 22095113 Free article.

2

Dual-energy X-ray absorptiometry study of body composition in patients with lipodystrophy.

Valerio CM, Godoy-Matos A, Moreira RO, Carraro L, Guedes EP, Moises RS, Mory PB, de Souza LL, Russo LA, Melazzi AC. Valerio CM, et al. Among authors: mory pb. Diabetes Care. 2007 Jul;30(7):1857-9. doi: 10.2337/dc07-0025. Epub 2007 Mar 23. Diabetes Care. 2007. PMID: 17384343 Free article. No abstract available.

3

Serum retinol binding protein 4 in patients with familial partial lipodystrophy.

Godoy-Matos AF, Moreira RO, MacDowell R, Bendet I, Mory PB, Moises RS. Godoy-Matos AF, et al. Among authors: mory pb. Clin Biochem. 2009 Jul;42(10-11):1183-6. doi: 10.1016/j.clinbiochem.2009.03.006. Epub 2009 Mar 18. Clin Biochem. 2009. PMID: 19303000

4

Body composition study by dual-energy x-ray absorptiometry in familial partial lipodystrophy: finding new tools for an objective evaluation.

Valerio CM, Zajdenverg L, de Oliveira JE, Mory PB, Moyses RS, Godoy-Matos AF. Valerio CM, et al. Among authors: mory pb. Diabetol Metab Syndr. 2012 Aug 31;4(1):40. doi: 10.1186/1758-5996-4-40. Diabetol Metab Syndr. 2012. PMID: 22938045 Free PMC article.

5

Phenotypic diversity in patients with lipodystrophy associated with LMNA mutations.

Mory PB, Crispim F, Freire MB, Salles JE, Valério CM, Godoy-Matos AF, Dib SA, Moisés RS. Mory PB, et al. Eur J Endocrinol. 2012 Sep;167(3):423-31. doi: 10.1530/EJE-12-0268. Epub 2012 Jun 14. Eur J Endocrinol. 2012. PMID: 22700598

6

Erratum: Body composition study by dual-energy x-ray absorptiometry in familial partial lipodystrophy: finding new tools for an objective evaluation.

Valerio CM, Zajdenverg L, de Oliveira JE, Mory PB, Moises RS, Godoy-Matos AF. Valerio CM, et al. Among authors: mory pb. Diabetol Metab Syndr. 2015 Mar 14;7:19. doi: 10.1186/s13098-015-0007-6. eCollection 2015. Diabetol Metab Syndr. 2015. PMID: 25774228 Free PMC article.

7

Atypical generalized lipoatrophy and severe insulin resistance due to a heterozygous LMNA p.T10I mutation.

Mory PB, Crispim F, Kasamatsu T, Gabbay MA, Dib SA, Moisés RS. Mory PB, et al. Arq Bras Endocrinol Metabol. 2008 Nov;52(8):1252-6. doi: 10.1590/s0004-27302008000800008. Arq Bras Endocrinol Metabol. 2008. PMID: 19169477

8

Maternally-inherited diabetes with deafness (MIDD) and hyporeninemic hypoaldosteronism.

Mory PB, Santos MC, Kater CE, Moisés RS. Mory PB, et al. Arq Bras Endocrinol Metabol. 2012 Nov;56(8):574-7. doi: 10.1590/s0004-27302012000800019. Arq Bras Endocrinol Metabol. 2012. PMID: 23295301

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