Moisés RS - Search Results

1

Unusual occurrence of intestinal pseudo obstruction in a patient with maternally inherited diabetes and deafness (MIDD) and favorable outcome with coenzyme Q10.

Bergamin CS, Rolim LC, Dib SA, Moisés RS. Bergamin CS, et al. Among authors: moises rs. Arq Bras Endocrinol Metabol. 2008 Nov;52(8):1345-9. doi: 10.1590/s0004-27302008000800023. Arq Bras Endocrinol Metabol. 2008. PMID: 19169492

2

Prevalence of maturity-onset diabetes of the young mutations in Brazilian families with autosomal-dominant early-onset type 2 diabetes.

Moises RS, Reis AF, Morel V, Chacra AR, Dib SA, Bellanne-Chantelot C, Velho G. Moises RS, et al. Diabetes Care. 2001 Apr;24(4):786-8. doi: 10.2337/diacare.24.4.786. Diabetes Care. 2001. PMID: 11315851 No abstract available.

3

Role of the Gly40Ser mutation in the glucagon receptor gene in Brazilian patients with type 2 diabetes mellitus.

Shiota D, Kasamatsu T, Dib SA, Chacra AR, Moisés RS. Shiota D, et al. Among authors: moises rs. Pancreas. 2002 May;24(4):386-90. doi: 10.1097/00006676-200205000-00010. Pancreas. 2002. PMID: 11961492

4

Myocardial dysfunction in mitochondrial diabetes treated with Coenzyme Q10.

Salles JE, Moisés VA, Almeida DR, Chacra AR, Moisés RS. Salles JE, et al. Among authors: moises rs, moises va. Diabetes Res Clin Pract. 2006 Apr;72(1):100-3. doi: 10.1016/j.diabres.2005.09.005. Epub 2005 Oct 25. Diabetes Res Clin Pract. 2006. PMID: 16253379

5

[Wolfram syndrome: from definition to molecular bases].

Ribeiro MR, Crispim F, Vendramini MF, Moisés RS. Ribeiro MR, et al. Among authors: moises rs. Arq Bras Endocrinol Metabol. 2006 Oct;50(5):839-44. doi: 10.1590/s0004-27302006000500003. Arq Bras Endocrinol Metabol. 2006. PMID: 17160206 Review. Portuguese.

6

Beta-cell function in individuals carrying the mitochondrial tRNA leu (UUR) mutation.

Salles JE, Kasamatsu TS, Dib SA, Moisés RS. Salles JE, et al. Among authors: moises rs. Pancreas. 2007 Jan;34(1):133-7. doi: 10.1097/01.mpa.0000246659.38375.4d. Pancreas. 2007. PMID: 17198195

7

[Diabetes mellitus associated with the mitochondrial mutation A3243G: frequency and clinical presentation].

Salles JE, Kalinin LB, Ferreira SR, Kasamatsu T, Moisés RS. Salles JE, et al. Among authors: moises rs. Arq Bras Endocrinol Metabol. 2007 Jun;51(4):559-65. doi: 10.1590/s0004-27302007000400009. Arq Bras Endocrinol Metabol. 2007. PMID: 17684616 Portuguese.

8

[Neonatal diabetes mellitus].

Gurgel LC, Moisés RS. Gurgel LC, et al. Among authors: moises rs. Arq Bras Endocrinol Metabol. 2008 Mar;52(2):181-7. doi: 10.1590/s0004-27302008000200005. Arq Bras Endocrinol Metabol. 2008. PMID: 18438528 Review. Portuguese.

9

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. Among authors: moises rs. Arq Bras Endocrinol Metabol. 2008 Nov;52(8):1252-6. doi: 10.1590/s0004-27302008000800008. Arq Bras Endocrinol Metabol. 2008. PMID: 19169477

10

Hyperinsulinemic hypoglycemia evolving to gestational diabetes and diabetes mellitus in a family carrying the inactivating ABCC8 E1506K mutation.

Vieira TC, Bergamin CS, Gurgel LC, Moisés RS. Vieira TC, et al. Among authors: moises rs. Pediatr Diabetes. 2010 Nov;11(7):505-8. doi: 10.1111/j.1399-5448.2009.00626.x. Pediatr Diabetes. 2010. PMID: 20042013

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