This page shows the publications Pierre Zalloua has written about Diabetes Mellitus, Type 1.
WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in Lebanon. Hum Mol Genet. 2008 Dec 15; 17(24):4012-21.
Patients with early onset of type 1 diabetes have significantly higher GG genotype at position 49 of the CTLA4 gene. Hum Immunol. 2004 Jul; 65(7):719-24.
No association between the -1031 polymorphism in the TNF-alpha promoter region and type 1 diabetes. Hum Immunol. 2003 Jun; 64(6):633-8.
Host and environmental factors defining the epidemiology of type 1 diabetes mellitus in a group of Lebanese children and young adults. J Pediatr Endocrinol Metab. 2003 Jun; 16(5):759-69.
Type-2 diabetes family history delays the onset of type-1 diabetes. J Clin Endocrinol Metab. 2002 Jul; 87(7):3192-6.
Higher serum leptin level in women than in men with type 1 diabetes. Am J Med Sci. 2002 Apr; 323(4):206-9.
A novel ALMS1 splice mutation in a non-obese juvenile-onset insulin-dependent syndromic diabetic patient. Eur J Hum Genet. 2014 Jan; 22(1):140-3.
Prevalence of asthmatic symptoms in Lebanese patients with type 1 diabetes and their unaffected siblings compared to age-matched controls. Acta Diabetol. 2010 Dec; 47 Suppl 1:13-8.
Leptin levels in patients with type 1 diabetes receiving intensive insulin therapy compared with those in patients receiving conventional insulin therapy. J Endocrinol Invest. 2002 Sep; 25(8):724-6.
The DD genotype of the ACE gene polymorphism is associated with diabetic nephropathy in the type-1 diabetics. Endocr Res. 2001 Feb-May; 27(1-2):99-108.
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