Annalisa Brozzetti

Lack of association of CCR2-64I and CCR5-Delta 32 with type 1 diabetes and latent autoimmune diabetes in adults.

Diabetes-related antibodies in adult diabetic patients.

MHC2TA single nucleotide polymorphism and genetic risk for autoimmune adrenal insufficiency.

High serum inhibin concentration discriminates autoimmune oophoritis from other forms of primary ovarian insufficiency.

Primary ovarian insufficiency due to steroidogenic cell autoimmunity is associated with a preserved pool of functioning follicles.

Cytotoxic T lymphocyte antigen-4 Ala17 polymorphism is a genetic marker of autoimmune adrenal insufficiency: Italian association study and meta-analysis of European studies.

Recombinant human GAD65 accumulates to high levels in transgenic tobacco plants when expressed as an enzymatically inactive mutant.

Association of genetic polymorphisms and autoimmune Addison's disease.

Autoantibody responses in autoimmune ovarian insufficiency and in Addison's disease are IgG1 dominated and suggest a predominant, but not exclusive, Th1 type of response.

Primary ovarian insufficiency: autoimmune causes.

Non-food/feed seeds as biofactories for the high-yield production of recombinant pharmaceuticals.

Progressive decline of residual follicle pool after clinical diagnosis of autoimmune ovarian insufficiency.

BClI polymorphism of the glucocorticoid receptor gene is associated with increased obesity, impaired glucose metabolism and dyslipidaemia in patients with Addison's disease.

Comparative analysis of different biofactories for the production of a major diabetes autoantigen.

Anti-mullerian hormone concentration during the third trimester of pregnancy and puerperium: a longitudinal case-control study in normal and diabetic pregnancy.

Autoantibody response against NALP5/MATER in primary ovarian insufficiency and in autoimmune Addison's disease.