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All classifications not built on pathogenesis become inadequate sooner or later
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Sulfonylurea treatment outweighs insulin therapy in short-term metabolic control of patients with permanent neonatal diabetes mellitus due to activating mutations of the KCNJ11 (KIR6.2) gene
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40th EASD Annual Meeting of the European Association for the Study of Diabetes
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Low-protein diet and progression of retinal degeneration in gyrate atrophy of the choroid and retina: A twenty-six-year follow-up
Summary: Gyrate atrophy of the choroid and retina is an autosomal recessive chorioretinal dystrophy which leads to a slowly progressive loss of vision. The primary defect is due to a deficiency o...
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Permanent diabetes mellitus in the first year of life
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Permanent diabetes mellitus in the first year of life
Aims/hypothesis. The pathogenesis of permanent diabetes mellitus diagnosed early in life is heterogeneous and, in most cases, not known. We aimed at identifying markers differentiating between no...
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— to: Gragnoli C et al. (2001) Early-onset Type II diabetes mellitus in Italian families due to mutations in the genes encoding hepatic nuclear factor 1 alpha and glucokinase. Diabetologia 44: 1326–1329
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Large incidence variation of Type I diabetes in central-southern Italy 1990–1995: lower risk in rural areas
Aims/hypothesis. To evaluate the relation between the incidence of childhood Type I (insulin-dependent) diabetes mellitus and the degree of urbanization in the central-southern part of Italy. Met...
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Benign tyrosinaemia: an 18-year follow-up
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Late onset of cystinuria in a case of gyrate atrophy