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Johnny Ludvigsson

Researcher at Boston Children's Hospital

Publications -  571
Citations -  21683

Johnny Ludvigsson is an academic researcher from Boston Children's Hospital. The author has contributed to research in topics: Type 1 diabetes & Diabetes mellitus. The author has an hindex of 70, co-authored 529 publications receiving 19461 citations. Previous affiliations of Johnny Ludvigsson include Karolinska Institutet & Karolinska University Hospital.

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Autoantibodies in newly diagnosed diabetic children immunoprecipitate human pancreatic islet cell proteins

TL;DR: Sera from 8 out of 10 newly diagnosed diabetic children consistently immunoprecipitate a protein having a molecular weight of ∼64,000 (64K) and an additional protein was precipitated from islet cells obtained from a HLA-DR3-positive donor, suggesting that the 64K and/or 38K protein components may represent cell-specific target antigens in insulin-dependent diabetes.
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GAD treatment and insulin secretion in recent-onset type 1 diabetes

TL;DR: GAD-alum may contribute to the preservation of residual insulin secretion in patients with recent-onset type 1 diabetes, although it did not change the insulin requirement.
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Environmental risk factors for type 1 diabetes

TL;DR: A unified model in which immune tolerance to β cells can be broken by several environmental exposures that induce generation of hybrid peptides acting as neoautoantigens is suggested.
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Declining incidence of nephropathy in insulin-dependent diabetes mellitus

TL;DR: During the past decade the cumulative incidence of diabetic nephropathy, as manifested by persistent albuminuria, among patients who have had diabetes for 25 years has decreased substantially, probably as a result of improved glycemic control.
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Teplizumab for treatment of type 1 diabetes (Protege study): 1-year results from a randomised, placebo-controlled trial.

TL;DR: It is suggested that future studies of immunotherapeutic intervention with teplizumab might have increased success in prevention of a decline in β-cell function (measured by C-peptide) and provision of glycaemic control at reduced doses of insulin if they target patients early after diagnosis of diabetes and children.