2015
DOI: 10.1007/s13340-015-0210-6
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Erratum to: Diagnostic criteria for slowly progressive insulin-dependent (type 1) diabetes mellitus (SPIDDM) (2012): report by the Committee on Slowly Progressive Insulin-Dependent (Type 1) Diabetes Mellitus of the Japan Diabetes Society

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Cited by 5 publications
(20 citation statements)
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“… Islet autoantibodies include glutamic acid decarboxylate (GAD) antibodies, insulinoma‐associated protein‐2 (IA‐2) antibodies, insulin autoantibodies (IAA), zinc transporter 8 (ZnT8) antibodies, and islet cell antibodies (ICA) (adapted from). …”
Section: Guideline For the Diagnosis Of Diabetes Mellitusmentioning
confidence: 99%
See 4 more Smart Citations
“… Islet autoantibodies include glutamic acid decarboxylate (GAD) antibodies, insulinoma‐associated protein‐2 (IA‐2) antibodies, insulin autoantibodies (IAA), zinc transporter 8 (ZnT8) antibodies, and islet cell antibodies (ICA) (adapted from). …”
Section: Guideline For the Diagnosis Of Diabetes Mellitusmentioning
confidence: 99%
“… Type 1 diabetes is classified by the etiology as (A) autoimmune and (b) idiopathic and also classified by the manner of the disease onset as acute, slowly‐progressive, and fulminant. Patients with acute type 1 diabetes are generally likely to develop ketosis or ketoacidosis within 3 months of the onset of hyperglycemia and required insulin therapy immediately. Patients with slowly progressive (insulin‐dependent) type 1 diabetes do not develop ketosis or ketoacidosis and do not require insulin therapy immediately, although their diagnosis is established by a positive test for anti‐GAD antibodies or islet cell antibodies (ICA). Patients with fulminant type 1 diabetes frequently develop ketosis or ketoacidosis within 1 week of the onset of hyperglycemia, require insulin therapy immediately, and are characterized by having lower HbA1c values relative to their glucose values. …”
Section: Guideline For the Diagnosis Of Diabetes Mellitusmentioning
confidence: 99%
See 3 more Smart Citations