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Volumn 34, Issue 4, 2000, Pages 332-335

Unravelling the heterogeneity of non insulin dependent diabetes

Author keywords

[No Author keywords available]

Indexed keywords

AUTOANTIBODY; GLUTAMATE DECARBOXYLASE; INSULIN;

EID: 0033870207     PISSN: 00358819     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Short Survey
Times cited : (6)

References (14)
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    • O'Rahilly, S.1    Spivey, R.S.2    Holman, R.R.3    Nugent, Z.4
  • 2
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    • Crucial points at diagnosis. Type 2 diabetes or slow type 1 diabetes
    • Zimmet P, Turner R, McCarty D, Rowley M, et al. Crucial points at diagnosis. Type 2 diabetes or slow type 1 diabetes. Diabetes Care 1999;22(Suppl 2):B59-64.
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    • Zimmet, P.1    Turner, R.2    McCarty, D.3    Rowley, M.4
  • 3
    • 0027500697 scopus 로고
    • Antibodies to glutamic acid decarboxylase reveal latent autoimmune diabetes mellitus in adults with non-insulin-dependent onset of disease
    • Tuomi T, Groop LC, Zimmet PZ, Rowley MJ, et al. Antibodies to glutamic acid decarboxylase reveal latent autoimmune diabetes mellitus in adults with non-insulin-dependent onset of disease. Diabetes 1993;42:358-62.
    • (1993) Diabetes , vol.42 , pp. 358-362
    • Tuomi, T.1    Groop, L.C.2    Zimmet, P.Z.3    Rowley, M.J.4
  • 4
    • 0022570021 scopus 로고
    • Islet cell antibodies identify latent type 1 diabetes in patients aged 35-75 at diagnosis
    • Groop LC, Bottazzo GF, Doniach D. Islet cell antibodies identify latent type 1 diabetes in patients aged 35-75 at diagnosis. Diabetes 1986;35:237-41.
    • (1986) Diabetes , vol.35 , pp. 237-241
    • Groop, L.C.1    Bottazzo, G.F.2    Doniach, D.3
  • 5
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    • Mild familial diabetes with dominant inheritance
    • Tattersall RB. Mild familial diabetes with dominant inheritance. Q J Med 1974; 43:339-57.
    • (1974) Q J Med , vol.43 , pp. 339-357
    • Tattersall, R.B.1
  • 6
    • 0031914679 scopus 로고    scopus 로고
    • Maturity-onset diabetes of the young: Clinical heterogeneity explained by genetic heterogeneity
    • Hattersley AT. Maturity-onset diabetes of the young: clinical heterogeneity explained by genetic heterogeneity. Diabet Med 1998;15:15-24.
    • (1998) Diabet Med , vol.15 , pp. 15-24
    • Hattersley, A.T.1
  • 7
    • 0029914927 scopus 로고    scopus 로고
    • Maternally inherited diabetes and deafness: A new diabetes subtype
    • Maassen JA, Kadowaki T. Maternally inherited diabetes and deafness: a new diabetes subtype. Diabetologia 1996; 39:375-82.
    • (1996) Diabetologia , vol.39 , pp. 375-382
    • Maassen, J.A.1    Kadowaki, T.2
  • 8
    • 17344362695 scopus 로고    scopus 로고
    • A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)
    • Inoue H, Tanizawa Y, Wasson J, Behn P, et al. A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome). Nat Genet 1998;20: 143-8.
    • (1998) Nat Genet , vol.20 , pp. 143-148
    • Inoue, H.1    Tanizawa, Y.2    Wasson, J.3    Behn, P.4
  • 9
    • 0028808309 scopus 로고
    • Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome
    • Barrett TG, Bundey SE, Macleod AF. Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome. Lancet 1995; 346:1458-63.
    • (1995) Lancet , vol.346 , pp. 1458-1463
    • Barrett, T.G.1    Bundey, S.E.2    Macleod, A.F.3
  • 10
    • 0033062278 scopus 로고    scopus 로고
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    • Beales PL, Elcioglu N, Woolf AS, Parker D, et al. New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey. J Med Genet 1999;36: 437-46.
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    • Beales, P.L.1    Elcioglu, N.2    Woolf, A.S.3    Parker, D.4
  • 12
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    • American Society of Human Genetics/ American College of Medical GeneticsTest and Technology Transfer Committee: Diagnostic testing for Prader-Willi and Angelman syndromes
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  • 13
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    • Marshall JD, Ludman MD, Shea SE, Salisbury SR, et al. Genealogy, natural history and phenotype of Alstrom syndrome in a large Arcadian kindred and three additional families. Am J Med Genet 1997;73:150-61.
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    • Marshall, J.D.1    Ludman, M.D.2    Shea, S.E.3    Salisbury, S.R.4
  • 14
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    • Mutant insulin receptors in syndromes of insulin resistance
    • O'Rahilly S, Moller DE. Mutant insulin receptors in syndromes of insulin resistance. Clin Endocrinol 1992;36:121-32.
    • (1992) Clin Endocrinol , vol.36 , pp. 121-132
    • O'Rahilly, S.1    Moller, D.E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.