-
1
-
-
0032952815
-
Report of the expert committee on the diagnosis and classification of diabetes mellitus
-
1 Expert Committee: Report of the expert committee on the diagnosis and classification of diabetes mellitus. Diabetes Care 1999, 22(Suppl 1):5-19. This article provides a cogent summary of the latest recommendations from the American Diabetes Association on the diagnosis and classification of diabetes mellitus. As of year 2000, diabetes is classified according to etiology and not treatment. Since 1997, the diagnostic cut point for hyperglycemia has been lowered to 126 mg/dL.
-
(1999)
Diabetes Care
, vol.22
, Issue.SUPPL. 1
, pp. 5-19
-
-
-
3
-
-
0025057199
-
Scope and heterogeneous nature of MODY
-
3 Fajans SS: Scope and heterogeneous nature of MODY. Diabetes Care 1990, 13:49-64.
-
(1990)
Diabetes Care
, vol.13
, pp. 49-64
-
-
Fajans, S.S.1
-
4
-
-
0023123049
-
Maturity onset diabetes of youth in black Americans
-
4 Winter WE, Maclaren NK, Riley WJ, et al.: Maturity onset diabetes of youth in black Americans. New Engl J Med 1987, 316:285-291.
-
(1987)
New Engl J Med
, vol.316
, pp. 285-291
-
-
Winter, W.E.1
Maclaren, N.K.2
Riley, W.J.3
-
5
-
-
0030927342
-
The βcell transcription factors and development of the pancreas
-
5 Sander M, German M: The βcell transcription factors and development of the pancreas. J Mol Med 1997, 75:327-340.
-
(1997)
J Mol Med
, vol.75
, pp. 327-340
-
-
Sander, M.1
German, M.2
-
6
-
-
0031985396
-
A newly discovered role of transcription factors involved in pancreas development and the pathogenesis of diabetes mellitus
-
6 Habener JF, Stoffers DA: A newly discovered role of transcription factors involved in pancreas development and the pathogenesis of diabetes mellitus. Proc Ass Am Phys 1998, 110:12-21.
-
(1998)
Proc Ass Am Phys
, vol.110
, pp. 12-21
-
-
Habener, J.F.1
Stoffers, D.A.2
-
7
-
-
8544284816
-
Transcription factors contributing to the pancreatic βcell phenotype
-
7 Madsen OD, Jensen J, Petersen HV, et al: Transcription factors contributing to the pancreatic βcell phenotype. Horm Metab Res 1997, 29:265-270.
-
(1997)
Horm Metab Res
, vol.29
, pp. 265-270
-
-
Madsen, O.D.1
Jensen, J.2
Petersen, H.V.3
-
8
-
-
0030750728
-
Pancreatic islet expression studies and polymorphic DNA markers in the genes encoding hepatocyte nuclear factor-3α, -3β, -3γ, -4γ, and 6
-
8 Vaisse C, Kim J, Espinosa R, et al.: Pancreatic islet expression studies and polymorphic DNA markers in the genes encoding hepatocyte nuclear factor-3α, -3β, -3γ, -4γ, and 6. Diabetes 1997, 46:1364-1367.
-
(1997)
Diabetes
, vol.46
, pp. 1364-1367
-
-
Vaisse, C.1
Kim, J.2
Espinosa, R.3
-
9
-
-
0030850883
-
A missense mutation in the hepatocyte nuclear factor 4 alpha gene in a UK pedigree with maturityonset diabetes of the young
-
9 Bulman MP, Dronsfield MJ, Frayling T. et al.: A missense mutation in the hepatocyte nuclear factor 4 alpha gene in a UK pedigree with maturityonset diabetes of the young. Diabetologia 1997, 40:859-862.
-
(1997)
Diabetologia
, vol.40
, pp. 859-862
-
-
Bulman, M.P.1
Dronsfield, M.J.2
Frayling, T.3
-
10
-
-
0030779004
-
Hepatic function in a family with a nonsense mutation (R154X) in the hepatocyte nuclear factor-4α/MODY1 gene
-
10 Lindner T, Gragnoli C, Furuta H, et al.: Hepatic function in a family with a nonsense mutation (R154X) in the hepatocyte nuclear factor-4α/MODY1 gene J Clin Inv 1997, 100:1400-1405.
-
(1997)
J Clin Inv
, vol.100
, pp. 1400-1405
-
-
Lindner, T.1
Gragnoli, C.2
Furuta, H.3
-
11
-
-
0032589072
-
Mutation in the HNF-4α gene affects insulin secretion and triglyceride metabolism
-
11 Lehto M, Bitzén PO, Isomaa B, et al.: Mutation in the HNF-4α gene affects insulin secretion and triglyceride metabolism. Diabetes 1999, 48:423-425.
-
(1999)
Diabetes
, vol.48
, pp. 423-425
-
-
Lehto, M.1
Bitzén, P.O.2
Isomaa, B.3
-
12
-
-
0000309667
-
Organization and partial sequence of the hepatocyte nuclear factor-4α/MODY1 gene and identification of a missense mutation, R127W, in a Japanese family with MODY
-
12 Furuta H, Iwasaki N, Oda N, et al.: Organization and partial sequence of the hepatocyte nuclear factor-4α/MODY1 gene and identification of a missense mutation, R127W, in a Japanese family with MODY. Diabetes 1997, 46:1652-1657.
-
(1997)
Diabetes
, vol.46
, pp. 1652-1657
-
-
Furuta, H.1
Iwasaki, N.2
Oda, N.3
-
13
-
-
0031767978
-
Liver and kidney function in Japanese patients with maturityonset diabetes of the young
-
13 Iwasaki N, Ogata M, Tomonaga O, et al.: Liver and kidney function in Japanese patients with maturityonset diabetes of the young. Diabetes Care 1998, 21:2144-2148.
-
(1998)
Diabetes Care
, vol.21
, pp. 2144-2148
-
-
Iwasaki, N.1
Ogata, M.2
Tomonaga, O.3
-
14
-
-
0030798068
-
Studies of the genetic variability of the coding region of the hepatocyte nuclear factor-4α in Caucasians with maturity onset NIDDM
-
14 Moøller AM, Urhammer SA, Dalgaard LT, et al.: Studies of the genetic variability of the coding region of the hepatocyte nuclear factor-4α in Caucasians with maturity onset NIDDM. Diabetologia 1997, 40:980-983.
-
(1997)
Diabetologia
, vol.40
, pp. 980-983
-
-
Moøller, A.M.1
Urhammer, S.A.2
Dalgaard, L.T.3
-
15
-
-
0032955956
-
A novel Phe75fsdelT mutation in the hepatocyte nuclear factor-4α gene in a Danish pedigree with maturityonset diabetes of the young
-
15 Møller AM, Dalgaard LT, Ambye L, et al.: A novel Phe75fsdelT mutation in the hepatocyte nuclear factor-4α gene in a Danish pedigree with maturityonset diabetes of the young. J Clin Endo Metabol 1999, 84:367-369.
-
(1999)
J Clin Endo Metabol
, vol.84
, pp. 367-369
-
-
Møller, A.M.1
Dalgaard, L.T.2
Ambye, L.3
-
16
-
-
0026032055
-
Gene for noninsulindependent diabetes mellitus (maturityonset diabetes of the young subtype) is linked to DNA polymorphism on human chromosome 20q
-
16 Bell GI, Xiang KS, Newman MVD, et al.: Gene for noninsulindependent diabetes mellitus (maturityonset diabetes of the young subtype) is linked to DNA polymorphism on human chromosome 20q. Proc Natl Acad Sci U S A 1991, 88:1484-1488.
-
(1991)
Proc Natl Acad Sci U S A
, vol.88
, pp. 1484-1488
-
-
Bell, G.I.1
Xiang, K.S.2
Newman, M.V.D.3
-
17
-
-
0031802866
-
Exclusion of the hepatocyte nuclear factor 4α as a candidate gene for lateonset NIDDM linked with chromosome 20q
-
17 Malecki MT, Antonellis A, Casey P, et al.: Exclusion of the hepatocyte nuclear factor 4α as a candidate gene for lateonset NIDDM linked with chromosome 20q. Diabetes 1998, 47:970-972.
-
(1998)
Diabetes
, vol.47
, pp. 970-972
-
-
Malecki, M.T.1
Antonellis, A.2
Casey, P.3
-
18
-
-
0031031571
-
Pancreatic agenesis attributable to a single nucleotide deletion in the human IPF1 gene coding sequence
-
18 Stoffers DA, Zinkin NT, Stanojevic V, et al.: Pancreatic agenesis attributable to a single nucleotide deletion in the human IPF1 gene coding sequence. Nat Gen 1997, 15:106-110.
-
(1997)
Nat Gen
, vol.15
, pp. 106-110
-
-
Stoffers, D.A.1
Zinkin, N.T.2
Stanojevic, V.3
-
19
-
-
0031453186
-
Mutation in hepatocyte nuclear factor 1β gene (TCF2) associated with MODY
-
19 Horikawa Y, Iwasaki N, Hara M, et al.: Mutation in hepatocyte nuclear factor 1β gene (TCF2) associated with MODY. Nat Gen 1997, 17:384-385.
-
(1997)
Nat Gen
, vol.17
, pp. 384-385
-
-
Horikawa, Y.1
Iwasaki, N.2
Hara, M.3
-
20
-
-
0031848798
-
Frameshift mutation, A263fsinsGG, in the hepatocyte nuclear factor 1β gene associated with diabetes and renal dysfunction
-
20 Nishigori H, Yamada S, Kohama T, et al.: Frameshift mutation, A263fsinsGG, in the hepatocyte nuclear factor 1β gene associated with diabetes and renal dysfunction. Diabetes 1998, 47:1354-1355.
-
(1998)
Diabetes
, vol.47
, pp. 1354-1355
-
-
Nishigori, H.1
Yamada, S.2
Kohama, T.3
-
21
-
-
15444341853
-
Mutations in the hepatocyte nuclear factor-1alpha/MODY3 gene in Japanese subjects with early and lateonset NIDDM
-
21 Iwasaki N, Oda N, Ogata M, et al.: Mutations in the hepatocyte nuclear factor-1alpha/MODY3 gene in Japanese subjects with early and lateonset NIDDM. Diabetes 1997, 46:1504-1508.
-
(1997)
Diabetes
, vol.46
, pp. 1504-1508
-
-
Iwasaki, N.1
Oda, N.2
Ogata, M.3
-
22
-
-
0031760142
-
Linkage and molecular scanning analyses of MODY3/hepatocyte nuclear factor-1α gene in typical familial type 2 diabetes: Evidence for novel mutations in exons 8 and 10
-
22 Elbein SC, Teng K, Yount P, et al.: Linkage and molecular scanning analyses of MODY3/hepatocyte nuclear factor-1α gene in typical familial type 2 diabetes: evidence for novel mutations in exons 8 and 10. J Clin Endo Metabol 1998, 83:2059-2065.
-
(1998)
J Clin Endo Metabol
, vol.83
, pp. 2059-2065
-
-
Elbein, S.C.1
Teng, K.2
Yount, P.3
-
23
-
-
0030067124
-
A lesson in metabolic regulation inspired by the glucokinase glucose sensor paradigm
-
23 Matschinsky FM: A lesson in metabolic regulation inspired by the glucokinase glucose sensor paradigm. Diabetes 1996, 45:223-241.
-
(1996)
Diabetes
, vol.45
, pp. 223-241
-
-
Matschinsky, F.M.1
-
24
-
-
0031892853
-
Pancreatic βcell glucokinase, closing the gap between theoretical concepts and experimental realities
-
24 Matschinsky FM, Glaser B, Magnuson MA: Pancreatic βcell glucokinase, closing the gap between theoretical concepts and experimental realities. Diabetes 1998, 47:307-315.
-
(1998)
Diabetes
, vol.47
, pp. 307-315
-
-
Matschinsky, F.M.1
Glaser, B.2
Magnuson, M.A.3
-
25
-
-
0027472126
-
Familial hyperglycemia due to mutations in glucokinase: Definition of a subtype of diabetes mellitus
-
25 Froguel P, Zouali H, Vionnet N, et al.: Familial hyperglycemia due to mutations in glucokinase: definition of a subtype of diabetes mellitus. N Engl J Med 1993, 328:697-702.
-
(1993)
N Engl J Med
, vol.328
, pp. 697-702
-
-
Froguel, P.1
Zouali, H.2
Vionnet, N.3
-
26
-
-
0002165223
-
Novel mutation identified in the glucokinase (GCK) genes of a patient with atypical diabetes mellitus (ADM) of African Americans
-
26 Nakamura M, House DV, Winter WE: Novel mutation identified in the glucokinase (GCK) genes of a patient with atypical diabetes mellitus (ADM) of African Americans [abstract]. Diabetes 1996, 45(Suppl 2):76.
-
(1996)
Diabetes
, vol.45
, Issue.SUPPL. 2
, pp. 76
-
-
Nakamura, M.1
House, D.V.2
Winter, W.E.3
-
27
-
-
0000451245
-
A novel homoplasmic point mutation at mitochondrial DNA (mtDNA) nucleotide 3308 in a family with atypical diabetes mellitus (ADM) of African Americans (AA)
-
27 Nakamura M, House DV, Winter WE: A novel homoplasmic point mutation at mitochondrial DNA (mtDNA) nucleotide 3308 in a family with atypical diabetes mellitus (ADM) of African Americans (AA) [abstract]. Diabetes 1997, 46(Suppl 1):175.
-
(1997)
Diabetes
, vol.46
, Issue.SUPPL. 1
, pp. 175
-
-
Nakamura, M.1
House, D.V.2
Winter, W.E.3
-
28
-
-
0008531365
-
The insulin gene in atypical diabetes mellitus (ADM): No evidence for exon 2 mutations
-
28 Nakamura M, House DV, Winter WE: The insulin gene in atypical diabetes mellitus (ADM): no evidence for exon 2 mutations [abstract]. Diabetes 1997, 46(Suppl 1):177.
-
(1997)
Diabetes
, vol.46
, Issue.SUPPL. 1
, pp. 177
-
-
Nakamura, M.1
House, D.V.2
Winter, W.E.3
-
29
-
-
0032553439
-
SRC-1 and GRIP1 coactivate transcription with hepatocyte nuclear factor 4
-
29 Wang JC, Stafford JM, Granner DK: SRC-1 and GRIP1 coactivate transcription with hepatocyte nuclear factor 4. J Biol Chem 1998, 273:30847-30850.
-
(1998)
J Biol Chem
, vol.273
, pp. 30847-30850
-
-
Wang, J.C.1
Stafford, J.M.2
Granner, D.K.3
-
30
-
-
0032941790
-
Functional study of the E276Q mutant hepatocyte nuclear factor-4α found in type 1 maturity-onset diabetes of the young
-
30 Suaud L, Hemimou Y, Formstecher P, et al.: Functional study of the E276Q mutant hepatocyte nuclear factor-4α found in type 1 maturity-onset diabetes of the young. Diabetes 1999, 48:1162-1167.
-
(1999)
Diabetes
, vol.48
, pp. 1162-1167
-
-
Suaud, L.1
Hemimou, Y.2
Formstecher, P.3
-
31
-
-
0033199955
-
Cell biologic assessment of human glucokinase mutants causing maturity-onset diabetes of the young type 2 (MODY-2) or glucokinase-linked hyperinsulinemia (GK-HI)
-
31 Burke CV, Buettger CW, Davis EA, et al.: Cell biologic assessment of human glucokinase mutants causing maturity-onset diabetes of the young type 2 (MODY-2) or glucokinase-linked hyperinsulinemia (GK-HI). Biochem J 1999, 342:345-352.
-
(1999)
Biochem J
, vol.342
, pp. 345-352
-
-
Burke, C.V.1
Buettger, C.W.2
Davis, E.A.3
-
32
-
-
0032792499
-
Characterization of glucokinase mutations associated with maturity-onset diabetes of the young type 2 (MODY-2)
-
32 Miller SP, Anand GR, Karschnia EJ, et al.: Characterization of glucokinase mutations associated with maturity-onset diabetes of the young type 2 (MODY-2). Diabetes 1999, 48:1645-1651.
-
(1999)
Diabetes
, vol.48
, pp. 1645-1651
-
-
Miller, S.P.1
Anand, G.R.2
Karschnia, E.J.3
-
33
-
-
0031793698
-
Mutations in the hepatocyte nuclear factor-1α gene in Caucasian families originally classified as having type I diabetes
-
33 Møller AM, Dalgaard LT, Pociot F, et al.: Mutations in the hepatocyte nuclear factor-1α gene in Caucasian families originally classified as having type I diabetes. Diabetologia 1998, 41:1528-1531.
-
(1998)
Diabetologia
, vol.41
, pp. 1528-1531
-
-
Møller, A.M.1
Dalgaard, L.T.2
Pociot, F.3
-
34
-
-
0031684710
-
A low renal threshold for glucose in diabetic patients with a mutation in the hepatocyte nuclear factor-1α(HNF-1α) gene
-
34 Menzel R, Kaisaki PJ, Rjasanowski I, et al.: A low renal threshold for glucose in diabetic patients with a mutation in the hepatocyte nuclear factor-1α(HNF-1α) gene. Diabetic Med 1998, 15:816-820.
-
(1998)
Diabetic Med
, vol.15
, pp. 816-820
-
-
Menzel, R.1
Kaisaki, P.J.2
Rjasanowski, I.3
-
35
-
-
0032886896
-
Impaired maximum microvascular hyperaemia in patients with MODY3 hepatocyte nuclear factor gene mutations
-
35 Lee BC, Appleton M, Shore AC, et al.: Impaired maximum microvascular hyperaemia in patients with MODY3 hepatocyte nuclear factor gene mutations). Diabetic Med 1999, 16:731-735.
-
(1999)
Diabetic Med
, vol.16
, pp. 731-735
-
-
Lee, B.C.1
Appleton, M.2
Shore, A.C.3
-
36
-
-
0033600787
-
Human insulin gene is a target gene of hepatocyte nuclear factor-1α (HNF-1α) and HNF-1β
-
36 Okita K, Yang Q, Yamagata K, et al.: Human insulin gene is a target gene of hepatocyte nuclear factor-1α (HNF-1α) and HNF-1β. Biochem Biophys Res Commun 1999, 263:566-569.
-
(1999)
Biochem Biophys Res Commun
, vol.263
, pp. 566-569
-
-
Okita, K.1
Yang, Q.2
Yamagata, K.3
-
37
-
-
0032857518
-
High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes
-
37 Lehto M, Wipemo C, Ivarsson SA, et al.: High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes. Diabetologia 1999, 42:1131-1137.
-
(1999)
Diabetologia
, vol.42
, pp. 1131-1137
-
-
Lehto, M.1
Wipemo, C.2
Ivarsson, S.A.3
-
38
-
-
15144347575
-
Mutation screening in 18 Caucasian families suggest the existence of other MODY genes
-
38 Chèvre JC, Hani EH, Boutin P, et al.: Mutation screening in 18 Caucasian families suggest the existence of other MODY genes. Diabetologia 1998, 41:1017-1023.
-
(1998)
Diabetologia
, vol.41
, pp. 1017-1023
-
-
Chèvre, J.C.1
Hani, E.H.2
Boutin, P.3
-
39
-
-
0032956493
-
Phenotypic characteristics of earlyonset autosomal-dominant type 2 diabetes unlinked to known maturity-onset diabetes of the young (MODY) genes
-
39 Doria A, O'Keeffe C, Yang Y, et al.: Phenotypic characteristics of earlyonset autosomal-dominant type 2 diabetes unlinked to known maturity-onset diabetes of the young (MODY) genes. Diabetes Care 1999, 22:253-261.
-
(1999)
Diabetes Care
, vol.22
, pp. 253-261
-
-
Doria, A.1
O'Keeffe, C.2
Yang, Y.3
-
40
-
-
0031874185
-
Cell transcription factors and diabetes
-
40 Furuta H, Horikawa Y, Iwaski N, et al.: β Cell transcription factors and diabetes. Diabetes 1998, 47:1356-1358.
-
(1998)
Diabetes
, vol.47
, pp. 1356-1358
-
-
Furuta, H.1
Horikawa, Y.2
Iwaski, N.3
-
41
-
-
0032776011
-
Hepatocyte nuclear factor-6: Associations between genetic variability and type II diabetes and genetic variability and estimates of insulin secretion
-
41 Møller AM, Ek J, Durviaux SM, et al.: Hepatocyte nuclear factor-6: associations between genetic variability and type II diabetes and genetic variability and estimates of insulin secretion. Diabetologia 1999, 42:1011-1016.
-
(1999)
Diabetologia
, vol.42
, pp. 1011-1016
-
-
Møller, A.M.1
Ek, J.2
Durviaux, S.M.3
-
42
-
-
0033051861
-
No evidence of linkage or diabetes-associated mutations in the transcription factors BETA2/NEUROD1 and PAX4 in type II diabetes in France
-
42 Dupont S, Vionnet N, Chèvre JC, et al.: No evidence of linkage or diabetes-associated mutations in the transcription factors BETA2/NEUROD1 and PAX4 in type II diabetes in France. Diabetologia 1999, 42:480-484.
-
(1999)
Diabetologia
, vol.42
, pp. 480-484
-
-
Dupont, S.1
Vionnet, N.2
Chèvre, J.C.3
-
44
-
-
0032800875
-
Maturity-onset diabetes of the young (MODY): A new challenge for pediatric diabetologists
-
44 Guazzarotti L, Bartolotta E, Chiarelli F: Maturity-onset diabetes of the young (MODY): a new challenge for pediatric diabetologists. J Pediatr Endocrinol Metab 1999, 12:487-497. This practical article notifies pediatric endocrinologists and diabetologists that we must be aware of unusual forms of diabetes, particularly the MODY syndrome.
-
(1999)
J Pediatr Endocrinol Metab
, vol.12
, pp. 487-497
-
-
Guazzarotti, L.1
Bartolotta, E.2
Chiarelli, F.3
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