-
1
-
-
41149084500
-
Clinical implications of a molecular genetic classification of monogenic beta-cell diabetes
-
Murphy R., Ellard S., and Hattersley A.T. Clinical implications of a molecular genetic classification of monogenic beta-cell diabetes. Nat Clin Pract Endocrinol Metab 4 (2008) 200-213
-
(2008)
Nat Clin Pract Endocrinol Metab
, vol.4
, pp. 200-213
-
-
Murphy, R.1
Ellard, S.2
Hattersley, A.T.3
-
2
-
-
33646074794
-
Genetic basis of maturity-onset diabetes of the young
-
Vaxillaire M., and Froguel P. Genetic basis of maturity-onset diabetes of the young. Endocrinol Metab Clin North Am 35 (2006) 371-384
-
(2006)
Endocrinol Metab Clin North Am
, vol.35
, pp. 371-384
-
-
Vaxillaire, M.1
Froguel, P.2
-
3
-
-
0142186278
-
Genetic cause of hyperglycaemia and response to treatment in diabetes
-
Pearson E.R., Starkey B.J., Powell R.J., Gribble F.M., Clark P.M., and Hattersley A.T. Genetic cause of hyperglycaemia and response to treatment in diabetes. Lancet 362 (2003) 1275-1281
-
(2003)
Lancet
, vol.362
, pp. 1275-1281
-
-
Pearson, E.R.1
Starkey, B.J.2
Powell, R.J.3
Gribble, F.M.4
Clark, P.M.5
Hattersley, A.T.6
-
4
-
-
0035122350
-
beta-cell genes and diabetes: quantitative and qualitative differences in the pathophysiology of hepatic nuclear factor-1alpha and glucokinase mutations
-
Pearson E.R., Velho G., Clark P., Stride A., Shepherd M., Frayling T.M., et al. beta-cell genes and diabetes: quantitative and qualitative differences in the pathophysiology of hepatic nuclear factor-1alpha and glucokinase mutations. Diabetes 50 Suppl. 1 (2001) S101-S107
-
(2001)
Diabetes
, vol.50
, Issue.SUPPL. 1
-
-
Pearson, E.R.1
Velho, G.2
Clark, P.3
Stride, A.4
Shepherd, M.5
Frayling, T.M.6
-
5
-
-
0031684710
-
A low renal threshold for glucose in diabetic patients with a mutation in the hepatocyte nuclear factor-1alpha (HNF-1alpha) gene
-
Menzel R., Kaisaki P.J., Rjasanowski I., Heinke P., Kerner W., and Menzel S. A low renal threshold for glucose in diabetic patients with a mutation in the hepatocyte nuclear factor-1alpha (HNF-1alpha) gene. Diabet Med 15 (1998) 816-820
-
(1998)
Diabet Med
, vol.15
, pp. 816-820
-
-
Menzel, R.1
Kaisaki, P.J.2
Rjasanowski, I.3
Heinke, P.4
Kerner, W.5
Menzel, S.6
-
6
-
-
12144289307
-
Hepatocyte nuclear factor-1 alpha gene inactivation: cosegregation between liver adenomatosis and diabetes phenotypes in two maturity-onset diabetes of the young (MODY)3 families
-
Reznik Y., Dao T., Coutant R., Chiche L., Jeannot E., Clauin S., et al. Hepatocyte nuclear factor-1 alpha gene inactivation: cosegregation between liver adenomatosis and diabetes phenotypes in two maturity-onset diabetes of the young (MODY)3 families. J Clin Endocrinol Metab 89 (2004) 1476-1480
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 1476-1480
-
-
Reznik, Y.1
Dao, T.2
Coutant, R.3
Chiche, L.4
Jeannot, E.5
Clauin, S.6
-
7
-
-
42549124531
-
Pancreatic exocrine insufficiency is not common in HNF-1alpha MODY
-
Klupa T., Skupien J., Gorczynska-Kosiorz S., Wanic K., Kusnierz-Cabala B., Solnica B., et al. Pancreatic exocrine insufficiency is not common in HNF-1alpha MODY. Diabetes Med 25 (2008) 627-630
-
(2008)
Diabetes Med
, vol.25
, pp. 627-630
-
-
Klupa, T.1
Skupien, J.2
Gorczynska-Kosiorz, S.3
Wanic, K.4
Kusnierz-Cabala, B.5
Solnica, B.6
-
8
-
-
55849089906
-
The evaluation of apolipoprotein M serum concentration as a biomarker of HNF-1α MODY
-
Skupien J., Kepka G., Gorczynska-Kosiorz S., Gebska A., Klupa T., Wanic K., et al. The evaluation of apolipoprotein M serum concentration as a biomarker of HNF-1α MODY. Rev Diabetes Study 4 (2007) 231-235
-
(2007)
Rev Diabetes Study
, vol.4
, pp. 231-235
-
-
Skupien, J.1
Kepka, G.2
Gorczynska-Kosiorz, S.3
Gebska, A.4
Klupa, T.5
Wanic, K.6
-
9
-
-
33644813829
-
Renal malformations may be linked to mutations in the hepatocyte nuclear factor-1alpha (MODY3) gene
-
Malecki M.T., Skupien J., Gorczynska-Kosiorz S., Klupa T., Nazim J., Moczulski D.K., et al. Renal malformations may be linked to mutations in the hepatocyte nuclear factor-1alpha (MODY3) gene. Diabetes Care 28 (2005) 2774-2776
-
(2005)
Diabetes Care
, vol.28
, pp. 2774-2776
-
-
Malecki, M.T.1
Skupien, J.2
Gorczynska-Kosiorz, S.3
Klupa, T.4
Nazim, J.5
Moczulski, D.K.6
-
10
-
-
15144347575
-
Mutation screening in 18 Caucasian families suggest the existence of other MODY genes
-
Chèvre J.C., Hani E.H., Boutin P., Vaxillaire M., Blanché H., Vionnet N., et al. Mutation screening in 18 Caucasian families suggest the existence of other MODY genes. Diabetologia 41 (1998) 1017-1023
-
(1998)
Diabetologia
, vol.41
, pp. 1017-1023
-
-
Chèvre, J.C.1
Hani, E.H.2
Boutin, P.3
Vaxillaire, M.4
Blanché, H.5
Vionnet, N.6
-
11
-
-
17544403804
-
Genetic and clinical characterisation of maturity-onset diabetes of the young in Spanish families
-
Costa A., Bescós M., Velho G., Chêvre J., Vidal J., Sesmilo G., et al. Genetic and clinical characterisation of maturity-onset diabetes of the young in Spanish families. Eur J Endocrinol 142 (2000) 380-386
-
(2000)
Eur J Endocrinol
, vol.142
, pp. 380-386
-
-
Costa, A.1
Bescós, M.2
Velho, G.3
Chêvre, J.4
Vidal, J.5
Sesmilo, G.6
-
12
-
-
14444278300
-
Mutations in the hepatocyte nuclear factor-1alpha gene are a common cause of maturity-onset diabetes of the young in the U.K.
-
Frayling T.M., Bulamn M.P., Ellard S., Appleton M., Dronsfield M.J., Mackie A.D., et al. Mutations in the hepatocyte nuclear factor-1alpha gene are a common cause of maturity-onset diabetes of the young in the U.K. Diabetes 46 (1997) 720-725
-
(1997)
Diabetes
, vol.46
, pp. 720-725
-
-
Frayling, T.M.1
Bulamn, M.P.2
Ellard, S.3
Appleton, M.4
Dronsfield, M.J.5
Mackie, A.D.6
-
13
-
-
33748357551
-
Mutations in the genes encoding the transcription factors hepatocyte nuclear factor 1 alpha (HNF1A) and 4 alpha (HNF4A) in maturity-onset diabetes of the young
-
Ellard S., and Colclough K. Mutations in the genes encoding the transcription factors hepatocyte nuclear factor 1 alpha (HNF1A) and 4 alpha (HNF4A) in maturity-onset diabetes of the young. Hum Mutat 27 (2006) 854-869
-
(2006)
Hum Mutat
, vol.27
, pp. 854-869
-
-
Ellard, S.1
Colclough, K.2
-
14
-
-
0038691467
-
Determinants of the development of diabetes (maturity-onset diabetes of the young-3) in carriers of HNF-1alpha mutations: evidence for parent-of-origin effect
-
Klupa T., Warram J.H., Antonellis A., Pezzolesi M., Nam M., Malecki M.T., et al. Determinants of the development of diabetes (maturity-onset diabetes of the young-3) in carriers of HNF-1alpha mutations: evidence for parent-of-origin effect. Diabetes Care 25 (2002) 2292-2301
-
(2002)
Diabetes Care
, vol.25
, pp. 2292-2301
-
-
Klupa, T.1
Warram, J.H.2
Antonellis, A.3
Pezzolesi, M.4
Nam, M.5
Malecki, M.T.6
-
15
-
-
0013198186
-
Intrauterine hyperglycemia is associated with an earlier diagnosis of diabetes in HNF-1alpha gene mutation carriers
-
Stride A., Shepherd M., Frayling T.M., Bulman M.P., Ellard S., and Hattersley A.T. Intrauterine hyperglycemia is associated with an earlier diagnosis of diabetes in HNF-1alpha gene mutation carriers. Diabetes Care 25 (2002) 2287-2291
-
(2002)
Diabetes Care
, vol.25
, pp. 2287-2291
-
-
Stride, A.1
Shepherd, M.2
Frayling, T.M.3
Bulman, M.P.4
Ellard, S.5
Hattersley, A.T.6
-
16
-
-
0042265784
-
Genetic modifiers of the age at diagnosis of diabetes (MODY3) in carriers of hepatocyte nuclear factor-1alpha mutations map to chromosomes 5p15, 9q22, and 14q24
-
Kim S.H., Ma X., Klupa T., Powers C., Pezzolesi M., Warram J.H., et al. Genetic modifiers of the age at diagnosis of diabetes (MODY3) in carriers of hepatocyte nuclear factor-1alpha mutations map to chromosomes 5p15, 9q22, and 14q24. Diabetes 52 (2003) 2182-2186
-
(2003)
Diabetes
, vol.52
, pp. 2182-2186
-
-
Kim, S.H.1
Ma, X.2
Klupa, T.3
Powers, C.4
Pezzolesi, M.5
Warram, J.H.6
-
17
-
-
0031894649
-
Chronic diabetic complications in patients with MODY3 diabetes
-
Isomaa B., Henricsson M., Lehto M., Forsblom C., Karanko S., Sarelin L., et al. Chronic diabetic complications in patients with MODY3 diabetes. Diabetologia 41 (1998) 467-473
-
(1998)
Diabetologia
, vol.41
, pp. 467-473
-
-
Isomaa, B.1
Henricsson, M.2
Lehto, M.3
Forsblom, C.4
Karanko, S.5
Sarelin, L.6
-
18
-
-
0029762068
-
Diabetes complications in NIDDM kindreds linked to the MODY3 locus on chromosome 12q
-
Velho G., Vaxillaire M., Boccio V., Charpentier G., and Froguel P. Diabetes complications in NIDDM kindreds linked to the MODY3 locus on chromosome 12q. Diabetes Care 19 (1996) 915-919
-
(1996)
Diabetes Care
, vol.19
, pp. 915-919
-
-
Velho, G.1
Vaxillaire, M.2
Boccio, V.3
Charpentier, G.4
Froguel, P.5
-
19
-
-
0025349613
-
Ultrasound screening for fetal urinary tract malformations: a prospective study in general population
-
Rosendahl H. Ultrasound screening for fetal urinary tract malformations: a prospective study in general population. Eur J Obstet Gynecol Reprod Biol 36 (1990) 27-33
-
(1990)
Eur J Obstet Gynecol Reprod Biol
, vol.36
, pp. 27-33
-
-
Rosendahl, H.1
-
20
-
-
0024306083
-
Renal abnormalities in schoolchildren
-
Sheih C.P., Liu M.B., Hung C.S., Yang K.H., Chen W.Y., and Lin C.Y. Renal abnormalities in schoolchildren. Pediatrics 84 (1989) 1086-1090
-
(1989)
Pediatrics
, vol.84
, pp. 1086-1090
-
-
Sheih, C.P.1
Liu, M.B.2
Hung, C.S.3
Yang, K.H.4
Chen, W.Y.5
Lin, C.Y.6
|