-
1
-
-
0014453164
-
Transient diabetes of the newborn
-
Gentz JC, Cornblath M: Transient diabetes of the newborn. Adv Pediatr 16:345-363, 1969
-
(1969)
Adv Pediatr
, vol.16
, pp. 345-363
-
-
Gentz, J.C.1
Cornblath, M.2
-
2
-
-
0031394680
-
Aetiopathology and genetic basis of neonatal diabetes
-
Shield JP, Gardner RJ, Wadsworth EJ, Whiteford ML, James RS, Robinson DO, Baum JD, Temple IK: Aetiopathology and genetic basis of neonatal diabetes. Arch Dis Child Fetal Neonatal Ed 76:F39-F42, 1997
-
(1997)
Arch Dis Child Fetal Neonatal Ed
, vol.76
-
-
Shield, J.P.1
Gardner, R.J.2
Wadsworth, E.J.3
Whiteford, M.L.4
James, R.S.5
Robinson, D.O.6
Baum, J.D.7
Temple, I.K.8
-
4
-
-
0032847052
-
Neonatal diabetes mellitus and cerebellar hypoplasia/agenesis: Report of a new recessive syndrome
-
Hoveyda N, Shield JP, Garrett C, Chong WK, Beardsall K, Bentsi-Enchill E, Mallya H, Thompson MH: Neonatal diabetes mellitus and cerebellar hypoplasia/agenesis: report of a new recessive syndrome. J Med Genet 36:700-704, 1999
-
(1999)
J Med Genet
, vol.36
, pp. 700-704
-
-
Hoveyda, N.1
Shield, J.P.2
Garrett, C.3
Chong, W.K.4
Beardsall, K.5
Bentsi-Enchill, E.6
Mallya, H.7
Thompson, M.H.8
-
5
-
-
0028857541
-
Rapid multipoint linkage analysis of recessive traits in nuclear families, including homozygosity mapping
-
Kruglyak L, Daly MJ, Lander ES: Rapid multipoint linkage analysis of recessive traits in nuclear families, including homozygosity mapping. Am J Hum Genet 56:519-527, 1995
-
(1995)
Am J Hum Genet
, vol.56
, pp. 519-527
-
-
Kruglyak, L.1
Daly, M.J.2
Lander, E.S.3
-
6
-
-
0027529490
-
Is transient neonatal diabetes a risk factor for diabetes in later life?
-
Shield JP, Baum JD: Is transient neonatal diabetes a risk factor for diabetes in later life? Lancet 341:693, 1993
-
(1993)
Lancet
, vol.341
, pp. 693
-
-
Shield, J.P.1
Baum, J.D.2
-
7
-
-
0034425698
-
EIF2AK3, encoding translation initiation factor 2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndrome
-
Delepine M, Nicolino M, Barrett T, Golamaully M, Lathrop GM, Julier C: EIF2AK3, encoding translation initiation factor 2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndrome. Nat Genet 25:406-409, 2000
-
(2000)
Nat Genet
, vol.25
, pp. 406-409
-
-
Delepine, M.1
Nicolino, M.2
Barrett, T.3
Golamaully, M.4
Lathrop, G.M.5
Julier, C.6
-
8
-
-
0026497195
-
Distinct neurological syndrome in two brothers with hyperuricaemia
-
Christen HJ, Hanefeld F, Duley JA, Simmonds HA: Distinct neurological syndrome in two brothers with hyperuricaemia. Lancet 340:1167-1168, 1992
-
(1992)
Lancet
, vol.340
, pp. 1167-1168
-
-
Christen, H.J.1
Hanefeld, F.2
Duley, J.A.3
Simmonds, H.A.4
-
9
-
-
0342902204
-
Neonatal diabetes mellitus due to complete glucokinase deficiency
-
Njolstad PR, Sovik O, Cuesta-Munoz A, Bjorkhaug L, Massa O, Barbetti F, Undlien DE, Shiota C, Magnuson MA, Molven A, Matschinsky FM, Bell GI: Neonatal diabetes mellitus due to complete glucokinase deficiency. N Engl J Med 344:1588-1592, 2001
-
(2001)
N Engl J Med
, vol.344
, pp. 1588-1592
-
-
Njolstad, P.R.1
Sovik, O.2
Cuesta-Munoz, A.3
Bjorkhaug, L.4
Massa, O.5
Barbetti, F.6
Undlien, D.E.7
Shiota, C.8
Magnuson, M.A.9
Molven, A.10
Matschinsky, F.M.11
Bell, G.I.12
-
10
-
-
0029794055
-
Further evidence for an imprinted gene for neonatal diabetes localised to chromosome 6q22-q23
-
Temple IK, Gardner RJ, Robinson DO, Kibirige MS, Ferguson AW, Baum JD, Barber JC, James RS, Shield JP: Further evidence for an imprinted gene for neonatal diabetes localised to chromosome 6q22-q23. Hum Mol Genet 5:1117-1121, 1996
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1117-1121
-
-
Temple, I.K.1
Gardner, R.J.2
Robinson, D.O.3
Kibirige, M.S.4
Ferguson, A.W.5
Baum, J.D.6
Barber, J.C.7
James, R.S.8
Shield, J.P.9
-
11
-
-
0028292032
-
Isodisomy of chromosome 6 in a newborn with methylmalonic acidemia and agenesis of pancreatic beta cells causing diabetes mellitus
-
Abramowicz MJ, Andrien M, Dupont E, Dorchy H, Parma J, Duprez L, Ledley FD, Courtens W, Vamos E: Isodisomy of chromosome 6 in a newborn with methylmalonic acidemia and agenesis of pancreatic beta cells causing diabetes mellitus. J Clin Invest 94:418-421, 1994
-
(1994)
J Clin Invest
, vol.94
, pp. 418-421
-
-
Abramowicz, M.J.1
Andrien, M.2
Dupont, E.3
Dorchy, H.4
Parma, J.5
Duprez, L.6
Ledley, F.D.7
Courtens, W.8
Vamos, E.9
-
12
-
-
0027273990
-
Permanent neonatal diabetes mellitus and pancreatic exocrine insufficiency resulting from congenital pancreatic a genesis
-
Wright NM, Metzger DL, Borowitz SM, Clarke WL: Permanent neonatal diabetes mellitus and pancreatic exocrine insufficiency resulting from congenital pancreatic agenesis. Am J Dis Child 147:607-609, 1993
-
(1993)
Am J Dis Child
, vol.147
, pp. 607-609
-
-
Wright, N.M.1
Metzger, D.L.2
Borowitz, S.M.3
Clarke, W.L.4
-
13
-
-
0029058637
-
Neonatal diabetes mellitus associated with severe diarrhea, hyperimmunoglobulin E syndrome, and absence of islets of Langerhans
-
Roberts J, Searle J: Neonatal diabetes mellitus associated with severe diarrhea, hyperimmunoglobulin E syndrome, and absence of islets of Langerhans. Pediatr Pathol Lab Med 15:477-483, 1995
-
(1995)
Pediatr Pathol Lab Med
, vol.15
, pp. 477-483
-
-
Roberts, J.1
Searle, J.2
-
14
-
-
0028149890
-
Insulin-promoter-factor 1 is required for pancreas development in mice
-
Jonsson J, Carlsson L, Edlund T, Edlund H: Insulin-promoter-factor 1 is required for pancreas development in mice. Nature 371:606-609, 1994
-
(1994)
Nature
, vol.371
, pp. 606-609
-
-
Jonsson, J.1
Carlsson, L.2
Edlund, T.3
Edlund, H.4
-
15
-
-
0036180326
-
Pancreas duodenum homeobox-1 regulates pancreas development during embryogenesis and islet cell function in adulthood
-
Hui H, Perfetti R: Pancreas duodenum homeobox-1 regulates pancreas development during embryogenesis and islet cell function in adulthood. Eur J Endocrinol 146:129-141, 2002
-
(2002)
Eur J Endocrinol
, vol.146
, pp. 129-141
-
-
Hui, H.1
Perfetti, R.2
-
16
-
-
0031031571
-
Pancreatic agenesis attributable to a single nucleotide deletion in the human IPF1 gene coding sequence
-
Stoffers DA, Zinkin NT, Stanojevic V, Clarke WL, Habener JF: Pancreatic agenesis attributable to a single nucleotide deletion in the human IPF1 gene coding sequence. Nat Genet 15:106-110, 1997
-
(1997)
Nat Genet
, vol.15
, pp. 106-110
-
-
Stoffers, D.A.1
Zinkin, N.T.2
Stanojevic, V.3
Clarke, W.L.4
Habener, J.F.5
-
17
-
-
0032042095
-
Phosphatidylinositol signalling reactions
-
Zhang X, Majerus PW: Phosphatidylinositol signalling reactions. Semin Cell Dev Biol 9:153-160, 1998
-
(1998)
Semin Cell Dev Biol
, vol.9
, pp. 153-160
-
-
Zhang, X.1
Majerus, P.W.2
|