-
1
-
-
33746686369
-
Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations
-
Neonatal Diabetes International Collaborative Group
-
Pearson ER, Flechtner I, Njølstad PR, et al.; Neonatal Diabetes International Collaborative Group. Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations. N Engl J Med 2006;355:467-477
-
(2006)
N Engl J Med
, vol.355
, pp. 467-477
-
-
Pearson, E.R.1
Flechtner, I.2
Njølstad, P.R.3
-
2
-
-
2342633204
-
Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes
-
Gloyn AL, Pearson ER, Antcliff JF, et al. Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes. N Engl JMed 2004;350:1838-1849
-
(2004)
N Engl J Med
, vol.350
, pp. 1838-1849
-
-
Gloyn, A.L.1
Pearson, E.R.2
Antcliff, J.F.3
-
3
-
-
33646513278
-
Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype
-
Flanagan SE, Edghill EL, Gloyn AL, Ellard S, Hattersley AT. Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype. Diabetologia 2006;49:1190-1197
-
(2006)
Diabetologia
, vol.49
, pp. 1190-1197
-
-
Flanagan, S.E.1
Edghill, E.L.2
Gloyn, A.L.3
Ellard, S.4
Hattersley, A.T.5
-
4
-
-
77954840889
-
Muscle dysfunction caused by a KATP channel mutation in neonatal diabetes is neuronal in origin
-
Clark RH, McTaggart JS, Webster R, et al. Muscle dysfunction caused by a KATP channel mutation in neonatal diabetes is neuronal in origin. Science 2010;329:458-461
-
(2010)
Science
, vol.329
, pp. 458-461
-
-
Clark, R.H.1
McTaggart, J.S.2
Webster, R.3
-
5
-
-
0032517821
-
Distribution and phenotype of neurons containing the ATP-sensitive K+ channel in rat brain
-
Dunn-Meynell AA, Rawson NE, Levin BE. Distribution and phenotype of neurons containing the ATP-sensitive K+ channel in rat brain. Brain Res 1998;814:41-54
-
(1998)
Brain Res
, vol.814
, pp. 41-54
-
-
Dunn-Meynell, A.A.1
Rawson, N.E.2
Levin, B.E.3
-
6
-
-
24144467758
-
Activating mutations in Kir6.2 and neonatal diabetes: New clinical syndromes, new scientific insights, and new therapy
-
Hattersley AT, Ashcroft FM. Activating mutations in Kir6.2 and neonatal diabetes: new clinical syndromes, new scientific insights, and new therapy. Diabetes 2005;54:2503-2513
-
(2005)
Diabetes
, vol.54
, pp. 2503-2513
-
-
Hattersley, A.T.1
Ashcroft, F.M.2
-
7
-
-
20344380957
-
Mutations in the Kir6.2 subunit of the KATP channel and permanent neonatal diabetes: New insights and new treatment
-
Slingerland AS, Hattersley AT. Mutations in the Kir6.2 subunit of the KATP channel and permanent neonatal diabetes: new insights and new treatment. Ann Med 2005;37:186-195
-
(2005)
Ann Med
, vol.37
, pp. 186-195
-
-
Slingerland, A.S.1
Hattersley, A.T.2
-
8
-
-
33847363327
-
Improved motor development and good long-term glycaemic control with sulfonylurea treatment in a patient with the syndrome of intermediate developmental delay, early-onset generalised epilepsy and neonatal diabetes associated with the V59M mutation in the KCNJ11 gene
-
Slingerland AS, Nuboer R, Hadders-Algra M, Hattersley AT, Bruining GJ. Improved motor development and good long-term glycaemic control with sulfonylurea treatment in a patient with the syndrome of intermediate developmental delay, early-onset generalised epilepsy and neonatal diabetes associated with the V59M mutation in the KCNJ11 gene. Diabetologia 2006;49:2559-2563
-
(2006)
Diabetologia
, vol.49
, pp. 2559-2563
-
-
Slingerland, A.S.1
Nuboer, R.2
Hadders-Algra, M.3
Hattersley, A.T.4
Bruining, G.J.5
-
9
-
-
40049100688
-
Sulphonylurea therapy improves cognition in a patient with the V59M KCNJ11 mutation
-
Slingerland AS, Hurkx W, Noordam K, et al. Sulphonylurea therapy improves cognition in a patient with the V59M KCNJ11 mutation. Diabet Med 2008;25:277-281
-
(2008)
Diabet Med
, vol.25
, pp. 277-281
-
-
Slingerland, A.S.1
Hurkx, W.2
Noordam, K.3
-
10
-
-
35748967277
-
Sulfonylurea improves CNS function in a case of intermediate DEND syndrome caused by a mutation in KCNJ11
-
Mlynarski W, Tarasov AI, Gach A, et al. Sulfonylurea improves CNS function in a case of intermediate DEND syndrome caused by a mutation in KCNJ11. Nat Clin Pract Neurol 2007;3:640-645
-
(2007)
Nat Clin Pract Neurol
, vol.3
, pp. 640-645
-
-
Mlynarski, W.1
Tarasov, A.I.2
Gach, A.3
-
11
-
-
80755173306
-
Creation of the Web-based University of Chicago Monogenic Diabetes Registry: Using technology to facilitate longitudinal study of rare subtypes of diabetes
-
Greeley SA, Naylor RN, Cook LS, Tucker SE, Lipton RB, Philipson LH. Creation of the Web-based University of Chicago Monogenic Diabetes Registry: using technology to facilitate longitudinal study of rare subtypes of diabetes. J Diabetes Sci Tech 2011;5:879-886
-
(2011)
J Diabetes Sci Tech
, vol.5
, pp. 879-886
-
-
Greeley, S.A.1
Naylor, R.N.2
Cook, L.S.3
Tucker, S.E.4
Lipton, R.B.5
Philipson, L.H.6
-
12
-
-
59649090686
-
-
6th ed. San Antonio, TX, Pearson Psychological Corporation
-
Beery KE, Beery NA. The Beery-Buktenica Developmental Test of Visual-Motor Integration: Beery VMI Administration, Scoring, and Teaching. 6th ed. San Antonio, TX, Pearson Psychological Corporation, 2010
-
(2010)
The Beery-Buktenica Developmental Test of Visual-Motor Integration: Beery VMI Administration, Scoring, and Teaching
-
-
Beery, K.E.1
Beery, N.A.2
-
13
-
-
0031159365
-
Test of visual-motor integration: Construct validity in a comparison with the Beery-Buktenica Developmental Test of Visual-Motor Integration
-
Preda C. Test of visual-motor integration: construct validity in a comparison with the Beery-Buktenica Developmental Test of Visual-Motor Integration. Percept Mot Skills 1997;84:1439-1443
-
(1997)
Percept Mot Skills
, vol.84
, pp. 1439-1443
-
-
Preda, C.1
-
14
-
-
79953878418
-
From genes to brain development to phenotypic behavior: "dorsal-stream vulnerability" in relation to spatial cognition, attention, and planning of actions in Williams syndrome (WS) and other developmental disorders
-
Atkinson J, Braddick O. From genes to brain development to phenotypic behavior: "dorsal-stream vulnerability" in relation to spatial cognition, attention, and planning of actions in Williams syndrome (WS) and other developmental disorders. Prog Brain Res 2011;189:261-283
-
(2011)
Prog Brain Res
, vol.189
, pp. 261-283
-
-
Atkinson, J.1
Braddick, O.2
-
15
-
-
70349575972
-
Assessment and management of hypoglycemia in children and adolescents with diabetes
-
Clarke W, Jones T, Rewers A, Dunger D, Klingensmith GJ. Assessment and management of hypoglycemia in children and adolescents with diabetes. Pediatr Diabetes 2009;10(Suppl. 12):134-145
-
(2009)
Pediatr Diabetes
, vol.10
, Issue.SUPPL. 12
, pp. 134-145
-
-
Clarke, W.1
Jones, T.2
Rewers, A.3
Dunger, D.4
Klingensmith, G.J.5
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