SCOPUS 정보 검색 플랫폼

Volumn 30, Issue 11, 2007, Pages

Sulfonylrea treatment in permanent neonatal diabetes due to G53D mutation in the KCNJ11 gene [1]

(6) Gurgel, Lucimary C a Crispim, Felipe a Noffs, Maria Helena S a Belzunces, Erich a Rahal, Marcio A a Moisés, Regina S a

a FEDERAL UNIVERSITY OF SÃO PAULO (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

GLIBENCLAMIDE; INSULIN; PANCREAS ISLET CELL ANTIBODY; SULFONYLUREA;

ADULT; CASE REPORT; COGNITION; DIABETES MELLITUS; DRUG DOSE REDUCTION; DRUG EFFICACY; DRUG SUBSTITUTION; ELECTROENCEPHALOGRAM; GENE MUTATION; GLUCOSE BLOOD LEVEL; HISTORY OF MEDICINE; HUMAN; INSULIN TREATMENT; INTELLIGENCE QUOTIENT; LEARNING; LEARNING DISORDER; LETTER; LONG TERM MEMORY; MALE; METABOLIC REGULATION; NEUROLOGIC DISEASE; NEUROPSYCHOLOGICAL TEST; QUALITY OF LIFE; STATISTICAL SIGNIFICANCE; VERBAL BEHAVIOR;

ADULT; AGE OF ONSET; AMINO ACID SUBSTITUTION; DIABETES MELLITUS; HETEROZYGOTE DETECTION; HUMANS; INFANT; MALE; POTASSIUM CHANNELS, INWARDLY RECTIFYING; SULFONYLUREA COMPOUNDS;

EID: 36049015306 PISSN: 01495992 EISSN: 01495992 Source Type: Journal
DOI: 10.2337/dc07-1196 Document Type: Letter

Times cited : (27)

References (3)

1
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- Neonatal Diabetes International Collaborative Group: Switching from insulin to oral sulfonilureas in patients with diabetes due to Kir6.2 mutation
- Pearson ER, Flechtner I, Njostad PR, Malecki MT, Flanagan SE, Larkin B, Aschcroft FM, Klimes I, Codner E, Iotova V, Slingerland AS, Shield J, Robert JJ, Holst JJ, Clark PM, Ellard S, Sovik O, Pollak M, Hattersley AT, Neonatal Diabetes International Collaborative Group: Switching from insulin to oral sulfonilureas in patients with diabetes due to Kir6.2 mutation. N Engl J Med 355:467-477, 2006
- (2006) N Engl J Med , vol.355 , pp. 467-477
- Pearson, E.R.¹ Flechtner, I.² Njostad, P.R.³ Malecki, M.T.⁴ Flanagan, S.E.⁵ Larkin, B.⁶ Aschcroft, F.M.⁷ Klimes, I.⁸ Codner, E.⁹ Iotova, V.¹⁰ Slingerland, A.S.¹¹ Shield, J.¹² Robert, J.J.¹³ Holst, J.J.¹⁴ Clark, P.M.¹⁵ Ellard, S.¹⁶ Sovik, O.¹⁷ Pollak, M.¹⁸ Hattersley, A.T.¹⁹

2
- 27744546143
- the Early Onset Diabetes Study Group of the Italian Society of Pediatric Endocrinology and Diabetology: Transient neonatal diabetes is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation
- Colombo C, Delvecchio M, Zecchino C, Faienza MF, Cavallo L, Barbetti F, the Early Onset Diabetes Study Group of the Italian Society of Pediatric Endocrinology and Diabetology: Transient neonatal diabetes is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation. Diabetologia 48:2439-2441, 2005
- (2005) Diabetologia , vol.48 , pp. 2439-2441
- Colombo, C.¹ Delvecchio, M.² Zecchino, C.³ Faienza, M.F.⁴ Cavallo, L.⁵ Barbetti, F.⁶

3
- 33846008028
- Transfer to sulphonylrea therapy in adult subjects with permanent neonatal diabetes due to KCNJ11-activating mutations: Evidence for improvement in insulin sensitivity
- Malecki MT, Snupien J, Klupa T, Wanic K, Mlynarski W, Gach A, Solecka I, Sieradzki J: Transfer to sulphonylrea therapy in adult subjects with permanent neonatal diabetes due to KCNJ11-activating mutations: evidence for improvement in insulin sensitivity. Diabetes Care 30:147-149, 2007
- (2007) Diabetes Care , vol.30 , pp. 147-149
- Malecki, M.T.¹ Snupien, J.² Klupa, T.³ Wanic, K.⁴ Mlynarski, W.⁵ Gach, A.⁶ Solecka, I.⁷ Sieradzki, J.⁸

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.