메뉴 건너뛰기




Volumn 68, Issue 5, 2008, Pages 747-755

Non-insulinoma persistent hyperinsulinaemic hypoglycaemia caused by an activating glucokinase mutation: Hypoglycaemia unawareness and attacks

Author keywords

[No Author keywords available]

Indexed keywords

DIAZOXIDE; GLUCOKINASE; GLUCOSE; OCTREOTIDE; THIAZIDE DIURETIC AGENT;

EID: 42149161294     PISSN: 03000664     EISSN: 13652265     Source Type: Journal    
DOI: 10.1111/j.1365-2265.2008.03184.x     Document Type: Article
Times cited : (27)

References (44)
  • 2
    • 0029156713 scopus 로고
    • Clinical review 72: Diagnosis and management of functioning islet cell tumors
    • Perry, R.R. Vinik, A.I. (1995) Clinical review 72: diagnosis and management of functioning islet cell tumors. Journal of Clinical Endocrinology and Metabolism, 80, 2273 2278.
    • (1995) Journal of Clinical Endocrinology and Metabolism , vol.80 , pp. 2273-2278
    • Perry, R.R.1    Vinik, A.I.2
  • 6
    • 0035013533 scopus 로고    scopus 로고
    • Adult-onset nesidioblastosis causing hypoglycemia: An important clinical entity and continuing treatment dilemma
    • Witteles, R.M., Straus, F.H., I.I. Sugg, S.L., Koka, M.R., Costa, E.A. Kaplan, E.L. (2001) Adult-onset nesidioblastosis causing hypoglycemia: an important clinical entity and continuing treatment dilemma. Archives of Surgery, 136, 656 663.
    • (2001) Archives of Surgery , vol.136 , pp. 656-663
    • Witteles, R.M.1    Straus, F.H.2    I.I. Sugg, S.L.3    Koka, M.R.4    Costa, E.A.5    Kaplan, E.L.6
  • 8
    • 9744240247 scopus 로고    scopus 로고
    • Nesidioblastosis associated with hyperinsulinemic hypoglycemia in adults: Review of the literature
    • Jabri, A.L. Bayard, C. (2004) Nesidioblastosis associated with hyperinsulinemic hypoglycemia in adults: review of the literature. European Journal of Internal Medicine, 15, 407 410.
    • (2004) European Journal of Internal Medicine , vol.15 , pp. 407-410
    • Jabri, A.L.1    Bayard, C.2
  • 11
    • 34447320515 scopus 로고    scopus 로고
    • Noninsulinoma pancreatogenous hypoglycemia syndrome: Quantitative and immunohistochemical analyses of islet cells for insulin, glucagon, somatostatin, and pancreatic and duodenal homeobox protein
    • Sahloul, R., Yaqub, N., Driscoll, H.K., Leidy, J.W. Jr., Parkash, J., Matthews, K.A. Chertow, B.S. (2007) Noninsulinoma pancreatogenous hypoglycemia syndrome: quantitative and immunohistochemical analyses of islet cells for insulin, glucagon, somatostatin, and pancreatic and duodenal homeobox protein. Endocrine Practice, 13, 187 193.
    • (2007) Endocrine Practice , vol.13 , pp. 187-193
    • Sahloul, R.1    Yaqub, N.2    Driscoll, H.K.3    Leidy Jr., J.W.4    Parkash, J.5    Matthews, K.A.6    Chertow, B.S.7
  • 14
    • 0028941073 scopus 로고
    • Medical progress - Hypoglycemic disorders
    • Service, F.J. (1995) Medical progress - hypoglycemic disorders. New England Journal of Medicine, 332, 1144 1152.
    • (1995) New England Journal of Medicine , vol.332 , pp. 1144-1152
    • Service, F.J.1
  • 16
    • 0034119682 scopus 로고    scopus 로고
    • Persistent hyperinsulinaemic hypoglycaemia of infancy: A heterogeneous syndrome unrelated to nesidioblastosis
    • Rahier, J., Guiot, Y. Sempoux, C. (2000) Persistent hyperinsulinaemic hypoglycaemia of infancy: a heterogeneous syndrome unrelated to nesidioblastosis. Archives of Disease in Childhood. Fetal and Neonatal Edition, 82, F108 F112.
    • (2000) Archives of Disease in Childhood. Fetal and Neonatal Edition , vol.82
    • Rahier, J.1    Guiot, Y.2    Sempoux, C.3
  • 18
    • 0029836983 scopus 로고    scopus 로고
    • Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy
    • Thomas, P., Ye, Y. Lightner, E. (1996) Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy. Human Molecular Genetics, 5, 1809 1812.
    • (1996) Human Molecular Genetics , vol.5 , pp. 1809-1812
    • Thomas, P.1    Ye, Y.2    Lightner, E.3
  • 25
    • 25844501587 scopus 로고    scopus 로고
    • Serum glucagon counterregulatory hormonal response to hypoglycemia is blunted in congenital hyperinsulinism
    • Hussain, K., Bryan, J., Christesen, H.T., Brusgaard, K. guilar-Bryan, L. (2005) Serum glucagon counterregulatory hormonal response to hypoglycemia is blunted in congenital hyperinsulinism. Diabetes, 54, 2946 2951.
    • (2005) Diabetes , vol.54 , pp. 2946-2951
    • Hussain, K.1    Bryan, J.2    Christesen, H.T.3    Brusgaard, K.4    Guilar-Bryan, L.5
  • 27
    • 1642540203 scopus 로고    scopus 로고
    • Family with autosomal dominant hyperinsulinism associated with A456V mutation in the glucokinase gene
    • Dullaart, R.P., Hoogenberg, K., Rouwe, C.W. Stulp, B.K. (2004) Family with autosomal dominant hyperinsulinism associated with A456V mutation in the glucokinase gene. Journal of Internal Medicine, 255, 143 145.
    • (2004) Journal of Internal Medicine , vol.255 , pp. 143-145
    • Dullaart, R.P.1    Hoogenberg, K.2    Rouwe, C.W.3    Stulp, B.K.4
  • 33
    • 33644749337 scopus 로고    scopus 로고
    • The network of glucokinase-expressing cells in glucose homeostasis and the potential of glucokinase activators for diabetes therapy
    • Matschinsky, F.M., Magnuson, M.A., Zelent, D., Jetton, T.L., Doliba, N., Han, Y., Taub, R. Grimsby, J. (2006) The network of glucokinase-expressing cells in glucose homeostasis and the potential of glucokinase activators for diabetes therapy. Diabetes, 55, 1 12.
    • (2006) Diabetes , vol.55 , pp. 1-12
    • Matschinsky, F.M.1    Magnuson, M.A.2    Zelent, D.3    Jetton, T.L.4    Doliba, N.5    Han, Y.6    Taub, R.7    Grimsby, J.8
  • 34
    • 0033670425 scopus 로고    scopus 로고
    • Counterregulatory responses to hypoglycemia in patients with glucokinase gene mutations
    • Guenat, E., Seematter, G., Philippe, J., Temler, E., Jequier, E. Tappy, L. (2000) Counterregulatory responses to hypoglycemia in patients with glucokinase gene mutations. Diabetes Metabolism, 26, 377 384.
    • (2000) Diabetes Metabolism , vol.26 , pp. 377-384
    • Guenat, E.1    Seematter, G.2    Philippe, J.3    Temler, E.4    Jequier, E.5    Tappy, L.6
  • 37
    • 34249683855 scopus 로고    scopus 로고
    • Glucose-dependent modulation of insulin secretion and intracellular calcium ions by GKA50, a glucokinase activator
    • Johnson, D., Shepherd, R.M., Gill, D., Gorman, T., Smith, D.M. Dunne, M.J. (2007) Glucose-dependent modulation of insulin secretion and intracellular calcium ions by GKA50, a glucokinase activator. Diabetes, 56, 1694 1702.
    • (2007) Diabetes , vol.56 , pp. 1694-1702
    • Johnson, D.1    Shepherd, R.M.2    Gill, D.3    Gorman, T.4    Smith, D.M.5    Dunne, M.J.6
  • 40
    • 33644664033 scopus 로고    scopus 로고
    • Mechanisms of hypoglycemia-associated autonomic failure and its component syndromes in diabetes
    • Cryer, P.E. (2005) Mechanisms of hypoglycemia-associated autonomic failure and its component syndromes in diabetes. Diabetes, 54, 3592 3601.
    • (2005) Diabetes , vol.54 , pp. 3592-3601
    • Cryer, P.E.1
  • 42
    • 33746269205 scopus 로고    scopus 로고
    • Hypoglycemia in diabetes: Pathophysiological mechanisms and diurnal variation
    • Cryer, P.E. (2006) Hypoglycemia in diabetes: pathophysiological mechanisms and diurnal variation. Progress in Brain Research, 153, 361 365.
    • (2006) Progress in Brain Research , vol.153 , pp. 361-365
    • Cryer, P.E.1
  • 43
    • 2542610014 scopus 로고    scopus 로고
    • A novel syndrome of autosomal-dominant hyperinsulinemic hypoglycemia linked to a mutation in the human insulin receptor gene
    • Hojlund, K., Hansen, T., Lajer, M., Henriksen, J.E., Levin, K., Lindholm, J., Pedersen, O. Beck-Nielsen, H. (2004) A novel syndrome of autosomal-dominant hyperinsulinemic hypoglycemia linked to a mutation in the human insulin receptor gene. Diabetes, 53, 1592 1598.
    • (2004) Diabetes , vol.53 , pp. 1592-1598
    • Hojlund, K.1    Hansen, T.2    Lajer, M.3    Henriksen, J.E.4    Levin, K.5    Lindholm, J.6    Pedersen, O.7    Beck-Nielsen, H.8
  • 44
    • 0037464795 scopus 로고    scopus 로고
    • A new subtype of autosomal dominant diabetes attributable to a mutation in the gene for sulfonylurea receptor 1
    • Huopio, H., Otonkoski, T., Vauhkonen, I., Reimann, F., Ashcroft, F.M. Laakso, M. (2003) A new subtype of autosomal dominant diabetes attributable to a mutation in the gene for sulfonylurea receptor 1. Lancet, 361, 301 307.
    • (2003) Lancet , vol.361 , pp. 301-307
    • Huopio, H.1    Otonkoski, T.2    Vauhkonen, I.3    Reimann, F.4    Ashcroft, F.M.5    Laakso, M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.