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Volumn 146, Issue 5, 2008, Pages 570-577

Pituitary abnormalities in Prader-Willi syndrome and early onset morbid obesity

Author keywords

Early onset obesity; Pituitary gland; Prader Willi syndrome

Indexed keywords

HYPOPHYSIS HORMONE;

EID: 43049125542     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.31677     Document Type: Article
Times cited : (67)

References (35)
  • 1
    • 1342301761 scopus 로고    scopus 로고
    • Some exact conditional tests of independence for RxC cross-classification tables
    • Agresti A, Wackerly D. 1997. Some exact conditional tests of independence for RxC cross-classification tables. Psychometrika 42:111-126.
    • (1997) Psychometrika , vol.42 , pp. 111-126
    • Agresti, A.1    Wackerly, D.2
  • 2
    • 0033498345 scopus 로고    scopus 로고
    • Congenital hypogonadotropic hypogonadism and micropenis: Effect of testosterone treatment on adult penile size why sex reversal is not indicated
    • Bin-Abbas B, Conte FA, Grumbach MM, Kaplan SL. 1999. Congenital hypogonadotropic hypogonadism and micropenis: Effect of testosterone treatment on adult penile size why sex reversal is not indicated. J Pediatr 134:579-583.
    • (1999) J Pediatr , vol.134 , pp. 579-583
    • Bin-Abbas, B.1    Conte, F.A.2    Grumbach, M.M.3    Kaplan, S.L.4
  • 3
    • 31044455614 scopus 로고    scopus 로고
    • Prader-Willi syndrome: Clinical genetics, cytogenetics and molecular biology
    • Bittel DC, Butler MG. 2005. Prader-Willi syndrome: Clinical genetics, cytogenetics and molecular biology. Expert Rev Mol Med 7:1-20.
    • (2005) Expert Rev Mol Med , vol.7 , pp. 1-20
    • Bittel, D.C.1    Butler, M.G.2
  • 4
    • 15744364160 scopus 로고    scopus 로고
    • Increased abnormal pituitary findings on magnetic resonance in patients with male idiopathic hypogonadotrophic hypogonadism
    • Bolu SE, Tasar M, Uckaya G, Gonul E, Deniz F, Ozdemir IC. 2004. Increased abnormal pituitary findings on magnetic resonance in patients with male idiopathic hypogonadotrophic hypogonadism. J Endocrinol Invest 27:1029-1033.
    • (2004) J Endocrinol Invest , vol.27 , pp. 1029-1033
    • Bolu, S.E.1    Tasar, M.2    Uckaya, G.3    Gonul, E.4    Deniz, F.5    Ozdemir, I.C.6
  • 6
    • 0035719948 scopus 로고    scopus 로고
    • Endocrine dysfunction in Prader-Willi syndrome: A review with special reference to GH
    • Burman P, Ritzen EM, Lindgren AC. 2001. Endocrine dysfunction in Prader-Willi syndrome: A review with special reference to GH. Endocr Rev 22:787-799.
    • (2001) Endocr Rev , vol.22 , pp. 787-799
    • Burman, P.1    Ritzen, E.M.2    Lindgren, A.C.3
  • 7
    • 0025149577 scopus 로고
    • Endocrine function and morphological findings in patients with disorders of the hypothalamo-pituitary area: A study with magnetic resonance
    • Cacciari E, Zucchini S, Carla G, Pirazzoli P, Cicognani A, Mandini M, Busacca M, Trevisan C. 1990. Endocrine function and morphological findings in patients with disorders of the hypothalamo-pituitary area: A study with magnetic resonance. Arch Dis Child 65:1199-1202.
    • (1990) Arch Dis Child , vol.65 , pp. 1199-1202
    • Cacciari, E.1    Zucchini, S.2    Carla, G.3    Pirazzoli, P.4    Cicognani, A.5    Mandini, M.6    Busacca, M.7    Trevisan, C.8
  • 8
    • 0034527182 scopus 로고    scopus 로고
    • Fetal hypothalamic-pituitary adrenal (HPA) development and activation as a determinant of the timing of birth, and of postnatal disease
    • Challis J, Sloboda D, Matthews S, Holloway A, Alfaidy N, Howe D, Fraser M, Newnham J. 2000. Fetal hypothalamic-pituitary adrenal (HPA) development and activation as a determinant of the timing of birth, and of postnatal disease. Endocr Res 26:489-504.
    • (2000) Endocr Res , vol.26 , pp. 489-504
    • Challis, J.1    Sloboda, D.2    Matthews, S.3    Holloway, A.4    Alfaidy, N.5    Howe, D.6    Fraser, M.7    Newnham, J.8
  • 11
    • 14544272858 scopus 로고    scopus 로고
    • Monogenic obesity in humans
    • Farooqi IS, O'Rahilly S. 2005. Monogenic obesity in humans. Annu Rev Med 56:443-458.
    • (2005) Annu Rev Med , vol.56 , pp. 443-458
    • Farooqi, I.S.1    O'Rahilly, S.2
  • 14
    • 24344499528 scopus 로고    scopus 로고
    • The number of hypothalamic hypocretin (orexin) neurons is not affected in Prader-Willi syndrome
    • Fronczek R, Lammers GJ, Balesar R, Unmehopa UA, Swaab DF. 2005. The number of hypothalamic hypocretin (orexin) neurons is not affected in Prader-Willi syndrome. J Clin Endocrinol Metab 90:5466-5470.
    • (2005) J Clin Endocrinol Metab , vol.90 , pp. 5466-5470
    • Fronczek, R.1    Lammers, G.J.2    Balesar, R.3    Unmehopa, U.A.4    Swaab, D.F.5
  • 16
    • 0031114837 scopus 로고    scopus 로고
    • Genomic imprinting: Potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes
    • Glenn CG, Driscoll DJ, Thomas PY, Nicholls RD. 1997. Genomic imprinting: Potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes. Mol Hum Reprod 3:321-332.
    • (1997) Mol Hum Reprod , vol.3 , pp. 321-332
    • Glenn, C.G.1    Driscoll, D.J.2    Thomas, P.Y.3    Nicholls, R.D.4
  • 17
    • 1042267409 scopus 로고    scopus 로고
    • Prader-Willi syndrome: Advances in genetics, pathophysiology and treatment
    • Goldstone AP. 2004. Prader-Willi syndrome: Advances in genetics, pathophysiology and treatment. Trends Endocrinol Metab 15:12-20.
    • (2004) Trends Endocrinol Metab , vol.15 , pp. 12-20
    • Goldstone, A.P.1
  • 18
    • 0036172575 scopus 로고    scopus 로고
    • Hypothalamic NPY and agouti-related protein are increased in human illness but not in Prader-Willi syndrome and other obese subjects
    • Goldstone AP, Unmehopa UA, Bloom SR, Swaab DF. 2002. Hypothalamic NPY and agouti-related protein are increased in human illness but not in Prader-Willi syndrome and other obese subjects. J Clin Endocrinol Metab 87:927-937.
    • (2002) J Clin Endocrinol Metab , vol.87 , pp. 927-937
    • Goldstone, A.P.1    Unmehopa, U.A.2    Bloom, S.R.3    Swaab, D.F.4
  • 19
    • 0038469984 scopus 로고    scopus 로고
    • Hypothalamic growth hormone-releasing hormone (GHRH) cell number is increased in human illness, but is not reduced in Prader-Willi syndrome or obesity
    • Goldstone AP, Unmehopa UA, Swaab DF. 2003. Hypothalamic growth hormone-releasing hormone (GHRH) cell number is increased in human illness, but is not reduced in Prader-Willi syndrome or obesity. Clin Endocrinol (Oxf) 58:743-755.
    • (2003) Clin Endocrinol (Oxf) , vol.58 , pp. 743-755
    • Goldstone, A.P.1    Unmehopa, U.A.2    Swaab, D.F.3
  • 20
    • 0026535844 scopus 로고
    • A neuropathological study of a case of the Prader-Willi syndrome with an interstitial deletion of the proximal long arm of chromosome 15
    • Hayashi M, Itoh M, Kabasawa Y, Hayashi H, Satoh J, Morimatsu Y. 1992. A neuropathological study of a case of the Prader-Willi syndrome with an interstitial deletion of the proximal long arm of chromosome 15. Brain Dev 1:58-62.
    • (1992) Brain Dev , vol.1 , pp. 58-62
    • Hayashi, M.1    Itoh, M.2    Kabasawa, Y.3    Hayashi, H.4    Satoh, J.5    Morimatsu, Y.6
  • 21
    • 0038389384 scopus 로고    scopus 로고
    • Mutations in the human proopiomelanocortin gene
    • Krude H, Biebermann H, Gruters A. 2003. Mutations in the human proopiomelanocortin gene. Ann NY Acad Sci 994:233-239.
    • (2003) Ann NY Acad Sci , vol.994 , pp. 233-239
    • Krude, H.1    Biebermann, H.2    Gruters, A.3
  • 22
    • 0032704136 scopus 로고    scopus 로고
    • Prader-Labhart-Willi syndrome with central precocious puberty and empty sella syndrome
    • Linnemann K, Schroder C, Mix M, Kruger G, Fusch C. 1999. Prader-Labhart-Willi syndrome with central precocious puberty and empty sella syndrome. Acta Paediatr 88:1295-1297.
    • (1999) Acta Paediatr , vol.88 , pp. 1295-1297
    • Linnemann, K.1    Schroder, C.2    Mix, M.3    Kruger, G.4    Fusch, C.5
  • 23
  • 24
    • 0038021427 scopus 로고    scopus 로고
    • Pituitary magnetic resonance imaging in idiopathic and genetic growth hormone deficiency
    • Maghnie M, Loche S, Cappa M. 2003. Pituitary magnetic resonance imaging in idiopathic and genetic growth hormone deficiency. J Clin Endocrinol Metab 88:1911.
    • (2003) J Clin Endocrinol Metab , vol.88 , pp. 1911
    • Maghnie, M.1    Loche, S.2    Cappa, M.3
  • 25
    • 0030034236 scopus 로고    scopus 로고
    • MR of the pituitary in patients with Prader-Willi syndrome: Size determination and imaging findings
    • Miller L, Angulo M, Price D, Taneja S. 1996. MR of the pituitary in patients with Prader-Willi syndrome: Size determination and imaging findings. Pediatr Radiol 26:43-47.
    • (1996) Pediatr Radiol , vol.26 , pp. 43-47
    • Miller, L.1    Angulo, M.2    Price, D.3    Taneja, S.4
  • 28
    • 0035491217 scopus 로고    scopus 로고
    • Magnetic resonance diagnosis of congenital hypopituitarism in children with optic nerve hypoplasia
    • Phillips PH, Spear C, Brodsky MC. 2001. Magnetic resonance diagnosis of congenital hypopituitarism in children with optic nerve hypoplasia. J AAPOS 5:275-280.
    • (2001) J AAPOS , vol.5 , pp. 275-280
    • Phillips, P.H.1    Spear, C.2    Brodsky, M.C.3
  • 30
    • 0030727691 scopus 로고    scopus 로고
    • Prader-Willi syndrome and the hypothalamus
    • Swaab DF. 1997. Prader-Willi syndrome and the hypothalamus. Acta Paediatr Suppl 423:50-54.
    • (1997) Acta Paediatr , Issue.SUPPL. 423 , pp. 50-54
    • Swaab, D.F.1
  • 31
    • 0028852641 scopus 로고
    • Alterations in the hypothalamic paraventricular nucleus and its oxytocin neurons (putative satiety cells) in Prader-Willi syndrome: A study of five cases
    • Swaab DF, Purba JS, Hofman MA. 1995. Alterations in the hypothalamic paraventricular nucleus and its oxytocin neurons (putative satiety cells) in Prader-Willi syndrome: A study of five cases. J Clin Endocrinol Metab 80:573-579.
    • (1995) J Clin Endocrinol Metab , vol.80 , pp. 573-579
    • Swaab, D.F.1    Purba, J.S.2    Hofman, M.A.3
  • 32
    • 0034523408 scopus 로고    scopus 로고
    • Auxological and endocrine evolution of 28 children with Prader-Willi syndrome: Effect of GH therapy in 14 children
    • Tauber M, Barbeau C, Jouret B, Pienkowski C, Malzac P, Moncla A, Rochiccioli P. 2000. Auxological and endocrine evolution of 28 children with Prader-Willi syndrome: Effect of GH therapy in 14 children. Horm Res 53:279-287.
    • (2000) Horm Res , vol.53 , pp. 279-287
    • Tauber, M.1    Barbeau, C.2    Jouret, B.3    Pienkowski, C.4    Malzac, P.5    Moncla, A.6    Rochiccioli, P.7
  • 33
    • 0033927916 scopus 로고    scopus 로고
    • Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesity
    • Vaisse C, Clement K, Durand E, Hercberg S, Guy-Grand B, Froguel P. 2000. Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesity. J Clin Invest 106:253-262.
    • (2000) J Clin Invest , vol.106 , pp. 253-262
    • Vaisse, C.1    Clement, K.2    Durand, E.3    Hercberg, S.4    Guy-Grand, B.5    Froguel, P.6
  • 34
    • 33745612078 scopus 로고    scopus 로고
    • A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity
    • Varela MC, Simoes-Sato AY, Kim CA, Bertola DR, De Castro CI, Koiffmann CP. 2006. A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity. Eur J Med Genet 49:298-305.
    • (2006) Eur J Med Genet , vol.49 , pp. 298-305
    • Varela, M.C.1    Simoes-Sato, A.Y.2    Kim, C.A.3    Bertola, D.R.4    De Castro, C.I.5    Koiffmann, C.P.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.