메뉴 건너뛰기




Volumn 23, Issue , 2012, Pages 30-41

Spectrum of insulin-like growth factor deficiency

Author keywords

[No Author keywords available]

Indexed keywords


EID: 84871958509     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1159/000341739     Document Type: Chapter
Times cited : (13)

References (26)
  • 2
    • 79956157928 scopus 로고    scopus 로고
    • Consensus statement on the standardization and evaluation of growth hormone and insulin-like growth factor assays
    • Clemmons DR: Consensus statement on the standardization and evaluation of growth hormone and insulin-like growth factor assays. Clin Chem 2011; 57:555-559.
    • (2011) Clin Chem , vol.57 , pp. 555-559
    • Clemmons, D.R.1
  • 3
    • 0035217709 scopus 로고    scopus 로고
    • Reference values for IGF-1 throughout childhood and adolescence: a model that accounts simultaneously for the effect of gender, age, and puberty
    • Lofqvist C, Andersson E, Gelander L, Rosberg S, Blum WF, Albertsson WK: Reference values for IGF-1 throughout childhood and adolescence: a model that accounts simultaneously for the effect of gender, age, and puberty. J Clin Endocrinol Metab 2001;86:5870-5876.
    • (2001) J Clin Endocrinol Metab , vol.86 , pp. 5870-5876
    • Lofqvist, C.1    Andersson, E.2    Gelander, L.3    Rosberg, S.4    Blum, W.F.5    Albertsson, W.K.6
  • 9
    • 79952520636 scopus 로고    scopus 로고
    • Genetics of GHRH, GHRH-receptor, GH and GH-receptor: its impact on pharmacogenetics
    • Mullis PE: Genetics of GHRH, GHRH-receptor, GH and GH-receptor: its impact on pharmacogenetics. Best Pract Res Clin Endocrinol Metab 2011;25:25-41.
    • (2011) Best Pract Res Clin Endocrinol Metab , vol.25 , pp. 25-41
    • Mullis, P.E.1
  • 16
    • 66749151333 scopus 로고    scopus 로고
    • Noonan syndrome, the Ras-MAPK signalling pathway and short stature
    • Binder G: Noonan syndrome, the Ras-MAPK signalling pathway and short stature. Horm Res 2009; 71(suppl 2):64-70.
    • (2009) Horm Res , vol.71 , pp. 64-70
    • Binder, G.1
  • 17
    • 77749239998 scopus 로고    scopus 로고
    • Growth hormone and insulin-like growth factor I insensitivity of fibroblasts isolated from a patient with an I{kappa} B{alpha} mutation
    • Wu S, Walenkamp MJ, Lankester A, Bidlingmaier M, Wit JM, De Luca F: Growth hormone and insulin-like growth factor I insensitivity of fibroblasts isolated from a patient with an I{kappa} B{alpha} mutation. J Clin Endocrinol Metab 2010; 95:1220-1228.
    • (2010) J Clin Endocrinol Metab , vol.95 , pp. 1220-1228
    • Wu, S.1    Walenkamp, M.J.2    Lankester, A.3    Bidlingmaier, M.4    Wit, J.M.5    De Luca, F.6
  • 21
    • 0029879642 scopus 로고    scopus 로고
    • A homozygous splice site mutation affecting the intracellular domain of the growth hormone (GH) receptor resulting in Laron syndrome with elevated GH-binding protein [see comments]
    • Woods KA, Fraser NC, Postel Vinay MC, Savage MO, Clark AJ: A homozygous splice site mutation affecting the intracellular domain of the growth hormone (GH) receptor resulting in Laron syndrome with elevated GH-binding protein [see comments]. J Clin Endocrinol Metab 1996;81: 1686-1690.
    • (1996) J Clin Endocrinol Metab , vol.81 , pp. 1686-1690
    • Woods, K.A.1    Fraser, N.C.2    Postel Vinay, M.C.3    Savage, M.O.4    Clark, A.J.5
  • 24
    • 79952496635 scopus 로고    scopus 로고
    • IGF1 molecular anomalies demonstrate its critical role in fetal, postnatal growth and brain development
    • Netchine I, Azzi S, Le BY, Savage MO: IGF1 molecular anomalies demonstrate its critical role in fetal, postnatal growth and brain development. Best Pract Res Clin Endocrinol Metab 2011;25:181-190.
    • (2011) Best Pract Res Clin Endocrinol Metab , vol.25 , pp. 181-190
    • Netchine, I.1    Azzi, S.2    Le, B.Y.3    Savage, M.O.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.