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Volumn 74, Issue 10, 2007, Pages 959-961

Allgrove syndrome

Author keywords

Achalasia cardia; Adrenal failure; Alacrimia

Indexed keywords

FRESH FROZEN PLASMA; GLUCOSE; HYDROCORTISONE;

EID: 36949036231     PISSN: 00195456     EISSN: None     Source Type: Journal    
DOI: 10.1007/s12098-007-0179-7     Document Type: Article
Times cited : (15)

References (8)
  • 1
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    • Allgrove J, Clayton GS, Grant DB. Familial glucocorticoid deficiency with achalasia and deficient tear production. Lancet 1978; 1: 1284-1286.
    • (1978) Lancet , vol.1 , pp. 1284-1286
    • Allgrove, J.1    Clayton, G.S.2    Grant, D.B.3
  • 2
    • 0026934907 scopus 로고
    • Physical and sexual growth patteren of Indian affluent children from 5-18 yr of age
    • Agarwal et al. Physical and sexual growth patteren of Indian affluent children from 5-18 yr of age. Indian Pediatrics 1992; 29: 1203-1282.
    • (1992) Indian Pediatrics , vol.29 , pp. 1203-1282
    • Agarwal1
  • 3
    • 0000074410 scopus 로고
    • Familial Addison's disease. Case report of two sisters with corticoid deficiency unassociated with hypoaldosteronism
    • Sheppard TH, landing BH, Manson DG. Familial Addison's disease. Case report of two sisters with corticoid deficiency unassociated with hypoaldosteronism. J Chlid 1959; 97: 154-162.
    • (1959) J Chlid , vol.97 , pp. 154-162
    • Sheppard, T.H.1    Landing, B.H.2    Manson, D.G.3
  • 4
    • 0014353812 scopus 로고
    • The syndrome of congenital unresponsiveness to ACTH. Report of six cases
    • Migeon CJ, Kenny FM, kowarski A et al. The syndrome of congenital unresponsiveness to ACTH. Report of six cases. Pediatr Res 1968; 2: 501-513.
    • (1968) Pediatr Res , vol.2 , pp. 501-513
    • Migeon, C.J.1    Kenny, F.M.2    Kowarski, A.3
  • 6
    • 0027361220 scopus 로고
    • Localization of the gene encoding the melanocortin-2 (adrenocorticotrphic hormone) and melanocortin-3 receptor to chromosome 18p11.2 and 20q13.2-13.3 by fluorescence in situ hybridization
    • Gantz I, Tashiro T, Barcroft C et al. Localization of the gene encoding the melanocortin-2 (adrenocorticotrphic hormone) and melanocortin-3 receptor to chromosome 18p11.2 and 20q13.2-13.3 by fluorescence in situ hybridization. Genomics 1993; 18: 166-167.
    • (1993) Genomics , vol.18 , pp. 166-167
    • Gantz, I.1    Tashiro, T.2    Barcroft, C.3
  • 7
    • 0029827345 scopus 로고    scopus 로고
    • Linkage of the gene for Triple a syndrome to chromosome 12q13 near type-II keratin gene cluster
    • Weber A, wienker TF, Jung M et al. Linkage of the gene for Triple A syndrome to chromosome 12q13 near type-II keratin gene cluster. Hum Mol Gen 1996; 5: 2061-2066.
    • (1996) Hum Mol Gen , vol.5 , pp. 2061-2066
    • Weber, A.1    Wienker, T.F.2    Jung, M.3
  • 8
    • 0030769871 scopus 로고    scopus 로고
    • Segregation of Allgrove (Triple A) syndrome in Puerto Rican kindreds with chromosome 12 (12q13) polymorphic markers
    • Sratakis CA, Lin JPF, Pras E et al. Segregation of Allgrove (Triple A) syndrome in Puerto Rican kindreds with chromosome 12 (12q13) polymorphic markers. Proc Asso Am Physicians 1997; 109: 478-482.
    • (1997) Proc Asso Am Physicians , vol.109 , pp. 478-482
    • Sratakis, C.A.1    Lin, J.P.F.2    Pras, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.