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Volumn 54, Issue 1, 2007, Pages 59-62

A case of prolactin deficiency with familial puerperal alactogenesis accompanying impaired ACTH secretion

Author keywords

Combined pituitary hormone deficiency; Encephalitis; Lactogenesis; Polymerase chain reaction

Indexed keywords

CORTICOTROPIN; DEXAMETHASONE; FOLLITROPIN; GROWTH HORMONE; HYDROCORTISONE; LUTEINIZING HORMONE; METHYLPREDNISOLONE; PREDNISOLONE; PROLACTIN; THYROTROPIN;

EID: 33947609991     PISSN: 09188959     EISSN: 13484540     Source Type: Journal    
DOI: 10.1507/endocrj.K05-163     Document Type: Article
Times cited : (6)

References (14)
  • 2
    • 0022966503 scopus 로고
    • Post-traumatic hypopituitarism. Six cases and a review of the literature
    • Edwards OM, Clark JD (1986) Post-traumatic hypopituitarism. Six cases and a review of the literature. Medicine (Baltimore) 65: 281-902.
    • (1986) Medicine (Baltimore) , vol.65 , pp. 281-902
    • Edwards, O.M.1    Clark, J.D.2
  • 3
    • 0031752470 scopus 로고    scopus 로고
    • Sheehan's syndrome of more than 30 years' duration: An endocrine and MRI study of 6 cases
    • Otsuka F, Kageyama J, Ogura T, Hattori T, Makino H (1998) Sheehan's syndrome of more than 30 years' duration: an endocrine and MRI study of 6 cases. Endocr J 45: 451-458.
    • (1998) Endocr J , vol.45 , pp. 451-458
    • Otsuka, F.1    Kageyama, J.2    Ogura, T.3    Hattori, T.4    Makino, H.5
  • 5
    • 0031003241 scopus 로고    scopus 로고
    • Familial puerperal alactogenesis: Possibility of a genetically transmitted isolated prolactin deficiency
    • Zargar AH, Masoodi SR, Laway BA, Shah NA, Salahudin M (1997) Familial puerperal alactogenesis: possibility of a genetically transmitted isolated prolactin deficiency. Br J Obstet Gynaecol 104: 629-631.
    • (1997) Br J Obstet Gynaecol , vol.104 , pp. 629-631
    • Zargar, A.H.1    Masoodi, S.R.2    Laway, B.A.3    Shah, N.A.4    Salahudin, M.5
  • 7
    • 0026475362 scopus 로고
    • Isolated prolactin deficiency: A case report
    • Falk RJ (1992) Isolated prolactin deficiency: a case report. Fertil Steril 58: 1060-1062.
    • (1992) Fertil Steril , vol.58 , pp. 1060-1062
    • Falk, R.J.1
  • 9
    • 0030978612 scopus 로고    scopus 로고
    • Lymphocytic adrenohypophysitis and lymphocytic infundibuloneurohypophysitis
    • Hashimoto K, Takao T, Makino S (1997) Lymphocytic adrenohypophysitis and lymphocytic infundibuloneurohypophysitis. Endocr J 44: 1-10.
    • (1997) Endocr J , vol.44 , pp. 1-10
    • Hashimoto, K.1    Takao, T.2    Makino, S.3
  • 10
    • 0032989717 scopus 로고    scopus 로고
    • Longitudinal hormonal and pituitary imaging changes in two female with combined pituitary hormone deficiency due to deletion of A301, G302 in the Prop-1 gene
    • Mendonca BB, Osorio MGF, Latronico C, Estefan V, Lo LSS, Arnhold IJP (1999) Longitudinal hormonal and pituitary imaging changes in two female with combined pituitary hormone deficiency due to deletion of A301, G302 in the Prop-1 gene. J Clin Endocrinol Metab 84: 942-945.
    • (1999) J Clin Endocrinol Metab , vol.84 , pp. 942-945
    • Mendonca, B.B.1    Osorio, M.G.F.2    Latronico, C.3    Estefan, V.4    Lo, L.S.S.5    Arnhold, I.J.P.6
  • 11
    • 0031741771 scopus 로고    scopus 로고
    • Phenotypic variability in familial combined pituitary hormone deficiency caused by a Prop-1 gene mutation resulting in the substitution of Arg-Cys at codon 120 (R120C)
    • Fluck C, Deladoey J, Rutishauser K, Eble A, Marti U, Wu W, Mullis PE (1998) Phenotypic variability in familial combined pituitary hormone deficiency caused by a Prop-1 gene mutation resulting in the substitution of Arg-Cys at codon 120 (R120C). J Clin Endocrinol Metab 83: 3727-3734.
    • (1998) J Clin Endocrinol Metab , vol.83 , pp. 3727-3734
    • Fluck, C.1    Deladoey, J.2    Rutishauser, K.3    Eble, A.4    Marti, U.5    Wu, W.6    Mullis, P.E.7
  • 12
    • 0034038650 scopus 로고    scopus 로고
    • Combined pituitary hormone deficiency and pituitary hypoplasia due to a mutation of the Pit-1 gene
    • Frisch H, Kim C, Hausler G, Pfaffle R (2000) Combined pituitary hormone deficiency and pituitary hypoplasia due to a mutation of the Pit-1 gene. Clin Endocrinol 52: 661-665.
    • (2000) Clin Endocrinol , vol.52 , pp. 661-665
    • Frisch, H.1    Kim, C.2    Hausler, G.3    Pfaffle, R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.