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Volumn 46, Issue 8, 1999, Pages 514-517

Primary ovarian failure (Turner syndrome excluded). Presenting symptoms and outcome;Insuffisances ovariennes primitives (syndrome de Turner exclu). Circonstances cliniques de decouverte et evolution

Author keywords

Blepharophimosis; Hearing loss; Ovarian dysgenesis; Primary and secondary amenorrhea

Indexed keywords

GONADOTROPIN;

EID: 0032721177     PISSN: 00662097     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (1)

References (8)
  • 1
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    • PALLISTER P.D., OPITZ J.M. - The Perrault syndrome: autosomal recessive ovarian dysgenesis with facultative, non sex limited sensorineural deafness. Am J Med Genet, 1979, 4, 239-246.
    • (1979) Am J Med Genet , vol.4 , pp. 239-246
    • Pallister, P.D.1    Opitz, J.M.2
  • 2
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    • Familial blepharophimosis: Anuncommon marker of ovarian dysgenesis
    • NICOLINO M., BOST M., DAVID M., CHAUSSAIN J.L. -Familial blepharophimosis: anuncommon marker of ovarian dysgenesis. J Pediat Endocrinol. 1995, 8, 127-133.
    • (1995) J Pediat Endocrinol. , vol.8 , pp. 127-133
    • Nicolino, M.1    Bost, M.2    David, M.3    Chaussain, J.L.4
  • 4
    • 0029864808 scopus 로고    scopus 로고
    • A gene for premature ovarian failure associated with eyelid malformation maps to chromosome 3q22-q23
    • AMATI P., GASARINI P., ZLOTOGORA J. et al. - A gene for premature ovarian failure associated with eyelid malformation maps to chromosome 3q22-q23. Am J Hum Genet, 1996, 58, 1089-1092.
    • (1996) Am J Hum Genet , vol.58 , pp. 1089-1092
    • Amati, P.1    Gasarini, P.2    Zlotogora, J.3
  • 5
    • 0029838761 scopus 로고    scopus 로고
    • Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor gene
    • AITTOMAKI K., HERVA R., STENMAN ULF-HAKAN et al. -Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor gene. J Clin Endocrinol Metal, 1996, 81, 3722-3726.
    • (1996) J Clin Endocrinol Metal , vol.81 , pp. 3722-3726
    • Aittomaki, K.1    Herva, R.2    Ulf-Hakan, S.3
  • 6
    • 0030025051 scopus 로고    scopus 로고
    • Brief Report : Testicular and ovarian resistance to luteinizing hormone caused by inactivating mutations of the luteinizing hormone-receptor gene
    • LATRONICO A.C., ANASTI J., ARNHOLD I.J.P., RAPAPORT A. et al. - Brief Report : testicular and ovarian resistance to luteinizing hormone caused by inactivating mutations of the luteinizing hormone-receptor gene. N Eng J Med, 1996, 334, 8, 507-512.
    • (1996) N Eng J Med , vol.334 , Issue.8 , pp. 507-512
    • Latronico, A.C.1    Anasti, J.2    Arnhold, I.J.P.3    Rapaport, A.4
  • 7
    • 0029843814 scopus 로고    scopus 로고
    • An Inactivating Mutation of the Luteinizing Hormone Receptor Causes Amenorrhea in a 46,XX Female
    • SERGIO P., TOLEDO A., HAN G. BRUNNER, KRAAIJ R., POST M., DAHIA P.L.M. et al. - An Inactivating Mutation of the Luteinizing Hormone Receptor Causes Amenorrhea in a 46,XX Female. J Clin Endocrinol Metab, 1996, 81, 3850-3854.
    • (1996) J Clin Endocrinol Metab , vol.81 , pp. 3850-3854
    • Sergio, P.1    Toledo, A.2    Brunner, H.G.3    Kraaij, R.4    Post, M.5    Dahia, P.L.M.6
  • 8
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    • Pseudo-hypoparathyroïdies: Nouvelles approches diagnostiques et thérapeutiques
    • CAREL J.C., GARABEDIAN M., MALLET E., CHAUSSAIN J.L. - Pseudo-hypoparathyroïdies: nouvelles approches diagnostiques et thérapeutiques. Arch Pédiatr, 1997, 4 (suppl 2), 86s-90s.
    • (1997) Arch Pédiatr , vol.4 , Issue.2 SUPPL.
    • Carel, J.C.1    Garabedian, M.2    Mallet, E.3    Chaussain, J.L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.