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Volumn 174, Issue 2, 2000, Pages 555-559

MR imaging of the pituitary gland in children and young adults with congenital combined pituitary hormone deficiency associated with PROPI mutations

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL EXAMINATION; FEMALE; GENE MUTATION; HUMAN; HYPOPITUITARISM; IMAGE ANALYSIS; INFANT; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL;

EID: 0033971815     PISSN: 0361803X     EISSN: None     Source Type: Journal    
DOI: 10.2214/ajr.174.2.1740555     Document Type: Article
Times cited : (60)

References (13)
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  • 2
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    • Mutations in PROPI cause familial combined pituitary hormone deficiency
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  • 3
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    • A mutational hot spot in the Prop-I gene in Russian children with combined pituitary hormone deficiency
    • Fofanova OV, Takamura N, Kinoshita E-I, et al. A mutational hot spot in the Prop-I gene in Russian children with combined pituitary hormone deficiency. Pituitary 1998;1:45-49
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    • Fofanova, O.V.1    Takamura, N.2    Kinoshita, E.-I.3
  • 4
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    • Compound heterozygous deletion of the PROPI gene in children with combined pituitary hormone deficiency
    • Fofanova O, Takamura N, Kinoshita E, et al. Compound heterozygous deletion of the PROPI gene in children with combined pituitary hormone deficiency. J Clin Endocrinol Metab 1998; 83:2601-2604
    • (1998) J Clin Endocrinol Metab , vol.83 , pp. 2601-2604
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  • 5
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    • Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROPI gene mutation resulting in the substitution of Arg to Cys at codon 120 (R120C)
    • Fluck C, Deladoey J, Rutishauser K, et al. Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROPI gene mutation resulting in the substitution of Arg to Cys at codon 120 (R120C). J Clin Endocrinol Metab 1998;83:3727-3734
    • (1998) J Clin Endocrinol Metab , vol.83 , pp. 3727-3734
    • Fluck, C.1    Deladoey, J.2    Rutishauser, K.3
  • 6
    • 7844241236 scopus 로고    scopus 로고
    • The PROPI 2-base pair deletion is a common cause of combined pituitary hormone deficiency
    • Cogan JD, Wu W, Phillips JA III, et al. The PROPI 2-base pair deletion is a common cause of combined pituitary hormone deficiency. J Clin Endocrinol Metab 1998;83:3346-3349
    • (1998) J Clin Endocrinol Metab , vol.83 , pp. 3346-3349
    • Cogan, J.D.1    Wu, W.2    Phillips J.A. III3
  • 7
    • 0032561414 scopus 로고    scopus 로고
    • Human PROP-I: Cloning, mapping, genomic structure -mutations in familial combined pituitary hormone deficiency
    • Duquesnoy P, Roy A, Dastot F, et al. Human PROP-I: cloning, mapping, genomic structure -mutations in familial combined pituitary hormone deficiency. FEBS Lett 1998;437:216-220
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    • Clinical and biochemical phenotype of familial anterior hypopituitarism from mutation of the PROPI gene
    • Rosenbloom AL, Almonte AS, Brown MR, et al. Clinical and biochemical phenotype of familial anterior hypopituitarism from mutation of the PROPI gene. J Clin Endocrinol Metab 1999;84:50-57
    • (1999) J Clin Endocrinol Metab , vol.84 , pp. 50-57
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  • 10
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  • 13
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    • (1999) J Clin Endocrinol Metab , vol.84 , pp. 942-945
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.