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Volumn 850, Issue , 1998, Pages 475-478

Bone metabolism in thalassemia

Author keywords

[No Author keywords available]

Indexed keywords

HORMONE;

EID: 0031853952     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.1998.tb10526.x     Document Type: Conference Paper
Times cited : (19)

References (17)
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  • 2
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    • Calcium phosphate metabolism and bone disease in patients with homozygous thalassemia
    • DE VERNEJOUL, M. C. et al. 1982. Calcium phosphate metabolism and bone disease in patients with homozygous thalassemia. J. Clin. Endocrinol. Metabol. 54: 276-281.
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  • 3
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    • The contribution of hypogonadism to the development of osteoporosis in thalassemia major: New therapeutical approaches
    • ANAPLIOTOU, M. L. et al. 1995. The contribution of hypogonadism to the development of osteoporosis in thalassemia major: New therapeutical approaches. Clin. Endocrinol. 42: 279-287.
    • (1995) Clin. Endocrinol. , vol.42 , pp. 279-287
    • Anapliotou, M.L.1
  • 4
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    • Osteoporosis in haemocromatosis: Iron excess, gonadal deficiency or other factors?
    • DIAMOND, T. et al. 1989. Osteoporosis in haemocromatosis: Iron excess, gonadal deficiency or other factors? Ann. Int. Med. 110: 430-436.
    • (1989) Ann. Int. Med. , vol.110 , pp. 430-436
    • Diamond, T.1
  • 5
    • 0030848911 scopus 로고    scopus 로고
    • Incidence of enodcrine complications and clinical disease severity related to genotype analysis and iron overload in patients with beta-thalassaemia
    • JENSEN, C. E. et al. 1997. Incidence of enodcrine complications and clinical disease severity related to genotype analysis and iron overload in patients with beta-thalassaemia. Eur. J. Haematol. 59(2): 76-81.
    • (1997) Eur. J. Haematol. , vol.59 , Issue.2 , pp. 76-81
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  • 6
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    • Standards from birth to maturity for height, weight, height velocity and weight velocity: British Children, 1965
    • TANNER, J. M. et al. 1965. Standards from birth to maturity for height, weight, height velocity and weight velocity: British Children, 1965. Arch. Dis. Child. 41: 613-635.
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    • Tanner, J.M.1
  • 7
    • 0025317879 scopus 로고
    • Measurement of bone mineral content of the lumbar spine by Dual Energy X-Ray Absorptiometry in normal children: Correlations with growth parameters
    • GLASTRE, C. et al. 1990. Measurement of bone mineral content of the lumbar spine by Dual Energy X-Ray Absorptiometry in normal children: Correlations with growth parameters. J. Clin. Endocrinol. Metabol. 70: 1330-1333.
    • (1990) J. Clin. Endocrinol. Metabol. , vol.70 , pp. 1330-1333
    • Glastre, C.1
  • 8
    • 0028691003 scopus 로고
    • Growth patterns in patients with thalassemia major
    • PANTELAKIS, S. 1994. Growth patterns in patients with thalassemia major. Acta Paediatr. Suppl. 406: 109-110.
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  • 9
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    • Effect of different treatment regimens on linear growth and final height in β thalassemia major
    • DE SANCTIS, V. et al. 19943 Effect of different treatment regimens on linear growth and final height in β thalassemia major. Clin. Endocrinol. 40: 91.
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  • 10
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    • Bone density, mineral content, and cortical index in patients with thalassemia major and the correlation to their bone fractures, blood transfusions and the treatment with desferrioxamine
    • ORVIETO, R. et al. 1992. Bone density, mineral content, and cortical index in patients with thalassemia major and the correlation to their bone fractures, blood transfusions and the treatment with desferrioxamine. Calcif. Tissue Int. 50: 397-399.
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  • 11
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    • Fractures in thalassemia
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  • 12
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    • Urinary pyridinoline and doexypyrydynoline in healthy children and in children with GH deficiency
    • FUJIMOTO, S. et al. 1995. Urinary pyridinoline and doexypyrydynoline in healthy children and in children with GH deficiency. J. Clin. Endocrinol. Metabol. 80: 1922-1928.
    • (1995) J. Clin. Endocrinol. Metabol. , vol.80 , pp. 1922-1928
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    • High-dose desferrioxamine as a cause of growth failure in thalassemic patients
    • PIGA, A. et al. 1988. High-dose desferrioxamine as a cause of growth failure in thalassemic patients. Eur. J. Haematol. 40: 380-381.
    • (1988) Eur. J. Haematol. , vol.40 , pp. 380-381
    • Piga, A.1
  • 15
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    • Short stature in homozygous β-thalassemia is due to disproportionate truncal shortening
    • RODDA, C. P. et al. 1995. Short stature in homozygous β-thalassemia is due to disproportionate truncal shortening. Clin. Endocrinol. 42: 587-590.
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  • 17


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.