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Volumn 44, Issue 4, 2002, Pages 450-452

A rare rickets case: Hypophosphatemic rickets;Nadi̇r bi̇r ri̇kets olgusu: Hi̇pofosfatemi□k ri̇kets

Author keywords

Hypophosphatemia; Rickets; Vitamin D

Indexed keywords

ARTICLE; CASE REPORT; CHILDHOOD DISEASE; CLINICAL FEATURE; DISEASE COURSE; EARLY DIAGNOSIS; HUMAN; HYPOPHOSPHATEMIA; MALE; METABOLIC DISORDER; RICKETS; VITAMIN D DEFICIENCY;

EID: 0036984368     PISSN: 13020471     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (1)

References (8)
  • 1
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    • Bone Disease
    • Nelson, W.E., Behrman, R.E., Kliegran, R.M., Arvin, A.M., Pennsylvania, WB Saunders Co.
    • Chesney, W.R.: Bone Disease. Nelson, W.E., Behrman, R.E., Kliegran, R.M., Arvin, A.M.: in Nelson Textbook of Pediatrics. 15 eds., Pennsylvania, WB Saunders Co., 1996, p. 1984-1990.
    • (1996) Nelson Textbook of Pediatrics. 15 Eds. , pp. 1984-1990
    • Chesney, W.R.1
  • 2
    • 0035141957 scopus 로고    scopus 로고
    • Rickets: It's not just vitamin D deficiency
    • Hochberg, Z.: Rickets: it's not just vitamin D deficiency. Curr Opin Endocrinol & Diabetes 8:23-28, 2001.
    • (2001) Curr Opin Endocrinol & Diabetes , vol.8 , pp. 23-28
    • Hochberg, Z.1
  • 3
    • 0013077277 scopus 로고    scopus 로고
    • Hipofosfatemik riketsde uzun süreli izlem
    • Özalp, I., Tuncer, M., Ankara
    • Dursun, A., Coşkun, T.: Hipofosfatemik riketsde uzun süreli izlem. Eds: Özalp, I., Tuncer, M. Katki Pediatri Dergisi, Ankara, 20(4), 536-550, 1999.
    • (1999) Katki Pediatri Dergisi , vol.20 , Issue.4 , pp. 536-550
    • Dursun, A.1    Coşkun, T.2
  • 4
    • 0034265863 scopus 로고    scopus 로고
    • The many faces of vitamin D deficinency rickets
    • Joiner, T.A., Foster, C., Shope, T.: The many faces of vitamin D deficinency rickets. Pediatr Rev 21(9): 296-302, 2001.
    • (2001) Pediatr Rev , vol.21 , Issue.9 , pp. 296-302
    • Joiner, T.A.1    Foster, C.2    Shope, T.3
  • 5
    • 0034889880 scopus 로고    scopus 로고
    • Mutational analysis and genotype-phenotype correlation of the PHEX gene in X-linked hypophosphatemic rickets
    • Holm, I.A., Nelson, A.E., Robinson, B.G., et al.: Mutational analysis and genotype-phenotype correlation of the PHEX gene in X-linked hypophosphatemic rickets. J Clin Endocrinol Metab 86: 3889-99, 2001.
    • (2001) J Clin Endocrinol Metab , vol.86 , pp. 3889-3899
    • Holm, I.A.1    Nelson, A.E.2    Robinson, B.G.3
  • 6
    • 0035160055 scopus 로고    scopus 로고
    • Autosomal recessive hypophosphatemic rickets with hypercalciuria is not caused by mutations in the type II renal sodium/phosphate cotransporter gene
    • van den Heuvel, L., Koul, K.O., Knots, E.: Autosomal recessive hypophosphatemic rickets with hypercalciuria is not caused by mutations in the type II renal sodium/phosphate cotransporter gene. Nephrol Dial Transplant 16: 48-51, 2001.
    • (2001) Nephrol Dial Transplant , vol.16 , pp. 48-51
    • Van den Heuvel, L.1    Koul, K.O.2    Knots, E.3
  • 7
    • 0033892896 scopus 로고    scopus 로고
    • Infantile hypophosphatasia: Disappinting results of treatment
    • Deeb, A.A., Bruce, S.N., Morris, A.A., et al.: Infantile hypophosphatasia: disappinting results of treatment. Acta Pediatr 89 (6): 730-3, 2000.
    • (2000) Acta Pediatr , vol.89 , Issue.6 , pp. 730-733
    • Deeb, A.A.1    Bruce, S.N.2    Morris, A.A.3
  • 8
    • 0026672595 scopus 로고
    • A new kindred with hereditary hypophosphatemic rickets with hypercalciuria: Implications for correct diagnosis and treatment
    • Tieder, M., Arie, R., Bab, I.: A new kindred with hereditary hypophosphatemic rickets with hypercalciuria: Implications for correct diagnosis and treatment. Nephron 62: 178-181,1992.
    • (1992) Nephron , vol.62 , pp. 178-181
    • Tieder, M.1    Arie, R.2    Bab, I.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.