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Volumn 132, Issue 5, 1998, Pages 764-765

Making a 'dent' in hereditary hypercalciuric nephrolithiasis

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN E; HEMOGLOBIN F;

EID: 0031749036     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(98)70300-2     Document Type: Editorial
Times cited : (6)

References (13)
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    • (1990) , pp. 293-315
    • Stapleton, FB1    Jones, DP2
  • 2
    • 85119813480 scopus 로고
    • Clinical and laboratory studies of 207 consecutive patients in a kidney stone clinic
    • RA Melnick PH Henneman Clinical and laboratory studies of 207 consecutive patients in a kidney stone clinic N Engl J Med 259 1958 370 374
    • (1958) N Engl J Med , vol.259 , pp. 370-374
    • Melnick, RA1    Henneman, PH2
  • 3
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    • Urolithiasis in children: the role of hypercalciuria
    • FB Stapleton CP McKay HN Noe Urolithiasis in children: the role of hypercalciuria Pediatr Ann 16 1987 980 992
    • (1987) Pediatr Ann , vol.16 , pp. 980-992
    • Stapleton, FB1    McKay, CP2    Noe, HN3
  • 4
    • 0018644610 scopus 로고
    • Physiological basis for absorptive and renal hypercalciuria
    • CYC Pak Physiological basis for absorptive and renal hypercalciuria Am J Physiol 237 1979 F415 F423
    • (1979) Am J Physiol , vol.237 , pp. F415-F423
    • Pak, CYC1
  • 7
    • 0031748292 scopus 로고    scopus 로고
    • X-linked recessive nephrolithiasis: presentation and diagnosis in children
    • SJ Schurman AGW Norden SJ Scheinman X-linked recessive nephrolithiasis: presentation and diagnosis in children J Pediatr 132 1998 859 862
    • (1998) J Pediatr , vol.132 , pp. 859-862
    • Schurman, SJ1    Norden, AGW2    Scheinman, SJ3
  • 8
    • 8544254724 scopus 로고    scopus 로고
    • Characterization of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stone) disorders
    • SE Lloyd W Günther SHS Pearce A Thomson ML Bianchi M Bosio Characterization of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stone) disorders Hum Mol Genet 6 1997 1233 1239
    • (1997) Hum Mol Genet , vol.6 , pp. 1233-1239
    • Lloyd, SE1    Günther, W2    Pearce, SHS3    Thomson, A4    Bianchi, ML5    Bosio, M6
  • 9
    • 0028038212 scopus 로고
    • Dent's disease: a familial proximal renal tubular syndrome with low molecular weight proteinuria, hypercalciuria, nephrocalcinosis, metabolic bone disease, progressive renal failure and a marked male predominance
    • OM Wrong AGW Norden TG. Feest Dent's disease: a familial proximal renal tubular syndrome with low molecular weight proteinuria, hypercalciuria, nephrocalcinosis, metabolic bone disease, progressive renal failure and a marked male predominance Q J Med 87 1994 473 493
    • (1994) Q J Med , vol.87 , pp. 473-493
    • Wrong, OM1    Norden, AGW2    Feest, TG.3
  • 10
    • 0028957547 scopus 로고
    • Hypercalciuria and nephrocalcinosis in patients with idiopathic low molecular weight proteinuria in Japan
    • T Igarashi H Hayakawa H Shiraga H Kawato K Yan H Kawaguchi Hypercalciuria and nephrocalcinosis in patients with idiopathic low molecular weight proteinuria in Japan Nephron 69 1995 242 247
    • (1995) Nephron , vol.69 , pp. 242-247
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    • Genetic mapping in the Xp11.2 region of a new form of x-linked hypophosphatemic rickets
    • A Bolino M Devoto G Enia C Zoccali J Weissenbach G Romeo Genetic mapping in the Xp11.2 region of a new form of x-linked hypophosphatemic rickets Eur J Hum Genet 1 1993 269 279
    • (1993) Eur J Hum Genet , vol.1 , pp. 269-279
    • Bolino, A1    Devoto, M2    Enia, G3    Zoccali, C4    Weissenbach, J5    Romeo, G6
  • 12
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    • Crystal clear chloride channels
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  • 13
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    • Characterization of carrier females and affected males with X-linked recessive nephrolithiasis
    • SC Reinhart AGW Norden M Lapsley RV Thakker J Pang AM Moses Characterization of carrier females and affected males with X-linked recessive nephrolithiasis J Am Soc Nephrol 5 1995 1451 1461
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.