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Volumn 23, Issue 7, 2008, Pages 1183-1187

Glomerulocystic kidney disease in hypomelanosis of Ito

Author keywords

Cataract; Glomerulocystic kidney disease; Ito hypomelanosis; TCF2 gene

Indexed keywords

ALANINE AMINOTRANSFERASE; ASPARTATE AMINOTRANSFERASE; CONTRAST MEDIUM; GAMMA GLUTAMYLTRANSFERASE; RAMIPRIL;

EID: 44449094939     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-008-0797-y     Document Type: Article
Times cited : (11)

References (16)
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  • 2
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  • 3
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    • Hatchwell E, Robinson D, Crolla JA, Cockwell AE (1996) X inactivation analysis in a female with hypomelanosis of Ito associated with a balanced X:E7 translocation: evidence for functional disomy of Xp. J Med Genet 33:216-220
    • (1996) J Med Genet , vol.33 , pp. 216-220
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  • 4
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    • Bloch-Sulzberger incontinentia pigmenti based on 3 personal cases
    • Smolinska U, Filipowicz-Iwanowska T (1976) Bloch-Sulzberger incontinentia pigmenti based on 3 personal cases. Przegl Dermatol 63:649-652
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  • 5
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  • 9
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    • A cutaneous disease with multisystem involvement: Hypomelanosis of Ito may be associated with proteinuria, focal segmental glomerulosclerosis and end-stage renal disease
    • Gatter N, Hoppe B, Nützenadel F, Waldherr R, Querfeld U (2007) A cutaneous disease with multisystem involvement: Hypomelanosis of Ito may be associated with proteinuria, focal segmental glomerulosclerosis and end-stage renal disease. Nephrol Dial Transplant 22:1796-1798
    • (2007) Nephrol Dial Transplant , vol.22 , pp. 1796-1798
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    • Glomerulocystic kidney disease: Nosological considerations
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.