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Published by S. Karger AG. ISSN: 1660-2110.<br /><br />Nephron Clinical Practice is a subjournal of Nephron with its own citation and index. This part of Nephron provides readers with up-to-date, high-quality research and opinions on all aspects of clinical nephrology, dialysis and transplantation. Original articles report on innovative clinical studies and patient-based experimental work which has immediate relevance to clinical practice. Comment and Analysis provides expert opinion and a critical comment on selected original articles. Minireviews provide succinct, topical reviews of key issues in clinical practice: 'Current Practice' explores the management of specific renal diseases; 'Therapeutic Advances' focuses on newly introduced drugs and their therapeutic potential; 'From Laboratory to Clinic' examines how recent experimental evidence impacts on clinical practice; 'On the Horizon'.
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Comparison between 1alpha(OH)D3 and 1,25(OH)2D3 on the suppression of plasma PTH levels in uremic patients, evaluated by the 'whole' and 'intact' PTH assays.
被引量：1 发表：1970
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Mesangiocapillary glomerulonephritis type 2 associated with familial partial lipodystrophy (Dunnigan-Kobberling syndrome).
The lipodystrophies are a heterogeneous group of disorders of adipose tissue associated with insulin resistance. The sporadic form of partial lipodystrophy, characterised by fat loss from the face and upper body, is associated with complement abnormalities and mesangiocapillary glomerulonephritis type 2 (MCGN II) and the conditions are thought to have a shared autoimmune aetiology. We present the first case of the rare familial form of partial lipodystrophy, caused by a mutation in the LMNA gene, associated with MCGN II. This suggests that partial lipodystrophy of both the sporadic and familial subtypes may predispose to this condition and that the observed renal and complement abnormalities may be secondary to other factors associated with lipodystrophy.
被引量：11 发表：2004
