Literature DB >> 11812889

Focal segmental glomerulosclerosis, proteinuria and nephrocalcinosis associated with renal tubular acidosis.

Rasheed A Balogun1, Nancy D Adams, Joseph Palmisano, Harold Yamase, Irfans Chughtai, Andre A Kaplan.   

Abstract

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Year:  2002        PMID: 11812889     DOI: 10.1093/ndt/17.2.308

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN: 0931-0509            Impact factor:   5.992


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  4 in total

1.  Nephrotic range proteinuria as a presenting feature of classical nephropathic cystinosis.

Authors:  Gurdeep Singh Dhooria; Harmesh Singh Bains
Journal:  Indian J Pediatr       Date:  2013-06-18       Impact factor: 1.967

2.  An expanded syndrome of dRTA with hearing loss, hyperoxaluria and beta2-microglobulinuria.

Authors:  Lawrence Copelovitch; Bernard S Kaplan
Journal:  NDT Plus       Date:  2010-07-12

3.  Loss of kAE1 expression in collecting ducts of end-stage kidneys from a family with SLC4A1 G609R-associated distal renal tubular acidosis.

Authors:  Alfred A Vichot; Zsuzsanna K Zsengellér; Boris E Shmukler; Nancy D Adams; Neera K Dahl; Seth L Alper
Journal:  Clin Kidney J       Date:  2016-08-31

4.  Medullary nephrocalcinosis, distal renal tubular acidosis and polycythaemia in a patient with nephrotic syndrome.

Authors:  Suneth Karunarathne; Yapa Udayakumara; Dumitha Govindapala; Harshini Fernando
Journal:  BMC Nephrol       Date:  2012-07-26       Impact factor: 2.388

  4 in total

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