Zobrazeno 1 - 10
of 18
pro vyhledávání: '"D S, Milliner"'
Publikováno v:
Indian Journal of Nephrology, Vol 26, Iss 5, Pp 383-384 (2016)
Indian Journal of Nephrology
Indian Journal of Nephrology
A 31-year-old male presented with recurrent renal stones from the age of 12 years and renal failure secondary to nephrolithiasis on hemodialysis for the past 6 years. He had been born of a consanguineous union and one out of his five siblings also ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb8d05c7f5a381a4034ba1f45fd26432
https://doi.org/10.4103/0971-4065.189317
https://doi.org/10.4103/0971-4065.189317
Publikováno v:
BJU international. 88(9)
To evaluate the short-term efficacy of (l)-2-oxothiaolidine-4-carboxylate (OTZ, which reduces urinary oxalate excretion in normal subjects) in the treatment of primary hyperoxaluria type 1 (PH1) in a phase II study.Two patients with PH1 received intr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8cf4032829dc4217245e15131d275063
https://pubmed.ncbi.nlm.nih.gov/11851603
https://pubmed.ncbi.nlm.nih.gov/11851603
Publikováno v:
Pediatric nephrology (Berlin, Germany). 12(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e798862127fb40c05690eae26d60c59f
https://pubmed.ncbi.nlm.nih.gov/9745877
https://pubmed.ncbi.nlm.nih.gov/9745877
Publikováno v:
Journal of nephrology. 11
Primary hyperoxaluria, types 1 and 2, are rare disorders. Much of the information in the literature has been derived from case reports and data registries limited to patients requiring dialysis and/or transplantation. We present a single-center exper
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::00354c079e7d7e15498506f869c55633
https://pubmed.ncbi.nlm.nih.gov/9604813
https://pubmed.ncbi.nlm.nih.gov/9604813
Publikováno v:
Clinical chemistry. 43(8 Pt 1)
Primary hyperoxaluria (PH) is an autosomal recessive metabolic abnormality characterized by excessive oxalate excretion leading to nephrocalcinosis and progressive renal dysfunction. Type I primary hyperoxaluria (PH I) results from a deficiency of al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::815c343137e78e02802f447db37c5975
https://pubmed.ncbi.nlm.nih.gov/9267307
https://pubmed.ncbi.nlm.nih.gov/9267307
Publikováno v:
The Journal of urology. 156(2 Pt 2)
We determined the long-term prognosis of the pediatric patient presenting with simultaneous ureteropelvic junction obstruction and a renal calculus.We retrospectively reviewed all individuals younger than 17 years who presented to our institutions wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fa750ba0cb7d3090e7887840eded731
https://pubmed.ncbi.nlm.nih.gov/8683773
https://pubmed.ncbi.nlm.nih.gov/8683773
Publikováno v:
American journal of kidney diseases : the official journal of the National Kidney Foundation. 23(2)
Primary hyperoxaluria type II (PH-II) or L-glyceric aciduria was first reported by Williams and Smith in 1968 (N Engl J Med 278:233-239, 1968). Deficiencies of D-glycerate dehydrogenase and glyoxylate reductase activity in patients with this disorder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3c3c8f011ec5574faeceb48500db54e5
https://pubmed.ncbi.nlm.nih.gov/8311084
https://pubmed.ncbi.nlm.nih.gov/8311084
Publikováno v:
Transplantation proceedings. 26(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8bee4fa7a7dbb61372124e6f87922c9a
https://pubmed.ncbi.nlm.nih.gov/8108906
https://pubmed.ncbi.nlm.nih.gov/8108906
Publikováno v:
Transplantation proceedings. 26(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c37a0f1e1cd21cef253a8e6b68355b8e
https://pubmed.ncbi.nlm.nih.gov/8108898
https://pubmed.ncbi.nlm.nih.gov/8108898
Autor:
D. S. Milliner, L. H. Smith
Publikováno v:
Urolithiasis 2 ISBN: 9781461360919
Primary hyperoxaluria is a rare, autosomal recessive disorder. Although recognized earlier, it was not until the early 1950s that sufficient numbers of cases were described to permit its identification as a distinct clinical entity. During the decade
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::268732336e65f0f7a993a802614c9403
https://doi.org/10.1007/978-1-4615-2556-1_226
https://doi.org/10.1007/978-1-4615-2556-1_226
