Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Renal tubular defect"'
Akademický článek
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Akademický článek
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Publikováno v:
The Journal of Veterinary Medical Science
Renal Fanconi syndrome has recently been associated with the ingestion of pet jerky treats from China in mostly small breed dogs in North America, Australia and Europe. We report here about two dogs with Fanconi syndrome following pet jerky treats ex
Autor:
E. Furman, E. H. Hooijberg, Urs Giger, A. C. Sewell, D. Brandstetter, Ernst Leidinger, J. Leidinger, C. Hochleithner
Publikováno v:
Tierärztliche Praxis Ausgabe K: Kleintiere / Heimtiere. 43:188-192
SummaryTransient Fanconi syndrome without azotemia was diagnosed in a dog and was associated with ingestion of Chinese chicken jerky treats. Fanconi syndrome is a proximal renal tubular defect and a diagnosis was made based upon severe glucosuria wit
Autor:
Nazli Kuter, Harika Alpay, Asli Memisoglu, Zeynep Alp Ünkar, Kıvılcım Karadeniz Cerit, Hülya Bilgen, Eren Özek
Publikováno v:
International Journal of Clinical Pediatrics. 3:114-116
Hypochloremic metabolic alkalosis occurs in pseudo-Bartter’s syndrome (PBS) without a primary renal tubular defect. Usually seen in cystic fibrosis, this syndrome can also be caused by recurrent vomiting for various reasons. We present a case of mu
Autor:
Joseph W. Bartges, Lori A. Koehler, Sherry L. Sanderson, Kathleen A. Bird, Laura L. Swanson, Lisa K. Ulrich, Carl A. Osborne, Jody P. Lulich
Publikováno v:
Veterinary Clinics of North America: Small Animal Practice. 29:193-211
Cystine uroliths are a sequela to cystinuria, an inherited renal tubular defect in reabsorption of cystine and some other amino acids. At the Minnesota Urolith Center, 67 breeds of dogs were identified, including English Bulldogs, Dachshunds, Mastiff
Autor:
William van’t Hoff
Publikováno v:
Current Paediatrics. 7:147-152
Renal tubular disorders in childhood are rare, but, when present, may produce profound electrolyte and volume disturbances. Children with hereditary tubular dysfunction commonly present in the first year of life with failure to thrive and other non-s
Akademický článek
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Publikováno v:
Pediatric Nephrology. 7:83-85
Hypouricaemia due to an isolated renal tubular defect is a rare condition. Several members from an affected family are described. The propositus is a 12-year-old girl with hypouricaemia (0.7-1.1 mg/dl) and increased fractional excretion of uric acid
Changes in renal tubuli in patients with idiopathic membrane nephropathy(IMN)have not been sufficiently investigated, although it is known that essential pathomorphological changes occur in tubuli in addition to their functional lesion in some other
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::ff9f82507031e4a96a03b1f21a0d7964
https://www.bib.irb.hr/284967
https://www.bib.irb.hr/284967