The urinary excretion of total hydroxylysine and its glycosides in normal persons, and in patients suffering from Alport's syndrome―Contribution of the peptide-bound fraction
- Author
- SCHRODER, C. H1 ; MONNENS, L. A. H; VAN LITH-ZANDERS, H. M. A; TRIJBELS, J. M. F; VEERKAMP, J. H
[1] Univ. Nijmegen, dep. pediatrics, Nijmegen 9101, Netherlands - Source
Nephron. 1987, Vol 47, Num 4, pp 253-257 ; ref : 9 ref
- CODEN
- NPRNAY
- ISSN
- 0028-2766
- Scientific domain
- Urology, nephrology
- Publisher
- Karger, Basel
/
Karger, Freiburg
/
Karger, Paris
- Publication country
- Switzerland
- Document type
- Article
- Language
- English
- Keyword (fr)
- Alport syndrome Appareil urinaire pathologie Excrétion Homme Hydroxylysine Héréditaire Métabolite Néphropathie glomérulaire Urine
- Keyword (en)
- Alport syndrome Urinary system disease Excretion Human Hydroxylysine Hereditary Metabolite Glomerulonephritis Urine
- Keyword (es)
- Alport síndrome Aparato urinario patología Excreción Hombre Hidroxilisina Hereditario Metabolito Nefropatía glomerular Orina
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B14 Nephrology. Urinary tract diseases / 002B14A Nephropathies. Renovascular diseases. Renal failure / 002B14A01 Glomerulonephritis
- Discipline
- Nephrology. Urinary tract diseases
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 7647217
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1159/000184519 
https://dx.doi.org/10.1159/000184519
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