Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ovadia Shemesh"'
Publikováno v:
Kidney International. (4):916-923
Effect of colloid volume expansion on glomerular barrier size–selectivity in humans. Colloid volume expansion magnifies proteinuria in subjects with the nephrotic syndrome. To elucidate this phenomenon, we performed differential solute clearances p
Publikováno v:
The American journal of physiology. 256(1 Pt 2)
To elucidate the mechanisms by which indomethacin lowers proteinuria, we studied 20 patients with the nephrotic syndrome. We performed differential macromolecule clearances before and after 3 days of therapy (150 mg/24 h). The fractional clearances o
Publikováno v:
Nephrology ISBN: 9781461297703
Nephrology
Nephrology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3760d7d006ce408ec515dbc27f22a52a
https://doi.org/10.1007/978-1-4612-5284-9_95
https://doi.org/10.1007/978-1-4612-5284-9_95
Publikováno v:
The American journal of physiology. 257(4 Pt 2)
Angiotensin II (ANG II) infusion has been reported to impair barrier size selectivity and exacerbate proteinuria in the rat. To examine whether this is also true of humans, we infused a pressor dose of ANG II into seven healthy controls and seven nep
Publikováno v:
Archives of Internal Medicine. 145:1334
Boelaert et al are right in pointing out that C6, C7, and C8 are not the only hereditary complement deficiencies associated with recurrent neisserial sepsis, as illustrated by their family study and their list of previously published case studies. We
Publikováno v:
Journal of Urology. 135:1111-1111
Limitations of creatinine as a filtration marker in glomerulopathic patients. To determine the reliability of creatinine as a measure of the glomerular filtration rate (GFR), we compared the simultaneous clearance of creatinine to that of three true
Publikováno v:
Archives of Internal Medicine. 144:1481
• A 24-year-old man had repeated episodes of meningococcal meningitis. Selective deficiency of the eighth component of complement (C8) was demonstrated in the patient, his twin brother, and in one of five siblings. As the parents were first cousins