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Hereditary chronic nephritis in India
Annals of Tropical Paediatrics, 1985Forty-six patients from 23 Indian families with hereditary chronic nephritis (HCN) with or without Alport's syndrome are presented. The occurrence of this disease in diverse Indian races, communities and castes is now documented. Clinical and laboratory findings in these patients are similar to those reported from temperate regions.
A, Cariappa +4 more
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Archives of Pediatrics & Adolescent Medicine, 1960
J A, CHAPPELL, W M, KELSEY
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J A, CHAPPELL, W M, KELSEY
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Alport’S Syndrome (Hereditary Nephritis)
2010This is mainly an X-linked dominant inherited trait and the disease manifests in childhood and is progressive. The mutations are located in the COL4A5 gene encoding the α5 chain of type IV collagen. Autosomal Alport syndrome is caused by mutations in the COL4A3 and COL4A4 genes encoding the a3 and a4 chain of type IV collagen.
Margit Pavelka, Jürgen Roth
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The Journal of family practice, 1977
The diagnosis, prognosis, and heredity of glomerulonephritis, in 207 members of one family over five generations was determined. No evidence of significant renal insufficiency or renal associated mortality was found. A history of urinary tract infections was obtained from 58 percent of those with hematuria. Several of those with nephritis also had high-
A S, Peterson, J J, Schubert
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The diagnosis, prognosis, and heredity of glomerulonephritis, in 207 members of one family over five generations was determined. No evidence of significant renal insufficiency or renal associated mortality was found. A history of urinary tract infections was obtained from 58 percent of those with hematuria. Several of those with nephritis also had high-
A S, Peterson, J J, Schubert
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Genetic testing in prostate cancer management: Considerations informing primary care
Ca-A Cancer Journal for Clinicians, 2022Veda N Giri +2 more
exaly
[Dysembryogenesis in hereditary nephritis].
Genetika, 1976In 75 children with hereditary nephritis, in 27 ones with hematuric form of acquired nephritis and in 55 parents dysplastic symptoms were investigated. A high differential and diagnostic value of disembriogenetic stigmata for hereditary nephritis is demonstrated.
M S, Ignatova +3 more
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HYPERPROLINÆMIA AND HEREDITARY NEPHRITIS
The Lancet, 1964H, KOPELMAN, A M, ASATOOR, M D, MILNE
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