proline and Nephritis, Hereditary

proline has been researched along with Nephritis, Hereditary in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	2 (100.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
ASATOOR, AM; KOPELMAN, H; MILNE, MD	1
EFRON, ML	1

Other Studies

2 other study(ies) available for proline and Nephritis, Hereditary

Article	Year
HYPERPROLINAEMIA AND HEREDITARY NEPHRITIS. Lancet (London, England), 1964, Nov-21, Volume: 2, Issue:7369 Topics: 1-Pyrroline-5-Carboxylate Dehydrogenase; Amino Acid Metabolism, Inborn Errors; Blood; Blood Chemical Analysis; Chromatography; Diseases in Twins; Fluids and Secretions; Genetics, Medical; Glycine; Humans; Hydroxyproline; Nephritis, Hereditary; Nephrotic Syndrome; Pathology; Proline; Proline Oxidase; Proteinuria; Urine	1964
FAMILIAL HYPERPROLINEMIA. REPORT OF A SECOND CASE, ASSOCIATED WITH CONGENITAL RENAL MALFORMATIONS, HEREDITARY HEMATURIA AND MILD MENTAL RETARDATION, WITH DEMONSTRATION OF AN ENZYME DEFECT. The New England journal of medicine, 1965, Jun-17, Volume: 272 Topics: 1-Pyrroline-5-Carboxylate Dehydrogenase; Amino Acid Metabolism, Inborn Errors; Amino Acid Oxidoreductases; Blood; Cerebrospinal Fluid; Child; Clinical Enzyme Tests; Congenital Abnormalities; Genetics, Medical; Hematuria; Humans; Intellectual Disability; Kidney Diseases; Nephritis, Hereditary; Proline; Proline Oxidase; Urine	1965

Article

Year

HYPERPROLINAEMIA AND HEREDITARY NEPHRITIS.

Lancet (London, England), 1964, Nov-21, Volume: 2, Issue:7369

Topics: 1-Pyrroline-5-Carboxylate Dehydrogenase; Amino Acid Metabolism, Inborn Errors; Blood; Blood Chemical Analysis; Chromatography; Diseases in Twins; Fluids and Secretions; Genetics, Medical; Glycine; Humans; Hydroxyproline; Nephritis, Hereditary; Nephrotic Syndrome; Pathology; Proline; Proline Oxidase; Proteinuria; Urine

1964

FAMILIAL HYPERPROLINEMIA. REPORT OF A SECOND CASE, ASSOCIATED WITH CONGENITAL RENAL MALFORMATIONS, HEREDITARY HEMATURIA AND MILD MENTAL RETARDATION, WITH DEMONSTRATION OF AN ENZYME DEFECT.

The New England journal of medicine, 1965, Jun-17, Volume: 272

Topics: 1-Pyrroline-5-Carboxylate Dehydrogenase; Amino Acid Metabolism, Inborn Errors; Amino Acid Oxidoreductases; Blood; Cerebrospinal Fluid; Child; Clinical Enzyme Tests; Congenital Abnormalities; Genetics, Medical; Hematuria; Humans; Intellectual Disability; Kidney Diseases; Nephritis, Hereditary; Proline; Proline Oxidase; Urine

1965