Cystinuria

References

• Segal S., Thier S. O. Cystinuria, chap. 80. The Metabolic Basis of Inherited Disease, J. B. Stanbury, J. B. Wynganden, D. S. Fredrickson, J. L. Goldstein, M. S. Brown. McGraw-Hill, New York 1983
   Google Scholar
• Rosenberg L. E., Schriver C. R. Disorders of amino acid metabolism, chap. 11. Metabolic Control and Disease, P. K. Bondy, L. E. Rosenberg. W. B. Saunders, Philadelphia 1980
   Google Scholar
• Halperin E. C., Thier S. O. Cystinuria, chap. 10. Nephrolithiasis, F. L. Coe, B. M. Brenner, J. H. Stern. Churchill Livingstone, New York 1980
   Google Scholar
• Segal S. Cystinuria as a membrane transport disorder, chap. 19. Congenital Metabolic Diseases, R. A. Wapnir. Marcel Dekker, New York 1985
   Google Scholar
• Brand E., Harris M., Biloon S. The excretion of cystine complex which decomposes in the urine with the liberation of free cystine. J. Biol. Chem. 1930; 86: 315
   Google Scholar
• Rosenthal A. F., Yaseen A. Improved qualitative screening test for cystinuria and homocystinuria. Clin. Chim. Acta 1969; 26: 363
   PubMed Web of Science ®Google Scholar
• Georges R. J., Politzer W. M. pH dependency of the cyanide-nitroprusside colour reaction of cystine. Clin. Chim. Acta 1970; 30: 737
   PubMed Web of Science ®Google Scholar
• Middleton J. E. A simple, safe nitroprusside test using Ketostix reagent strips for detecting cystine and homocystine in urine. J. Clin. Pathol. 1970; 23: 90
   PubMed Web of Science ®Google Scholar
• David R. M., Shihabi Z. K., O'Connor M. L. Simplified method for cystinuria screening. Clin. Chem. 1986; 32: 1417
   PubMed Web of Science ®Google Scholar
• Spaeth G. L., Barber G. W. Prevalence of homocystinuria among the mentally retarded: evaluation of a specific screening test. Pediatrics 1967; 40: 586
   PubMed Web of Science ®Google Scholar
• Sullivan M. X., Hess W. C. The determination of cystine in urine. J. Biol. Chem. 1936; 116: 221
   Google Scholar
• Kallistratos G., Pantelidis C., Marketos S. Zystinuriennachweis mit Hilfe des Urocystin Test. Fortschr. Urol. Nephrol. 1977; 9: 210
   Google Scholar
• Roesel R. A., Coryell M. E. Determination of cystine excretion by the nitroprusside method during drug therapy of cystinuria. Clin. Chim. Acta 1974; 52: 343
   PubMed Web of Science ®Google Scholar
• Bremer J. H., Duran M., Kamerling J. P., Przyrembel H., Wadman S. K. Disturbances of Amino Acid Metabolism: Clinical Chemistry and Diagnosis. Urban and Schwarzenberg, Baltimore 1981; 423
   Google Scholar
• Schriver C. R., Rosenberg L. E. Amino Acid Metabolism and Its Disorders. W. B. Saunders, Philadelphia 1973
   Google Scholar
• Spackman D. H., Stein W. H., Moore S. Automatic recording apparatus for use in the chromatography of amino acids. Anal. Chem. 1958; 30: 1190
   Web of Science ®Google Scholar
• Kraffczy K. F., Helger R., Lang H., Bremer H. J. Thin layer chromatographic screening test for amino acid anomalies without desalting using internal standards. Clin. Chim. Acta 1971; 35: 345
   Web of Science ®Google Scholar
• Holmgren G., Jeppson J. O., Samuelson G. High voltage electrophoresis in urinary amino acid screening. Scand. J. Clin. Lab. Invest. 1970; 26: 313
   PubMed Web of Science ®Google Scholar
• Kuzel K. Simple polarographic determination of cystine in urine with cystinuria. Clin. Chim. Acta 1973; 48: 377
   PubMed Web of Science ®Google Scholar
• Bayer E., Grom E., Kaltenegger B., Uhmann R. Separation of amino acids by high performance liquid chromatography. Anal. Chem. 1976; 48: 1106
   PubMed Web of Science ®Google Scholar
• Adams R. F. Determination of amino acid profiles in biological samples by gas chromatography. J. Chromatogr. 1974; 95: 189
   PubMed Web of Science ®Google Scholar
• Williams K. M., Halpern B. The use of gas chromatography-mass spectrometry for the diagnosis and study of metabolic disorders. I. The screening and identification of urinary and serum amino acids. Aust. J. Biol. Sci. 1973; 26: 831
   PubMedGoogle Scholar
• Dent C. E., Senior B. Studies on the treatment of cystinuria. Br. J. Urol. 1955; 27: 317
   PubMedGoogle Scholar
• Dustin J. P., Moore S., Bidwood E. J. Chromatographic studies on the excretion of amino acids in early infancy. Metabolism 1955; 4: 75
   PubMed Web of Science ®Google Scholar
• Smith A. Evaluation of the nitroprusside test for the diagnosis of cystinuria. Med. J. Aust. 1977; 2: 153
   PubMed Web of Science ®Google Scholar
• Dahlberg P. J., Van Den Berg C. J., Kurtz S. B., Wilson D. M., Smith L. H. Clinical features and management of cystinuria. Mayo Clin. Proc 1977; 1352: 533
   Google Scholar
• Crawhall J. C., Watts R. W. E. Cystinuria. Am. J. Med. 1968; 45: 736
   PubMed Web of Science ®Google Scholar
• Bostrom H., Hambraeus L. Cystinuria in Sweden. VII. Clinical histopathological and medicosocial aspects of the disease. Acta Med. Scand. 1964; 41: 1, (Suppl.)
   Google Scholar
• Turner B., Brown D. A. Amino acid excretion in infancy and early childhood. Med. J. Aust. 1972; 1: 62
   PubMed Web of Science ®Google Scholar
• Smith A. Cystinuria. Med. J. Aust. 1976; 2: 961
   PubMedGoogle Scholar
• Weinberger A., Sperling O., Rabinovitz M., Brosh S., Adam A., de Vries A. High frequency of cystinuria among Jews of Libyan origin. Hum. Hered. 1974; 24: 568
   PubMed Web of Science ®Google Scholar
• Fleming W. H., Avery G. B., Morgan R. I., et al. Gastrointestinal malabsorption associated with cystinuria: report of a case in a Negro. Pediatrics 1963; 32: 358
   PubMed Web of Science ®Google Scholar
• Broadus A. E., Thier S. O. Metabolic basis of renal stone disease. N. Engl. J. Med. 1979; 300: 839
   PubMed Web of Science ®Google Scholar
• Adibi S. A. The influence of molecular structure of neutral amino acids on their absorptive kinetics in the jejunum and ileum of human intestine in vivo. Gastroenterology 1969; 56: 903
   PubMed Web of Science ®Google Scholar
• Silk D. B. A. Disorders of nitrogen absorption. Clin. Gast. 1982; 11: 47
   PubMedGoogle Scholar
• Matthews D. M. Protein absorption. J. Clin. Pathol. 1971; 5(Suppl. 24)29
   Google Scholar
• Rosenberg I. H., Coleman A. L., Rosenberg L. E. The role of sodium in the transport of amino acids by the intestine. Biochim. Biophys. Acta 1965; 102: 161
   PubMed Web of Science ®Google Scholar
• Thier S. O., Alpers D. H. Disorders of intestinal transport of amino acids. Am. J. Dis. Child. 1969; 117: 13
   PubMedGoogle Scholar
• Matthews D. M. Absorption of amino acids and peptides from the intestine. Clin. Endocrinol. Metab. 1974; 3: 3
   PubMedGoogle Scholar
• Segal S. Disorders of renal amino acid transport. N. Engl. J. Med. 1976; 294: 1044
   PubMed Web of Science ®Google Scholar
• Buehler B. A. Inherited disorders of amino acid transport in relation to the kidney. Ann. Clin. Lab. Sci. 1981; 11: 274
   PubMed Web of Science ®Google Scholar
• Segal S. Disorders of amino acid transport. Biochem. Soc. Trans. 1983; 11: 633
   PubMed Web of Science ®Google Scholar
• Laner J. A Review of Amino Acid and Transport Processes in Animal Cells and Tissues. University of Maine Press, Drono 1978
   Google Scholar
• Defronzo R. A., Thier S. O. Inherited tubule disorders. Hosp. Pract. 1982; 17: 111
   Web of Science ®Google Scholar
• Craft I. L., Geddes D., Hyde C. W., Wise L. J., Matthews D. M. Absorption and malabsorption of glycine and glycine peptides in man. Gut 1968; 9: 425
   PubMed Web of Science ®Google Scholar
• Silk D. B. A., Hegarty J. E., Fairclough P. D., Clark M. L. Characterization and nutritional significance of peptide transport in man. Ann. Nutr. Metab. 1982; 26: 337
   PubMed Web of Science ®Google Scholar
• Wollaston W. H. On cystic oxide, a new species of urinary calculus. Trans. R. Soc. London 1810; 100: 223
   Google Scholar
• Marcet A. An Essay on the Chemical History and Medical Treatment of Calculus Disorders. London 1817
   Google Scholar
• Stromeyer L. Ann. Chim. Phys. 1824; 27: 221
   Google Scholar
• Toel F. Beobachteingen ureter cystinbilding. Ann. Chem. Pharmakol. 1855; 96: 247
   Google Scholar
• Niemann A. Beitrag Zur Lehre Von Cystinurie beim mensachen. Dtsch. Arch. Klin. Med. 1876; 18: 232
   Google Scholar
• Garrod A. E. The Croonian lectures. Lancet 1908; 2: 1
   Google Scholar
• Alaberg A., Fobin O. Protein metabolism in cystinuria. Am. J. Physiol. 1905; 14: 54
   Google Scholar
• Wolff C. G. L., Skiffer P. A. Protein metabolism in cystinuria. J. Biol. Chem. 1908; 4: 439
   Google Scholar
• Schriver C. R., Roseberg L. E. Amino Acid Metabolism and Its Disorders. W. B. Saunders, Philadelphia 1973
   Google Scholar
• Yeh H. L., Frankl W., Dunn M. S., Parker P., Hughes B., Gyorgey P. The urinary excretion of amino acids by a cystinurie subject. Am. J. Med. Sci. 1947; 214: 507
   PubMed Web of Science ®Google Scholar
• Stein W. H. Excretion of amino acids in cystinuria. Proc. Soc. Exp. Biol. Med. 1951; 78: 705
   PubMed Web of Science ®Google Scholar
• Dent C. E., Rose G. A. Amino acid metabolism in cystinuria. Q. J. Med. 1951; 20: 205
   PubMedGoogle Scholar
• Milne M. D., Asatoor A. M., Edwards K. D. G., Loughridge L. W. The intestinal absorption defect in cystinuria. Gut 1961; 2: 323
   PubMed Web of Science ®Google Scholar
• Robson E. B., Rose G. A. The effect of intravenous lysine on the renal clearance of cystine, arginine, and ornithine in normal subjects, in patients with cystinuria and Fanconi syndrome and in their relatives. Clin. Sci. 1957; 16: 75
   PubMed Web of Science ®Google Scholar
• Dent C. E., Senior B., Walshe J. M. The pathogenesis of cystinuria. II. Polarographic studies of the metabolism of sulphur containing amino acids. J. Clin. Invest. 1954; 33: 1216
   PubMed Web of Science ®Google Scholar
• Frimpter G. W., Horwith M., Furth E., Fellows R. E., Thompson D. D. Inulin and endogenous amino acid renal clearances in cystinuria: evidence for tubular secretion. J. Clin. Invest. 1962; 41: 281
   PubMed Web of Science ®Google Scholar
• Arrow U. K., Westall R. G. Amino acid clearances in cystinuria. J. Physiol. 1958; 142: 141
   PubMed Web of Science ®Google Scholar
• Crawhall J. C., Scowen E. F., Thompson C. J., Watts R. W. E. The renal clearance of amino acids in cystinuria. J. Clin. Invest. 1967; 46: 1162
   PubMed Web of Science ®Google Scholar
• Rosenberg L. E., Downing S. J., Segal S. Competitive inhibition dibasic amino acid transport in rat kidney. J. Biol. Chem. 1962; 237: 2265
   PubMed Web of Science ®Google Scholar
• Fox M., Thier S., Rosenberg L. E., Kiser W., Segal S. Evidence against a single renal transport defect in cystinuria. N. Engl. J. Med. 1964; 270: 556
   PubMed Web of Science ®Google Scholar
• Brodehl J., Gillisen K., Kowalewsko S. Isolated cystinuria (without lysine-omithine-argininuria) in a family with hypocalcemic tetany. Proc. 3rd Int. Congr. on Nephrology. Washington, DC 1966
   Google Scholar
• Perheentupa J., Visakorpi J. K. Protein intolerance with deficient transport of basic amino acids: another inborn error of metabolism. Lancet 1965; 2: 813
   PubMed Web of Science ®Google Scholar
• Kato T. Renal handling of dibasic amino acids and cystine in cystinuria. Clin. Sci. Mol. Med. 1977; 53: 9
   PubMedGoogle Scholar
• Foreman J. W., Hwang S. M., Segal S. Transport interactions of cystine and dibasic amino acids in isolated rat renal tubules. Metabolism 1980; 29: 53
   PubMed Web of Science ®Google Scholar
• Thier S., Fox M., Segal S., Rosenberg L. E. Cystinuria: in vitro demonstration of an intestinal transport defect. Science 1964; 143: 482
   PubMed Web of Science ®Google Scholar
• McCarthy C. F., Borland J. L., Lynch J. H., Owen E. E., Tyori M. P. Defective uptake of basic amino acids and L-cystine by intestinal mucosa of patients with cystinuria. J. Clin. Invest. 1964; 43: 1518
   PubMed Web of Science ®Google Scholar
• Thier S., Segal S., Fox M., Blair A., Rosenberg L. E. Defective intestinal transport of dibasic amino acids and cystine. J. Clin. Invest. 1965; 44: 442
   PubMed Web of Science ®Google Scholar
• London D. R., Foley T. H. Cystine metabolism in cystinuria. Clin. Sci. 1965; 29: 133
   Web of Science ®Google Scholar
• Silk D. B., Perrett D., Stephens A. D., Clark M. L., Scowen E. F. Intestinal absorption of cystine and cysteine in normal subjects and patients with cystinuria. Clin. Sci. Mol. Med. 1974; 47: 393
   PubMedGoogle Scholar
• Desjeux J. F., Vonlanthen M., Dumontier A. M., Simell O., Legrain M. Cystine fluxes across the isolated jejunal epithelium in cystinuria: increased effux permeability at the luminal membrane. Pediatr. Res. 1987; 21: 477
   PubMed Web of Science ®Google Scholar
• Arrow V. K., Westall R. G. Amino acid clearances in cystinuria. J. Physiol. 1958; 142: 141
   PubMed Web of Science ®Google Scholar
• Asatoor A. M., Crouchman M. R., Harrison A. R., Light F. W., Loughridge L. W., Milne M. D., Richards A. J. Intestinal absorption of oligopeptides in cystinuria. Clin. Sci. 1971; 41: 23
   PubMed Web of Science ®Google Scholar
• Asatoor A. M., Harrison B. D. W., Milne M. D., Prosser D. I. Intestinal absorption of an arginine-containing peptide in cystinuria. Gut 1972; 13: 95
   PubMed Web of Science ®Google Scholar
• Hellier M. D., Holdsworth C. D., Perrett D., Thirumalai C. Intestinal dipeptide transport in normal and cystinurie subjects. Clin. Sci. 1972; 43: 659
   PubMed Web of Science ®Google Scholar
• Hellier M. D., Perrett D., Holdsworth C. D. Dipeptide absorption in cystinuria. Br. Med. J. 1970; 4: 782
   PubMedGoogle Scholar
• Rosenberg L. E., Downing S. J. Transport of neutral and dibasic amino acids by human leukocytes: absence of a defect in cystinuria. J. Clin. Invest. 1965; 44: 1382
   PubMed Web of Science ®Google Scholar
• Gardner J. E., Levy A. G. Transport of dibasic amino acids in human erythrocytes. Metabolism 1972; 21: 413
   PubMed Web of Science ®Google Scholar
• Groth V., Rosenberg L. E. Transport of dibasic amino acids, cystine, and tryptophan by cultured human fibroblasts: absence of a defect in cystinuria and Hartnup disease. J. Clin. Invest. 1972; 51: 2130
   PubMed Web of Science ®Google Scholar
• Becker F. E., Green H. Incorporation of cystine and lysine by normal and “cystinuric” leukocytes. Proc. Soc. Exp. Biol. Med. 1958; 99: 694
   PubMed Web of Science ®Google Scholar
• Foreman J. W., McNamara P. D., Bowring M. A., Lee J., Rea C., Segal S. Cystine-glutamate transport interacting in rat renal cortical tubules, brush border vesicles, and cultured renal tubular cells. Biol. Sci. Rep. 1986; 6: 113
   PubMed Web of Science ®Google Scholar
• Gahl W. A., Rizzo W. G. Normal free dibasic amino acids in breast milk of a woman with cystinuria. N. Engl. J. Med. 1983; 309: 1388
   PubMed Web of Science ®Google Scholar
• Stein W. H. Excretion of amino acids in cystinuria. Proc. Soc. Exp. Biol. (N.Y.) 1951; 78: 705
   PubMed Web of Science ®Google Scholar
• Harris H., Mittwoch V., Robson E. B., Warren F. L. Phenotypes and genotypes in cystinuria. Ann. Hum. Genet. 1955; 20: 57
   PubMed Web of Science ®Google Scholar
• Harris H., Robson E. B. Variation in homozygous cystinuria. Acta Genet. (Basel) 1955; 5: 581
   Google Scholar
• Rosenberg L. E., Downing S., Durant J. L., Segal S. Cystinuria: biochemical evidence for three genetically distinct diseases. J. Clin. Invest. 1966; 45: 365
   PubMed Web of Science ®Google Scholar
• Hershko L., Ben-Ami E., Pacrorkovski J., Levin N. Allelomorphism in cystinuria. Proc. Tel-Hashomer Hasp. 1965; 4: 21
   Google Scholar
• Rosenberg L. E. Genetic heterogeneity in cystinuria. Amino Acid Metabolism and Genetic Variation, W. L. Nyhan. McGraw-Hill, New York 1962; 341
   Google Scholar
• Morin C. L., Thompson M. W., Jackson S. H., Sass-Kortsak A. Biochemical and genetic studies in cystinuria: observations on double heterozygotes of genotype I/II. J. Clin. Invest. 1971; 50: 1961
   PubMed Web of Science ®Google Scholar
• Rosenberg L. E. Cystinuria: genetic heterogeneity and allelism. Science 1966; 154: 1341
   PubMed Web of Science ®Google Scholar
• Rosenberg L. E., Durant J. L., Albrecht I. Genetic heterogeneity in cystinuria: evidence for allelism. Trans. Assoc. Am. Phys. 1966; 79: 284
   PubMedGoogle Scholar
• Kelly S., Copeland W. Amino acid patterns in cystinuric families. J. Med. Genet. 1968; 5: 281
   PubMedGoogle Scholar
• Crawhall J. C., Purkiss P., Watts R. W. E., Young E. P. The excretion of amino acids by cystinuric patients and their relatives. Ann. Hum. Genet (London) 1969; 33: 149
   PubMed Web of Science ®Google Scholar
• Kelly S. Cystinuria genotypes predicted from excretion patterns. Am. J. Med. Genet. 1978; 2: 175
   PubMed Web of Science ®Google Scholar
• Caldwell R. J., Townsend J., Smith M. J. V. Genetics of cystinuria in an inbred population. J. Urol. 1978; 119: 531
   PubMed Web of Science ®Google Scholar
• Kallistratos G., Marketos S., Lapatzanis P., Demopoulous K. Findings in kidney stone patients. Metabolic and clinical anomalies. Experience in Greece. Scand. J. Urol. Nephrol. 1980; 53: 195, (Suppl.)
   Google Scholar
• Meloni C. R., Canary J. J. Cystinuria with hyperuricemia. JAMA 1967; 200: 169
   PubMed Web of Science ®Google Scholar
• Vergis J. G., Walker B. R. Cystinuria, hyperuricemia and uric acid nephrolithiasis. Nephron 1970; 7: 577
   PubMedGoogle Scholar
• Linari F., Marangella M., Malfi B., Vacha G., Bruno M., Giorcelli G., Fritteri B. Hyperuricemia and cystinuria. Adv. Exp. Med. Biol. 1980; 122A: 135
   PubMedGoogle Scholar
• Evans W. P., Resnick M. J., Boyce W. H. Homozygous cystinuria evaluation of 35 patients. J. Urol. 1982; 127: 707
   PubMed Web of Science ®Google Scholar
• Nyhan W. L. Abnormalities in Amino Acid Metabolism in Clinical Medicine. Appleton-Century-Crofts, Norwalk, CT 1984; 373
   Google Scholar
• Brooks W. D. W., Heasman M. A., Lovell R. R. H. Retinitis pigmentosa associated with cystinuria: 2 uncommon inherited conditions occurring in family. Lancet 1949; 1: 1096
   PubMedGoogle Scholar
• Hurwitz L. J., Carson N. A. J., Allen I. V., Fannin T. F., Lyttle J. A., Neill D. W. Clinical, biochemical, and histopathological findings in a family with muscular dystrophy. Brain 1967; 90: 799
   PubMed Web of Science ®Google Scholar
• Tanguay R. B., Galindo J. Cystinuria associated with mongolism and identification of an abnormal pyrrolidine compound in urine. Am J. Clin. Pathol. 1966; 46: 442
   PubMed Web of Science ®Google Scholar
• Gross T. B., Ulrich J. A., Jones J. D. Urinary excretion of amino acids in a kindred with hereditary pancreatitis and aminoaciduria. Gastroenterology 1964; 47: 41
   PubMed Web of Science ®Google Scholar
• Dent C. E., Harris H. The genetics of cystinuria. Ann. Hum. Genet. 1951; 16: 160
   Google Scholar
• Kurczynski T. Neurological complications of cystinuria. Dev. Med. Child Neurol. 1979; 21: 811
   PubMed Web of Science ®Google Scholar
• Dennis J., Taylor D. C. Neurological complications of cystinuria. Dev. Med. Child Neurol. 1980; 22: 402
   PubMed Web of Science ®Google Scholar
• Myer W. D., Gebhard R. L. Subacute combined degeneration of the spinal cord with cystinuria. Neurology 1975; 25: 994
   PubMed Web of Science ®Google Scholar
• Blackburn C. R. B., McLeod J. G. CNS lesions in cystinuria. Arch. Neurol 1977; 34: 638
   PubMedGoogle Scholar
• Cavanagh N. P. C., Bicknell J., Howard F. Cystinuria with mental retardation and paroxysmal dyskinesia in 2 brothers. Arch. Dis. Child. 1974; 49: 662
   PubMed Web of Science ®Google Scholar
• Bailey R. R., Carrell R. W., Shannon F. T. Homozygous cystinuria and occulo-cerebro-renal dystrophy of Lowe in same family. Arch. Dis. Child. 1976; 51: 558
   PubMed Web of Science ®Google Scholar
• Radu H., Tanese-Mogos I., Rosu A. M., Killyen I., Ionescu V. A new polygenic disturbance: cystinuria, leucinuria and spinal muscular atrophy. J. Neurol. 1974; 207: 73
   PubMed Web of Science ®Google Scholar
• Banerji N. K., Millar J. H. D. Paraplegia associated with cystinuria. J. Neurol. Sci. 1971; 12: 101
   PubMed Web of Science ®Google Scholar
• Schriver C. R., Whelan D. T., Clow C. L., Dallaire L. Cystinuria: increased prevalence in patients with mental disease. N. Engl. J. Med. 1970; 283: 783
   PubMed Web of Science ®Google Scholar
• Smith D. R., Kolb F. O., Harper H. A. Management of cystinuria and cystine stone disease. J. Urol. 1959; 81: 61
   PubMed Web of Science ®Google Scholar
• Rodman J. S., Blackburn P., Williams J. J., Brown A., Pospischil M. A., Peterson C. M. The effect of dietary protein on cystine excretion in patients with cystinuria. Clin. Nephrol. 1984; 22: 273
   PubMed Web of Science ®Google Scholar
• Kolb F. O., Earll J. M., Harper H. A. “Disappearance” of cystinuria in a patient treated with prolonged low methionine diet. Metabolism 1967; 16: 378
   PubMed Web of Science ®Google Scholar
• Zinneman H. H., Jones J. E. Dietary methionine and its influence on cystine excretion in cystinuric patients. Metabolism 1966; 15: 915
   PubMedGoogle Scholar
• Dent C. E., Senior B. Studies on the treatment of cystinuria. Br. J. Urol. 1955; 27: 317
   PubMedGoogle Scholar
• Weinberg S. R., Tabenkin P. A. Observations on therapy of cystine calculus disease. Arch. Int. Med. 1952; 90: 850
   Google Scholar
• Dent C. E., Friedmann M., Green H., Watson L. C. A. Treatment of cystinuria. Br. Med. J. 1965; 1: 403
   PubMed Web of Science ®Google Scholar
• Crawhall J. C., Scowen E. F., Watts R. C. E. Effects of penicillamine on cystinuria. Br. Med. J. 1963; 1: 588
   PubMedGoogle Scholar
• Crawhall J. C., Scowen E. F., Watts R. C. E. Further observations on use of D-penicillamine in cystinuria. Br. Med. J. 1964; 1: 1411
   PubMedGoogle Scholar
• Multicenter Trial Group. Controlled trial of D-penicillamine in severe rheumatoid arthritis. Lancet 1973; 1: 275
   PubMed Web of Science ®Google Scholar
• Walshe J. M. Penicillamine: a new oral therapy for Wilson's disease. Am. J. Med. 1956; 2: 487
   Google Scholar
• Sachs H. K., Blanksma L. A., Murray E. F., O'Connell M. J. Ambulatory treatment of lead poisoning. Report of 1,555 cases. Pediatrics 1970; 46: 389
   PubMed Web of Science ®Google Scholar
• Perrett D. The metabolism and pharmacology of D-pencillamine in man. J. Rheum. 1981; 7: 41, (Suppl.)
   Google Scholar
• Crawhall J. C., Thompson C. J. Cystinuria: effect of D-penicillamine on plasma and urinary cystine concentrations. Science 1965; 147: 1459
   PubMed Web of Science ®Google Scholar
• Lota M., Potts J. T. Quantitation of the effects of penicillamine therapy in cystinuria. J. Clin. Invest. 1964; 43: 1293
   Web of Science ®Google Scholar
• Ekberg M., Jeppsson J. O., Denneberg T. Penicillamine treatment of cystinuria. Acta Med. Scand. 1974; 195: 415
   PubMedGoogle Scholar
• Crawhall J. C. Cystinuria—an experience in management over 18 years. Mineral Elec. Metab. 1987; 13: 286
   PubMedGoogle Scholar
• Asatoor A. Pyridoxine deficiency in the rat produced by D-penicillamine. Nature (London) 1964; 203: 1382
   PubMed Web of Science ®Google Scholar
• Jaffe I. A., Altman K., Merryman P. The antipyridoxine effect of penicillamine in man. J. Clin. Invest. 1964; 43: 1869
   PubMed Web of Science ®Google Scholar
• Lotz M., Bartter F. C. Stone dissolution with D-penicillamine in cystinuria. Br. Med. J. 1965; 1408
   PubMedGoogle Scholar
• Van Dugteren G. R., Wiggelinkhuizen J. Dissolution of bilateral staghorn cystine renal calculi. Arch. Dis. Child. 1979; 54: 795
   PubMed Web of Science ®Google Scholar
• Shaw D. G., Sutor D. J. Cystine stone dissolution. Br. J. Radiol. 1972; 45: 664
   PubMed Web of Science ®Google Scholar
• Crawhall J. C., Watts R. C. E. Some complications in the treatment of of cystinuria with D-penicillamine and N-acetyl-D-pencillamine. Postgrad. Med. J. October, 1968; 8, (Suppl.)
   Web of Science ®Google Scholar
• Halperin E. C., Thier S. O., Rosenberg L. E. The use of D-penicillamine in cystinuria: efficacy and untoward reactions. Yale J. Biol. Med. 1981; 54: 439
   PubMed Web of Science ®Google Scholar
• Jaffe I. Induction of autoimmune syndromes by penicillamine therapy in rheumatoid arthritis and other diseases. Springer Semin. Immunopathol. 1981; 4: 193
   PubMed Web of Science ®Google Scholar
• Oliver I., Liberman U. A., DeVries A. Lupus-like syndrome induced by penicillamine in cystinuria. JAMA 1972; 200: 588
   Google Scholar
• Gefel D., Harats N., Lijovetsky G., Eliakim M. Cholestatic jaundice associated with D-pencillamine therapy. Scand. J. Rheum. 1985; 14: 303
   PubMed Web of Science ®Google Scholar
• Fellers F. X., Shahida N. T. The nephrotic syndrome induced by penicillamine therapy. Am. J. Dis. Child. 1959; 98: 669
   Google Scholar
• Rosenberg L. E., Hayslett J. P. Nephrotoxic effects of penicillamine in cystinuria. JAMA 1967; 201: 128
   Web of Science ®Google Scholar
• Corcos J. M., Soler-Bechera J., Mayer K., Freyberg R. H., Goldstein R., Jaffe I. Neutrophilc agranulocytosis during administration of penicillamine. JAMA 1964; 189: 265
   PubMed Web of Science ®Google Scholar
• Luke R. G., Briggs J. D., Fell G. S., Kennedy A. C. Proteinuria associated with D-penicillamine therapy of cystinuria. J. Urol. 1968; 99: 207
   PubMed Web of Science ®Google Scholar
• Steinmann B., Otten A., Gitzelmann R. Skin and bone lesions (dermato-osteolathyrism), possible side effects of D-penicillamine treatment in a boy with cystinuria. Helv. Paediatr. Acta 1979; 34: 281
   PubMedGoogle Scholar
• Kean W. F., Bellamy N., Lock C. J. L., Adachi J. Bio-inorganic effects of D-penicillamine in children and in the elderly. Clin. Invest. Med. 1984; 7: 77
   PubMed Web of Science ®Google Scholar
• Endres W. D-Penicillamine in pregnancy — to ban or not to ban?. Klin. Wochenschr. 1981; 59: 535
   PubMedGoogle Scholar
• Laver M., Fairley K. F. D-Pencillamine treatment in pregnancy. Lancet 1971; 1: 1019
   PubMed Web of Science ®Google Scholar
• Gregory M. C., Mansell M. A. Pregnancy and cystinuria. Lancet 1983; 2: 1158
   PubMed Web of Science ®Google Scholar
• King J. S. Treatment of cystinuria with a-mercaptopropionlglycine: a preliminary report with some notes on column chromatography of mercaptans. Proc. Soc. Exp. Biol. Med. 1968; 129: 927
   PubMed Web of Science ®Google Scholar
• Remien A., Kallistratos G., Burchart P. Treatment of cystinuria with thiola (a-mercaptopropionylglycine). Eur. Urol. 1975; 1: 227
   PubMedGoogle Scholar
• Hautmann R., Terhorst B., Stuhlsatz H. W., Lutzeyer W. Mercaptopropionylglycine: a progress in cystine stone therapy. J. Urol. 1977; 117: 628
   PubMed Web of Science ®Google Scholar
• Johansen K., Gammelgard P. A., Jorgensen F. S. Treatment of cystinuria with alpha-mercaptopropionylglycine. Scand.J. Urol. Nephrol. 1980; 14: 189
   PubMed Web of Science ®Google Scholar
• Lucky P. A., Skovby F., Thier S. O. Pemphigus foliaceus and proteinuria induced by a-mercaptopropionylglycine. J. Am. Acad. Dermatol. 1983; 8: 667
   PubMed Web of Science ®Google Scholar
• Rizzoni F., Pavanello N., Dussini N., Chiandetti L., Zacchelo G. Nephrotic syndrome during treatment with alpha-mercaptopropionylglycine. J. Urol. 1979; 122: 381
   PubMed Web of Science ®Google Scholar
• Pak C. Y. C., Fuller C., Sakahee K., Zerwekh J. E., Adams B. V. Management of cystine nephrolithiasis with alpha-mercaptoproprionylglycine. J. Urol. 1986; 136: 1003
   PubMed Web of Science ®Google Scholar
• Harbar J. A., Cusworth D. C., Lawes L. C., Wrong O. M. Comparison of a-mercaptopropion-ylglycine and D-penicillamine in the treatment of cystinuria. J. Urol. 1986; 136: 146
   PubMed Web of Science ®Google Scholar
• Stephens A. D., Watts R. W. E. The treatment of cystinuria with N-acetyl-D-penicillamine — a comparison with the results of D-penicillamine treatment. Q. J. Med. 1971; 159: 355
   Google Scholar
• Mulvaney W. P., Quilter T., Mortera A. Experiences with acetylcysteine in cystinuric patients. J. Urol 1975; 114: 107
   PubMed Web of Science ®Google Scholar
• Blackburn P., Peterson C. M. Thioldisulfide interchange between cystine and N-2-mercaptoethy 1–1, 3-diaminopropane as a potential treatment for cystinuria. Anal. Biochem. 1984; 136: 31
   PubMedGoogle Scholar
• Miyagi K., Nakada F., Ohshiro S. Effect of glutamine on cystine excretion in a patient with cystinuria. N. Engl. J. Med. 1979; 301: 196
   PubMed Web of Science ®Google Scholar
• Skovby F., Rosenberg L. E., Thier S. O. No effect of L-glutamine on cystinuria. N. Engl. J. Med. 1980; 302: 236
   PubMed Web of Science ®Google Scholar
• Joost J., Jarosch E. Glutamine: a new anticystinuric drug?. Eur. Urol. 1981; 7: 363
   PubMed Web of Science ®Google Scholar
• Van Den Berg C. J., Jones J. D., Wilson D. M., Smith L. H. Glutamine therapy of cystinuria. Invest. Urol. 1980; 18: 155
   PubMedGoogle Scholar
• Jaeger P., Portman L., Saunders A., Rosenberg L. E., Thier S. O. Anticystinuric effect of glutamine and of dietary sodium restriction. N. Engl. J. Med. 1986; 315: 1120
   PubMed Web of Science ®Google Scholar
• Egghart G., Marquardt H. D., Kastert H. B., Feizelmeier F. Percutaneous nephrostomy and irrigation lithochemolysis. Int. Urol. Nephrol. 1983; 15: 131
   PubMedGoogle Scholar
• Stark H., Savir A. Dissolution of cystine calculi by pelviocaliceal irrigation with D-penicillamine. J. Urol. 1980; 124: 895
   PubMed Web of Science ®Google Scholar
• Smith A. D., Lange P. H., Miller R. P., Reinke D. B. Dissolution of cystine calculi by irrigation with acetylcysteine through percutaneous nephrostomy. Urology 1979; 13: 422
   PubMed Web of Science ®Google Scholar
• Tseng C. H., Talwalkar Y. B., Tank E. S., Hatch T., Alexander S. R. Dissolution of cystine calculi by pelviocaliceal irrigation with tromethamine-E. J. Urol. 1982; 128: 1281
   PubMed Web of Science ®Google Scholar
• Dretler S. P., Pfister R. C., Newhouse J. H., Prien E. L. Percutaneous catheter dissolution of cystine calculi. J. Urol. 1984; 131: 216
   PubMed Web of Science ®Google Scholar
• Millet V. G., Praga M., Miranda B., Bello I., Ruilope L., Gonzalez R. D., Leyva O., Alcazar J. M., Barrkentos A., Ridicio J. L. Ureolytic citrobacter freundii infection of the urine as a cause of dissolution of cystine renal calculi. J. Urol. 1985; 133: 443
   PubMed Web of Science ®Google Scholar
• Hoctsma A. J., Koene R. A. P., Trijbels F. J. M., Monneks L. A. H. Disappearance of cystinuria after renal transplantation. JAMA 1983; 250: 615
   Web of Science ®Google Scholar
• Krizek V., Erben J., Lazne M., Navratil P., Svab J. Disappearance of cystinuria after kidney transplantation. Br. J. Urol. 1983; 55: 575
   PubMedGoogle Scholar
• Kelly S., Nolan E. P. Postscript on excretion rates in posttransplant cystinuric patient. JAMA 1980; 243: 1897
   PubMed Web of Science ®Google Scholar
• Bovee K. Canine cystine urolithiasis. Vet. Clin. N.A. 1986; 16: 211
   Google Scholar
• Holtzapple P. G., Rea C., Bovee K., Segal S. Cystine and lysine transport in renal and jejunal tissue from cystinuric dogs. Metabolism 1971; 20: 1016
   PubMed Web of Science ®Google Scholar
• Tsan M. F., Jones T. C., Thornton G. W., Levey H. L., Gilmore C., Wilson T. H. Canine cystinuria: its urinary amino acid pattern and genetic analysis. Am. J. Vet. Res. 1972; 33: 2455
   PubMed Web of Science ®Google Scholar
• Tsan M. F., Jones T. C., Wilson T. H. Canine cystinuria: intestinal and renal amino acid transport. Am. J. Vet. Res. 1972; 33: 2463
   PubMed Web of Science ®Google Scholar
• Bush M., Bovee K. Cystinuria in a maned wolf. J. Am. Vet. Med. Assoc 1978; 173: 1159
   PubMed Web of Science ®Google Scholar
• Craan A. G. Cystinuria: the disease and its models. Life Sci. 1981; 28: 5
   PubMed Web of Science ®Google Scholar