{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,3]],"date-time":"2026-01-03T06:45:32Z","timestamp":1767422732802},"reference-count":29,"publisher":"Elsevier BV","issue":"1","license":[{"start":{"date-parts":[[1968,7,1]],"date-time":"1968-07-01T00:00:00Z","timestamp":-47433600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["The Journal of Pediatrics"],"published-print":{"date-parts":[[1968,7]]},"DOI":"10.1016\/s0022-3476(68)80041-1","type":"journal-article","created":{"date-parts":[[2006,8,18]],"date-time":"2006-08-18T11:13:09Z","timestamp":1155899589000},"page":"77-83","source":"Crossref","is-referenced-by-count":19,"title":["Familial juvenile nephronophthisis and medullary cystic disease"],"prefix":"10.1016","volume":"73","author":[{"given":"Frank A.","family":"Pedreira","sequence":"first","affiliation":[]},{"given":"Ellen L.","family":"Marmer","sequence":"additional","affiliation":[]},{"given":"William H.","family":"Bergstrom","sequence":"additional","affiliation":[]}],"member":"78","reference":[{"key":"10.1016\/S0022-3476(68)80041-1_bib1","first-page":"1","article-title":"Die famili\u00e4re juvenile nephronophthise (die idiopathische parenchymatose Schrumpfniere)","volume":"6","author":"Fanconi","year":"1951","journal-title":"Helvet. paediat. acta"},{"key":"10.1016\/S0022-3476(68)80041-1_bib2","doi-asserted-by":"crossref","first-page":"428","DOI":"10.1111\/j.1651-2227.1958.tb07655.x","article-title":"Familial juvenile nephronophthisis","volume":"47","author":"Hackzell","year":"1958","journal-title":"Acta paediat."},{"key":"10.1016\/S0022-3476(68)80041-1_bib3","first-page":"217","article-title":"A case of Fanconis familial juvenile nephronophthisis","volume":"14","author":"Hooft","year":"1959","journal-title":"Helvet. paediat. acta"},{"key":"10.1016\/S0022-3476(68)80041-1_bib4","doi-asserted-by":"crossref","first-page":"470","DOI":"10.1111\/j.1651-2227.1960.tb07761.x","article-title":"Juvenile nephronophthisis. Part I. A genetically determined nephropathy with hypotonic polyuria and azotemia","volume":"49","author":"Broberger","year":"1960","journal-title":"Acta paediat."},{"key":"10.1016\/S0022-3476(68)80041-1_bib5","doi-asserted-by":"crossref","first-page":"489","DOI":"10.1111\/j.1651-2227.1960.tb07762.x","article-title":"Juvenile nephronophthisis. Part II. A histologic and microangiographic study","volume":"49","author":"Ivemark","year":"1960","journal-title":"Acta paediat."},{"key":"10.1016\/S0022-3476(68)80041-1_bib6","doi-asserted-by":"crossref","first-page":"561","DOI":"10.1111\/j.1651-2227.1962.tb06582.x","article-title":"Familial juvenile nephronophthisis","volume":"51","author":"Sydow","year":"1962","journal-title":"Acta paediat."},{"key":"10.1016\/S0022-3476(68)80041-1_bib7","doi-asserted-by":"crossref","first-page":"625","DOI":"10.1016\/0002-9394(61)90147-7","article-title":"Juvenile familial nephropathy with tapetoretinal degeneration","volume":"52","author":"Senior","year":"1961","journal-title":"Am. J. Ophth."},{"key":"10.1016\/S0022-3476(68)80041-1_bib8","first-page":"337","article-title":"Familial juvenile nephronophthisis: An unrecognized renal disease in the United States","volume":"34","author":"Mangos","year":"1964","journal-title":"Pediatrics"},{"key":"10.1016\/S0022-3476(68)80041-1_bib9","doi-asserted-by":"crossref","first-page":"984","DOI":"10.1056\/NEJM196605052741802","article-title":"Hereditary occurrence of cystic disease of the renal medulla","volume":"274","author":"Goldman","year":"1966","journal-title":"New England J. Med."},{"key":"10.1016\/S0022-3476(68)80041-1_bib10","doi-asserted-by":"crossref","first-page":"1029","DOI":"10.1056\/NEJM196605052741813","article-title":"Cystic diseases of the kidney","volume":"274","year":"1966","journal-title":"New England J. Med."},{"key":"10.1016\/S0022-3476(68)80041-1_bib11","doi-asserted-by":"crossref","first-page":"373","DOI":"10.7326\/0003-4819-57-3-373","article-title":"Clinical and pathological aspects of cystic disease of renal medulla: Analysis of eighteen cases","volume":"57","author":"Strauss","year":"1962","journal-title":"Ann. Int. Med."},{"key":"10.1016\/S0022-3476(68)80041-1_bib12","series-title":"Diseases of the kidney: 43 contributors; Medullary cystic disease","first-page":"938","year":"1963"},{"key":"10.1016\/S0022-3476(68)80041-1_bib13","series-title":"Transactions Midwest Society of Pediatric Research","first-page":"4","article-title":"Medullary cystic disease: Studies of affected family","author":"Herdman","year":"1964"},{"key":"10.1016\/S0022-3476(68)80041-1_bib14","first-page":"369","article-title":"Congenital medullary cysts of kidneys with severe refractory anemia","volume":"69","author":"Smith","year":"1945","journal-title":"Am. J. Dis. Child."},{"key":"10.1016\/S0022-3476(68)80041-1_bib15","doi-asserted-by":"crossref","first-page":"750","DOI":"10.1001\/archinte.1952.00240120025003","article-title":"Studies of sodium and potassium metabolism in salt losing nephritis","volume":"90","author":"Murphy","year":"1952","journal-title":"Arch. Int. Med."},{"key":"10.1016\/S0022-3476(68)80041-1_bib16","first-page":"750","article-title":"Medullary cysts of kidneys","volume":"90","author":"Hogness","year":"1960","journal-title":"Arch. Int. Med."},{"key":"10.1016\/S0022-3476(68)80041-1_bib17","doi-asserted-by":"crossref","first-page":"1139","DOI":"10.1016\/S0025-7125(16)33953-0","article-title":"Hormonal studies in salt losing nephritis","volume":"44","author":"Thorn","year":"1960","journal-title":"M. Clin. North America"},{"key":"10.1016\/S0022-3476(68)80041-1_bib18","doi-asserted-by":"crossref","first-page":"277","DOI":"10.1001\/archpedi.1964.02080060279009","article-title":"Congenital cysts of renal medulla: Case with severe refractory anemia","volume":"107","author":"Faigel","year":"1964","journal-title":"Am. J. Dis. Child."},{"key":"10.1016\/S0022-3476(68)80041-1_bib19","doi-asserted-by":"crossref","first-page":"158","DOI":"10.1016\/0002-9343(57)90347-9","article-title":"Salt-losing nephritis with fixed urinary composition","volume":"22","author":"Knowles","year":"1957","journal-title":"Am. J. Med."},{"key":"10.1016\/S0022-3476(68)80041-1_bib20","first-page":"330","article-title":"Cystic disease of the renal medulla","volume":"56","author":"Kerlan","year":"1963","journal-title":"J. Tennessee M. A."},{"key":"10.1016\/S0022-3476(68)80041-1_bib21","first-page":"82","article-title":"The anemia associated with renal disease","volume":"52","author":"Kaye","year":"1958","journal-title":"J. Lab. & Clin. Med."},{"key":"10.1016\/S0022-3476(68)80041-1_bib22","doi-asserted-by":"crossref","first-page":"563","DOI":"10.1016\/S0031-3955(16)31583-8","article-title":"Growth aberrations in renal disease","volume":"11","author":"Bergstrom","year":"1964","journal-title":"Pediat. Clin. North America"},{"key":"10.1016\/S0022-3476(68)80041-1_bib23","doi-asserted-by":"crossref","first-page":"1537","DOI":"10.1055\/s-0028-1112966","article-title":"Ein kongenitales Syndrom von Minderwuchs und anomalies des uropoetischen Systems ohne Niereninsuffizienz","volume":"86","author":"Loeschke","year":"1961","journal-title":"Deutsche med. Wchnschr."},{"key":"10.1016\/S0022-3476(68)80041-1_bib24","first-page":"363","article-title":"Kidney abnormalities","author":"Potter","year":"1952"},{"key":"10.1016\/S0022-3476(68)80041-1_bib25","doi-asserted-by":"crossref","first-page":"504","DOI":"10.1136\/bmj.1.3454.504","article-title":"Hereditary familial congenital haemorrhagic nephritis","volume":"1","author":"Alport","year":"1927","journal-title":"Brit. M. J."},{"key":"10.1016\/S0022-3476(68)80041-1_bib26","doi-asserted-by":"crossref","first-page":"58","DOI":"10.1016\/0002-9343(65)90245-7","article-title":"Familial nephropathy with retinitis pigmentosa: New oculorenal syndrome in adults","volume":"39","author":"Meier","year":"1965","journal-title":"Am. J. Med."},{"key":"10.1016\/S0022-3476(68)80041-1_bib27","doi-asserted-by":"crossref","first-page":"1060","DOI":"10.1136\/bmj.1.5337.1060","article-title":"Familial visual defects associated with polycystic kidney and medullary sponge kidney","volume":"1","author":"Fairley","year":"1963","journal-title":"Brit. M. J."},{"key":"10.1016\/S0022-3476(68)80041-1_bib28","first-page":"39","article-title":"Principles of human genetics","author":"Stern","year":"1949"},{"key":"10.1016\/S0022-3476(68)80041-1_bib29","first-page":"91","article-title":"Renal tubular dysfunction","author":"Woolf","year":"1966"}],"container-title":["The Journal of Pediatrics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022347668800411?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022347668800411?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,1,14]],"date-time":"2019-01-14T06:50:52Z","timestamp":1547448652000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0022347668800411"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1968,7]]},"references-count":29,"journal-issue":{"issue":"1","published-print":{"date-parts":[[1968,7]]}},"alternative-id":["S0022347668800411"],"URL":"https:\/\/doi.org\/10.1016\/s0022-3476(68)80041-1","relation":{},"ISSN":["0022-3476"],"issn-type":[{"value":"0022-3476","type":"print"}],"subject":[],"published":{"date-parts":[[1968,7]]}}}