{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,4,3]],"date-time":"2022-04-03T01:19:11Z","timestamp":1648948751180},"reference-count":15,"publisher":"Springer Science and Business Media LLC","issue":"3","license":[{"start":{"date-parts":[[1989,12,1]],"date-time":"1989-12-01T00:00:00Z","timestamp":628473600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Eur J Pediatr"],"published-print":{"date-parts":[[1989,12]]},"DOI":"10.1007\/bf01958283","type":"journal-article","created":{"date-parts":[[2005,8,2]],"date-time":"2005-08-02T06:58:12Z","timestamp":1122965892000},"page":"205-207","source":"Crossref","is-referenced-by-count":5,"title":["Frequent relapser minimal change nephrosis: An unrecognized X-linked disorder?"],"prefix":"10.1007","volume":"149","author":[{"given":"N. B.","family":"Awadalla","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A. S.","family":"Teebi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A. Y.","family":"Elzouki","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Shaltout","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"BF01958283_CR1","first-page":"40","volume-title":"The kidney in genetic disease","author":"AY Barakat","year":"1986","unstructured":"Barakat AY, Der Kaloustian VM, Mufarrij AA, Birbari AE (1986) The kidney in genetic disease. Churchill Livingstone, London, pp 40\u201341"},{"key":"BF01958283_CR2","doi-asserted-by":"crossref","first-page":"253","DOI":"10.1136\/adc.59.3.253","volume":"59","author":"AY Elzouki","year":"1984","unstructured":"Elzouki AY, Amin F, Jaiswal OP (1984) Primary nephrotic syndrome in Arab children. Arch Dis Child 59:253\u2013255","journal-title":"Arch Dis Child"},{"key":"BF01958283_CR3","first-page":"427","volume":"13","author":"G Gonzales","year":"1977","unstructured":"Gonzales G, Kleinkencht C, Gubler MC, Lenoir G (1977) Syndromes nephrotiques familiaux. Rev Pediatr 13:427\u2013433","journal-title":"Rev Pediatr"},{"key":"BF01958283_CR4","first-page":"91","volume":"28","author":"R Habib","year":"1973","unstructured":"Habib R, Bois E (1973) Heterogenit\u00e9 des syndromes nephrotiques a debut precoce du norrison (syndrome nephrotique \u201cinfantile\u201d). Helv Paediatr Acta 28:91\u2013107","journal-title":"Helv Paediatr Acta"},{"key":"BF01958283_CR5","first-page":"165","volume-title":"Pathology annual","author":"R Habib","year":"1971","unstructured":"Habib R, Kleinknecht C (1971) The primary nephrotic syndrome of childhood. Classification and clinicopathologic study of 406 cases. In: Sommers SC (ed) Pathology annual. Appleton Century-Crofts, New York, p 165"},{"key":"BF01958283_CR6","doi-asserted-by":"crossref","first-page":"765","DOI":"10.1038\/ki.1981.209","volume":"20","author":"International Study of Kidney Disease in Children","year":"1981","unstructured":"International Study of Kidney Disease in Children (1981) Primary nephrotic syndrome in children: clinical significance of histopathologic variants of minimal change and of difference mesangial hypercellularity. Kidney Int 20:765\u2013771","journal-title":"Kidney Int"},{"key":"BF01958283_CR7","volume-title":"Mendelian inheritance in man. Catalogs of autosomal dominant, autosomal recessive and X-linked phenotypes","author":"VA McKusick","year":"1988","unstructured":"McKusick VA (1988) Mendelian inheritance in man. Catalogs of autosomal dominant, autosomal recessive and X-linked phenotypes, 8th edn. John Hopkins University Press, Baltimore","edition":"8th edn."},{"key":"BF01958283_CR8","doi-asserted-by":"crossref","first-page":"753","DOI":"10.1111\/j.1651-2227.1982.tb09514.x","volume":"71","author":"HB Mendelsohn","year":"1982","unstructured":"Mendelsohn HB, Krauss M, Berant M, Lichtig C (1982) Familial early-onset nephrotic syndrome: diffuse mesangial sclerosis: clinico-pathological study of a kindred. Acta Paediatr Scand 71:753\u2013758","journal-title":"Acta Paediatr Scand"},{"key":"BF01958283_CR9","first-page":"220","volume":"1","author":"MW Moncrieff","year":"1973","unstructured":"Moncrieff MW, White RHR, Glasgow EF, Winterborn MH, Cameron JS, Ogg CS (1973) The familial nephrotic syndrome: II. A clinicopathological study. Clin Nephrol 1:220","journal-title":"Clin Nephrol"},{"key":"BF01958283_CR10","doi-asserted-by":"crossref","first-page":"109","DOI":"10.1097\/00000441-198009000-00007","volume":"280","author":"T Naruse","year":"1980","unstructured":"Naruse T, Hirokawa N, Maekawa T, Azato H, Ito K, Kaya H (1980) Familial nephrotic syndrome with focal glomerulaer sclerosis. Am J Med Sci 280:109\u2013113","journal-title":"Am J Med Sci"},{"key":"BF01958283_CR11","doi-asserted-by":"crossref","first-page":"113","DOI":"10.1159\/000152208","volume":"19","author":"R Norio","year":"1969","unstructured":"Norio R (1969) The nephrotic syndrome and heredity. Hum Hered 19:113","journal-title":"Hum Hered"},{"key":"BF01958283_CR12","first-page":"223","volume":"10","author":"R Norio","year":"1964","unstructured":"Norio R, Hjelt L, Hallman N (1964) Congenital nephrotic syndrome: an inherited disease? A preliminary report. Ann Paediatr Fenn 10:223\u2013227","journal-title":"Ann Paediatr Fenn"},{"key":"BF01958283_CR13","doi-asserted-by":"crossref","first-page":"348","DOI":"10.1055\/s-0028-1110575","volume":"91","author":"HG Rossenbeck","year":"1966","unstructured":"Rossenbeck HG, Margraf O, Hofmann D (1966) \u00dcber das infantile nephrotische Syndrom bei kongenitaler Glomerulonephritis. Dtsch Med Wochenschr 91:348\u2013355","journal-title":"Dtsch Med Wochenschr"},{"key":"BF01958283_CR14","first-page":"548","volume":"88","author":"R Schwarz","year":"1976","unstructured":"Schwarz R, Stoegmann W, Fischbach H (1976) Famili\u00e4res nephrotisches Syndrom, mit fokaler Glomerulosklerose. Wien Klin Wochenschr 88:548\u2013554","journal-title":"Wien Klin Wochenschr"},{"key":"BF01958283_CR15","first-page":"215","volume":"1","author":"RHR White","year":"1973","unstructured":"White RHR (1973) The familial nephrotic syndrome I.A. European survey. Clin Nephrol 1:215","journal-title":"Clin Nephrol"}],"container-title":["European Journal of Pediatrics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF01958283.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF01958283\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF01958283","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,13]],"date-time":"2019-05-13T17:30:33Z","timestamp":1557768633000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF01958283"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1989,12]]},"references-count":15,"journal-issue":{"issue":"3","published-print":{"date-parts":[[1989,12]]}},"alternative-id":["BF01958283"],"URL":"https:\/\/doi.org\/10.1007\/bf01958283","relation":{},"ISSN":["0340-6199","1432-1076"],"issn-type":[{"value":"0340-6199","type":"print"},{"value":"1432-1076","type":"electronic"}],"subject":[],"published":{"date-parts":[[1989,12]]}}}