{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,1,26]],"date-time":"2024-01-26T18:08:02Z","timestamp":1706292482051},"reference-count":26,"publisher":"Springer Science and Business Media LLC","issue":"18","license":[{"start":{"date-parts":[[1982,9,1]],"date-time":"1982-09-01T00:00:00Z","timestamp":399686400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Klin Wochenschr"],"published-print":{"date-parts":[[1982,9]]},"DOI":"10.1007\/bf01715841","type":"journal-article","created":{"date-parts":[[2005,6,12]],"date-time":"2005-06-12T07:16:10Z","timestamp":1118560570000},"page":"1115-1125","source":"Crossref","is-referenced-by-count":2,"title":["Long-term management of inherited renal tubular disorders","Langzeitbetreuung von Patienten mit angeborenen Tubulopathien"],"prefix":"10.1007","volume":"60","author":[{"given":"F.","family":"Manz","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"K.","family":"Sch\u00e4rer","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"BF01715841_CR1","doi-asserted-by":"crossref","first-page":"370","DOI":"10.1542\/peds.58.3.370","volume":"58","author":"BS Arant","year":"1976","unstructured":"Arant BS, Greifer I, Edelmann CM, Spitzer A (1976) Effect of chronic salt and water loading on the tubular defects of a child with Fanconi syndrome (cystinosis). Pediatrics 58:370\u2013377","journal-title":"Pediatrics"},{"key":"BF01715841_CR2","doi-asserted-by":"crossref","first-page":"148","DOI":"10.1001\/jama.1975.03250020022018","volume":"232","author":"BA Barnes","year":"1975","unstructured":"Barnes BA, Bergan JJ, Braun WE, Fraumeni JF, Kountz SL, Mickey MR, Rubin AL, Simmons RL, Stevens LE, Wilson RE (1975) Renal transplantation in congenital-and metabolic diseases. JAMA 232:148\u2013153","journal-title":"JAMA"},{"key":"BF01715841_CR3","first-page":"339","volume":"34","author":"B B\u00e9tend","year":"1979","unstructured":"B\u00e9tend B, David L, Vincent M, Hermier M, Francois R (1979) Successful indomethacin treatment of two paediatric patients with severe tubulopathies. Helv Paediat Acta 34:339\u2013344","journal-title":"Helv Paediat Acta"},{"key":"BF01715841_CR4","doi-asserted-by":"crossref","first-page":"199","DOI":"10.1016\/S0140-6736(79)91464-8","volume":"II","author":"E Beutler","year":"1979","unstructured":"Beutler E (1979) Nature's transplant in Fabry's disease. Lancet II:199","journal-title":"Lancet"},{"key":"BF01715841_CR5","doi-asserted-by":"crossref","first-page":"937","DOI":"10.1515\/9783112327203-166","volume-title":"Vitamin D, biochemical, chemical and clinical aspects related to calcium metabolism","author":"ED Brewer","year":"1977","unstructured":"Brewer ED, Tsai H, Morris C (1977) Fanconi syndrome and its relationship to vitamin D. In: Norman AW, Schaefer K, Coburn JW, DeLuca HF, Fraser D, Grigoleit HG, Herrath D (eds) Vitamin D, biochemical, chemical and clinical aspects related to calcium metabolism. De Gruyter, Berlin, pp 937\u2013949"},{"key":"BF01715841_CR6","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1056\/NEJM197201062860107","volume":"286","author":"WA Briggs","year":"1972","unstructured":"Briggs WA, Kominami N, Wilson RE, Merrill JP (1972) Kidney transplantation in Fanconi syndrome. N Engl J Med 286:25","journal-title":"N Engl J Med"},{"key":"BF01715841_CR7","first-page":"955","volume-title":"Pediatric kidney disease","author":"J Brodehl","year":"1978","unstructured":"Brodehl J (1978) The Fanconi syndrome. In: Edelmann CM (ed) Pediatric kidney disease. Little, Brown and Company, Boston, Vol II, pp 955\u2013987"},{"key":"BF01715841_CR8","unstructured":"Broyer M, Guillot M, Gubler MC, Habib R (1980) La cystinose infantile, r\u00e9\u00e9valuation des sympt\u00f4mes pr\u00e9coces et tardifs. Actual N\u00e9phrol pp 127\u2013157"},{"key":"BF01715841_CR9","first-page":"602","volume":"25","author":"L Callis","year":"1970","unstructured":"Callis L, Castello F, Fortuny G, Vallo A, Ballabriga A (1970) Effect of hydrochlorothiazide on rickets and on renal tubular acidosis in two patients with cystinosis. Helv Paediat Acta 25:602\u2013619","journal-title":"Helv Paediat Acta"},{"key":"BF01715841_CR10","first-page":"49","volume":"18","author":"RA Donckerwolcke","year":"1981","unstructured":"Donckerwolcke RA, Broyer M, Brunner FP, Brynger H, Jacobs C, Kramer P, Selwood NH, Wing AJ (1981) Combined report on regular dialysis and transplantation of children in Europe. Proc. EDTA 18:49\u201368","journal-title":"Proc. EDTA"},{"key":"BF01715841_CR11","first-page":"247","volume-title":"Observations on results of management of galactosemic patients","author":"GN Donnell","year":"1969","unstructured":"Donnell GN, Koch R, Berger WR (1969) Observations on results of management of galactosemic patients. In: Hsia DYY (ed) Galactosemia Thomas, Springfield, pp 247\u2013259"},{"key":"BF01715841_CR12","first-page":"589","volume-title":"The metabolic basis of inherited disease","author":"E Gj\u00f8ne","year":"1978","unstructured":"Gj\u00f8ne E, Norum KR, Glomset JA (1978) Familial hecithin: cholesterol acyltransferase deficiency. In: Stanbury JB, Wyngaarden JB, Fredrickson DS (eds) The metabolic basis of inherited disease. McGraw-Hill Book Company, New York, pp 589\u2013603"},{"key":"BF01715841_CR13","first-page":"497","volume":"37","author":"M Guillot","year":"1980","unstructured":"Guillot M, Broyer M, Cathelineau L, Boulegue D, Dartois AM, Folio D, Guimbaud P (1980) Nutrition ent\u00e9rale a d\u00e9bit constant en n\u00e9phrologie p\u00e9diatrique. Arch Franc P\u00e9diat 37:497\u2013505","journal-title":"Arch Franc P\u00e9diat"},{"key":"BF01715841_CR14","doi-asserted-by":"crossref","first-page":"354","DOI":"10.1016\/0002-9343(82)90826-9","volume":"72","author":"DJ Levenson","year":"1982","unstructured":"Levenson DJ, Simmons CD, Brenner BM (1982) Arachidonic acid metabolism, prostaglandins and the kidney. Am J Med 72:354\u2013374","journal-title":"Am J Med"},{"key":"BF01715841_CR15","doi-asserted-by":"crossref","first-page":"67","DOI":"10.1007\/BF00496992","volume":"128","author":"F Manz","year":"1978","unstructured":"Manz F, Sch\u00e4rer K, Janka P, Lombeck J (1978) Renal magnesium wasting, incomplete tubular acidosis, hypercalciuria and nephrocalcinosis in siblings. Eur J Pediatr 128:67\u201379","journal-title":"Eur J Pediatr"},{"key":"BF01715841_CR16","unstructured":"Manz F, Gretz N, Bender-G\u00f6tze C, Brandis M, Bremer HJ, Brodehl J, Bulla M, Diekmann L, Ehrich JHH, Endres W, Feldhoff C, Gekle D, Gesch\u00f6ll-Bauer B, Grote K, Gr\u00fcttner R, Hagge W, Hennemann H, Klare B, Leupold D, L\u00f6hr H, Michalk D, Ott F, Pistor K, Schindera F, Schmidt H, Schulte-Wissermann H, Weber HP, Willenbockel U, Wolf H (1982) Epidemiologie der Zystinose in der Bundesrepublik Deutschland. Eine multizentrische Studie. Mschr. Kinderheilk, Abstract (in press)"},{"key":"BF01715841_CR17","first-page":"289","volume":"16","author":"A Patrick","year":"1981","unstructured":"Patrick A, Cameron JS, Ogg CS (1981) A family with a dominant form of idiopathic Fanconi syndrome leading to renal failure in adult life. Clin Nephrol 16:289\u2013292","journal-title":"Clin Nephrol"},{"key":"BF01715841_CR18","doi-asserted-by":"crossref","first-page":"381","DOI":"10.1016\/S0022-5347(17)56420-4","volume":"122","author":"G Rizzoni","year":"1979","unstructured":"Rizzoni G, Pavanello L, Dussini N, Chiandetti L, Zacchallo G (1979) Nephrotic syndrome during treatment with alphamercaptopropionylglycine. J Urol 122:381\u2013382","journal-title":"J Urol"},{"key":"BF01715841_CR19","volume-title":"Klinische Nephrologie","author":"K Sch\u00e4rer","year":"1982","unstructured":"Sch\u00e4rer K, Manz F (1982) Heredit\u00e4re Tubulopathien. In: Losse H, Renner E (eds) Klinische Nephrologie. Thieme, Stuttgart, Bd II (in press)"},{"key":"BF01715841_CR20","first-page":"171","volume":"121","author":"H Schmidt","year":"1973","unstructured":"Schmidt H, Lutz P, Bickel H (1973) Wertbeurteilung der di\u00e4tetischen Behandlung der Cystinose. Mschr Kinderheilk 121:171\u2013173","journal-title":"Mschr Kinderheilk"},{"key":"BF01715841_CR21","first-page":"1660","volume-title":"The metabolic basis of inherited disease","author":"JA Schneider","year":"1978","unstructured":"Schneider JA, Schulmann JD, Seegmiller JE (1978) Cystinosis and the Fanconi syndrome. In: Stanbury JB, Wyngaarden JB, Fredrickson DS (eds) The metabolic basis of inherited disease. McGraw-Hill Book Company, New York, pp 1660\u20131682"},{"key":"BF01715841_CR22","doi-asserted-by":"crossref","first-page":"756","DOI":"10.1056\/NEJM197904053001403","volume":"300","author":"JA Schneider","year":"1979","unstructured":"Schneider JA, Schlesselman JJ, Mendoza SA, Orloff S, Thoene JG, Kroll W, Godfrey AD, Schulman JD (1979) Ineffectiveness of ascorbic acid therapy in nephropathic cystinosis. N Engl J Med 300:756\u2013759","journal-title":"N Engl J Med"},{"key":"BF01715841_CR23","unstructured":"Schulte M, Lenz W (1977) Todesf\u00e4lle durch Sorbit-Infusionen. Dt \u00c4rztebl p. 1947\u20131950"},{"key":"BF01715841_CR24","first-page":"1079","volume-title":"Pediatric kidney disease","author":"GJ Schwartz","year":"1978","unstructured":"Schwartz GJ, Spitzer A (1978) Disorders of renal transport of sodium, potassium and magnesium. In: Edelmann CM (ed) Pediatric kidney disease. Little, Brown and Company, Boston, Vol II, pp 1079\u20131093"},{"key":"BF01715841_CR25","first-page":"307","volume-title":"Pediatric Nephrology","author":"A Spitzer","year":"1976","unstructured":"Spitzer A (1976) Pathophysiology and management of renal tubular disorders. In: Strauss J (ed) Pediatric Nephrology. Plenum Press, New York, pp 307\u2013319"},{"key":"BF01715841_CR26","doi-asserted-by":"crossref","first-page":"643","DOI":"10.1016\/S0140-6736(82)92201-2","volume":"I","author":"JM Walshe","year":"1982","unstructured":"Walshe JM (1982) Treatment of Wilson's disease with trientine (triethylene tetramine) dihydrochloride. Lancet I:643\u2013647","journal-title":"Lancet"}],"container-title":["Klinische Wochenschrift"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF01715841.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF01715841\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF01715841","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,1,26]],"date-time":"2024-01-26T17:07:21Z","timestamp":1706288841000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF01715841"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1982,9]]},"references-count":26,"journal-issue":{"issue":"18","published-print":{"date-parts":[[1982,9]]}},"alternative-id":["BF01715841"],"URL":"https:\/\/doi.org\/10.1007\/bf01715841","relation":{},"ISSN":["0023-2173","1432-1440"],"issn-type":[{"value":"0023-2173","type":"print"},{"value":"1432-1440","type":"electronic"}],"subject":[],"published":{"date-parts":[[1982,9]]}}}