{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,25]],"date-time":"2026-03-25T11:57:59Z","timestamp":1774439879695,"version":"3.50.1"},"reference-count":23,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[1974,7,1]],"date-time":"1974-07-01T00:00:00Z","timestamp":141868800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Blut"],"published-print":{"date-parts":[[1974,7]]},"DOI":"10.1007\/bf01631580","type":"journal-article","created":{"date-parts":[[2005,5,6]],"date-time":"2005-05-06T09:18:01Z","timestamp":1115371081000},"page":"43-49","source":"Crossref","is-referenced-by-count":2,"title":["Enterogene Meth\u00e4moglobin\u00e4mie bei heterozygoter NADH-Meth\u00e4moglobin-Reduktase-Defizienz der Erythrozyten"],"prefix":"10.1007","volume":"29","author":[{"given":"Karlheinz","family":"Schmidt","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Klaus","family":"Faber","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Felix","family":"Heni","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"CR1","series-title":"Biochemical Society Symposia","first-page":"55","volume-title":"Methemoglobin and Sulfhemoglobin","author":"Q. H. Gibson","year":"1954","unstructured":"Gibson, Q. H.: Methemoglobin and Sulfhemoglobin, Biochemical Society Symposia, No. 12, p. 55, Cambridge University Press, London 1954."},{"key":"CR2","doi-asserted-by":"crossref","first-page":"13","DOI":"10.1042\/bj0420013","volume":"42","author":"Q. H. Gibson","year":"1948","unstructured":"Gibson, Q. H.: The Reduktion of Methemoglobin in Red Blood Cells and Studies of Idiopathic Methemoglobinemia, Biochem. J.42, 13 (1948).","journal-title":"Biochem. J."},{"key":"CR3","doi-asserted-by":"crossref","first-page":"941","DOI":"10.1016\/S0140-6736(47)91326-3","volume":"2","author":"Q. H. Gibson","year":"1947","unstructured":"Gibson, Q. H., D. C. Harrison: Familial Idiopathic Methemoglobinemia: Five Cases in one Family, Lancet2, 941 (1947).","journal-title":"Lancet"},{"key":"CR4","first-page":"339","volume":"72","author":"E. Hegesh","year":"1968","unstructured":"Hegesh, E., N. Calmanovici and M. Avron: New Method for Determining Ferrihemoglobin Reductase in Erythrocytes, J. Lab. Clin. Med.72, 339 (1968).","journal-title":"J. Lab. Clin. Med."},{"key":"CR5","doi-asserted-by":"crossref","unstructured":"H\u00f6rlein, H. und G. Weber: \u00dcber chronische famili\u00e4re Meth\u00e4moglobin\u00e4mie und eine neue Modifikation des Meth\u00e4moglobins, Dtsch. med. Wschr.476 (1948).","DOI":"10.1055\/s-0028-1118186"},{"key":"CR6","doi-asserted-by":"crossref","first-page":"196","DOI":"10.1172\/JCI106473","volume":"50","author":"H. Hsieh","year":"1971","unstructured":"Hsieh, H. and E. R. Jaff\u00e9: Electrophoretic and Functional Variants of NADH-Methemoglobin Reductase in Hereditary Methemoglobinemia, J. Clin. Invest.50, 196 (1971).","journal-title":"J. Clin. Invest."},{"key":"CR7","first-page":"231","volume-title":"Biochemical Methods in Red Cell Genetics","author":"E. R. Jaff\u00e9","year":"1969","unstructured":"Jaff\u00e9, E. R.: DPNH-Methemoglobin Reductase (Diaphorase), in: Biochemical Methods in Red Cell Genetics J. Yunis (ed.), Chap 9, p. 231. Acad. Press, New York 1969."},{"key":"CR8","unstructured":"Jaff\u00e9, E. R. and P. Heller: Methemoglobinemia in Man, in: Progress in Hematology, C. V. Moore and E. B. Brown, eds.4, 48 (1965)."},{"key":"CR9","doi-asserted-by":"crossref","first-page":"795","DOI":"10.1111\/j.1749-6632.1968.tb48262.x","volume":"151","author":"E. R. Jaff\u00e9","year":"1968","unstructured":"Jaff\u00e9, E. R. and G. Neumann: Hereditary Methemoglobinemia, Toxic Methemoglobinemia and the Reduction of Methemoglobin. Ann. N. Y. Acad. Sci.151, 795 (1968).","journal-title":"Ann. N. Y. Acad. Sci."},{"key":"CR10","doi-asserted-by":"crossref","first-page":"1818","DOI":"10.1172\/JCI104206","volume":"39","author":"J. H. Jandl","year":"1960","unstructured":"Jandl, J. H., L. K. Engle and D. W. Allen: Oxidative Hemolysis and Precipitation of Hemoglobin. J. Clin. Invest.39, 1818 (1960).","journal-title":"J. Clin. Invest."},{"key":"CR11","doi-asserted-by":"crossref","first-page":"605","DOI":"10.1016\/0006-291X(67)90529-3","volume":"29","author":"J. C. Kaplan","year":"1967","unstructured":"Kaplan, J. C. and E. Beutler: Electrophoresis of Red Cell NADH and NADH-Diaphorases in Normal Subjects and Patients with Congential Methemoglobinemia. Biochem. Biophys. Res. Commun.29, 605 (1967).","journal-title":"Biochem. Biophys. Res. Commun."},{"key":"CR12","doi-asserted-by":"crossref","first-page":"330","DOI":"10.1182\/blood.V36.3.330.330","volume":"36","author":"J. C. Kaplan","year":"1970","unstructured":"Kaplan, J. C., A. M. Nicolas, A. Hanzlickova and E. Beutler: A Simple Spot Screening-Test for Fast Detection of Red-Cell NADH-Diaphorase Deficiency. Blood36, 330 (1970).","journal-title":"Blood"},{"key":"CR13","first-page":"264","volume":"316","author":"M. Kiese","year":"1944","unstructured":"Kiese, M.: Die Reduktion des H\u00e4moglobins, Biochem. J.316, 264 (1944).","journal-title":"Biochem. J."},{"key":"CR14","first-page":"158","volume":"231","author":"M. Kiese","year":"1957","unstructured":"Kiese, M., D. Schneider und H. D. Waller: H\u00e4moglobinreduktase, Arch exp. Path u. Pharm.231, 158 (1957).","journal-title":"Arch exp. Path u. Pharm."},{"key":"CR15","unstructured":"Recknagel, K. und H. H\u00f6rlein: \u00dcber einen Fall kongenitaler idiopathischer Meth\u00e4moglobin\u00e4mie, Medizinische Welt1954, 463."},{"key":"CR16","doi-asserted-by":"crossref","first-page":"440","DOI":"10.1016\/0002-9343(66)90138-0","volume":"40","author":"E. C. Rossi","year":"1966","unstructured":"Rossi, E. C., G. T. Bryan, R. F. Schilling and D. V. Clatanoff: Remission of Chronic Methemoglobinemia Following Neomycin Therapy. Am. J. Med.40, 440 (1966).","journal-title":"Am. J. Med."},{"key":"CR17","first-page":"194","volume":"19","author":"E. M. Scott","year":"1960","unstructured":"Scott, E. M.: Erythrocyte Diaphorase: The Enzymatic Defect of Hereditary Methemoglobinemia. Fed. Proc.19, 194 (1960).","journal-title":"Fed. Proc."},{"key":"CR18","doi-asserted-by":"crossref","first-page":"1176","DOI":"10.1172\/JCI104131","volume":"39","author":"E. M. Scott","year":"1960","unstructured":"Scott, E. M.: Relation of Diaphorase of Human Erythrocytes to Inheritance of Methemoglobinemia. J. Clin. Invest.39, 1176 (1960).","journal-title":"J. Clin. Invest."},{"key":"CR19","doi-asserted-by":"crossref","first-page":"584","DOI":"10.1016\/0006-3002(59)90324-5","volume":"34","author":"E. M. Scott","year":"1959","unstructured":"Scott, E. M. and I. V. Griffith The Enzymic Defect of Hereditary Methemoglobinemia: Diaphorase. Biochem. Biophys. Acta34, 584 (1959).","journal-title":"Biochem. Biophys. Acta"},{"key":"CR20","doi-asserted-by":"crossref","first-page":"18","DOI":"10.1182\/blood.V18.1.18.18","volume":"18","author":"P. L. Townes","year":"1961","unstructured":"Townes, P. L. and G. R. Lovell: Hereditary Methemoglobinemia: A New Variant Exhibiting Dominant Inheritence of Methemoglobin A. Blood18, 18 (1961).","journal-title":"Blood"},{"key":"CR21","doi-asserted-by":"crossref","first-page":"60","DOI":"10.1182\/blood.V19.1.60.60","volume":"19","author":"P. L. Townes","year":"1962","unstructured":"Townes, P. L. and M. Morrison: Investigation of the Defect in a Variant of Hereditary Methemoglobinemia. Blood19, 60 (1962).","journal-title":"Blood"},{"key":"CR22","first-page":"494","volume":"221","author":"O. Warburg","year":"1930","unstructured":"Warburg, O., F. Kubowitz und W. Christian: Kohlenhydratverbrennung durch Meth\u00e4moglobin. Biochem. Z.221, 494 (1930).","journal-title":"Biochem. Z."},{"key":"CR23","doi-asserted-by":"crossref","first-page":"212","DOI":"10.1136\/bmj.4.5573.212","volume":"4","author":"C. A. West","year":"1967","unstructured":"West, C. A., B. D. Gomperts, E. R. Huehns, I. Kessel and J. R. Ashby: Demonstration of an Enzyme Variant in a Case of Congenital Methemoglobinemia. Brit. Med. J.4, 212 (1967).","journal-title":"Brit. Med. J."}],"container-title":["Blut Zeitschrift f\u00fcr die Gesamte Blutforschung"],"original-title":[],"language":"de","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF01631580.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF01631580\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF01631580","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2020,4,7]],"date-time":"2020-04-07T07:13:25Z","timestamp":1586243605000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF01631580"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1974,7]]},"references-count":23,"journal-issue":{"issue":"1","published-print":{"date-parts":[[1974,7]]}},"alternative-id":["BF01631580"],"URL":"https:\/\/doi.org\/10.1007\/bf01631580","relation":{},"ISSN":["0006-5242","1432-0584"],"issn-type":[{"value":"0006-5242","type":"print"},{"value":"1432-0584","type":"electronic"}],"subject":[],"published":{"date-parts":[[1974,7]]}}}