Fructose intolerance
Nakamura, N.; Uga, N.
Nihon Rinsho. Japanese Journal of Clinical Medicine Suppl: 1368-1369
1978
ISSN/ISBN: 0047-1852 PMID: 691359 Document Number: 126570
Document emailed within 1 workday
Related Documents
Hackl, J.M.; Balogh, D.; Kunz, F.; Dworzak, E.; Puschendorf, B.; Decristoforo, A.; Maier, F. 1978: Postoperative fructose infusion in a case of presumed hereditary fructose intolerance Wiener Klinische Wochenschrift 90(7): 237-240McInnes, R.R. 1982: ProSobee and fructose intolerance Canadian Medical Association Journal 127(11): 1077
Steinmann, B.; Gitzelmann, R. 1981: The diagnosis of hereditary fructose intolerance Helvetica Paediatrica Acta 36(4): 297-316
Aussannaire, M.; Gallet, J.P.; Joly, C.; Alain, J.; Lalande, J.; Bertrand, N. 1973: A case of edematous fructose intolerance Archives Francaises de Pediatrie 30(5): 558
Brauman, J.; Kentos, P.; Frisque, P.; Gepts, W.; Verbanck, M. 1971: Hereditary fructose intolerance in an 83-year-old woman Acta Clinica Belgica 26(2): 65-77
Mercier, J.C.; Bourrillon, A.; Beaufils, F.; Odievre, M. 1976: Hereditary fructose intolerance with early onset Archives Francaises de Pediatrie 33(10): 945-953
Larsen, K.; Adnanes, O.; Aarskog, N.K.; Runde, I.; Ogreid, D. 1994: Congenital fructose intolerance. new molecular aspects Tidsskrift for den Norske Laegeforening: Tidsskrift for Praktisk Medicin Ny Raekke 114(28): 3312-3314
Coşkun, T.; Ozalp, I.; Tekinalp, G. 1991: Hereditary fructose intolerance in a patient with phenylketonuria Turkish Journal of Pediatrics 33(3): 181-184
Mattes, S.; Schmidt, G. 1979: Hereditary fructose intolerance and therapeutic problems Kinderarztliche Praxis 47(1): 26-30
Willems, C.; Heusden, A.; Renson, P.; Legat, C.; Monard, Y.; Stainier, L. 1971: Hypertyrosinemia with hypermethioninemia in the newborn in a case of fructose intolerance Helvetica Paediatrica Acta 26(4): 467-481
Dreyfus, J.C.; Schapira, F.; Besmond, C.; Gregori, C.; Kahn, A. 1985: Study of hereditary fructose intolerance by methods of molecular biology Annales de Medecine Interne 136(6): 456-458
Celiker, V.; Dural, O.; Erdem, K. 1993: Anesthetic management of a patient with hereditary fructose intolerance and phenylketonuria Turkish Journal of Pediatrics 35(2): 127-130
Di Martino, L.; Iorio, G.; Guandalini, S.; Iannuzzi, S.; Battaglia, A.; Andria, G. 1980: Hereditary fructose intolerance: description of 2 cases with early onset La Pediatria 88(1): 99-110
Bell, L.; Sherwood, W.G. 1987: Current practices and improved recommendations for treating hereditary fructose intolerance Journal of the American Dietetic Association 87(6): 721-728
Costa, C.; Costa, J.M.; Deleuze, J.F.; Legrand, A.; Hadchouel, M.; Baussan, C. 1998: Simple, rapid nonradioactive method to detect the three most prevalent hereditary fructose intolerance mutations Clinical Chemistry 44(5): 1041-1043
Nüssli, R. 1971: Growth of patients with hereditary fructose intolerance or hereditary saccharose-isomaltose malabsorption Helvetica Paediatrica Acta 26(5): 637-647
Costas, M.J.; Cameselle, J.C. 1988: The inhibition of fructose 1,6-bisphosphatase by fructose 2,6-bisphosphate is enhanced by EDTA and diminished by zinc(II) Biochemistry International 16(4): 747-753
Landau, B.R.; Marshall, J.S.; Craig, J.W.; Hostetler, K.Y.; Genuth, S.M. 1971: Quantitation of the pathways of fructose metabolism in normal and fructose-intolerant subjects Journal of Laboratory and Clinical Medicine 78(4): 608-618
Kelch, L.; Adlung, J.; Grazikowske, H.; Ritter, U. 1976: Milk intolerance, lactose intolerance and lactase deficiency in partial resection of the stomach Der Chirurg; Zeitschrift für Alle Gebiete der Operativen Medizen 47(5): 280-283
Fisherman, E.W.; Cohen, G. 1973: Chemical intolerance to butylated-hydroxyanisole (BHA) and butylated-hydroxytoluene (BHT) and vascular response as an indicator and monitor of drug intolerance Annals of Allergy 31(3): 126-133