Value of genetic diagnosis of C282Y mutation in patients with hereditary hemochromatosis
Ocran, K.; Schmidt, H.H.
Zeitschrift für Gastroenterologie 38(2): 205-207
2000
ISSN/ISBN: 0044-2771 PMID: 10721178 Document Number: 520823
Document emailed within 1 workday
Related Documents
Foss Haug, K.B.; Kierulf, P.; Sandset, P.M.; Urdal, P.; Wisløff, F. 1998: Hereditary hemochromatosis and use of genetic tests Tidsskrift for den Norske Laegeforening: Tidsskrift for Praktisk Medicin Ny Raekke 118(12): 1911Zlocha, J.; Kovács, L.; Pozgayová, S.; Kupcová, V.; Durínová, S. 2006: Molecular genetic diagnostics and screening of hereditary hemochromatosis Vnitrni Lekarstvi 52(6): 602-608
Settarova, D.A.; Settarov, I.A. 1991: Differential diagnosis of hereditary hemochromatosis in children Pediatriia 1: 76-80
Zdárský, E.; Horák, J.; Stríteský, J.; Heirler, F. 1999: Hemochromatosis. Determination of the C282Y mutation frequency in the population of the Czech Republic and sensitivity of hemochromatosis detection using Guthrie cards Casopis Lekaru Ceskych 138(16): 497-499
Moreno, L.; Vallcorba, P.; Boixeda, D.; Cabello, P.; Bermejo, F.; San Román, C. 1999: The usefulness of the detection of Cys282Tyr and His63Asp mutations in the diagnosis of hereditary hemochromatosis Revista Clinica Espanola 199(10): 632-636
Settarova, D.A.; Sharandak, A.P.; Tokarev, I.N. 1989: Characteristics of central hemodynamics in patients with hereditary hemochromatosis with cardiac lesions Kardiologiia 29(9): 98-99
Svendsen, I.H.; Steensgaard-Hansen, F.; Nordvåg, B.Y. 1999: Hereditary amyloid cardiomyopathy related to a mutation at transthyretin protein number 111. a clinical, genetic and echocardiographic study of an affected Danish family Ugeskrift for Laeger 161(36): 4995-4999
Dumur, V.; Lalau, G.; Boone, P.; Roussel, P.; Francois, P.; Hache, J.C.; Hemery, B.; Puech, B. 1992: Rapid diagnosis of mitochondrial mutation at position 11778-associated Leber hereditary optic neuropathy Clinical Chemistry 38(7): 1390
Nørby, S.; Rosenberg, T. 1990: Leber's hereditary optic atrophy. a hereditary disease caused by mitochondrial DNA mutation Ugeskrift for Laeger 152(43): 3149-3152
Sharandak, A.P.; Settarova, D.A.; Sokolov, S.S.; Tokarev, I.N. 1989: Physical work capacity studied by measured physical loading in patients with hereditary hemochromatosis Terapevticheskii Arkhiv 61(11): 120-122
Yano, K.; Miki, Y. 2000: Genetic diagnosis of hereditary breast cancer Nihon Rinsho. Japanese Journal of Clinical Medicine 58 Suppl: 527-532
Chinitz, M.A. 1990: Hereditary hemochromatosis American Journal of Gastroenterology 85(1): 99-100
Cojocariu, C.; Trifan, A.; Stanciu, C. 2007: Hereditary hemochromatosis Revista Medico-Chirurgicala a Societatii de Medici Si Naturalisti Din Iasi 111(3): 584-592
Olschwang, S. 1996: Hereditary non-polyposis colorectal cancer: genetic diagnosis Gastroenterologie Clinique et Biologique 20(5 Part 2): B5-B8
Stone, E.M.; Newman, N.J.; Miller, N.R.; Johns, D.R.; Lott, M.T.; Wallace, D.C. 1992: Visual recovery in patients with Leber's hereditary optic neuropathy and the 11778 mutation Journal of Clinical Neuro-Ophthalmology 12(1): 10-14
Liu, Y.-h.; Yuan, H.-j. 2013: Gene diagnosis and genetic counseling in hereditary hearing loss Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi 48(12): 1051-1056
Mangold, E.; Friedl, W.; Propping, P. 2001: Hereditary colorectal carcinoma: predictive diagnosis and genetic counseling Praxis 90(12): 490-496
Brittenham, G.M.; Franks, A.L.; Rickles, F.R. 1998: Research priorities in hereditary hemochromatosis Annals of Internal Medicine 129(11): 993-996
Nielsen, F.C.; Tygstrup, N. 1998: Hereditary hemochromatosis--new diagnostic possibilities Ugeskrift for Laeger 160(3): 254
Raszeja-Wyszomirska, J.; Ławniczak, M.łg.; Milkiewicz, P. 2008: Novel aspects of pathogenesis of hereditary hemochromatosis Polski Merkuriusz Lekarski: Organ Polskiego Towarzystwa Lekarskiego 24(139): 54-58