Expression of the ceruloplasmin gene in Wilson-Konovalov disease
Neĭfakh, S.A.; Vakharlovskiĭ, V.G.; Gaĭtskhoki, V.S.; Monakhov, N.K.; Puchkova, L.V.
Vestnik Akademii Meditsinskikh Nauk SSSR 1: 53-63
1982
ISSN/ISBN: 0002-3027 PMID: 7064533 Document Number: 187176
Document emailed within 1 workday
Related Documents
Bogolitsyn, I.G.; Krasavtsev, E.L. 1986: Diagnosis of Wilson-Konovalov disease Sovetskaia Meditsina 7: 112-113Starikov, A.S.; Obraztsova, R.G. 1981: Pathohistological characteristics of hepatocerebral dystrophy (Wilson-Konovalov disease) Zhurnal Nevropatologii i Psikhiatrii Imeni S.S. Korsakova 81(11): 1612-1616
Prokhorova, M.V.; Krel', P.E. 1992: Diagnostic difficulties and therapeutic success in Wilson-Konovalov disease Terapevticheskii Arkhiv 64(8): 99-100
Padrul, M.M.; Olina, A.A.; Sadykova, G.K. 2018: A favorable outcome of pregnancy with Wilson-Konovalov disease (a clinical case) Wiadomosci Lekarskie 71(5): 1109-1113
Rakhimova, O.I.; Rozina, T.P.; Popova, E.N.; Lopatkina, T.N.; Ignatova, T.M. 2004: Fibrosing alveolitis as a complication due to D-penicillamine therapy for Wilson-Konovalov disease Klinicheskaia Meditsina 82(11): 57-60
Yüce, A.; Koçak, N.; Ozen, H.; Gürakan, F. 1999: Wilson's disease patients with normal ceruloplasmin levels Turkish Journal of Pediatrics 41(1): 99-102
Kinoshita, Y.; Yamakami, Y.; Mori, Y.; Haruki, E.; Kikuchi, N. 1999: Studies of mass infant screening for Wilson disease by urinary ceruloplasmin Southeast Asian Journal of Tropical Medicine and Public Health 30(Suppl 2): 149-150
Starikov, A.S. 1990: The electromyographic analysis of trembling hyperkinesis in Wilson-Konovalov's hepatocerebral dystrophy Zhurnal Voprosy Neirokhirurgii Imeni N. N. Burdenko 3: 29-31
Pan, F.; Cai, G.; Liu, B.; Zou, C. 1998: Ceruloplasmin gene expression in silicotic rat lung Wei Sheng Yan Jiu 27(4): 227-228; 232
Stapelbroek, J.M.; Ploos van Amstel, J.K.; van Hattum, J.; van den Berg, L.H.; Klomp, L.W.J.; Houwen, R.H.J. 2003: From gene to disease; Wilson disease: copper storage due to mutations in ATP7B Nederlands Tijdschrift Voor Geneeskunde 147(13): 603-605
Riedel, H.D.; Fitscher, B.A.; Hefter, H.; Strohmeyer, G.; Stremmel, W. 1994: Cloning the Wilson disease gene Zeitschrift für Gastroenterologie 32(8): 472-473
Yang, R.; Fan, Y.; Yu, L. 1997: Identification of a novel missense mutation in Wilson disease gene Zhonghua Yi Xue Za Zhi 77(5): 344-347
Fan, Y.; Yang, R.; Yu, L.; Wu, M.; Shi, S.; Ren, M.; Han, Y.; Hu, J.; Zhao, S. 1997: Identification of a novel missense mutation in Wilson's disease gene Chinese Medical Journal 110(11): 887-890
Yuzbasiyan-Gurkan, V.; Brewer, G.J.; Abrams, G.D.; Main, B.; Giacherio, D. 1989: Treatment of Wilson's disease with zinc. V. Changes in serum levels of lipase, amylase, and alkaline phosphatase in patients with Wilson's disease Journal of Laboratory and Clinical Medicine 114(5): 520-526
Degli Esposti, A.; Antener, I.; Ambrosioni, G.; Bonfiglioli, G. 1976: Wilson's disease. Summary of studies carried out in a family group with Wilson's disease. Significance of amino-acid balance in homo and heterozygotes for the detection of liver damage Minerva Pediatrica 28(34): 2063-2086
Keandaungjuntr, J.; Busabaratana, M.; Kositchaiwat, C.; Sura, T.; Pulkes, T. 2011: Analysis of exon 8 of ATP7B gene in Thai patients with Wilson disease Journal of the Medical Association of Thailand 94(10): 1184-1188
Fan, Y.; Yu, L.; Jiang, Y.; Xu, Y.; Yang, R.; Han, Y.; Cui, Y.; Ren, M.; Zhao, S. 2000: Identification of a mutation hotspot in exon 8 of Wilson disease gene by cycle sequencing Chinese Medical Journal 113(2): 172-174
Seidel, J.; Caca, K.; Schwab, S.G.; Berr, F.; Wildenauer, D.B.; Mentzel, H.J.; Horn, N.; Kauf, E. 2001: Disturbed copper transport in humans. Part 2: mutations of the ATP7B gene lead to Wilson disease (WD) Cellular and Molecular Biology 47 Online Pub: Ol149-Ol157
Kamoun, P.; Cadoudal, M.; Rabier, D.; Jérôme, H. 1986: Detection of Wilson's disease in sibs of a patient with Wilson's disease Clinical Chemistry 32(2): 392
Kobayashi, S.; Ochiai, T.; Hori, S.; Suzuki, T.; Shimizu, T.; Gunji, Y.; Shimada, H.; Yamamoto, S.; Ogawa, A.; Kohno, Y.; Sunaga, M.; Shimazu, M.; Tanaka, K. 2001: Copper metabolism after living donor liver transplantation for hepatic failure of Wilson's disease from a gene mutated donor Hepato-Gastroenterology 48(41): 1259-1261