109 related articles for article (PubMed ID: 2633562)
1. [Experience in heterozygote detection in Wilson-Konovalov mutation based on the study of molecular forms of ceruloplasmin].
Puchkova LV; Verbina IA; Vakharlovskiĭ VG; Gaĭtskhoki VS; Neĭfakh SA
Zh Nevropatol Psikhiatr Im S S Korsakova; 1989; 89(12):14-8. PubMed ID: 2633562
[TBL] [Abstract][Full Text] [Related]
2. Molecular forms of ceruloplasmin in hepatolenticular degeneration and their interaction with human erythrocyte ceruloplasmin receptor.
Puchkova LV; Verbina IA; Denezhkina VV; Vakharlovskii VG; Voitsekhovskii BL; Gaitskhoki VS; Neifakh SA
Biomed Sci; 1990; 1(5):460-6. PubMed ID: 1966785
[TBL] [Abstract][Full Text] [Related]
3. [Interaction of molecular forms of ceruloplasmin with specific membrane receptors from healthy persons and patients with hepatolenticular degeneration].
Puchkova LV; Verbina IA; Gaĭtskoki VS; Neĭfakh SA
Biokhimiia; 1991 Dec; 56(12):2261-9. PubMed ID: 1666959
[TBL] [Abstract][Full Text] [Related]
4. Immunoenzyme determination of total serum ceruloplasmin. Application to Wilson disease.
Saenko EL; Skorobogatko OV; Yaropolov AI
Biochem Int; 1991 Mar; 23(5):819-24. PubMed ID: 1883396
[TBL] [Abstract][Full Text] [Related]
5. [Isolation and characteristics of a protein similar to ceruloplasmin from the serum of a patient with hepatolenticular degeneration (Wilson-Konovalov disease)].
Verbina IA; Puchkova LV
Dokl Akad Nauk SSSR; 1985; 283(2):478-80. PubMed ID: 4042831
[No Abstract] [Full Text] [Related]
6. Wilson's disease: diagnostic difficulties in the patient with chronic hepatitis and hypoceruloplasminemia.
Spechler SJ; Koff RS
Gastroenterology; 1980 Apr; 78(4):803-6. PubMed ID: 7353765
[TBL] [Abstract][Full Text] [Related]
7. Early and presymptomatic detection of Wilson's disease at the mandatory 3-year-old medical health care examination in Hokkaido Prefecture with the use of a novel automated urinary ceruloplasmin assay.
Nakayama K; Kubota M; Katoh Y; Sawada Y; Saito A; Nishimura K; Katsura E; Ichihara N; Suzuki T; Kouguchi H; Tamura M; Honma H; Kanzaki S; Itami H; Ohtake A; Kobayashi K; Ariga T; Fujieda K; Shimizu N; Aoki T
Mol Genet Metab; 2008 Jul; 94(3):363-7. PubMed ID: 18424137
[TBL] [Abstract][Full Text] [Related]
8. Serum ceruloplasmin oxidase activity is a sensitive and highly specific diagnostic marker for Wilson's disease.
Merle U; Eisenbach C; Weiss KH; Tuma S; Stremmel W
J Hepatol; 2009 Nov; 51(5):925-30. PubMed ID: 19720421
[TBL] [Abstract][Full Text] [Related]
9. [Factors affecting the concentration of serum ceruloplasmin in Wilson-Konovalov disease].
Mzhel'skaia TI; Ivanova-Smolenskaia IA; Korobova NV
Vopr Med Khim; 1994; 40(6):48-53. PubMed ID: 7618303
[TBL] [Abstract][Full Text] [Related]
10. Isolation and partial characterization of molecular forms of ceruloplasmin from human bile.
Verbina IA; Puchkova LV; Gaitskhoki VS; Neifakh SA
FEBS Lett; 1992 Feb; 298(2-3):105-8. PubMed ID: 1544429
[TBL] [Abstract][Full Text] [Related]
11. Analysis of seven pedigrees of childhood Wilson's disease characterized by abdominal symptoms.
Ikei N; Abe J; Shin S; Kohsaka T
Acta Paediatr Jpn; 1995 Apr; 37(2):141-4. PubMed ID: 7793244
[TBL] [Abstract][Full Text] [Related]
12. A study of the caeruloplasmin concentrations found in 75 patients with Wilson's disease, their kinships and various control groups.
Gibbs K; Walshe JM
Q J Med; 1979 Jul; 48(191):447-63. PubMed ID: 396544
[No Abstract] [Full Text] [Related]
13. Wilson's disease patients with normal ceruloplasmin levels.
Yüce A; Koçak N; Ozen H; Gürakan F
Turk J Pediatr; 1999; 41(1):99-102. PubMed ID: 10770682
[TBL] [Abstract][Full Text] [Related]
14. [On hepato-lenticular degeneration (Wilson's disease). I. Detection and early diagnosis].
Campanella G; Gillardi U; Germinario L
Acta Neurol (Napoli); 1971; 26(4):403-22. PubMed ID: 5132823
[No Abstract] [Full Text] [Related]
15. [Molecular defect of ceruloplasmin synthesis and maturation in Wilson-Konovalov disease].
Puchkova LV; Vakharlovskiĭ VG; Gaĭtskhoki VS; Monakhov NK; Shvartsman AL
Genetika; 1982 May; 18(5):703-12. PubMed ID: 7201432
[TBL] [Abstract][Full Text] [Related]
16. Wilson's disease: a patient undiagnosed for 18 years.
Mak CM; Tam S; Fan ST; Liu CL; Lam CW
Hong Kong Med J; 2006 Apr; 12(2):154-8. PubMed ID: 16603785
[TBL] [Abstract][Full Text] [Related]
17. Cytochrome oxidase deficiency in Wilson's disease: a suggested ceruloplasmin function.
Shokeir MH; Shreffler DC
Proc Natl Acad Sci U S A; 1969 Mar; 62(3):867-72. PubMed ID: 4308098
[TBL] [Abstract][Full Text] [Related]
18. Prevention of Wilson's disease in asymptomatic patients.
Sternlieb I; Scheinberg IH
N Engl J Med; 1968 Feb; 278(7):352-9. PubMed ID: 5635646
[No Abstract] [Full Text] [Related]
19. Ceruloplasmin in Wilson's disease.
Holtzman NA; Naughton MA; Iber FL; Gaumnitz BM
J Clin Invest; 1967 Jun; 46(6):993-1002. PubMed ID: 6026104
[TBL] [Abstract][Full Text] [Related]
20. Screening asymptomatic family members for Wilson's disease.
Lindahl JA; Sharp HL
Minn Med; 1982 Aug; 65(8):473-5. PubMed ID: 6752690
[No Abstract] [Full Text] [Related]
[Next] [New Search]