PubRank

V G Vakharlovskiĭ

Author PubWeight™ 0.78‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 [Molecular genetic basis of proximal spinal muscular atrophy and experience in its pharmaceutical treatment]. Genetika 2008 0.78
2 [Expression of the ceruloplasmin gene in Wilson-Konovalov disease]. Vestn Akad Med Nauk SSSR 1982 0.75
3 [Characteristics of visceral manifestations of Wilson-Konovalov disease]. Sov Med 1989 0.75
4 [Contents of alpha-fetoprotein in the blood of pregnant women as a criterion of the presence of congenital heart defects in the fetus]. Akush Ginekol (Mosk) 1995 0.75
5 [Experience in heterozygote detection in Wilson-Konovalov mutation based on the study of molecular forms of ceruloplasmin]. Zh Nevropatol Psikhiatr Im S S Korsakova 1989 0.75
6 [Successful treatment of a patient with hepatolenticular degeneration with the terminal stage of liver disease]. Gematol Transfuziol 1991 0.75
7 [Molecular defect of ceruloplasmin synthesis and maturation in Wilson-Konovalov disease]. Genetika 1982 0.75
8 [Activity of enzymes in amniotic fluid in prenatal diagnosis of cystic fibrosis]. Genetika 1989 0.75
9 [Clinical polymorphism in respiratory oxalosis]. Ter Arkh 2001 0.75
10 [I-131 absorption by the thyroid gland in hepatolenticular generation]. Klin Med (Mosk) 1974 0.75
11 [Changes in the bioelectrical activity of the brain in hepato-cerebral dystrophy (Wilson--Konovalov disease)]. Zh Nevropatol Psikhiatr Im S S Korsakova 1977 0.75
12 [Complex medical and surgical treatment of hepatolenticular degeneration]. Vopr Neirokhir 1975 0.75
13 [Prenatal diagnosis and prevention of congenital and hereditary diseases]. Akush Ginekol (Mosk) 1994 0.75
14 [Genetic defect in ceruloplasmin synthesis in liver polyribosomes in Wilson-Konovalov disease]. Dokl Akad Nauk SSSR 1975 0.75
15 [Idiopathic torsion dystonia]. Zh Nevrol Psikhiatr Im S S Korsakova 2009 0.75
16 [Clinical polymorphism and ceruloplasmin variants in hepatolenticular degeneration]. Genetika 1977 0.75
17 [Early diagnosis of hepatolenticular degeneration in children]. Vopr Okhr Materin Det 1975 0.75
18 [Use of penicillamine in Wilson-Konovalov disease]. Klin Med (Mosk) 1980 0.75
19 [Partial aldosterone and vasopressin deficiency syndrome as a cause of epileptiform paroxysms in homozygotic twins]. Fiziol Cheloveka 1991 0.75
20 [Clinical manifestation of Wilson-Konovalov disease and current theories on its pathogenesis]. Ter Arkh 1974 0.75
21 [Molecular structure of the human ceruloplasmin gene and its expression in the Wilson-Konovalov mutation]. Dokl Akad Nauk SSSR 1981 0.75