PubRank

M G Bliumina

Author PubWeight™ 2.47‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 [The frequency of X-linked mental retardation]. Genetika 1989 0.97
2 [A schizophrenia-like variant of phenylketonuria]. Zh Nevropatol Psikhiatr Im S S Korsakova 1975 0.76
3 [Heterochromatic regions of human chromosomes 1, 9, 16 and Y and the phenotype]. Genetika 1984 0.75
4 [Obstetrical problems of phenylketonuria]. Akush Ginekol (Mosk) 1976 0.75
5 [Medico-genetic consultation in monosymptomatic sensorineural deafness]. Vestn Otorinolaringol 1985 0.75
6 [Genetic forms of rapidly progressive neurosensory hearing loss]. Vestn Otorinolaringol 1986 0.75
7 [Children with ring chromosome 13]. Pediatriia 1981 0.75
8 [Experience with treatment of children with phenylketonuria]. Zh Nevropatol Psikhiatr Im S S Korsakova 1969 0.75
9 [Classification of hereditary sensorineural deafness]. Vestn Otorinolaringol 1986 0.75
10 [The intellectual defect in phenylketonuria, its dynamics and structure]. Zh Nevropatol Psikhiatr Im S S Korsakova 1972 0.75
11 [Polymorphism of the heterochromatic regions of chromosomes 1, 9, 16 and Y and mental retardation]. Genetika 1984 0.75
12 [Incidence of oligophrenia with fragile X chromosome (FraXq27)]. Genetika 1987 0.75
13 [Etiology of neurosensory hearing loss in children with normal-hearing parents]. Vestn Otorinolaringol 1982 0.75
14 [Clinical and electroencephalographic features of the convulsive syndrome in phenylketonuria in children]. Zh Nevropatol Psikhiatr Im S S Korsakova 1969 0.75
15 [Malignant forms of phenylketonuria]. Zh Nevropatol Psikhiatr Im S S Korsakova 1984 0.75
16 [Autosomal anomalies in a specially selected group of children with mental retardation without signs of Down's syndrome]. Zh Nevropatol Psikhiatr Im S S Korsakova 1982 0.75
17 [Phenylalanine level in the serum of heterozygotes for phenylketonuria under intensified protein catabolism]. Genetika 1981 0.75
18 [Phenylketonuria with congenital megaloblastic anemia]. Pediatriia 1981 0.75
19 [Characteristics of medical genetic counseling in hearing disorders]. Vestn Otorinolaringol 1982 0.75
20 [A simplified method of determining the serum concentration of phenylalanine]. Lab Delo 1972 0.75
21 [Genetic study of sensorineural hearing loss]. Genetika 1982 0.75
22 [Problem of the clinical aspects and treatment of phenylketonuria in children]. Vopr Okhr Materin Det 1969 0.75
23 [Organizational forms of medical genetic assistance to the population]. Vestn Akad Med Nauk SSSR 1973 0.75
24 [Clinical manifestations of oligophrenia with fragile X syndrome in boys in the pre- and post-pubertal age]. Zh Nevropatol Psikhiatr Im S S Korsakova 1989 0.75
25 [Modern concepts of the role of heredity in the origin of monosymptomatic hearing disorders in children]. Vestn Otorinolaringol 1980 0.75
26 [A supposed deletion in the long arm of one of the group B chromosomes in a peculiar form of oligophrenia]. Tsitologiia 1968 0.75
27 [Multiple birth and Down's disease]. Genetika 1975 0.75
28 [Frequency and types of inheritance of genetic neurosensory hearing loss in children]. Vestn Otorinolaringol 1981 0.75
29 [Clinical polymorphism of the Waardenburg-Klein syndrome in children]. Pediatriia 1987 0.75
30 [Families with recurrent cases of Waardenburg-Klein syndrome]. Genetika 1985 0.75
31 [On the dynamics of psychopathologic manifestations in phenylketonuria (phenylpyruvic oligophrenia)]. Zh Nevropatol Psikhiatr Im S S Korsakova 1967 0.75
32 [Differential approach to genetic prognosis for progeny in cases of sporadic sensorineural deafness in children]. Vestn Otorinolaringol 1983 0.75
33 [Relationship between the severity of brain damage in phenylketonuria and the degree of hyperphenylalaninemia]. Zh Nevropatol Psikhiatr Im S S Korsakova 1980 0.75
34 [Polymorphism of clinical manifestations and characteristics of imbecility in the Laurence-Moon-Biedl syndrome]. Zh Nevropatol Psikhiatr Im S S Korsakova 1989 0.75
35 [Effect of maternal genetic heterozygosity]. Genetika 1975 0.75
36 [Spontaneous abortions in women-carriers of the phenylketonuria gene]. Akush Ginekol (Mosk) 1972 0.75
37 [Syndrome of supravalvular aortic stenosis in children]. Pediatriia 1984 0.75
38 [Medico-genetic consultation for families with neurosensory hypoacusis of unknown etiology in both spouses]. Vestn Otorinolaringol 1987 0.75
39 [Clinico-electroencephalographic evaluation of the effectiveness of diet therapy in patients with phenylketonuria]. Zh Nevropatol Psikhiatr Im S S Korsakova 1972 0.75
40 [State of nuclear chromatin of peripheral blood lymphocytes in Down's syndrome and phenylketonuria detected by a cytospectrofluorometric method]. Biull Eksp Biol Med 1971 0.75
41 [Pressing problems of phenylketonuria]. Pediatriia 1980 0.75
42 [Heterochromatic regions of chromosomes 1, 9, 16 and Y in children with signs of embryonic development disorder]. Genetika 1982 0.75
43 [Genetic characteristics of recessive sensorineural hearing loss]. Genetika 1987 0.75
44 [New form of dominant hereditary neurosensory hearing loss]. Vestn Otorinolaringol 1982 0.75