Zobrazeno 1 - 10
of 45
pro vyhledávání: '"M G, Bliumina"'
Autor:
M G, Bliumina
Publikováno v:
Vestnik otorinolaringologii. (3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fd7e43e68b4d9260ac3607992e677cc3
https://pubmed.ncbi.nlm.nih.gov/3727263
https://pubmed.ncbi.nlm.nih.gov/3727263
Autor:
M G, Bliumina
Publikováno v:
Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952). 89(8)
Psychopathological, neurological and somatic manifestations of oligophrenia-with fragile X chromosome were investigated in 13 mentally retarded boys in prepuberty and in 9 such post-puberty++ patients. Age-related features of several psychopathologic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::828773674e26f5b38466a70c5074f801
https://pubmed.ncbi.nlm.nih.gov/2588887
https://pubmed.ncbi.nlm.nih.gov/2588887
Publikováno v:
Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952). 80(12)
The frequency of the various degrees of the intellectual defect and convulsive syndrome was studied in 473 patients with phenylketonuria divided into four groups as regards the phenylalanine blood level, that was 150 to 199 mg/l in group I, 200 to 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4b2e48e3b355832ff5f99c3cb648769c
https://pubmed.ncbi.nlm.nih.gov/7223198
https://pubmed.ncbi.nlm.nih.gov/7223198
Autor:
M G, Bliumina
Publikováno v:
Genetika. 25(6)
600 mentally retarded children, 339 boys and 261 girls aged 5-9 years were examined. Boys to girls ratio (B:G) was found in the total group to be 1.3. Among 257 children with mental retardation of confirmed genetic origin B:G = 1.4, in 129 children w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9ed5e18668d2441d5ce366829694085b
https://pubmed.ncbi.nlm.nih.gov/2806899
https://pubmed.ncbi.nlm.nih.gov/2806899
Autor:
M G, Bliumina
Publikováno v:
Vestnik otorinolaringologii. (5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cb7344e5be7d716f744bb5eb57053f87
https://pubmed.ncbi.nlm.nih.gov/7147565
https://pubmed.ncbi.nlm.nih.gov/7147565
Publikováno v:
Genetika. 20(1)
Polymorphism of the heterochromatic regions (HR) on chromosomes 1, 9, 16 and in three groups of boys at the age of 3 to 14 years was studied. Two groups of boys with olygophrenia of unknown etiology differed by the extent of mental defect, the latter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6efc7f5712dee429fa3b9960b9c63e08
https://pubmed.ncbi.nlm.nih.gov/6538157
https://pubmed.ncbi.nlm.nih.gov/6538157
Autor:
M G, Bliumina
Publikováno v:
Genetika. 23(1)
The study of 50 retarded males imbezilitat and idiots, and 100 males with oligophrenia-debilitat in 16-18 years. Severe macroorchism (1.8-4.5 times more, then anthropometric norma for this years) was found at 5 males in first group (10%), and in 8 ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fec5cd614dc1d4591f585d93b853927c
https://pubmed.ncbi.nlm.nih.gov/3817470
https://pubmed.ncbi.nlm.nih.gov/3817470
Autor:
M G, Bliumina
Publikováno v:
Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952). 84(10)
Forty-eight patients with pernicious phenylketonuria (PKU) were examined. It was revealed that the prognostically unfavourable symptoms in relation to the malignant course of the disease included early development of epileptic attacks and neurologica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::92da152b9e8eacf6023882e702d7f720
https://pubmed.ncbi.nlm.nih.gov/6506948
https://pubmed.ncbi.nlm.nih.gov/6506948