Zobrazeno 1 - 2
of 2
pro vyhledávání: '"L V, Dubchak"'
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 97(12)
Bulbospinal muscular atrophy--a rare disease with X-linked recessive type of inheritance. It is caused by expansion of trinucleotide repetitions in the gene of androgenic receptor (AR). We elaborated a method of DNA-testing with usage of nonradioacti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::94261c1d2648e24d42357f47fd9e1969
https://pubmed.ncbi.nlm.nih.gov/9591063
https://pubmed.ncbi.nlm.nih.gov/9591063
Autor:
N A, Sokolina, M A, Ronkin, I M, Maksimenko, E A, Dubanova, N V, Vinogradova, L V, Logunova, L V, Dubchak, I M, Tsoĭ
Publikováno v:
Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952). 90(9)
The authors describe a rare and little studied form (distal) of spinal amyotrophy. 12 patients were placed under observation. A group of patients with symmetric distal pareses of the hands and legs has been distinguished. Patients with long existent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d8a1226dbb52960319f7c83600ab1534
https://pubmed.ncbi.nlm.nih.gov/2176036
https://pubmed.ncbi.nlm.nih.gov/2176036