Zobrazeno 1 - 3
of 3
pro vyhledávání: '"I V, Jevneronok"'
Autor:
T V, Asadchuk, N V, Rumiantseva, I V, Naumchik, S A, Likhachev, I V, Pleshko, L V, Shalkevich, I V, Jevneronok, J P, Kachan
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 116(1)
To analyze the molecular defect, a phenotype of hereditary neuropathy with liability to pressure palsies (HNPP, OMIM 162500), in patients with PMP22 gene mutation caused by 1.5 Mb deletion at 17p11.2. and present the principles of diagnosis and genet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e39def5a50fbd08912d5e74181969132
https://pubmed.ncbi.nlm.nih.gov/26977628
https://pubmed.ncbi.nlm.nih.gov/26977628
Autor:
I. V. Pleshko, J. P. Kachan, I. V. Jevneronok, I. V. Naumchik, S. A. Likhachev, L. V. Shalkevich, T. V. Asadchuk, N. V. Rumiantseva
Publikováno v:
Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova. 116:64
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b568c9f051da44d2b422842e5cddc8f
https://doi.org/10.17116/jnevro20161161164-69
https://doi.org/10.17116/jnevro20161161164-69
Publikováno v:
Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova. 116:10
Moyamoya disease in children is a rarely diagnosed entity. Frequent headache is the first symptom of the disease. Headache associated with moya-moya disease (HAMD) is a separated entity reported in the literature. Variants of onset, a spectrum of pri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b4888518f9563942c5e174b7c1892f7
https://doi.org/10.17116/jnevro20161161110-17
https://doi.org/10.17116/jnevro20161161110-17