1. Repository of Kharkiv National Medical University

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PreviewIssue DateTitleAuthor(s)
Гентики_1_13.pdf.jpg2013Double blind placebo control trial of large neutral amino Acids in treatment of PKU: effect on blood phenylalanineMatalon, R.; Bhatia, G.; Michals-Matalon, K.; Burlina, A.; Burlina, A.; Braga, C.; Fiori, L.; Giovannini, M.; Grechanina, E.; Novikov, P.; Tyring, S.; Guttler, F.
2017-09-10Studying influence of mtDNA polymorphisms and polymorphic gene variants C677T MTHFR and A66G MTRR on clinical manifestations of mitochondrial dysfunctionGrechanina, Elena; Grechanina, Juliya
2017-04-25Selective screening of mitochondrial dysfunction in a region with a high level of neurological diseasesGrechanina, Elena; Grechanina, Juliya
2017-04-25A rare disease of the mitochondrial respiratory chain – 3-methylglutaconic aciduria. Approach to diagnosis and rehabilitationGrechanina, Elena; Grechanina, Juliya; Biletska, Svetlana; Maksutina, Irina
Титул содержание.pdf.jpg2014-06Effectiveness of qualifying diagnostics of hereditary metabolic diseases with the use of gas chromatography / mass spectrometry by the example of the HHH syndromeGrechanina, Elena; Grechanina, Juliya; Zdybska, Olena; Kaniuka, Maksim; Molodan, Ludmila; Senatorova, Ganna
med290 Статья Ю.Б.ГРЕЧАНИНОЙ_128-end(1)_1-4.pdf.jpg2019-05-04Successful rehabilitation of patient disabled by the autistic spectrum disorder and the modified epigenetic staGrechanina, Juliya; Bugaeva, Olena; Lisniak, Svetlana; Staruseva, V.; Shmulich, O.
The discoverer of Canavan syndrome gene.pdf.jpg2019-06-04The discoverer of Canavan syndrome gene: how problems of diagnosis and treatment are being changed over timeGrechanina, Elena; Grechanina, Juliya; Matalon, Reuben; Delgado, Listvania; Tyring, Stephen

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