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PreviewIssue DateTitleAuthor(s)
Тези(3).pdf.jpg2014Case of the combination of cystic fibrosis with metabolic disorders of fatty acids and sulfur containing amino acidsYanovska, Anna; Grechanina, Juliya; Grechanina, Elena; Zdybskaya, Elena
Гречаніна Рorphyria Порфірія англ .pdf.jpg2019Porphyria : Guidelines for the training of interns, 5th year studentsGrechanina, Elena; Grechanina, Juliya; Molodan, Ludmila; Zdybskaya, Olena; Bugaeva, Olena; Efremova, Olesya; Oliinyk, Daria
Гречаніна Shereshevsky-Turner Syndrome Синдром Шерешевского-Тернера англ .pdf.jpg2019Shereshevsky-Turner Syndrome : Guidelines for the training of interns, 5th year studentsGrechanina, Elena; Grechanina, Juliya; Molodan, Ludmila; Zdybskaya, Olena; Bugaeva, Olena; Efremova, Olesya; Oliinyk, Daria
Тези(2).pdf.jpg2014An early manifestation of LBSL (leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation) syndrom, case descriptionGrechanina, Elena; Zdubskaya, Elena
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
2013Medical genetics. Contents module 4. Monogenic diseases. Diagnosis of disorders of sulphur-containing amino acidsGrechanina, Elena; Grechanina, Juliya; Molodan, L.; Zdubskaya, E.; Bugaeva, Olena
Тези(10).pdf.jpg2014A new variant of Ehlers-Danlos syndrome with inborn errors of mucopolysaccharide metabolism in the mother and sonBugaeva, Olena; Grechanina, Elena; Grechanina, Juliya
2013Monogenic diseases. Inherent diseases of CNSGrechanina, Elena; Grechanina, Juliya; Molodan, L.V.; Zdubskaya, E.P.; Bugaeva, Olena
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
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