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1

Newborn screening for severe combined immunodeficiency: lessons from a pilot study and prospects by O.R. Boyarchuk, N.M. Yarema, H.V. Makukh

Published 2023-04-01

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2

Markers of fibrillogenic disorders in children with different variants of pyelonephritis by N.S. Lukianenko, M.Yu. Iskiv, K.A. Kens, H.V. Makukh

Published 2018-03-01

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3

Висока частота гомозиготного генотипу 472АА COMT (Val158) гена катехол-О-метилтрансферази (COMT) у дітей із синдромом подразненого кишечника... by M.O. Semen, O.L. Lychkovska, I.E. Shymanska, V.D. Semen, H.V. Makukh

Published 2022-10-01

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4

Клінічний випадок комбінованого імунодефіциту, діагностованого за допомогою визначення TREC by N.M. Yarema, H.V. Makukh, L.M. Virstyuk, O.V. Fedynska, O.R. Boyarchuk

Published 2022-09-01

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5

Polymorphisms in genes involved in folate metabolism as maternal risk factors for congenital heart diseases of the fеtus by Y.B. Sharhorodska, H.V. Makukh, L.B. Chorna, O.K. Yefimenko, H.R. Akopyan

Published 2019-09-01

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6

INHERITED 15Q DUPLICATION IN THREE NOT RELATED UKRAINIAN FAMILIES by S. H. Levandivska, M. I. Dushar, O. V. Tyshchenko, N. L. Huleyuk, E. Y. Patskun, H. V. Makukh

Published 2023-06-01

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