A Case of Prenatal Diagnosis of Apert Syndrome in the Second Trimester of Pregnancy
Anastasiia Kornutii, Oleksandr Kornutii, Ivanna Shymanska, Maiia Bondarenko et autres
0 citationsOBM Genetics
Ivanna Shymanska
Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.
10Publications signalées
38Citations signalées
2Affiliations récentes
Institutions déclarées
Domaines associés
Immunodeficiency and Autoimmune DisordersTuberculosis Research and EpidemiologyAsthma and respiratory diseasesChronic Obstructive Pulmonary Disease (COPD) ResearchMitochondrial Function and Pathology
Publications récentes
The Homozygous c.612C>G Mutation in C1QBP is Associated with Late-Onset Progressive External Ophthalmoplegia
Ivanna Shymanska, Sofiia Levandivska, Margarita Marchuk, Anastasiya Honchar et autres
0 citationsOBM Genetics
Application of molecular-genetic approaches in Cftr gene variant diagnostics: historical perspective and personal experience
O. Tyshchenko, M. Tyrkus, Ivanna Shymanska, N. P. Matiytsiv et autres
0 citationsFaktori eksperimental noi evolucii organizmiv
Fatal HLH in patients with X-linked lymphoproliferative disease 1 due to a novel variant in SH2D1A: case report
Oksana Boyarchuk, Алла Волоха, Nataliia Yarema, Tetyana Tomashivska et autres
4 citationsFrontiers in Immunology
Two case reports of B-cell lymphopenia associated with IGLL1 variants identified through newborn screening in Ukraine
Oksana Boyarchuk, Yaryna Romanyshyn, Ihor Savchak, Volodymyr Kravets et autres
0 citationsFrontiers in Pediatrics
Comparative analysis of two TREC/KREC quantification methods for newborn screening of primary immunodeficiency with T- and B-lymphopenia used in Ukraine
Volodymyr Kravets, Ivanna Shymanska, Oksana Boyarchuk, N. P. Matiytsiv et autres
1 citationStudia Biologica
Novel causal insights into idiopathic pregnancy loss
Yevheniya Sharhorodska, Anna Ulrich, Л. Б. Чорна, Ivanna Shymanska et autres
0 citationsBiopolymers and Cell
High frequency of the 472AA COMT (Val158) homozygous genotype of the catechol-O-methyltransferase (COMT) gene in children with irritable bowel syndrome
M.O. Semen, Ivanna Shymanska, V.D. Semen, Halyna Makukh
2 citationsModern pediatrics Ukraine
Newborn screening for severe combined immunodeficiency: The results of the first pilot TREC and KREC study in Ukraine with involving of 10,350 neonates
Oksana Boyarchuk, Nataliia Yarema, Volodymyr Kravets, О.М. Shulhai et autres
30 citationsFrontiers in Immunology
Genetic testing of allelic variants of PIZ (GLU342Lys, RS28929474) and PIS (GLU264Val, RS17580) of SERPINA1 gene in children with bronchial asthma
Ivanna Shymanska, Оlena Trutiak, O.L. Lychkovska, Halyna Makukh
1 citationEUREKA Life Sciences
BNTIC News n’est pas le producteur de ces données. Métadonnées interrogées à la demande auprès de OpenAlex (CC0). Sources et limites.