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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2020 | 1 |
2022 | 3 |
2023 | 1 |
2024 | 0 |
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5 results
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Page 1
Rare IFT140-Associated Phenotype of Cranioectodermal Dysplasia and Features of Diagnostic Journey in Patients with Suspected Ciliopathies.
Genes (Basel). 2023 Jul 28;14(8):1553. doi: 10.3390/genes14081553.
Genes (Basel). 2023.
PMID: 37628605
Free PMC article.
Glycated hemoglobin level dynamics in COVID-19 survivors: 12 months follow-up study after discharge from hospital.
Shestakova M, Kononenko I, Kalmykovа Z, Markova T, Kaplun E, Lysenko M, Mokrysheva N.
Shestakova M, et al. Among authors: markova t.
PLoS One. 2022 Nov 9;17(11):e0275381. doi: 10.1371/journal.pone.0275381. eCollection 2022.
PLoS One. 2022.
PMID: 36350895
Free PMC article.
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Does the c.-14C>T Mutation in the IFITM5 Gene Provide Identical Phenotypes for Osteogenesis Imperfecta Type V? Data from Russia and a Literature Review.
Tyurin A, Merkuryeva E, Zaripova A, Markova T, Nagornova T, Dantsev I, Nadyrshina D, Zakharova E, Khusainova R.
Tyurin A, et al. Among authors: markova t.
Biomedicines. 2022 Sep 22;10(10):2363. doi: 10.3390/biomedicines10102363.
Biomedicines. 2022.
PMID: 36289625
Free PMC article.
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Clinical and Genetic Characteristics of COL2A1-Associated Skeletal Dysplasias in 60 Russian Patients: Part I.
Markova T, Kenis V, Melchenko E, Osipova D, Nagornova T, Orlova A, Zakharova E, Dadali E, Kutsev S.
Markova T, et al.
Genes (Basel). 2022 Jan 13;13(1):137. doi: 10.3390/genes13010137.
Genes (Basel). 2022.
PMID: 35052477
Free PMC article.
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Identification of a Novel de Novo Variant in the SYT2 Gene Causing a Rare Type of Distal Hereditary Motor Neuropathy.
Mironovich O, Dadali E, Malmberg S, Markova T, Ryzhkova O, Poliakov A.
Mironovich O, et al. Among authors: markova t.
Genes (Basel). 2020 Oct 22;11(11):1238. doi: 10.3390/genes11111238.
Genes (Basel). 2020.
PMID: 33105646
Free PMC article.
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