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Year Number of Results
2019 1
2020 9
2021 5
2022 1
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14 results
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Page 1
Mendelian obesity, molecular pathways and pharmacological therapies: a review.
Paolacci S, Borrelli A, Stuppia L, Campanile FC, Dallavilla T, Krajčovič J, Veselenyiova D, Beccari T, Unfer V, Bertelli M; Geneob Project. Paolacci S, et al. Among authors: veselenyiova d. Eur Rev Med Pharmacol Sci. 2019 Feb;23(3):1357-1378. doi: 10.26355/eurrev_201902_17031. Eur Rev Med Pharmacol Sci. 2019. PMID: 30779104 Free article. Review.
Rare PECAM1 variants in three families with lymphedema.
Michelini S, Amato B, Kenanoglu S, Veselenyiova D, Dautaj A, Kurti D, Baglivo M, Dundar M, Krajcovic J, Miggiano GA, Aquilanti B, Matera G, Velluti V, Gagliardi L, Basha SH, Bertelli M. Michelini S, et al. Among authors: veselenyiova d. Lymphology. 2020;53(3):141-151. Lymphology. 2020. PMID: 33350288
Recessive multiple epiphyseal dysplasia and Stargardt disease in two sisters.
Gatticchi L, Vešelényiová D, Miertus J, Enrico Maltese P, Manara E, Costantini A, Benedetti S, Ďurovčíková D, Krajcovic J, Bertelli M. Gatticchi L, et al. Among authors: veselenyiova d. Mol Genet Genomic Med. 2021 Apr;9(4):e1630. doi: 10.1002/mgg3.1630. Epub 2021 Mar 16. Mol Genet Genomic Med. 2021. PMID: 33724725 Free PMC article.
CDH5, a Possible New Candidate Gene for Genetic Testing of Lymphedema.
Michelini S, Ricci M, Amato B, Gentileschi S, Veselenyiova D, Kenanoglu S, Fiorentino A, Kurti D, Baglivo M, Manara E, Basha SH, Priya S, Krajcovic J, Dundar M, Belgrado JP, Dautaj A, Bertelli M. Michelini S, et al. Among authors: veselenyiova d. Lymphat Res Biol. 2021 Dec 8. doi: 10.1089/lrb.2020.0089. Online ahead of print. Lymphat Res Biol. 2021. PMID: 34882481
TIE1 as a Candidate Gene for Lymphatic Malformations with or without Lymphedema.
Michelini S, Ricci M, Veselenyiova D, Kenanoglu S, Kurti D, Baglivo M, Fiorentino A, Basha SH, Priya S, Serrani R, Krajcovic J, Dundar M, Dautaj A, Bertelli M. Michelini S, et al. Among authors: veselenyiova d. Int J Mol Sci. 2020 Sep 16;21(18):6780. doi: 10.3390/ijms21186780. Int J Mol Sci. 2020. PMID: 32947856 Free PMC article.
Possible Role of the RORC Gene in Primary and Secondary Lymphedema: Review of the Literature and Genetic Study of Two Rare Causative Variants.
Michelini S, Ricci M, Serrani R, Stuppia L, Beccari T, Veselenyiova D, Kenanoglu S, Barati S, Kurti D, Baglivo M, Basha SH, Krajcovic J, Dundar M, Bertelli M. Michelini S, et al. Among authors: veselenyiova d. Lymphat Res Biol. 2021 Apr;19(2):129-133. doi: 10.1089/lrb.2020.0030. Epub 2020 Sep 22. Lymphat Res Biol. 2021. PMID: 32960152 Review.
Two rare PROX1 variants in patients with lymphedema.
Ricci M, Amato B, Barati S, Compagna R, Veselenyiova D, Kenanoglu S, Stuppia L, Beccari T, Baglivo M, Kurti D, Krajcovic J, Serrani R, Dundar M, Basha SH, Chiurazzi P, Bertelli M. Ricci M, et al. Among authors: veselenyiova d. Mol Genet Genomic Med. 2020 Oct;8(10):e1424. doi: 10.1002/mgg3.1424. Epub 2020 Aug 5. Mol Genet Genomic Med. 2020. PMID: 32757260 Free PMC article.
NOTCH1: Review of its role in lymphatic development and study of seven families with rare pathogenic variants.
Michelini S, Ricci M, Serrani R, Barati S, Kenanoglu S, Veselenyiova D, Kurti D, Baglivo M, Basha SH, Priya S, Dautaj A, Dundar M, Krajcovic J, Bertelli M. Michelini S, et al. Among authors: veselenyiova d. Mol Genet Genomic Med. 2021 Jan;9(1):e1529. doi: 10.1002/mgg3.1529. Epub 2020 Nov 28. Mol Genet Genomic Med. 2021. PMID: 33247628 Free PMC article.
Segregation Analysis of Rare NRP1 and NRP2 Variants in Families with Lymphedema.
Michelini S, Amato B, Ricci M, Kenanoglu S, Veselenyiova D, Kurti D, Baglivo M, Manara E, Dundar M, Krajcovic J, Basha SH, Priya S, Serrani R, Miggiano GAD, Aquilanti B, Matera G, Velluti V, Gagliardi L, Dautaj A, Bertelli M. Michelini S, et al. Among authors: veselenyiova d. Genes (Basel). 2020 Nov 17;11(11):1361. doi: 10.3390/genes11111361. Genes (Basel). 2020. PMID: 33212964 Free PMC article.
14 results