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231 results

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Page 1
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: amato b. 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.
Mutations in the ARAP3 Gene in Three Families with Primary Lymphedema Negative for Mutations in Known Lymphedema-Associated Genes.
Ricci M, Compagna R, Amato B, Kenanoglu S, Veselenyiova D, Kurti D, Baglivo M, Basha SH, Serrani R, Miggiano GAD, Aquilanti B, Matera G, Marceddu G, Velluti V, Gagliardi L, Dundar M, Krajcovic J, Bertelli M. Ricci M, et al. Among authors: amato b. Int J Genomics. 2020 Aug 25;2020:3781791. doi: 10.1155/2020/3781791. eCollection 2020. Int J Genomics. 2020. PMID: 32908855 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: amato b. Genes (Basel). 2020 Nov 17;11(11):1361. doi: 10.3390/genes11111361. Genes (Basel). 2020. PMID: 33212964 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: amato b. Lymphat Res Biol. 2022 Oct;20(5):496-506. doi: 10.1089/lrb.2020.0089. Epub 2021 Dec 8. Lymphat Res Biol. 2022. PMID: 34882481
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: amato b. Lymphology. 2020;53(3):141-151. Lymphology. 2020. PMID: 33350288
Genetic test for Mendelian fatigue and muscle weakness syndromes.
Kiani AK, Amato B, Maitz S, Nodari S, Benedetti S, Agostini F, Lorusso L, Capelli E, Dautaj A, Bertelli M. Kiani AK, et al. Among authors: amato b. Acta Biomed. 2020 Nov 9;91(13-S):e2020001. doi: 10.23750/abm.v91i13-S.10642. Acta Biomed. 2020. PMID: 33170160 Free PMC article. Review.
231 results