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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: basha sh. 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: basha sh. 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: basha sh. Int J Genomics. 2020 Aug 25;2020:3781791. doi: 10.1155/2020/3781791. eCollection 2020. Int J Genomics. 2020. PMID: 32908855 Free PMC article.
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: basha sh. Int J Mol Sci. 2020 Sep 16;21(18):6780. doi: 10.3390/ijms21186780. Int J Mol Sci. 2020. PMID: 32947856 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: basha sh. Genes (Basel). 2020 Nov 17;11(11):1361. doi: 10.3390/genes11111361. Genes (Basel). 2020. PMID: 33212964 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: basha sh. 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.
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: basha sh. Lymphology. 2020;53(3):141-151. Lymphology. 2020. PMID: 33350288
34 results