Similar articles for PMID: 22768468

Year	Number of Results
1984	1
1992	1
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2002	5
2003	8
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2013	7
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2018	10
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2024	0

1

Clinical and genetic study of 46 Italian patients with primary lymphedema.

Michelini S, Degiorgio D, Cestari M, Corda D, Ricci M, Cardone M, Mander A, Famoso L, Contini E, Serrani R, Pinelli L, Cecchin S, Bertelli M. Michelini S, et al. Lymphology. 2012 Mar;45(1):3-12. Lymphology. 2012. PMID: 22768468

2

Age of onset in hereditary lymphedema.

Levinson KL, Feingold E, Ferrell RE, Glover TW, Traboulsi EI, Finegold DN. Levinson KL, et al. J Pediatr. 2003 Jun;142(6):704-8. doi: 10.1067/mpd.2003.235. J Pediatr. 2003. PMID: 12838201

3

Rare Variants in LAMA5 Gene associated with FLT4 and FOXC2 Mutations in Primary Lymphedema May Contribute to Severity.

Liu NF, Yu ZY, Sun D, Lou Y. Liu NF, et al. Lymphology. 2016 Dec;49(4):192-204. Lymphology. 2016. PMID: 29908552

4

Defective valves and abnormal mural cell recruitment underlie lymphatic vascular failure in lymphedema distichiasis.

Petrova TV, Karpanen T, Norrmén C, Mellor R, Tamakoshi T, Finegold D, Ferrell R, Kerjaschki D, Mortimer P, Ylä-Herttuala S, Miura N, Alitalo K. Petrova TV, et al. Nat Med. 2004 Sep;10(9):974-81. doi: 10.1038/nm1094. Epub 2004 Aug 22. Nat Med. 2004. PMID: 15322537

5

The establishment of a predictive mutational model of the forkhead domain through the analyses of FOXC2 missense mutations identified in patients with hereditary lymphedema with distichiasis.

Berry FB, Tamimi Y, Carle MV, Lehmann OJ, Walter MA. Berry FB, et al. Hum Mol Genet. 2005 Sep 15;14(18):2619-27. doi: 10.1093/hmg/ddi295. Epub 2005 Aug 4. Hum Mol Genet. 2005. PMID: 16081467

6

A novel missense mutation and two microrearrangements in the FOXC2 gene of three families with lymphedema-distichiasis syndrome.

Fauret AL, Tuleja E, Jeunemaitre X, Vignes S. Fauret AL, et al. Lymphology. 2010 Mar;43(1):14-8. Lymphology. 2010. PMID: 20552815

7

Mutation in vascular endothelial growth factor-C, a ligand for vascular endothelial growth factor receptor-3, is associated with autosomal dominant milroy-like primary lymphedema.

Gordon K, Schulte D, Brice G, Simpson MA, Roukens MG, van Impel A, Connell F, Kalidas K, Jeffery S, Mortimer PS, Mansour S, Schulte-Merker S, Ostergaard P. Gordon K, et al. Circ Res. 2013 Mar 15;112(6):956-60. doi: 10.1161/CIRCRESAHA.113.300350. Epub 2013 Feb 14. Circ Res. 2013. PMID: 23410910

8

Lymphedema-distichiasis syndrome: a distinct type of primary lymphedema caused by mutations in the FOXC2 gene.

Vreeburg M, Heitink MV, Damstra RJ, Moog U, van Geel M, van Steensel MA. Vreeburg M, et al. Int J Dermatol. 2008 Nov;47 Suppl 1:52-5. doi: 10.1111/j.1365-4632.2008.03962.x. Int J Dermatol. 2008. PMID: 18986489

9

FOXC2 and FLT4 Gene Variants in Lymphatic Filariasis.

Sheik Y, Qureshi SF, Mohhammed B, Nallari P. Sheik Y, et al. Lymphat Res Biol. 2015 Jun;13(2):112-9. doi: 10.1089/lrb.2014.0025. Epub 2015 Jun 2. Lymphat Res Biol. 2015. PMID: 26091406

10

Genetic Screening in a Large Cohort of Italian Patients Affected by Primary Lymphedema Using a Next Generation Sequencing (NGS) Approach.

Michelini S, Vettori A, Maltese PE, Cardone M, Bruson A, Fiorentino A, Cappellino F, Sainato V, Guerri G, Marceddu G, Tezzele S, Bertelli M. Michelini S, et al. Lymphology. 2016 Jun;49(2):57-72. Lymphology. 2016. PMID: 29906362

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