PubMed (cited) for id: 153100

Year	Number of Results
1964	1
1965	1
1978	2
1985	1
1986	1
1998	1
1999	1
2000	1
2001	1
2003	1
2005	1
2006	2
2008	1
2009	2
2012	1
2013	1
2014	1
2024	0

1

A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease.

Balboa-Beltran E, Fernández-Seara MJ, Pérez-Muñuzuri A, Lago R, García-Magán C, Couce ML, Sobrino B, Amigo J, Carracedo A, Barros F. Balboa-Beltran E, et al. J Med Genet. 2014 Jul;51(7):475-8. doi: 10.1136/jmedgenet-2013-102020. Epub 2014 Apr 17. J Med Genet. 2014. PMID: 24744435

2

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

3

Classification of lymphatic-system malformations in primary lymphoedema based on MR lymphangiography.

Liu NF, Yan ZX, Wu XF. Liu NF, et al. Eur J Vasc Endovasc Surg. 2012 Sep;44(3):345-9. doi: 10.1016/j.ejvs.2012.06.019. Epub 2012 Jul 23. Eur J Vasc Endovasc Surg. 2012. PMID: 22831870 Free article.

4

Recessive primary congenital lymphoedema caused by a VEGFR3 mutation.

Ghalamkarpour A, Holnthoner W, Saharinen P, Boon LM, Mulliken JB, Alitalo K, Vikkula M. Ghalamkarpour A, et al. J Med Genet. 2009 Jun;46(6):399-404. doi: 10.1136/jmg.2008.064469. Epub 2009 Mar 15. J Med Genet. 2009. PMID: 19289394

5

Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas.

Connell FC, Ostergaard P, Carver C, Brice G, Williams N, Mansour S, Mortimer PS, Jeffery S; Lymphoedema Consortium. Connell FC, et al. Hum Genet. 2009 Jan;124(6):625-31. doi: 10.1007/s00439-008-0586-5. Epub 2008 Nov 12. Hum Genet. 2009. PMID: 19002718

6

Hereditary lymphedema type I associated with VEGFR3 mutation: the first de novo case and atypical presentations.

Ghalamkarpour A, Morlot S, Raas-Rothschild A, Utkus A, Mulliken JB, Boon LM, Vikkula M. Ghalamkarpour A, et al. Clin Genet. 2006 Oct;70(4):330-5. doi: 10.1111/j.1399-0004.2006.00687.x. Clin Genet. 2006. PMID: 16965327

7

Wide clinical spectrum in a family with hereditary lymphedema type I due to a novel missense mutation in VEGFR3.

Spiegel R, Ghalamkarpour A, Daniel-Spiegel E, Vikkula M, A Shalev S. Spiegel R, et al. J Hum Genet. 2006;51(10):846-850. doi: 10.1007/s10038-006-0031-3. Epub 2006 Aug 19. J Hum Genet. 2006. PMID: 16924388

8

Milroy disease and the VEGFR-3 mutation phenotype.

Brice G, Child AH, Evans A, Bell R, Mansour S, Burnand K, Sarfarazi M, Jeffery S, Mortimer P. Brice G, et al. J Med Genet. 2005 Feb;42(2):98-102. doi: 10.1136/jmg.2004.024802. J Med Genet. 2005. PMID: 15689446 Free PMC article. Review.

9

CONGENITAL HEREDITARY LYMPHOEDEMA.

ESTERLY JR. ESTERLY JR. J Med Genet. 1965 Jun;2(2):93-8. doi: 10.1136/jmg.2.2.93. J Med Genet. 1965. PMID: 14295660 Free PMC article. No abstract available.

10

PLEURAL EFFUSION IN CHRONIC HEREDITARY LYMPHEDEMA (NONNE, MILROY, MEIGE'S DISEASE). REPORT OF TWO CASES.

HURWITZ PA, PINALS DJ. HURWITZ PA, et al. Radiology. 1964 Feb;82:246-8. doi: 10.1148/82.2.246. Radiology. 1964. PMID: 14115303 No abstract available.

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