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Items: 1 to 20 of 22

1.

A Novel Splice-Site Mutation in VEGFC Is Associated with Congenital Primary Lymphoedema of Gordon.

Nadarajah N, Schulte D, McConnell V, Martin-Almedina S, Karapouliou C, Mortimer PS, Jeffery S, Schulte-Merker S, Gordon K, Mansour S, Ostergaard P.

Int J Mol Sci. 2018 Aug 1;19(8). pii: E2259. doi: 10.3390/ijms19082259.

2.

A Genetic Approach to the Classification of Primary Lymphoedema and Lymphatic Malformations.

Ho B, Gordon K, Mortimer PS.

Eur J Vasc Endovasc Surg. 2018 Oct;56(4):465-466. doi: 10.1016/j.ejvs.2018.07.001. Epub 2018 Jul 25. No abstract available.

PMID:
30055909
3.

Emberger syndrome: A rare association with hearing loss.

Zawawi F, Sokolov M, Mawby T, Gordon KA, Papsin BC, Cushing SL.

Int J Pediatr Otorhinolaryngol. 2018 May;108:82-84. doi: 10.1016/j.ijporl.2018.02.014. Epub 2018 Feb 7.

PMID:
29605372
4.

VIPAR, a quantitative approach to 3D histopathology applied to lymphatic malformations.

Hägerling R, Drees D, Scherzinger A, Dierkes C, Martin-Almedina S, Butz S, Gordon K, Schäfers M, Hinrichs K, Ostergaard P, Vestweber D, Goerge T, Mansour S, Jiang X, Mortimer PS, Kiefer F.

JCI Insight. 2017 Aug 17;2(16). pii: 93424. doi: 10.1172/jci.insight.93424. [Epub ahead of print]

5.

Magnetic Resonance Imaging-Based Assessment of Breast Cancer-Related Lymphoedema Tissue Composition.

Borri M, Gordon KD, Hughes JC, Scurr ED, Koh DM, Leach MO, Mortimer PS, Schmidt MA.

Invest Radiol. 2017 Sep;52(9):554-561. doi: 10.1097/RLI.0000000000000386.

6.

Ano-genital Granulomatosis and Crohn's Disease: A Case Series of Males Presenting with Genital Lymphoedema.

Alexakis C, Gordon K, Mellor R, Chong H, Mortimer P, Pollok R.

J Crohns Colitis. 2017 Apr 1;11(4):454-459. doi: 10.1093/ecco-jcc/jjw173.

PMID:
27683802
7.

Lymph vessels: the forgotten second circulation in health and disease.

Adamczyk LA, Gordon K, Kholová I, Meijer-Jorna LB, Telinius N, Gallagher PJ, van der Wal AC, Baandrup U.

Virchows Arch. 2016 Jul;469(1):3-17. doi: 10.1007/s00428-016-1945-6. Epub 2016 May 12. Review.

8.

Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.

Fotiou E, Martin-Almedina S, Simpson MA, Lin S, Gordon K, Brice G, Atton G, Jeffery I, Rees DC, Mignot C, Vogt J, Homfray T, Snyder MP, Rockson SG, Jeffery S, Mortimer PS, Mansour S, Ostergaard P.

Nat Commun. 2015 Sep 3;6:8085. doi: 10.1038/ncomms9085.

9.

The lymphatic phenotype in Noonan and Cardiofaciocutaneous syndrome.

Joyce S, Gordon K, Brice G, Ostergaard P, Nagaraja R, Short J, Moore S, Mortimer P, Mansour S.

Eur J Hum Genet. 2016 May;24(5):690-6. doi: 10.1038/ejhg.2015.175. Epub 2015 Aug 5.

10.

The lymphatic phenotype in Turner syndrome: an evaluation of nineteen patients and literature review.

Atton G, Gordon K, Brice G, Keeley V, Riches K, Ostergaard P, Mortimer P, Mansour S.

Eur J Hum Genet. 2015 Dec;23(12):1634-9. doi: 10.1038/ejhg.2015.41. Epub 2015 Mar 25. Review.

11.

Quantitative Contrast-Enhanced Magnetic Resonance Lymphangiography of the Upper Limbs in Breast Cancer Related Lymphedema: An Exploratory Study.

Borri M, Schmidt MA, Gordon KD, Wallace TA, Hughes JC, Scurr ED, Koh DM, Leach MO, Mortimer PS.

Lymphat Res Biol. 2015 Jun;13(2):100-6. doi: 10.1089/lrb.2014.0039. Epub 2015 Mar 16.

12.

Surgical procedures in lymphedema management.

Hadamitzky C, Pabst R, Gordon K, Vogt PM.

J Vasc Surg Venous Lymphat Disord. 2014 Oct;2(4):461-8. doi: 10.1016/j.jvsv.2014.02.001. Epub 2014 Mar 22. Review.

PMID:
26993555
13.

Rapid resolution of hidradenitis suppurativa after bariatric surgical intervention.

Thomas CL, Gordon KD, Mortimer PS.

Clin Exp Dermatol. 2014 Apr;39(3):315-7; quiz 317-8. doi: 10.1111/ced.12269.

PMID:
24635068
14.

Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations.

Jones GE, Ostergaard P, Moore AT, Connell FC, Williams D, Quarrell O, Brady AF, Spier I, Hazan F, Moldovan O, Wieczorek D, Mikat B, Petit F, Coubes C, Saul RA, Brice G, Gordon K, Jeffery S, Mortimer PS, Vasudevan PC, Mansour S.

Eur J Hum Genet. 2014 Jul;22(7):881-7. doi: 10.1038/ejhg.2013.263. Epub 2013 Nov 27.

15.

An unusual case of genital swelling.

Foley CC, McMenamin M, Gordon KD, Irvine AD.

Clin Exp Dermatol. 2013 Dec;38(8):946-8. doi: 10.1111/ced.12131. Epub 2013 May 10. No abstract available.

PMID:
23659728
16.

The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings.

Connell FC, Gordon K, Brice G, Keeley V, Jeffery S, Mortimer PS, Mansour S, Ostergaard P.

Clin Genet. 2013 Oct;84(4):303-14. doi: 10.1111/cge.12173. Epub 2013 Jun 27. Review.

PMID:
23621851
17.

A novel mutation in GJA1 causing oculodentodigital syndrome and primary lymphoedema in a three generation family.

Brice G, Ostergaard P, Jeffery S, Gordon K, Mortimer PS, Mansour S.

Clin Genet. 2013 Oct;84(4):378-81. doi: 10.1111/cge.12158. Epub 2013 Apr 26.

PMID:
23550541
18.

Genital lymphoedema due to ano-genital granulomatosis.

Gordon KD, Brice G, Walker Y, Pollok R, Mortimer P, Slater C.

Int J STD AIDS. 2013 Feb;24(2):149-51. doi: 10.1258/ijsa.2012.012183. Epub 2013 May 6.

PMID:
23514830
19.

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.

Circ Res. 2013 Mar 15;112(6):956-60. doi: 10.1161/CIRCRESAHA.113.300350. Epub 2013 Feb 14.

PMID:
23410910
20.

FLT4/VEGFR3 and Milroy disease: novel mutations, a review of published variants and database update.

Gordon K, Spiden SL, Connell FC, Brice G, Cottrell S, Short J, Taylor R, Jeffery S, Mortimer PS, Mansour S, Ostergaard P.

Hum Mutat. 2013 Jan;34(1):23-31. doi: 10.1002/humu.22223. Epub 2012 Oct 16. Review.

PMID:
23074044

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