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Journal Abstract Search
124 related items for PubMed ID: 30055909
1. 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. PubMed ID: 30055909 [No Abstract] [Full Text] [Related]
2. Genetic tests in lymphatic vascular malformations and lymphedema. Michelini S, Paolacci S, Manara E, Eretta C, Mattassi R, Lee BB, Bertelli M. J Med Genet; 2018 Apr; 55(4):222-232. PubMed ID: 29440349 [Abstract] [Full Text] [Related]
4. Update and audit of the St George's classification algorithm of primary lymphatic anomalies: a clinical and molecular approach to diagnosis. Gordon K, Varney R, Keeley V, Riches K, Jeffery S, Van Zanten M, Mortimer P, Ostergaard P, Mansour S. J Med Genet; 2020 Oct; 57(10):653-659. PubMed ID: 32409509 [Abstract] [Full Text] [Related]
5. Study of a supplement and a genetic test for lymphedema management. Michelini S, Cestari M, Michelini S, Camilleri G, De Antoni L, Sonna WN, Bertelli M. Acta Biomed; 2020 Nov 09; 91(13-S):e2020013. PubMed ID: 33170163 [Abstract] [Full Text] [Related]
6. An approach to familial lymphoedema. Jones GE, Mansour S. Clin Med (Lond); 2017 Dec 09; 17(6):552-557. PubMed ID: 29196357 [Abstract] [Full Text] [Related]
7. Paediatric lymphoedema: An audit of patients seen by the paediatric and primary lymphoedema group of vascular European Reference Network (VASCERN). Devoogdt N, Van Zanten M, Damstra R, Van Duinen K, Dickinson-Blok JL, Thomis S, Giacalone G, Belva F, Suominen S, Kavola H, Oberlin M, Rossler J, Rucigaj TP, Riches K, Mansour S, Gordon K, Vignes S, Keeley V. Eur J Med Genet; 2022 Dec 09; 65(12):104641. PubMed ID: 36243335 [Abstract] [Full Text] [Related]
10. Early detection of chronic progressive lymphoedema susceptibility in Belgian draught horse stallions by means of ELISA. De Keyser K, Oosterlinck M, Raes E, Ducatelle R, Janssens S, Buys N. Commun Agric Appl Biol Sci; 2012 Dec 09; 77(1):183-7. PubMed ID: 22558778 [No Abstract] [Full Text] [Related]
11. Primary lymphoedema in a kitten. Jacobsen JO, Eggers C. J Small Anim Pract; 1997 Jan 09; 38(1):18-20. PubMed ID: 9121128 [Abstract] [Full Text] [Related]
12. [Primary lymphedema of limbs]. Vaillant L, Tauveron V. Presse Med; 2010 Dec 09; 39(12):1279-86. PubMed ID: 21035299 [Abstract] [Full Text] [Related]
13. [Primary conjunctival-palpebral lymphedema and Milroy disease]. Offret H, Labrune B. J Fr Ophtalmol; 1994 Dec 09; 17(11):679-82. PubMed ID: 7722228 [Abstract] [Full Text] [Related]
14. Splice-site mutations in VEGFC cause loss of function and Nonne-Milroy-like primary lymphedema. Fastré E, Lanteigne LE, Helaers R, Giacalone G, Revencu N, Dionyssiou D, Demiri E, Brouillard P, Vikkula M. Clin Genet; 2018 Jul 09; 94(1):179-181. PubMed ID: 29542815 [No Abstract] [Full Text] [Related]
15. Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24. Brice G, Mansour S, Bell R, Collin JR, Child AH, Brady AF, Sarfarazi M, Burnand KG, Jeffery S, Mortimer P, Murday VA. J Med Genet; 2002 Jul 09; 39(7):478-83. PubMed ID: 12114478 [Abstract] [Full Text] [Related]
16. A Novel Genetic Candidate for Primary Lymphedema. Rockson SG. Lymphat Res Biol; 2022 Oct 09; 20(5):467. PubMed ID: 36302177 [No Abstract] [Full Text] [Related]
17. Lymphoedema and cellulitis: chicken or egg? Keeley VL. Br J Dermatol; 2008 Jun 09; 158(6):1175-6. PubMed ID: 18482406 [No Abstract] [Full Text] [Related]
18. 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. Int J Mol Sci; 2020 Sep 16; 21(18):. PubMed ID: 32947856 [Abstract] [Full Text] [Related]
20. An unusual case of familial lymphedema. Dean SM, Starr J. Ann Vasc Surg; 2014 Jul 16; 28(5):1314.e1-3. PubMed ID: 24333525 [Abstract] [Full Text] [Related] Page: [Next] [New Search]