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249 related items for PubMed ID: 222308
1. Brief communication: nevus unis lateris and Klippel-Trenaunay-Weber syndrome with the Sturge Weber anomalady in a consanguineous Puerto Rican family. Rivera-Reyes LR, Toro-Solá MA. Bol Asoc Med P R; 1979 Feb; 71(2):69-71. PubMed ID: 222308 [No Abstract] [Full Text] [Related]
2. [Association on Sturge Weber and Klippel Trenaunay Weber syndromes. Apropos of 2 cases]. Guízar Vázquez J, Navarrete Cadena C, Barrón Uribe C, Velázquez E, Armendares S. Bol Med Hosp Infant Mex; 1979 Feb; 36(3):415-24. PubMed ID: 218598 [Abstract] [Full Text] [Related]
3. [Sturge-Weber-Dimitri syndrome associated with Klippel-Trenaunay syndrome]. Belli L, Delmar A, Abulafia J, González Rescigno GR, Estrada E, Repetto A, Calvo E. Med Cutan Ibero Lat Am; 1980 Feb; 8(1-3):59-63. PubMed ID: 6267388 [Abstract] [Full Text] [Related]
4. Sturge-Weber-Klippel-Trenaunay syndrome: what's in a name? Happle R. Eur J Dermatol; 2003 Feb; 13(3):223. PubMed ID: 12804977 [No Abstract] [Full Text] [Related]
10. An infantile case of Sturge-Weber syndrome in association with Klippel-Trenaunay-Weber syndrome and phakomatosis pigmentovascularis. Lee CW, Choi DY, Oh YG, Yoon HS, Kim JD. J Korean Med Sci; 2005 Dec; 20(6):1082-4. PubMed ID: 16361829 [Abstract] [Full Text] [Related]
13. The Klippel-Trenaunay-Sturge-Weber syndrome. Neetens A, Martin JJ, Neetens I, Smets RM. Bull Soc Belge Ophtalmol; 1987 Apr; 224():123-37. PubMed ID: 2855036 [No Abstract] [Full Text] [Related]
14. Klippel-Trenaunay syndrome and Sturge-Weber syndrome: variations on a theme? Vissers W, Van Steensel M, Steijlen P, Renier W, Van De Kerkhof P, Van Der Vleuten C. Eur J Dermatol; 2003 Apr; 13(3):238-41. PubMed ID: 12804981 [Abstract] [Full Text] [Related]
15. Klippel-Trenaunay--Weber syndrome. Ofodile FA. East Afr Med J; 1981 Apr; 58(4):298-302. PubMed ID: 6266801 [No Abstract] [Full Text] [Related]
16. Co-occurrence of Sturge-Weber syndrome and Klippel-Trenaunay-Weber syndrome phenotype: Consideration of the historical aspect. Sakaguchi Y, Takenouchi T, Uehara T, Kishi K, Takahashi T, Kosaki K. Am J Med Genet A; 2017 Oct; 173(10):2831-2833. PubMed ID: 28782176 [No Abstract] [Full Text] [Related]
17. Klippel-Trenaunay and Sturge-Weber Overlap Syndrome with KRAS and GNAQ mutations. He R, Liao S, Yao X, Huang R, Zeng J, Zhang J, Yu J. Ann Clin Transl Neurol; 2020 Jul; 7(7):1258-1264. PubMed ID: 32613723 [Abstract] [Full Text] [Related]
18. Neuroradiologic findings in a young patient with characteristics of Sturge-Weber syndrome and Klippel-Trenaunay syndrome. Verhelst H, Van Coster R. J Child Neurol; 2005 Nov; 20(11):911-3. PubMed ID: 16417862 [Abstract] [Full Text] [Related]
20. Two reports of phacomatosis pigmentovascularis type IIb, one in association with Sturge-Weber syndrome and Klippel-Trenaunay syndrome. Finklea LB, Mohr MR, Warthan MM, Darrow DH, Williams JV. Pediatr Dermatol; 2010 Nov; 27(3):303-5. PubMed ID: 20609155 [Abstract] [Full Text] [Related] Page: [Next] [New Search]