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For: Lacerda Lda S, Alves UD, Zanier JF, Machado DC, Camilo GB, Lopes AJ. Differential diagnoses of overgrowth syndromes: the most important clinical and radiological disease manifestations. Radiol Res Pract 2014;2014:947451. [PMID: 25009745 DOI: 10.1155/2014/947451] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Snee IA, Mazzola CA, Sikorskyj T. Chiari I malformation with Klippel-Trenaunay syndrome: case report and review of the literature. Childs Nerv Syst 2021;37:2369-73. [PMID: 33492467 DOI: 10.1007/s00381-020-04992-x] [Reference Citation Analysis]
2 Arts FA, Chand D, Pecquet C, Velghe AI, Constantinescu S, Hallberg B, Demoulin JB. PDGFRB mutants found in patients with familial infantile myofibromatosis or overgrowth syndrome are oncogenic and sensitive to imatinib. Oncogene 2016;35:3239-48. [PMID: 26455322 DOI: 10.1038/onc.2015.383] [Cited by in Crossref: 46] [Cited by in F6Publishing: 41] [Article Influence: 6.6] [Reference Citation Analysis]
3 Abdolrahimzadeh S, Scavella V, Felli L, Cruciani F, Contestabile MT, Recupero SM. Ophthalmic Alterations in the Sturge-Weber Syndrome, Klippel-Trenaunay Syndrome, and the Phakomatosis Pigmentovascularis: An Independent Group of Conditions? Biomed Res Int 2015;2015:786519. [PMID: 26451379 DOI: 10.1155/2015/786519] [Cited by in Crossref: 23] [Cited by in F6Publishing: 25] [Article Influence: 3.3] [Reference Citation Analysis]
4 Ivanitskaya O, Andreeva E, Odegova N. Prenatal diagnosis of Klippel-Trenaunay syndrome: Series of four cases and review of the literature. Ultrasound 2020;28:91-102. [PMID: 32528545 DOI: 10.1177/1742271X19880327] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
5 Edmondson AC, Kalish JM. Overgrowth Syndromes. J Pediatr Genet 2015;4:136-43. [PMID: 27617124 DOI: 10.1055/s-0035-1564440] [Cited by in Crossref: 35] [Cited by in F6Publishing: 20] [Article Influence: 5.0] [Reference Citation Analysis]
6 Zhai J, Zhong ME, Shen J, Tan H, Li Z. Kyphoscoliosis with Klippel-Trenaunay syndrome: a case report and literature review. BMC Musculoskelet Disord 2019;20:10. [PMID: 30611239 DOI: 10.1186/s12891-018-2393-z] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
7 Chenbhanich J, Leelayuwatanakul N, Phowthongkum P. Klippel-Trenaunay-Weber syndrome as a cause of chronic thromboembolic pulmonary hypertension. BMJ Case Rep 2018;2018:bcr-2018-224621. [PMID: 29572375 DOI: 10.1136/bcr-2018-224621] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
8 Mussa A, Carli D, Cardaropoli S, Ferrero GB, Resta N. Lateralized and Segmental Overgrowth in Children. Cancers (Basel) 2021;13:6166. [PMID: 34944785 DOI: 10.3390/cancers13246166] [Reference Citation Analysis]
9 Sikakulya FK, Egesa WI, Kiyaka SM, Anyama P. A neonate with Klippel-Trénaunay syndrome: a case report. J Med Case Rep 2021;15:447. [PMID: 34488883 DOI: 10.1186/s13256-021-03029-4] [Reference Citation Analysis]
10 Arafa OM, Alzuhair AR, Alharbi SK, Alromaih NI. Surgical correction of foot equino-cavocarus deformity in Klippel-Trénaunay-Weber syndrome: a case report. J Surg Case Rep 2021;2021:rjab434. [PMID: 34650788 DOI: 10.1093/jscr/rjab434] [Reference Citation Analysis]
11 Hayek F. Pallister-Hall syndrome with orofacial narrowing and tethered cord: a case report. J Med Case Rep 2018;12:354. [PMID: 30486853 DOI: 10.1186/s13256-018-1868-8] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]