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Journal Abstract Search

225 related items for PubMed ID: 25602158

  • 1. Fibroadipose hyperplasia versus Proteus syndrome: segmental overgrowth with a mosaic mutation in the PIK3CA gene.
    Youssefian L, Vahidnezhad H, Baghdadi T, Ghaznavi A, Li Q, Tabrizi M, Uitto J.
    J Invest Dermatol; 2015 May; 135(5):1450-1453. PubMed ID: 25602158
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  • 2. Clinical delineation and natural history of the PIK3CA-related overgrowth spectrum.
    Keppler-Noreuil KM, Sapp JC, Lindhurst MJ, Parker VE, Blumhorst C, Darling T, Tosi LL, Huson SM, Whitehouse RW, Jakkula E, Grant I, Balasubramanian M, Chandler KE, Fraser JL, Gucev Z, Crow YJ, Brennan LM, Clark R, Sellars EA, Pena LD, Krishnamurty V, Shuen A, Braverman N, Cunningham ML, Sutton VR, Tasic V, Graham JM, Geer J, Henderson A, Semple RK, Biesecker LG.
    Am J Med Genet A; 2014 Jul; 164A(7):1713-33. PubMed ID: 24782230
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  • 4. Klippel-Trenaunay syndrome belongs to the PIK3CA-related overgrowth spectrum (PROS).
    Vahidnezhad H, Youssefian L, Uitto J.
    Exp Dermatol; 2016 Jan; 25(1):17-9. PubMed ID: 26268729
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  • 5. Molecular Diagnosis of Mosaic Overgrowth Syndromes Using a Custom-Designed Next-Generation Sequencing Panel.
    Chang F, Liu L, Fang E, Zhang G, Chen T, Cao K, Li Y, Li MM.
    J Mol Diagn; 2017 Jul; 19(4):613-624. PubMed ID: 28502725
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  • 6. Molecular diagnosis of somatic overgrowth conditions: A single-center experience.
    Lalonde E, Ebrahimzadeh J, Rafferty K, Richards-Yutz J, Grant R, Toorens E, Marie Rosado J, Schindewolf E, Ganguly T, Kalish JM, Deardorff MA, Ganguly A.
    Mol Genet Genomic Med; 2019 Mar; 7(3):e536. PubMed ID: 30761771
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  • 8. A case of congenital lipomatous overgrowth, vascular malformations, epidermal nevi, spinal/skeletal anomalies and/or scoliosis syndrome with lipoatrophy as an important clinical manifestation.
    Schreiber A, Grenier PO, Auger I.
    Pediatr Dermatol; 2017 Nov; 34(6):735-736. PubMed ID: 28833506
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  • 10. Cloves syndrome: a case report and perinatal diagnostic findings.
    Puvabanditsin S, Memon N, Chekmareva M, Di Stefano V, Mehta R.
    Genet Couns; 2014 Nov; 25(3):265-70. PubMed ID: 25365848
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  • 12. [CLOVES syndrome: a malformational syndrome closely resembling Proteus syndrome].
    Guillet A, Aubert H, Tessier MH, David A, Perret C, Penhoat M, Stalder JF, Barbarot S.
    Ann Dermatol Venereol; 2014 Nov; 141(8-9):507-13. PubMed ID: 25209813
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  • 13. What's New in Genetic Skin Diseases.
    Hill CR, Theos A.
    Dermatol Clin; 2019 Apr; 37(2):229-239. PubMed ID: 30850045
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  • 15. Molecular analysis of a uterine broad ligament leiomyoma in a patient with CLOVES syndrome.
    Karpathiou G, Chauleur C, Picot T, Peoc'h M.
    Pathol Res Pract; 2020 Dec; 216(12):153285. PubMed ID: 33190013
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  • 18. Proteus Syndrome: Case Report with Anatomopathological Correlation.
    Arredondo Montero J, Bronte Anaut M, López-Gutiérrez JC.
    Fetal Pediatr Pathol; 2022 Oct; 41(5):861-864. PubMed ID: 34668833
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  • 19. Recent advances in the study of somatic mosaicism and diseases other than cancer.
    Erickson RP.
    Curr Opin Genet Dev; 2014 Jun; 26():73-8. PubMed ID: 25050467
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  • 20. Somatic frameshift mutation in PIK3CA causes CLOVES syndrome by provoking PI3K/AKT/mTOR pathway.
    Yan W, Zhang B, Wang H, Mo R, Jiang X, Qin W, Ma L, Lin Z.
    Hereditas; 2021 Jun 01; 158(1):18. PubMed ID: 34074347
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