179 related articles for article (PubMed ID: 32662096)
1. Keratinocytic epidermal nevi associated with localized fibro-osseous lesions without hypophosphatemia.
Mestach L; Polubothu S; Calder A; Denayer E; Gholam K; Legius E; Levtchenko E; Van Laethem A; Brems H; Kinsler VA; Morren MA
Pediatr Dermatol; 2020 Sep; 37(5):890-895. PubMed ID: 32662096
[TBL] [Abstract][Full Text] [Related]
2. Postzygotic HRAS mutation causing both keratinocytic epidermal nevus and thymoma and associated with bone dysplasia and hypophosphatemia due to elevated FGF23.
Avitan-Hersh E; Tatur S; Indelman M; Gepstein V; Shreter R; Hershkovitz D; Brick R; Bergman R; Tiosano D
J Clin Endocrinol Metab; 2014 Jan; 99(1):E132-6. PubMed ID: 24243633
[TBL] [Abstract][Full Text] [Related]
3. Keratinocytic epidermal nevi are associated with mosaic RAS mutations.
Hafner C; Toll A; Gantner S; Mauerer A; Lurkin I; Acquadro F; Fernández-Casado A; Zwarthoff EC; Dietmaier W; Baselga E; Parera E; Vicente A; Casanova A; Cigudosa J; Mentzel T; Pujol RM; Landthaler M; Real FX
J Med Genet; 2012 Apr; 49(4):249-53. PubMed ID: 22499344
[TBL] [Abstract][Full Text] [Related]
4. Cutaneous skeletal hypophosphatemia syndrome: clinical spectrum, natural history, and treatment.
Ovejero D; Lim YH; Boyce AM; Gafni RI; McCarthy E; Nguyen TA; Eichenfield LF; DeKlotz CM; Guthrie LC; Tosi LL; Thornton PS; Choate KA; Collins MT
Osteoporos Int; 2016 Dec; 27(12):3615-3626. PubMed ID: 27497815
[TBL] [Abstract][Full Text] [Related]
5. Murine models of HRAS-mediated cutaneous skeletal hypophosphatemia syndrome suggest bone as the FGF23 excess source.
Ovejero D; Michel Z; Cataisson C; Saikali A; Galisteo R; Yuspa SH; Collins MT; de Castro LF
J Clin Invest; 2023 May; 133(9):. PubMed ID: 36943390
[TBL] [Abstract][Full Text] [Related]
6. Multilineage somatic activating mutations in HRAS and NRAS cause mosaic cutaneous and skeletal lesions, elevated FGF23 and hypophosphatemia.
Lim YH; Ovejero D; Sugarman JS; Deklotz CM; Maruri A; Eichenfield LF; Kelley PK; Jüppner H; Gottschalk M; Tifft CJ; Gafni RI; Boyce AM; Cowen EW; Bhattacharyya N; Guthrie LC; Gahl WA; Golas G; Loring EC; Overton JD; Mane SM; Lifton RP; Levy ML; Collins MT; Choate KA
Hum Mol Genet; 2014 Jan; 23(2):397-407. PubMed ID: 24006476
[TBL] [Abstract][Full Text] [Related]
7. Cutaneous skeletal hypophosphatemia syndrome (CSHS) is a multilineage somatic mosaic RASopathy.
Lim YH; Ovejero D; Derrick KM; ; Collins MT; Choate KA
J Am Acad Dermatol; 2016 Aug; 75(2):420-7. PubMed ID: 27444071
[TBL] [Abstract][Full Text] [Related]
8. Epidermal nevus syndromes: New insights into whorls and swirls.
Asch S; Sugarman JL
Pediatr Dermatol; 2018 Jan; 35(1):21-29. PubMed ID: 29044700
[TBL] [Abstract][Full Text] [Related]
9. Mosaic RASopathies concept: different skin lesions, same systemic manifestations?
Morren MA; Fodstad H; Brems H; Bedoni N; Guenova E; Jacot-Guillarmod M; Busiah K; Giuliano F; Gilliet M; Atallah I
J Med Genet; 2024 Apr; 61(5):411-419. PubMed ID: 38290824
[TBL] [Abstract][Full Text] [Related]
10. Epidermal Nevi and Related Syndromes -- Part 1: Keratinocytic Nevi.
Garcias-Ladaria J; Cuadrado Rosón M; Pascual-López M
Actas Dermosifiliogr (Engl Ed); 2018 Oct; 109(8):677-686. PubMed ID: 29983155
[TBL] [Abstract][Full Text] [Related]
11. Phacomatosis spilosebacea: A new name for a distinctive binary genodermatosis.
Torchia D; Happle R
J Am Acad Dermatol; 2023 Oct; 89(4):764-773. PubMed ID: 33583608
[TBL] [Abstract][Full Text] [Related]
12. HRAS-related epidermal nevus syndromes: Expansion of the spectrum with first branchial arch defects.
Beyens A; Lietaer C; Claes K; De Baere E; Goeteyn M; Lerut B; Syryn H; Vanakker O; Van der Meulen J; Vanwalleghem L; Callewaert B
Clin Genet; 2023 Jun; 103(6):709-713. PubMed ID: 36896710
[TBL] [Abstract][Full Text] [Related]
13. Phenotype/genotype correlations in epidermal nevus syndrome as a neurocristopathy.
Flores-Sarnat L; Sarnat HB
Handb Clin Neurol; 2015; 132():9-25. PubMed ID: 26564069
[TBL] [Abstract][Full Text] [Related]
14. Papular nevus spilus syndrome: old and new aspects of a mosaic RASopathy.
Torchia D; Happle R
Eur J Dermatol; 2019 Feb; 29(1):2-5. PubMed ID: 30827948
[TBL] [Abstract][Full Text] [Related]
15. Cutaneous Skeletal Hypophosphatemia Syndrome in Association with a Mosaic
Park PG; Park E; Hyun HS; Kang HG; Ha IS; Cho TJ; Ko JM; Cheong HI
Ann Clin Lab Sci; 2018 Sep; 48(5):665-669. PubMed ID: 30373874
[TBL] [Abstract][Full Text] [Related]
16. Molecular characterisation of oncogenic urothelial mosaic mutations in patients with extensive keratinocytic epidermal naevi.
Gadea A; Hernández-Muñoz I; Vicente A; Andrades E; García-Calvente M; Camacho L; Fernandez-Rodríguez C; Bellosillo B; Pujol R; Toll A
J Med Genet; 2020 Sep; 57(9):601-604. PubMed ID: 31937562
[No Abstract] [Full Text] [Related]
17. Epidermal nevus syndrome with hypophosphatemic rickets in a young girl.
Sukkhojaiwaratkul D; Mahachoklertwattana P; Poomthavorn P
J Paediatr Child Health; 2014 Jul; 50(7):566-9. PubMed ID: 24372733
[TBL] [Abstract][Full Text] [Related]
18. Successful treatment with MEK-inhibitor in a patient with NRAS-related cutaneous skeletal hypophosphatemia syndrome.
Carli D; Cardaropoli S; Tessaris D; Coppo P; La Selva R; Cesario C; Lepri FR; Pullano V; Palumbo M; Ramenghi U; Brusco A; Medico E; De Sanctis L; Ferrero GB; Mussa A
Genes Chromosomes Cancer; 2022 Dec; 61(12):740-746. PubMed ID: 35999193
[TBL] [Abstract][Full Text] [Related]
19. Papular epidermal nevus with "skyline" basal cell layer (PENS) following a Blaschko linear pattern.
Faure E; Tadini G; Brena M; Cassulini LR
Pediatr Dermatol; 2013; 30(6):e270-1. PubMed ID: 23600737
[TBL] [Abstract][Full Text] [Related]
20. Nevus marginatus: a distinct type of epidermal nevus or merely a variant of nevus sebaceus?
Hafner C; Landthaler M; Happle R; Vogt T
Dermatology; 2008; 216(3):236-8. PubMed ID: 18182817
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]