138 related articles for article (PubMed ID: 36376059)
1. Report of a case of RAVEN, hair heterochromia and autism in the setting of FGFR2 mutation.
Gracia-Darder I; Llull Ramos A; Giacaman A; Gómez Bellvert C; Obrador-Hevia A; Jubert Esteve E; Martín-Santiago A
Pediatr Dermatol; 2023 Mar; 40(2):382-384. PubMed ID: 36376059
[TBL] [Abstract][Full Text] [Related]
2. Cerebriform sebaceous nevus: a subtype of organoid nevus due to specific postzygotic FGFR2 mutations.
Theiler M; Weibel L; Christen-Zaech S; Carmignac V; Sorlin A; Neuhaus K; Chevarin M; Thauvin-Robinet C; Philippe C; Faivre L; Vabres P; Kuentz P
J Eur Acad Dermatol Venereol; 2021 Oct; 35(10):2085-2090. PubMed ID: 33930231
[TBL] [Abstract][Full Text] [Related]
3. Naevoid acanthosis nigricans or RAVEN (rounded and velvety epidermal naevus) and mosaic FGFR3 and FGFR2 mutations.
Bessis D; Petit A; Battistella M; Bourrat E; Girard C; Pallure V; Marque M; Lacour JP; Vitetta A; Bieth É; Selves J; Solassol J; Vendrell J
Br J Dermatol; 2019 Apr; 180(4):955-957. PubMed ID: 30580445
[No Abstract] [Full Text] [Related]
4. Mosaic-activating FGFR2 mutation in two fetuses with papillomatous pedunculated sebaceous naevus.
Kuentz P; Fraitag S; Gonzales M; Dhombres F; St-Onge J; Duffourd Y; Joyé N; Jouannic JM; Picard A; Marle N; Thevenon J; Thauvin-Robinet C; Faivre L; Rivière JB; Vabres P
Br J Dermatol; 2017 Jan; 176(1):204-208. PubMed ID: 27095246
[TBL] [Abstract][Full Text] [Related]
5. Mosaic mutations in FGFR3 and FGFR2 are associated with naevoid acanthosis nigricans or RAVEN (round and velvety epidermal naevus).
Larsabal M; Cogrel O; Caumont C; Jegou MH; Taïeb A; Morice-Picard F
Br J Dermatol; 2019 Jan; 180(1):201-202. PubMed ID: 30117157
[No Abstract] [Full Text] [Related]
6. [Nevoid acanthosis nigricans or RAVEN (rounded and velvety epidermal nevus): three cases].
Petit A; Lemarchand-Venencie F; Pinquier L; Lebbe C; Bourrat E
Ann Dermatol Venereol; 2012 Mar; 139(3):183-8. PubMed ID: 22401682
[TBL] [Abstract][Full Text] [Related]
7. Linear keratinocytic epidermal nevi on trunk skin caused by a somatic FGFR2 p.C382R mutation.
Tanaka R; Umegaki-Arao N; Sasaki T; Aoki S; Yoshida K; Niizeki H; Kubo A
J Dermatol; 2018 Nov; 45(11):e302-e303. PubMed ID: 29701304
[No Abstract] [Full Text] [Related]
8. Novel postzygotic KRAS mutation in a Japanese case of epidermal nevus syndrome presenting with two distinct clinical features, keratinocytic epidermal nevi and sebaceous nevi.
Igawa S; Honma M; Minami-Hori M; Tsuchida E; Iizuka H; Ishida-Yamamoto A
J Dermatol; 2016 Jan; 43(1):103-4. PubMed ID: 26498739
[No Abstract] [Full Text] [Related]
9. Somatic Embryonic FGFR2 Mutations in Keratinocytic Epidermal Nevi.
Toll A; Fernández LC; Pons T; Groesser L; Sagrera A; Carrillo-de Santa Pau E; Vicente A; Baselga E; Vázquez M; Beltrán S; Pisano DG; Rueda D; Gut M; Pujol RM; Hafner C; Gut I; Valencia A; Real FX
J Invest Dermatol; 2016 Aug; 136(8):1718-1721. PubMed ID: 27103312
[No Abstract] [Full Text] [Related]
10. Expansion of the complex genotypic and phenotypic spectrum of FGFR2-associated neurocutaneous syndromes.
Schmidt J; Kaulfuß S; Ott H; Gaubert M; Reintjes N; Bremmer F; Dreha-Kulaczewski S; Stroebel P; Yigit G; Wollnik B
Hum Genet; 2024 Feb; 143(2):159-168. PubMed ID: 38265560
[TBL] [Abstract][Full Text] [Related]
11. Epidermal nevi.
Brandling-Bennett HA; Morel KD
Pediatr Clin North Am; 2010 Oct; 57(5):1177-98. PubMed ID: 20888465
[TBL] [Abstract][Full Text] [Related]
12. Analysis of mutations in the PIK3CA and FGFR3 genes in verrucous epidermal nevus.
Miranda LQ; Fracaroli TS; Fonseca JC; Fontenelle E; Curvo RP; Porto LC; Souto R
An Bras Dermatol; 2013; 88(6 Suppl 1):36-8. PubMed ID: 24346875
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. The spectrum of epidermal nevi: a case of verrucous epidermal nevus contiguous with nevus sebaceus.
Waltz KM; Helm KF; Billingsley EM
Pediatr Dermatol; 1999; 16(3):211-3. PubMed ID: 10383778
[TBL] [Abstract][Full Text] [Related]
15. Wooly hair nevus.
Fernandes KAP; Fernandes KAP; Vargas TJS; Melo DF
An Bras Dermatol; 2017; 92(5 Suppl 1):163-165. PubMed ID: 29267480
[TBL] [Abstract][Full Text] [Related]
16. Pedunculated lesion of the scalp with surrounding long, dark hair in a newborn. Nevus sebaceus of Jadassohn with the hair collar sign.
Hernández-Núñez A; Nájera L; Martínez-Sánchez D; Meseguer C; Espinosa P; Borbujo J
Pediatr Dermatol; 2010; 27(5):525-6. PubMed ID: 21182643
[No Abstract] [Full Text] [Related]
17. The group of epidermal nevus syndromes Part I. Well defined phenotypes.
Happle R
J Am Acad Dermatol; 2010 Jul; 63(1):1-22; quiz 23-4. PubMed ID: 20542174
[TBL] [Abstract][Full Text] [Related]
18. Identification of a novel S249C FGFR3 mutation in a keratinocytic epidermal naevus syndrome.
Ousager LB; Bygum A; Hafner C
Br J Dermatol; 2012 Jul; 167(1):202-4. PubMed ID: 22229528
[No Abstract] [Full Text] [Related]
19. Epidermal nevus syndromes.
Sugarman JL
Semin Cutan Med Surg; 2007 Dec; 26(4):221-30. PubMed ID: 18395670
[TBL] [Abstract][Full Text] [Related]
20. Differential effects of FGFR2 mutation in ophthalmic findings in Apert syndrome.
Khong JJ; Anderson PJ; Hammerton M; Roscioli T; Selva D; David DJ
J Craniofac Surg; 2007 Jan; 18(1):39-42. PubMed ID: 17251833
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
