98 related articles for article (PubMed ID: 22434048)
1. Splicing aberration in naevoid basal cell carcinoma syndrome.
Ishitsuka Y; Furuta J; Miyashita T; Otsuka F
Acta Derm Venereol; 2012 Nov; 92(6):619-20. PubMed ID: 22434048
[No Abstract] [Full Text] [Related]
2. A Japanese case of naevoid basal cell carcinoma syndrome associated with segmental vitiligo.
Muramatsu S; Suga Y; Mizuno Y; Haseegawa T; Komuro Y; Kubo Y; Imakado S; Ogawa H
Br J Dermatol; 2005 Apr; 152(4):812-4. PubMed ID: 15840128
[No Abstract] [Full Text] [Related]
3. Palmar pits associated with the nevoid basal cell carcinoma syndrome.
North JP; McCalmont TH; LeBoit P
J Cutan Pathol; 2012 Aug; 39(8):735-8. PubMed ID: 22845656
[No Abstract] [Full Text] [Related]
4. Naevoid basal cell carcinoma syndrome in a 22-month-old child presenting with multiple basal cell carcinomas and a fetal rhabdomyoma.
Diociaiuti A; Inserra A; De Vega IF; Rota C; Surrenti T; Giraldi L; Piemontese MR; Giovannoni I; Callea F; El Hachem M
Acta Derm Venereol; 2015 Feb; 95(2):243-4. PubMed ID: 24816767
[No Abstract] [Full Text] [Related]
5. Variable expression of naevoid basal cell carcinoma syndrome in a family with a novel mutation in the PTCH1 gene.
Alonso-González J; Gutiérrez-González E; Fernández-Redondo V; Vega-Gliemmo A; Toribio J
Clin Exp Dermatol; 2012 Apr; 37(3):311-3. PubMed ID: 22007994
[No Abstract] [Full Text] [Related]
6. A novel germ-line mutation of PTCH1 gene in a Japanese family of nevoid basal cell carcinoma syndrome: are the palmoplantar pits associated with true basal cell carcinoma?
Otsubo S; Honma M; Asano K; Takahashi H; Iizuka H
J Dermatol Sci; 2008 Aug; 51(2):144-6. PubMed ID: 18436435
[No Abstract] [Full Text] [Related]
7. The dermoscopy of Gorlin syndrome: pursuit of the pits revisited.
Jarrett R; Walker L; Bowling J
Arch Dermatol; 2010 May; 146(5):582. PubMed ID: 20479325
[No Abstract] [Full Text] [Related]
8. Identification of mutations in the human PATCHED gene in sporadic basal cell carcinomas and in patients with the basal cell nevus syndrome.
Aszterbaum M; Rothman A; Johnson RL; Fisher M; Xie J; Bonifas JM; Zhang X; Scott MP; Epstein EH
J Invest Dermatol; 1998 Jun; 110(6):885-8. PubMed ID: 9620294
[TBL] [Abstract][Full Text] [Related]
9. A novel PTCH1 mutation in a patient of nevoid basal cell carcinoma syndrome.
Honma M; Ohishi Y; Uehara J; Ibe M; Kinouchi M; Ishida-Yamamoto A; Iizuka H
J Dermatol Sci; 2008 Apr; 50(1):73-5. PubMed ID: 18068337
[No Abstract] [Full Text] [Related]
10. Nevoid basal cell carcinoma (Gorlin) syndrome: unanswered issues.
Gorlin RJ
J Lab Clin Med; 1999 Dec; 134(6):551-2. PubMed ID: 10595780
[No Abstract] [Full Text] [Related]
11. Early-onset acral basal cell carcinomas in Gorlin syndrome.
Torrelo A; Vicente A; Navarro L; Planaguma M; Bueno E; González-Sarmiento R; Hernández-Martín A; Noguera-Morel L; Requena L; Colmenero I; Parareda A; González-Enseñat MA; Happle R
Br J Dermatol; 2014 Nov; 171(5):1227-9. PubMed ID: 24837096
[TBL] [Abstract][Full Text] [Related]
12. A novel missense mutation in the PTCH1 gene in a premature case of nevoid basal cell carcinoma syndrome.
Nakamura M; Tokura Y
Eur J Dermatol; 2009; 19(3):262-3. PubMed ID: 19213655
[No Abstract] [Full Text] [Related]
13. Late onset of cardiac tumour in naevoid Basal cell carcinoma (Gorlin) syndrome.
Kluger N; Marco-Baertich I; Guillot B
Acta Derm Venereol; 2007; 87(3):272-3. PubMed ID: 17533500
[No Abstract] [Full Text] [Related]
14. Novel mutation in the PTCH1 gene in a patient with Gorlin syndrome with prominent clinical features.
Valdivielso-Ramos M; Solera J; Mauleon C; Hernanz JM; Amiñoso C; Galiano S; De la Cueva P
Clin Exp Dermatol; 2014 Apr; 39(3):406-7. PubMed ID: 24635088
[No Abstract] [Full Text] [Related]
15. [Dermal fibroblasts exert a key influence in the development of basal-cell skin cancers: the model of Gorlin syndrome].
Valin A; Avril MF; Magnaldo T
Med Sci (Paris); 2010 Jan; 26(1):22-5. PubMed ID: 20132767
[No Abstract] [Full Text] [Related]
16. [Neonatal Gorlin syndrome associated to hemimegalencephaly confirmed by genetic study].
García-Oguiza A; Miralbés-Terraza S; Calvo-Martín M; Labarta-Aizpun J; López-Pisón J; Marco-Tello A; Rebage V
Rev Neurol; 2006 Aug 16-31; 43(4):251-2. PubMed ID: 16883514
[No Abstract] [Full Text] [Related]
17. Coincident two mutations and one single nucleotide polymorphism of the PTCH1 gene in a family with naevoid basal cell carcinoma syndrome.
Abe S; Kabashima K; Sakabe J; Shimauchi T; Yan Z; Okamoto T; Tokura Y
Acta Derm Venereol; 2008; 88(6):635-6. PubMed ID: 19002359
[No Abstract] [Full Text] [Related]
18. Merkel cell polyomavirus in naevoid basal cell carcinoma syndrome-associated basal cell carcinomas and sporadic trichoblastomas.
Kassem A; Pantulu D; Technau K; Kurz AK; Diaz C; Hörster S; Nashan D; Weyers W; Zur Hausen A
J Dermatol Sci; 2010 Aug; 59(2):140-2. PubMed ID: 20654786
[No Abstract] [Full Text] [Related]
19. Nevoid basal carcinoma syndrome (Gorlin syndrome) and pronounced androgenic alopecia in a woman with a novel mutation p.Leu1159fsx32 in the PTCH gene.
Kitsiou-Tzeli S; Willems P; Kosmadaki M; Leze E; Vrettou C; Kanavakis E; Katsarou A
J Dermatol; 2011 Dec; 38(12):1205-8. PubMed ID: 21950490
[No Abstract] [Full Text] [Related]
20. Unexpected manifestation of naevoid basal cell carcinoma (Gorlin) syndrome with a novel mutation in the PTCH1 gene in a female patient with long-lasting pemphigus vulgaris.
Goetze S; Raessler F; Hipler UC; Schulz S; Kohlhase J; Elsner P
J Eur Acad Dermatol Venereol; 2016 Mar; 30(3):493-4. PubMed ID: 25600101
[No Abstract] [Full Text] [Related]
[Next] [New Search]
