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Items: 1 to 20 of 1041

1.

Nonhealing eroded plaque on an interdigital web space of the foot.

Stasko T, Levin J, Nguyen N, Dawson N, Crowson AN.

Cutis. 2019 Jan;103(1):8; 14; 15. No abstract available.

PMID:
30758337
2.

Imaging features of uterine and ovarian fibromatosis in Nevoid Basal Cell Carcinoma Syndrome.

Scalia AC, Farulla A, Fiocchi F, Alboni C, Torricelli P.

J Radiol Case Rep. 2018 Sep 30;12(9):21-30. doi: 10.3941/jrcr.v12i9.3390. eCollection 2018 Sep.

3.

An Update of Gorlin-Goltz Syndrome.

Hasan A, Akintola D.

Prim Dent J. 2018 Sep 1;7(3):38-41.

PMID:
30428966
4.

Whole-exome sequencing of nevoid basal cell carcinoma syndrome families and review of Human Gene Mutation Database PTCH1 mutation data.

Gianferante DM, Rotunno M, Dean M, Zhou W, Hicks BD, Wyatt K, Jones K, Wang M, Zhu B, Goldstein AM, Mirabello L.

Mol Genet Genomic Med. 2018 Nov;6(6):1168-1180. doi: 10.1002/mgg3.498. Epub 2018 Nov 8.

5.

Programmed death-1 blockade for multiple basal cell carcinomas: clearing the field systemically?

Haug V, Schilling B.

Br J Dermatol. 2018 Sep;179(3):566-567. doi: 10.1111/bjd.16991. No abstract available.

PMID:
30222888
6.

Severe PATCHED1 Deficiency in Cancer-Prone Gorlin Patient Cells Results in Intrinsic Radiosensitivity.

Vulin A, Sedkaoui M, Moratille S, Sevenet N, Soularue P, Rigaud O, Guibbal L, Dulong J, Jeggo P, Deleuze JF, Lamartine J, Martin MT.

Int J Radiat Oncol Biol Phys. 2018 Oct 1;102(2):417-425. doi: 10.1016/j.ijrobp.2018.05.057. Epub 2018 Jun 2.

7.

Generalized basaloid follicular hamartoma syndrome versus Gorlin syndrome: A diagnostic challenge.

Shevchenko A, Durkin JR, Moon AT.

Pediatr Dermatol. 2018 Nov;35(6):e396-e397. doi: 10.1111/pde.13614. Epub 2018 Aug 28.

PMID:
30152544
8.

Gorlin-Goltz syndrome: a case series from north Italy.

Veronese F, Miglino B, Boggio P, Tiberio R, Zavattaro E, Colombo E, Savoia P.

Eur J Dermatol. 2018 Oct 1;28(5):687-688. doi: 10.1684/ejd.2018.3338. No abstract available.

PMID:
30129523
9.

Multiple Odontogenic Cysts and Intracranial Calcification: Gorlin-Goltz Syndrome.

Mo X, Zhang S.

Radiology. 2018 Oct;289(1):29. doi: 10.1148/radiol.2018180876. Epub 2018 Aug 14. No abstract available.

PMID:
30106350
10.

PTCH1 isoform 1b is the major transcript in the development of basal cell nevus syndrome.

Gielen RCAM, Reinders MGHC, Koillinen HK, Paulussen ADC, Mosterd K, van Geel M.

J Hum Genet. 2018 Sep;63(9):965-969. doi: 10.1038/s10038-018-0485-0. Epub 2018 Jun 21.

PMID:
29930296
11.

Gorlin-Goltz syndrome: first reported case of bullae in the lungs complicated with tension pneumothorax.

Yap D.

BMJ Case Rep. 2018 Jun 20;2018. pii: bcr-2017-223689. doi: 10.1136/bcr-2017-223689.

PMID:
29930167
12.

Supraclavicular Dermo-Muscular Agenesis in an Infant With Gorlin-Goltz Syndrome.

Demir CY, Kocak OF.

J Craniofac Surg. 2018 Oct;29(7):e654-e656. doi: 10.1097/SCS.0000000000004667.

PMID:
29894462
13.

Rhabdomyosarcoma and rhabdomyoma associated with nevoid basal cell carcinoma syndrome: Local treatment strategy.

Kerbrat A, Beaufrere A, Neiva-Vaz C, Galmiche L, Belhous K, Orbach D, Gauthier-Villars M, Picard A, Kadlub N.

Pediatr Dermatol. 2018 Jul;35(4):e245-e247. doi: 10.1111/pde.13536. Epub 2018 May 25.

PMID:
29799139
14.

Cells to Surgery Quiz: May 2018.

Mudigonda T, Dietert JB, Hurst EA.

J Invest Dermatol. 2018 May;138(5):e41. doi: 10.1016/j.jid.2018.03.1512. No abstract available.

PMID:
29681392
15.

Illuminating Alternative Strategies to Treat Targeted Chemotherapy-Resistant Sporadic Basal Cell Carcinoma.

Nguyen TTL, Atwood SX.

J Invest Dermatol. 2018 May;138(5):1017-1019. doi: 10.1016/j.jid.2017.11.013.

PMID:
29681387
16.

Odontogenic Keratocysts as First Manifestation of Nevoid Basal Cell Carcinoma Syndrome: Surgical Management and Immunohistochemical Analysis.

Dos Santos JL, Delgado RZR, de Oliveira GR, Rangel ALCA.

J Craniofac Surg. 2018 Sep;29(6):1588-1590. doi: 10.1097/SCS.0000000000004564.

PMID:
29621081
17.

Immunohistochemical evaluation of Sonic Hedgehog signaling pathway proteins (Shh, Ptch1, Ptch2, Smo, Gli1, Gli2, and Gli3) in sporadic and syndromic odontogenic keratocysts.

Hoyos Cadavid AM, Kaminagakura E, Rodrigues MFSD, Pinto CAL, Teshima THN, Alves FA.

Clin Oral Investig. 2019 Jan;23(1):153-159. doi: 10.1007/s00784-018-2421-2. Epub 2018 Mar 21.

PMID:
29564556
18.

A Novel PTCH1 Frameshift Mutation Leading to Nevoid Basal Cell Carcinoma Syndrome.

Durmaz CD, Evans G, Smith MJ, Ertop P, Akay BN, Tuncalı T.

Cytogenet Genome Res. 2018;154(2):57-61. doi: 10.1159/000487747. Epub 2018 Mar 16.

PMID:
29544218
19.

Delayed Diagnosis of Gorlin-Goltz Syndrome: The Importance of the Multidisciplinary Approach.

Figueira JA, Batista FRS, Rosso K, Veltrini VC, Pavan AJ.

J Craniofac Surg. 2018 Sep;29(6):e530-e531. doi: 10.1097/SCS.0000000000004438.

PMID:
29521748
20.

Potential hot spot for de novo mutations in PTCH1 gene in Gorlin syndrome patients: a case report of twins from Croatia.

Musani V, Ozretić P, Trnski D, Sabol M, Poduje S, Tošić M, Šitum M, Levanat S.

Croat Med J. 2018 Feb 28;59(1):20-24.

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