Results 111 to 120 of about 4,068 (202)

Novel mutation in PTCH1 gene in a patient with basal cell nevus syndrome and uterus bicornis. [PDF]

An Bras Dermatol, 2019
Miyashiro D, Torezan LA, Grinblat BM, Festa Neto C.   +3 more
europepmc   +1 more source

Epidermal nevus syndrome: epithelial and cutaneous tumours without systemic disorders: a case report

, 2013
Epidermal nevus syndrome (ENS) is a rare disease characterized by the association of epidermal nevi with abnormalities in other organs and districts affecting prevalently pediatric patients1.
Favia G, LO MUZIO, LORENZO, Muzio LL, Di Leva AP, Paderni C, Santarelli A, FAVIA, Gianfranco   +6 more
core  

Basal Cell Nevus Syndrome Treated With Laser Therapy: Novel Approach for Young Adults. [PDF]

Int J Dermatol
Briatico G, Scharf C, Di Brizzi EV, Brancaccio G, Drmac N.   +4 more
europepmc   +1 more source

Alteration in DNA replication in inirradiated basal cell nevus syndrome fibroblasts and effect of ionizing radiation.

, 1989
Analysis of DNA fiber autoradiograms from basal cell nevus syndrome (BCNS) skin fibroblasts has revealed for the first time a new defect in DNA replication earlier unknown in other chromosomal instability syndromes, that involves a significantly ...
Bil'din NV, Pleskach N, Barenfeld LS, Mikhelson VM, NERGADZE, SOLOMON, Andreeva LF   +5 more
core  

A novel PTCH1 mutation in basal cell nevus syndrome with rare craniofacial features. [PDF]

Hum Genome Var, 2019
Murata Y, Kurosaka H, Ohata Y, Aikawa T, Takahata S, Fujii K, Miyashita T, Morita C, Inubushi T, Kubota T, Sakai N, Ozono K, Kogo M, Yamashiro T.   +13 more
europepmc   +1 more source

Acquisition of Drug Resistance in Basal Cell Nevus Syndrome Tumors through Basal to Squamous Cell Carcinoma Transition. [PDF]

J Invest Dermatol
Jussila AR, Haensel D, Gaddam S, Oro AE.
europepmc   +1 more source

FURTHER LOCALIZATION OF THE GENE FOR NEVOID BASAL-CELL CARCINOMA SYNDROME (NBCCS) IN 15 AUSTRALASIAN FAMILIES - LINKAGE AND LOSS OF HETEROZYGOSITY

, 1993
Nevoid basal cell carcinoma syndrome (NBCCS; basal cell nevus syndrome or Gorlin syndrome) is a cancer-predisposition syndrome characterized by multiple basal cell carcinomas (BCCs) and diverse developmental defects. The gene for NBCCS has been mapped to
TURNER, A, WAINWRIGHT, B, HOCKEY, A, SHARPE, H, GOLDGAR, D, HAAN, E, SEARLE, J, BERKMAN, J, RAVINE, D, CHENEVIXTRENCH, G, OLEY, C, WICKING, C   +11 more
core  

Basal Cell Nevus Syndrome

Skin research, 1975
F, Kern, G W, Hambrick
openaire   +3 more sources

Basal cell nevus syndrome (Gorlin-Goltz syndrome): genetic predisposition, clinical picture and treatment. [PDF]

Postepy Dermatol Alergol, 2017
Witmanowski H, Szychta P, Błochowiak K, Jundziłł A, Czajkowski R.   +4 more
europepmc   +1 more source

Extensive Mandibular Odontogenic Keratocysts Associated with Basal Cell Nevus Syndrome Treated with Carnoy's Solution versus Marsupialization.

Ann Maxillofac Surg, 2020
Abdoola I, Munzhelele IT, Ibrahim M.
europepmc   +1 more source