Disease: Nevoid basal cell carcinoma syndrome
- (18)F-FDG PET/CT findings in nevoid basal cell carcinoma syndrome: a systematic review and a new case report
- <sup>18</sup>F-FDG PET/CT and Whole-Body Bone Scan Findings in Gorlin-Goltz Syndrome
- A case of multiple basal cell carcinomas in an immunocompromised skin district: The aetiopathogenetic role of congenital lymphqedema
- A nonsense mutation in SUFU associated with multiple infundibulocystic basal cell carcinomas
- A novel de novo canonical splice site mutation in the PTCH1 gene in a male patient with mild psychomotor retardation and autistic traits: a case report
- A recurrence odontogenic keratocyst formation of mandible with distinctive features: a case report
- A Variant of Gorlin-Goltz Syndrome with Synchronous Malignant and Multiple Benign Lesions of the Jaws - A Case Report
- Acquisition of drug resistance in basal cell nevus syndrome tumors through basal to squamous cell carcinoma transition
- Acquisition of Drug Resistance in Basal Cell Nevus Syndrome Tumors through Basal to Squamous Cell Carcinoma Transition
- An Easily Missed But Life-Threatening Diagnosis: A Case Report of Gorlin Syndrome
- An Institutional Experience of a Tertiary Referral Center in Surgically Managing Patients With Gorlin Syndrome
- Basal cell nevus syndrome: the interface between dentistry and dermatology
- Basaloid follicular hamartoma syndrome: acquired sporadic variant with hypothyroidism, hypohidrosis and alopecia, a rare case
- Basaloid Follicular Hamartoma: A Histologic Clue for Diagnosis of Nevoid Basal Cell Carcinoma Syndrome
- Bilateral ovarian fibromas as the sole manifestation of Gorlin syndrome in a 22-year-old woman: a case report and literature review
- Cardiac Fibroma
- Cardiac Fibroma
- Case report: A novel PTCH1 frameshift mutation leading to nevoid basal cell carcinoma syndrome
- Comparison of the effectiveness of 5-Fluorouracil and modified Carnoy's solution in reducing the recurrence of odontogenic keratocyst
- Concurrent medulloblastoma and cardiac fibroma: a rare presentation of Gorlin-Goltz syndrome
- Conservative management of multiple odontogenic keratocysts in a child with nevoid basal cell carcinoma syndrome: A case report
- Depicting dermoscopic and confocal findings in patients with Gorlin-Goltz Syndrome
- Detection of PTCH1 Copy-Number Variants in Mosaic Basal Cell Nevus Syndrome
- Developing expert consensus for the use of hedgehog inhibitors in basal cell nevus syndrome
- Digital pathology-based artificial intelligence models for differential diagnosis and prognosis of sporadic odontogenic keratocysts
- Efficacy, tolerability, and quality of life evaluation in six patients affected by Gorlin-Goltz syndrome and treated with vismodegib 150 mg/die: a retrospective monocentric cohort analysis
- Establishment of induced pluripotent stem cells derived from patients and healthy siblings of a nevoid basal cell carcinoma syndrome family
- Exploring the Changing Diagnostic Criteria of Gorlin-Goltz Syndrome: A Case Report
- Factors and management techniques in odontogenic keratocysts: a systematic review
- Frameshift mutation in exon 17 of PTCH1 gene in Nevoid basal cell carcinoma syndrome: A case report
- Further Expanding the Mutational Spectrum of Gorlin Syndrome in Three Unrelated Families
- Gorlin Syndrome
- Gorlin Syndrome-Associated Basal Cell Carcinomas Treated with Vismodegib or Sonidegib: A Retrospective Study
- Gorlin-Goltz Syndrome - A Rare Case Entity in Young Child
- Gorlin-Goltz Syndrome: A Case Report and Literature Review with <em>PTCH1</em> Gene Sequencing
- Gorlin-Like Phenotype in a Young Girl With a De Novo PTCH2 Variant Mutation of Uncertain Significance
- Halo Phenomenon in Lobular Capillary Hemangioma: A Case Report of a Pyogenic Granuloma With Surrounding Cutaneous Hypopigmentation and Review of Tumors With Halo Phenomenon
- Hedgehog-Related Mutation Causes Bone Malformations with or without Hereditary Gene Mutations
- Imaging approaches for the diagnosis of genetic diseases affecting the female reproductive organs and beyond
- Incidental cardiac fibroma as first manifestation of naevoid basal cell carcinoma syndrome
- Interpretation on genetic tumour syndromes in the 5th WHO classification of paediatric tumours: part Ⅱ
- Medulloblastoma and other neoplasms in patients with heterozygous germline SUFU variants: A scoping review
- Minimally Invasive Plasma Device Management of Multiple Benign Skin Cancers Associated with Rare Genodermatoses-Case Series and Review of the Therapeutic Methods
- Mosaic SUFU mutation associated with a mild phenotype of multiple hereditary infundibulocystic basal cell carcinoma syndrome
- Mutations of <em>PTCH1</em> gene in two pedigrees with bifid rib-basal cell nevus-jaw cyst syndrome
- Neoadjuvant photodynamic therapy as a therapeutic alternative in multiple basal cell carcinoma induced by radiotherapy
- Nevoid basal cell carcinoma (Gorlin-Goltz) syndrome: an incidental finding
- Nevoid Basal Cell Carcinoma Syndrome
- Nevoid basal cell carcinoma syndrome with anophthalmia: a case report
- Nonsense-Mutation in SUFU ist mit multiplen infundibulozystischen Basalzellkarzinomen assoziiert: A nonsense mutation in SUFU associated with multiple infundibulocystic basal cell carcinomas
- Novel PTCH1 Mutation Causes Gorlin-Goltz Syndrome
- Odontogenic keratocysts: A retrospective histopathological study
- Oral smoothened inhibitors for Gorlin syndrome: A clinical review
- Pediatric odontogenic keratocyst and early diagnosis of Gorlin syndrome: Clinicopathological aids
- Performance of the eHealth decision support tool, MIPOGG, for recognising children with Li-Fraumeni, DICER1, Constitutional mismatch repair deficiency and Gorlin syndromes
- Radiological evaluation of odontogenic keratocysts in patients with nevoid basal cell carcinoma syndrome: A review
- Recurrence Patterns of Odontogenic Keratocysts in Syndromic and Non-Syndromic Patients
- Recurrent central odontogenic fibroma in a patient with nevoid basal cell carcinoma syndrome: case report and in vitro analysis
- Sebaceous Hyperplasia
- Sebaceous Hyperplasia
- Siblings with Gorlin-Goltz syndrome associated with cardiac tumors: a case report and review of literature
- Surveillance of a large cardiac fibroma in a patient with Gorlin syndrome
- Sustained Suppression of Gorlin Syndrome-Associated Basal Cell Carcinomas with Vismodegib or Sonidegib: A Case Series
- Targeted intradermal delivery of alpha-arbutin-loaded dissolving polymeric microneedles visualized by three-dimensional Orbitrap secondary ion mass spectrometry (3D OrbiSIMS)
- The role of the dentist and the orthodontist in early diagnosis of Gorlin-Goltz syndrome: a cephalometric and photometric study
- Tolerance of sonidegib after intolerance of vismodegib-Experience in two patients with nevoid basal cell carcinoma syndrome (Gorlin syndrome)
- Trichilemmoma
- Understanding Nevoid Basal Cell Carcinoma Syndrome (Gorlin Syndrome): A Case Report
- Update on Cancer Predisposition Syndromes and Surveillance Guidelines for Childhood Brain Tumors
- Vismodegib in Gorlin-Goltz syndrome: A systematic review
- Whole-Exome Sequencing Identified Two Novel Pathogenic Mutations in the <em>PTCH1</em> Gene in BCNS