• <em>Son of Sevenless</em>-1 genetic status in an Indian family with nonsyndromic hereditary gingival fibromatosis
• A bird's-eye view of pathologist over diagnostic confusion of oral cavity lesions
• A clinicopathological retrospective epidemiological analysis of benign tumors and tumor-like lesions in the oral and maxillofacial region, diagnosed at the University of Szeged, Department of Oral Medicine (1960-2014)
• A distinctive oral phenotype points to FAM20A mutations not identified by Sanger sequencing
• A novel gene <em>ZNF862</em> causes hereditary gingival fibromatosis
• A novel gene ZNF862 causes hereditary gingival fibromatosis
• Activated KCNQ1 channel promotes fibrogenic response in hereditary gingival fibromatosis via clustering and activation of Ras
• An Unusually Large Irritation Fibroma Associated with Gingiva of Lower Left Posterior Teeth Region
• Anesthetic Management of an Adult Patient With Hyaline Fibromatosis Syndrome Undergoing Laparoscopic Colectomy: A Case Report
• Anti-proliferative impact of resveratrol on gingival fibroblasts from juvenile hyaline fibromatosis
• Antifibrotic Potential of MiR-335-3p in Hereditary Gingival Fibromatosis
• Association of 17q24.2-q24.3 deletions with recognizable phenotype and short telomeres
• Case Report: A Case of Hereditary Gingival Fibromatosis With a High Level of Human beta Defensins in Gingival Epithelium
• Case Report: A Case of Hereditary Gingival Fibromatosis With a High Level of Human β Defensins in Gingival Epithelium
• Central odontogenic fibroma of the mandible: A case report with diagnostic considerations
• Clinical and genetic evaluations of Zimmermann-Laband syndrome with gingival fibromatosis: a rare case report
• Delayed Eruption of Tooth Due to Peripheral Giant-Cell Granuloma: An Unusual Presentation and Treatment in 15-Year-Old Child Patient
• Diagnosis implications of the whole genome sequencing in a large Lebanese family with hyaline fibromatosis syndrome
• Diode laser-assisted management of intraoral soft tissue overgrowth: a case series
• Distribution of biopsied non plaque-induced gingival lesions in a Chilean population according to the classification of periodontal diseases
• Double heterozygous pathogenic mutations in KIF3C and ZNF513 cause hereditary gingival fibromatosis
• Effective Anticoagulation Therapy Prior to Surgical Excision of an Aortic Valve Papillary Fibroelastoma Diagnosed after a Transient Cerebral Ischemic Attack;Report of a Case
• Electro-surgical management of a traumatic fibroma with clinical assessment of re-epithelialization using methylene blue assay: A clinico-histopathological case report
• Enamel renal syndrome: A case report with calcifications in pulp, gingivae, dental follicle and kidneys
• Epidemiology of oral mucosal lesions in Slovenia
• Establishment and characterization of ZJUCHi003: an induced pluripotent stem cell line from a patient with Temple-Baraitser/Zimmermann-Laband syndrome carrying KCNH1 c.1070G &gt; A (p.R357Q) variant
• Evaluation of clinico-pathological reports and recurrence of 20 cases of localized gingival overgrowths
• Ex vivo nonviral gene delivery of μ-opioid receptor to attenuate cancer-induced pain
• Exophytic gingival growth of the maxillary canine region in a young individual: Extremely rare case report of peripheral dentinogenic ghost cell tumor
• Expression of CD163 in hereditary gingival fibromatosis: A possible association with TGF-beta1
• Expression of CD163 in hereditary gingival fibromatosis: A possible association with TGF-β1
• Expression of TGF-beta and MMP-2 in hereditary gingival fibromatosis epithelial cells. A possible contribution of the epithelium to its pathogenesis
• Expression of TGF-β and MMP-2 in hereditary gingival fibromatosis epithelial cells. A possible contribution of the epithelium to its pathogenesis
• Fibro-epithelial polyps in children: A report of two cases with a literature review
• Fibroblasts from recurrent fibrotic overgrowths reveal high rate of proliferation in vitro - findings from the study of hereditary and idiopathic gingival fibromatosis
• Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca²⁺-Activated K⁺ Channel SK3 Cause Zimmermann-Laband Syndrome
• Giant Aggressive Odontogenic Fibroma in a 15-month-old Female: Case Report and Review of Literature
• Gingival enlargement: Practical management
• Gingival Fibroma: An Emerging Distinct Gingival Lesion with Well-Defined Histopathology
• Hereditary gingival fibromatosis in children: a systematic review of the literature
• Hereditary Gingival Fibromatosis: a Case Report with Seven-Year Follow-up
• Hereditary Gingival Fibromatosis: A Report of a Rare Case in Siblings and Its Management Using Diode Laser
• Hereditary Gingival Fibromatosis: A Report of a Severe Case
• Homozygous mutation in ELMO2 may cause Ramon syndrome
• Hyaline fibromatosis syndrome: a case presenting with gingival enlargement as the only clinical manifestation and a report of two new mutations in the ANTXR2 gene
• Hyaline fibromatosis syndrome: a rare, yet recognizable syndrome
• Hypercalcemia as a rare presentation of hyaline fibromatosis syndrome from different Sudanese families: two case reports
• Incidence of reactive hyperplastic lesions in the oral cavity: a 10 year retrospective study in Santa Catarina, Brazil
• Infantile Systemic Hyalinosis: Novel Founder Mutation in the Initiation Codon among "Malis (Farmers)" in Jodhpur
• Juvenile Hyaline Fibromatosis
• Juvenile Hyaline Fibromatosis Management With a Diode Laser: A Rare Case Report
• Loss of epithelial FAM20A in mice causes amelogenesis imperfecta, tooth eruption delay and gingival overgrowth
• Management of Traumatic Fibroma in a Patient with Cerebral Palsy Using 810nm Diode Laser
• Minimally Invasive Excision of Epulides with a CO₂ Laser: A Retrospective Study of 90 Patients
• Modeling RASopathies with Genetically Modified Mouse Models
• New evidence of genetic heterogeneity causing hereditary gingival fibromatosis and ALK and CD36 as new candidate genes
• Nonsyndromic Gingival Fibromatosis: A Rare Case Report
• Nonsyndromic hereditary gingival fibromatosis: Characterization of a family and review of genetic etiology
• Nonsyndromic with Recurrent Idiopathic Gingival Fibromatosis: A Rare Case Report
• Novel <em>REST</em> Truncation Mutations Causing Hereditary Gingival Fibromatosis
• Novel REST Truncation Mutations Causing Hereditary Gingival Fibromatosis
• Odontogenic Fibromyxoma in a Cat: First Confirmed Case in This Species
• Odontogenic myxofibroma of gingiva in a pediatric patient with tuberous sclerosis: A rare case report
• Oral lesions and periodontal status in diabetics and non-diabetics: A hospital based study
• Oral Lesions in Captive Nondomestic Felids With a Focus on Odontogenic Lesions
• Oral Pathology in Portuguese Dogs: An Eight-Year Biopsy-Based Retrospective Study
• Oral Pathology Quiz #91. Case number 3
• Oral Verruciform Xanthoma: A Series of 212 Cases and Review of the Literature
• Ossifying fibroma from surgical excision to periodontal management: case report
• Osteopontin expression and clinicopathologic correlation of oral hyperplastic reactive lesions: An institutional 6-year retrospective study
• Periodontology Part 3: Hereditary Gingival Fibromatosis (HGF): from diagnosis to treatment in the paediatric age
• Peripheral ameloblastic fibroma: a rare case report
• Peripheral Ossifying Fibroma and Peripheral Odontogenic Fibroma: Close Relatives or Family?
• Peripheral Ossifying Fibroma Evolved From Pyogenic Granuloma
• Peripheral ossifying fibroma: A 20-year retrospective study with focus on clinical and morphological features
• Peripheral ossifying fibroma: A rare case affecting maxillary region
• Preserving periodontal tissue in the treatment of a large peripheral ossifying fibroma: a case study
• Prevalence and Distribution of Oral Mucosal Lesions by Sex and Age Categories: A Retrospective Study of Patients Attending Lebanese School of Dentistry
• Prevalence of Histopathologic Types of Gingival Lesions in the Iranian Population: A 22-Year Retrospective Study
• Quandary in Diagnosing Peripheral Ossifying Fibroma and Pyogenic Granuloma: A Case Report with Mini Review
• REST Final-Exon-Truncating Mutations Cause Hereditary Gingival Fibromatosis
• Retrospective study of oral lesions biopsied in babies and toddlers
• Salivary and serum biomarkers of inflammation in a man with metastatic medullary thyroid carcinoma and hyperreactive gingiva: a fourteen year odyssey
• SATB2 Immunoexpression in Peripheral Ossifying Fibroma and Peripheral Odontogenic Fibroma
• SATB2 is frequently expressed in ossifying and non-ossifying peripheral oral fibroma of the gingival region but not in reactive fibromatous lesions from other intraoral sites
• Son of Sevenless-1 genetic status in an Indian family with nonsyndromic hereditary gingival fibromatosis
• Spongiotic hyperplasia of the oral mucosa: case series and immunohistochemical analysis
• Successful management of recurrent irritational fibroma and associated residual soft tissue defect in the posterior teeth through single-stage surgery: A rare case report
• Surgical Treatment of a Peripheral Ossifying Fibroma and Reconstruction with a Porcine Collagen Matrix: A Case Report
• Surgical treatment of hereditary gingival fibromatosis by diode laser: Report of five rare cases in the same family
• Symmetrical palatal fibromatosis: Five new cases and a review of the literature
• The Role of <em>KCNQ1</em> Mutations and Maternal Beta Blocker Use During Pregnancy in the Growth of Children With Long QT Syndrome
• Treatment of Different Oral Soft Tissue Lesions With Surgical Neodymium: Yttrium-Aluminum-Garnet Laser: Case Series
• Two missense mutations in KCNQ1 cause pituitary hormone deficiency and maternally inherited gingival fibromatosis
• Unusual clinical and histologic findings in a child with mixed dentition with hereditary gingival fibromatosis: a case report
• Unusual exophytic gingival lesion in a newborn treated with diode laser
• Unusual presentation of familial gingival fibromatosis among male siblings
• Use of GaAlAs Diode Laser for Excisional Biopsy of Gingival Giant Cell Fibroma: A Case Report of a Rare Lesion
• Zimmermann-Laband-1 Syndrome: Clinical, Histological, and Proteomic Findings of a 3-Year-Old Patient with Hereditary Gingival Fibromatosis
• ZNF862 induces cytostasis and apoptosis via the p21-RB1 and Bcl-xL-Caspase 3 signaling pathways in human gingival fibroblasts