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211 results on '"Fibromatosis, Gingival"'

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1. <scp>Zimmermann–Laband</scp> syndrome in monozygotic twins with a mild neurobehavioral phenotype lacking gingival overgrowth—A case report of a novel <scp> KCNN3 </scp> gene variant

2. Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3—a subgroup of K+ channelopathies

3. A 15-year Follow-Up of a Gingivectomy Procedure for Idiopathic Gingival Fibromatosis: A Case Report and Literature Review

4. Seven-year follow-up of a patient with hereditary gingival fibromatosis treated with a multidisciplinary approach: case report

5. A novel gene

6. Cantú syndrome versus Zimmermann-Laband syndrome: Report of nine individuals with ABCC9 variants

7. Homozygous mutation in ELMO2 may cause Ramon syndrome

8. Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca

9. Fibroblasts from recurrent fibrotic overgrowths reveal high rate of proliferation in vitro : findings from the study of hereditary and idiopathic gingival fibromatosis

10. Genetic analysis of hereditary gingival fibromatosis using whole exome sequencing and bioinformatics

11. Epilepsy in KCNH1-related syndromes

12. The Autosomal Dominant Inheritance of Hereditary Gingival Fibromatosis: A Case Report

13. TIMP-1 association with collagen type I overproduction in hereditary gingival fibromatosis

14. De Novo 17q24.2-q24.3 microdeletion presenting with generalized hypertrichosis terminalis, gingival fibromatous hyperplasia, and distinctive facial features

15. The Effect of MMP-13, MMP-12, and AMBN on Gingival Enlargement and Root Deformation In a New Type of Gingival Fibromatosis

16. Association of 17q24.2-q24.3 deletions with recognizable phenotype and short telomeres

17. REST Final-Exon-Truncating Mutations Cause Hereditary Gingival Fibromatosis

18. Analysis of mutations in the SOS-1 gene in two Polish families with hereditary gingival fibromatosis: SOS-1 analysis of hereditary gingival fibromatosis

19. Two missense mutations in KCNQ1 cause pituitary hormone deficiency and maternally inherited gingival fibromatosis

20. Enamel-Renal-Gingival syndrome, hypodontia, and a novelFAM20Amutation

21. Enamel-renal-gingival syndrome andFAM20Amutations

22. Giant maxillary gingival fibromatosis

23. The significance of electron microscopic examination of gingiva in cases of Hunter syndrome and hereditary gingival fibromatosis

24. [Unilateral idiopathic gingival fibromatosis--a case report]

25. Gingival Fibromatosis with Significant De Novo Formation of Fibrotic Tissue and a High Rate of Recurrence

26. Delineating the 17q24.2–q24.3 microdeletion syndrome phenotype

27. Linkage analysis confirms heterogeneity of hereditary gingival fibromatosis

28. Identification of 2 novel ANTXR2 mutations in patients with hyaline fibromatosis syndrome and proposal of a modified grading system

29. Minichromosome maintenance 2 and 5 expressions are increased in the epithelium of hereditary gingival fibromatosis associated with dental abnormalities

30. Gingival Hyperplasia Associated With Juvenile Hyaline Fibromatosis: A Case Report and Review of the Literature

31. Report of a case of Zimmermann–Laband syndrome with new manifestations

32. Cherubism Combined with Epilepsy, Mental Retardation and Gingival Fibromatosis (Ramon Syndrome): A Case Report

33. Familial cherubism: the experience of the Moscow Central Institute for Stomatology and Maxillo-Facial Surgery

34. Idiopathic Familial Gingival Fibromatosis Associated with Mental Retardation, Epilepsy and Hypertrichosis

35. Case Reports of a New Syndrome Associating Gingival Fibromatosis and Dental Abnormalities in a Consanguineous Family

36. Clinical and histomorphometric characteristics of three different families with hereditary gingival fibromatosis

37. Increased expression of collagen prolyl 4-hydroxylases in Chinese patients with hereditary gingival fibromatosis

38. An update on crown lengthening. Part 1: Gingival tissue excess

39. Splitting versus lumping : Temple–Baraitser and Zimmermann–Laband syndromes

40. Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome

41. Hereditary gingival fibromatosis: clinical and ultrastructural features of a new family

42. Hereditary Gingival Fibromatosis

43. Platelet-derived growth factor (PDGF) isoform and PDGF receptor expression in drug-induced gingival overgrowth and hereditary gingival fibrosis

44. Histopathological Evaluation of Five Unusual Gingival Enlargement Cases

45. A Case of Bullous Pemphigoid Arising in Juvenile Hyaline Fibromatosis with Oral Squamous Cell Carcinoma

46. Proliferation of Fibroblasts Cultured From Normal Gingiva and Hereditary Gingival Fibromatosis Is Dependent on Fatty Acid Synthase Activity

47. Infantile Systemic Hyalinosis

48. A Case of Zimmermann-Laband Syndrome with Supernumerary Teeth

49. Histomorphometric characteristics and expression of epidermal growth factor and its receptor by epithelial cells of normal gingiva and hereditary gingival fibromatosis

50. Effect of Transforming Growth Factor-β1, Interleukin-6, and Interferon-γ on the Expression of Type I Collagen, Heat Shock Protein 47, Matrix Metalloproteinase (MMP)-1 and MMP-2 by Fibroblasts from Normal Gingiva and Hereditary Gingival Fibromatosis

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