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410 related items for PubMed ID: 20470917
41. Juvenile hyaline fibromatosis and infantile systemic hyalinosis: divergent expressions of the same genetic defect? Dhingra M, Amladi S, Savant S, Nayak C. Indian J Dermatol Venereol Leprol; 2008; 74(4):371-4. PubMed ID: 18797061 [Abstract] [Full Text] [Related]
42. Juvenile systemic hyalinosis--a rare cause of gingival hypertrophy: a case report. Hutchinson I. Int J Paediatr Dent; 1996 Mar; 6(1):39-43. PubMed ID: 8695589 [Abstract] [Full Text] [Related]
43. A solitary calvarial lytic lesion with typical histopathological findings of juvenile hyaline fibromatosis. Bas NS, Güzey FK, Emel E, Cefle K, Turgut H, Alatas I, Sel B, Palanduz S, Ozturk S, Bas SC. J Neurosurg; 2005 Sep; 103(3 Suppl):285-8. PubMed ID: 16238086 [Abstract] [Full Text] [Related]
45. A rare cause of protein-losing enteropathy and growth retardation in infancy: infantile systemic hyalinosis. Büyükgebiz B, Oztürk Y, Arslan N, Ozer E. Turk J Pediatr; 2003 Sep; 45(3):258-60. PubMed ID: 14696808 [Abstract] [Full Text] [Related]
51. Infantile systemic hyalinosis associated with a putative splice-site mutation in the ANTXR2 gene. Fong K, Rama Devi AR, Lai-Cheong JE, Chirla D, Panda SK, Liu L, Tosi I, McGrath JA. Clin Exp Dermatol; 2012 Aug; 37(6):635-8. PubMed ID: 22300424 [Abstract] [Full Text] [Related]
52. Clinical aspects of Hyaline Fibromatosis Syndrome and identification of a novel mutation. Härter B, Benedicenti F, Karall D, Lausch E, Schweigmann G, Stanzial F, Superti-Furga A, Scholl-Bürgi S. Mol Genet Genomic Med; 2020 Jun; 8(6):e1203. PubMed ID: 32196989 [Abstract] [Full Text] [Related]
53. [Microstructure of subcutaneous lesions in juvenile hyaline fibromatosis]. Adamicová K, Fetisovová Z, Mellová Y, Statelová D, Hutka Z. Cesk Patol; 1998 Jul; 34(3):99-104. PubMed ID: 9750422 [Abstract] [Full Text] [Related]
54. Hereditary gingival fibromatosis: review of the literature and a case report. Bittencourt LP, Campos V, Moliterno LF, Ribeiro DP, Sampaio RK. Quintessence Int; 2000 Jun; 31(6):415-8. PubMed ID: 11203959 [Abstract] [Full Text] [Related]
55. Infantile systemic hyalinosis: report of three Iranian children and review of the literature. Aghighi Y, Bahremand S, Nematollahi LR. Clin Rheumatol; 2007 Jan; 26(1):128-30. PubMed ID: 16328093 [Abstract] [Full Text] [Related]
60. 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. Liu Y, Zeng X, Ding Y, Xu Y, Duan D. BMC Oral Health; 2021 Oct 09; 21(1):508. PubMed ID: 34627224 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]