Results 31 to 40 of about 22,397 (232)

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

open access: yesClinics, 2011
INTRODUCTION: Gingiva fibromatosis is a relatively rare condition characterized by diffuse enlargement of the gingiva, which is caused by expansion and accumulation of the connective tissue.
Hercílio Martelli-Júnior   +6 more
doaj   +1 more source

Hyaline fibromatosis syndrome (juvenile hyaline fibromatosis): whole-body MR findings in two siblings with different subcutaneous nodules distribution [PDF]

open access: yes, 2017
: Hyaline fibromatosis syndrome (juvenile hyaline fibromatosis) is a rare, progressive, autosomal recessive disorder whose main hallmark is the deposition of amorphous hyaline material in soft tissues, with an evolutionary course and health impairment ...
Castiglione, D.   +4 more
core   +1 more source

Fibroblasts Collagen Production and Histological Alterations in Hereditary Gingival Fibromatosis [PDF]

open access: yes, 2019
Hereditary gingival fibromatosis is a disorder for which the etiology remains unknown. We aimed to evaluate the fibroblasts and histological alterations to give new clues.
Bullon, Pedro   +3 more
core   +1 more source

Clinical aspects of Hyaline Fibromatosis Syndrome and identification of a novel mutation

open access: yesMolecular Genetics & Genomic Medicine, 2020
Background Hyaline fibromatosis syndrome is an autosomal recessive disease caused by mutations in ANTXR2 which leads to loss of function of the transmembrane protein anthrax toxin receptor 2.
Bettina Härter   +7 more
doaj   +1 more source

Hyaline fibromatosis syndrome inducing mutations in the ectodomain of anthrax toxin receptor 2 can be rescued by proteasome inhibitors. [PDF]

open access: yes, 2011
Hyaline Fibromatosis Syndrome (HFS) is a human genetic disease caused by mutations in the anthrax toxin receptor 2 (or cmg2) gene, which encodes a membrane protein thought to be involved in the homeostasis of the extracellular matrix.
Andrea Superti‐Furga   +13 more
core   +3 more sources

Idiopathic desmoid-type fibromatosis of the pancreatic head: case report and literature review [PDF]

open access: yes, 2014
Desmoid-type fibromatosis (DTF) is an uncommon nonmetastatic fibrous neoplasm. Sporadic intraperitoneal DTF is rarely described in current literature. We herein report a case of DTF of unknown cause involving the pancreatic head.
Baoling Tian   +5 more
core   +2 more sources

Le Fibromatosis colli: une tumeur cervicale rare du nourrisson

open access: yesThe Pan African Medical Journal, 2020
Le fibromatosis colli ou pseudotumeur infantile du muscle sternocléidomastoïdien est une cause rare de masse cervicale bénigne du nouveau-né et du nourrisson.
Nogognan Ignace Lengane   +7 more
doaj   +1 more source

Hereditary gingival fibromatosis : characteristics and treatment approach [PDF]

open access: yes, 2017
Hereditary gingival fibromatosis (HGF) is a rare disorder characterized by a benign, non-hemorrhagic, fibrous gingival overgrowth that can appear in isolation or as part of a syndrome.
Almiñana Pastor, Pedro J.   +3 more
core   +1 more source

MESENTERIC FIBROMATOSIS

open access: yesInternational Journal of Clinical Practice, 1994
SUMMARY Mesenteric fibromatosis is commonly associated with Gardner's syndrome and familial polyposis. These lesions may have an insidious onset via compression of the small or large intestines, or may be noted for the first time during abdominal exploration for some other cause. Differential diagnosis may be difficult.
A C, Tsamandas   +4 more
openaire   +2 more sources

Recapitulation of fibromatosis nodule by multipotential stem cells in immunodeficient mice. [PDF]

open access: yesPLoS ONE, 2011
Musculoskeletal fibromatosis remains a disease of unknown etiology. Surgical excision is the standard of care, but the recurrence rate remains high.
Jung-Pan Wang   +8 more
doaj   +1 more source

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