Results 121 to 130 of about 20,986 (228)

Clinical study of the treatment of digital exostosis by introducing a biocompatible gel [PDF]

Antecedentes. La exóstosis digital es una patología común que se presenta con frecuencia en las consultas de podología. A pesar del alto grado de incidencia es una entidad clínica muy poco estudiada.
Bonill a Toyos, Elvira Mª, de Planell Mas, Elena, Giralt de Veciana, Enrique, Manzanares Céspedes, Mª Cristina, Novel Martí, Virginia, Truchero Coma, Consuelo   +5 more
core   +2 more sources

Hereditary Multiple Exostoses: Clinical, Molecular and Radiologic Survey in 9 Families

Prague Medical Report, 2017
Hereditary multiple exostoses (HME) represents a heterogeneous group of diseases often associated with progressive skeletal deformities. Most frequently, mutations in EXT1 and EXT2 genes with autosomal dominant inheritance are responsible for HME. In our
Karel Medek, Jiří Zeman, Tomáš Honzík, Hana Hansíková, Štěpánka Švecová, Kamila Beránková, Vendula Kučerová Vidrová, Miloslav Kuklík, Jiří Chomiak, Markéta Tesařová   +9 more
doaj   +1 more source

A novel nonsense mutation of EXT1 gene in an Argentinian patient with Multiple Hereditary Exostoses [PDF]

, 2012
Multiple hereditary exostoses (MHE), also known as multiple osteochondromatosis, is an autosomal-dominant O-linked glycosylation disorder recently classified as EXT1/EXT2-CDG in the congenital disorder of glycosylation (CDG)nomenclature.
Asteggiano, Carla Gabriela, Azar, Nydia Beatríz, Balcells, Susana, Delgado, María Andrea, Dodelson de Kremer, Raquel, Grinberg Vaisman, Daniel Raúl, Robledo, Hector Hugo, Sarrión, Patricia, Segura, Florencio Vicente, Zecchini, Lorena del Valle   +9 more
core   +1 more source

Osteochondroma of the mandibular condyle: Resection and reconstruction using vertical sliding osteotomy of the mandibular ramus [PDF]

, 2009
Osteochondroma is one of the most common benign bone tumours, although not in the craniofacial region. More than half of these appear in the coronoid process.
Escrig de Teigeiro, M., Fernández-Alba Luengo, Javier, González, Sergio A., Navarro Cuéllar, C., Navarro Vila, C.   +4 more
core  

Hereditary multiple exostoses and porencephaly in a Nigerian child: a case report

The Pan African Medical Journal, 2018
Hereditary multiple exostoses (HME) is a rare condition that is characterised by the outgrowth of bony swellings, usually from the growth ends of long bones. It is autosomal dominant, and may result in debilitating deformities.
Idris Abiodun Adedeji, Hamza Mustapha Ahmed, Abdulazeez Olalekan Tella, Muhammad Faruk Bashir, Yusuf Aliyu Saliu   +4 more
doaj   +1 more source

Osteoporosis risk factors in HIV positive women with osteoporosis: A retrospective analysis [PDF]

, 2017
Multifactorial risk factors such as HIV/HCV co-infection and antiretroviral therapy (ARV) have been associated with osteoporosis in HIV+ women. We retrospectively analysed which known risk factors were associated with the diagnosis of osteoporosis ...
Colomba, C, DI CARLO, P, Gambino, A, Giannitrapani, L., La Galla, R, LI VECCHI, V., LO CASTO, A, Lo Re, G, Midiri, M., Montalto, G., Serra, N, Soresi, M.   +11 more
core  

Hereditary multiple exostosis : a study in abnormal bone growth [PDF]

, 2020
Hereditary multiple exostosis is a generalised, heritable disorder of bone, characterised by the appearance of numerous cartilagecappecl exostoses at the juxta-epiphysial regions of the endochondral skeleton.
Solomon, Louis
core   +1 more source

Biplanar EOS screening in children with hereditary multiple osteochondromas: a feasible screening method?

Frontiers in Pediatrics
BackgroundChildren with Hereditary Multiple Ostechondromas (HMO) require regular screening to identify gradual dysplasia or osteochondromas that need surgery.
Henrik Hedelin, Henrik Hedelin, Jenny Ahlin, Jenny Ahlin, Aina Danielsson, Aina Danielsson, Helena Brisby, Helena Brisby, Kerstin Lagerstrand, Kerstin Lagerstrand   +9 more
doaj   +1 more source

Hereditary multiple exostoses. [PDF]

Journal of Medical Genetics, 1991
openaire   +3 more sources

Experience of chronic pain and stigma in an adolescent with hereditary multiple osteochondromas: a case report

Journal of Rare Diseases
Experiencing the effects of a rare disease during childhood shapes development. Children with rare diseases may experience mental health challenges, bullying, and/or stigmatization, along with missing key opportunities for social development such as ...
Emily A. Holz
doaj   +1 more source