Results 121 to 130 of about 12,028 (243)

Síndrome de Mc Cune Albright: a propósito de un caso [PDF]

open access: yes, 2010
Se presenta el caso de un niño varón de 6 años que tras presentar una clínica de claudicación a la marcha progresiva durante 3 meses, sin antecedente de traumatismo, es diagnosticado de fractura patológica de cuello femoral izquierdo en el contexto de un
Amor, M.   +3 more
core  

The paradox of cancer genes in non-malignant conditions: implications for precision medicine. [PDF]

open access: yes, 2020
Next-generation sequencing has enabled patient selection for targeted drugs, some of which have shown remarkable efficacy in cancers that have the cognate molecular signatures.
Adashek, Jacob J   +3 more
core  

Diagnosis and conservative treatment of a rare case of femoral intraosseous arteriovenous malformation in a patient with polyostotic fibrous dysplasia: A case report

open access: yesMolecular and clinical oncology, 2019
Pure intraosseous arteriovenous malformation (AVM) in a limb bone is extremely rare. Furthermore, there is currently insufficient information on the diagnostic and therapeutic strategies for pure intraosseous AVMs.
S. Ohshika   +3 more
semanticscholar   +1 more source

Rare diseases: matching wheelchair users with rare metabolic, neuromuscular or neurological disorders to electric powered indoor/outdoor wheelchairs (EPIOCs) [PDF]

open access: yes, 2015
Purpose: To describe the clinical features of electric powered indoor/outdoor wheelchair (EPIOC) users with rare diseases (RD) impacting on EPIOC provision and seating. Method: Retrospective review by a consultant in rehabilitation medicine of electronic
Andrew O. Frank   +18 more
core   +3 more sources

Polyostotic fibrous dysplasia: report of a patient

open access: yesActa Médica del Centro, 2013
Polyostotic fibrous dysplasia is a benign fibro-osseous lesion in which the normal structure of the bone is replaced by fibrous tissue and by nonfunctional bony structures that show a trabecular aspect and have an unknown etiology.
Esteban Hernández Ruiz   +1 more
doaj  

Fibrous dysplasia: A tale of two syndromes

open access: yesSouth African Journal of Radiology
Fibrous dysplasia (FD) is a rare, non-inherited, congenital bone disorder which may be monostotic or polyostotic. The polyostotic form may rarely present in syndromic forms when associated with extra-skeletal manifestations.
Jacques Fourie   +3 more
doaj   +1 more source

Quadruple osteotomy: A simple approach to treat “O” deformity in hypophosphatemic rickets

open access: yesJournal of Orthopedics, Traumatology and Rehabilitation, 2018
Multiple deformities of femur and tibia in a child are known to occur in various conditions such as multiple hereditary exostosis, polyostotic fibrous dysplasia, Osteogenesis imperfecta, achondroplasia, multiple epiphyseal dysplasia, and rickets.
Alok Chandra Agarwal   +4 more
doaj   +1 more source

The surgical management of fibrous dysplasia of bone [PDF]

open access: yes, 2012
The surgical management of Polyostotic Fibrous Dysplasia (FD) of bone is technically demanding. The most effective methods to manage the associated bone deformity remain unclear. The marked variation in the degree and pattern of bone involvement has made
Ippolito, Ernesto   +5 more
core   +4 more sources

Polyostotic fibrous dysplasia of the ribs: An unusual cause of chest pain and dyspnea

open access: yesInternational Medical Case Reports Journal, 2009
Sevket Ozkaya1, Serhat Findik2, Hasan Demir1, Canan Yuksel3, Atilla Guven Atici21Samsun Chest Disease and Chest Surgery Hospital, Samsun, Turkey; 2Ondokuz Mayis University, Faculty of Medicine, Department of Pulmonary Medicine, Samsun, Turkey; 3Samsun ...
Sevket Ozkaya   +3 more
doaj  

Cytomorphological Diagnosis of Giant Cell Tumour of Distal End Radius in Elderly Patient [PDF]

open access: yes, 2013
Giant cell tumours (GCTs) of bone have been described as the most challenging benign bone tumors. It is very unusual for GCT to occur in patients younger than 20 yrs or older than 55 years. GCT is seen with a slightly increased frequency in females.
Bagale, P   +4 more
core   +1 more source

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