Results 81 to 90 of about 3,824 (214)
Equine Veterinary Education, Volume 36, Issue 12, Page e302-e307, December 2024.Summary To the authors' knowledge there is only one report in the literature describing plasma cell paramedullary myeloma in horses as so‐called ‘break out lesions’, originating from vertebral bone marrow and invading the epidural space. This report describes clinical and pathomorphological findings of such.
Anna Pelli +6 more
wiley +1 more source
Nasu-Hakola disease (PLOSL) : report of five cases and review of the literature [PDF]
, 2006 The combination of bilateral lytic lesions in the bones of the lower and upper extremities and presenile dementia is characteristic of polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy, also known as Nasu-Hakola disease.
Freyschmidt, Jürgen +3 more
core +2 more sources
Clinical findings and outcome in goats with discospondylitis and vertebral osteomyelitis
Journal of Veterinary Internal Medicine, Volume 38, Issue 3, Page 1925-1931, May/June 2024.Abstract Background Vertebral infections, including vertebral osteomyelitis, septic physitis, and discospondylitis, are rarely reported in goats, and when reported, have been largely limited to necropsy case reports. Objective Describe clinical findings and outcome in goats with vertebral infections evaluated by computed tomography (CT).
Alyssa Sullivan +4 more
wiley +1 more source
Molecular effect of an OPTN common variant associated to Paget's disease of bone [PDF]
, 2018 Paget's disease of bone (PDB) is a chronic bone disorder and although genetic factors appear to play an important role in its pathogenesis, to date PDB causing mutations were identified only in the Sequestosome 1 (SQSTM1) gene at the PDB3 locus.
Brown, Jacques P. +5 more
core +3 more sources
Spinal polyostotic fibrous dysplasia in two adults: Does only biopsy unravel the mystery?
Indian Journal of Endocrinology and Metabolism, 2013 Polyostotic fibrous dysplasia is a rare non-inheritable genetic disease due to mutation in GNAS gene. Here we present two adults who were accidentally detected lytic lesions in spine and after extensive evaluation for malignancies; was diagnosed on ...
Abhay Gundgurthi +7 more
doaj +1 more source
Use of Zoledronic Acid in the Treatment of Paget's Disease [PDF]
, 2011 This review examines the use of zoledronic acid in the treatment of Paget’s disease of bone. It begins with a brief discussion of the theories of pathogenesis of Paget’s disease, its clinical manifestations, and the history of bisphosphonate treatment in
Krane, Stephen Martin +1 more
core
Fulvestrant treatment of precocious puberty in girls with McCune-Albright syndrome [PDF]
, 2012 BACKGROUND: McCune-Albright Syndrome (MAS) is usually characterized by the triad of precocious puberty (PP), fibrous dysplasia, and café au lait spots. Previous treatments investigated for PP have included aromatase inhibitors and the estrogen receptor ...
Charles Sultan +6 more
core +1 more source
Síndrome de Mazabraud: Presentación de un caso clínico y revisión de la literatura [PDF]
, 2000 El síndrome de Mazabraud se define como la asociación de una tumoración de partes blandas, el mixoma intramuscular, y un tumor óseo, la displasia fibrosa.
Maqueda Abreu, V. +4 more
core
Treatment of Peripheral Precocious Puberty [PDF]
, 2015 There are many etiologies of peripheral precocious puberty (PPP) with diverse manifestations resulting from exposure to androgens, estrogens, or both. The clinical presentation depends on the underlying process and may be acute or gradual.
Eugster, Erica A., Schoelwer, Melissa
core +1 more source
Journal of Indian Academy of Oral Medicine and Radiology, 2006 Osteitis deformans or Paget′s disease of bone, fondly referred to as the ′collage of matrix madness′, is a unique skeletal disease characterized by furious osteoclastic bone resorption followed by a period of hectic bone formation, resulting in again in ...
B Sivapatha Sundharam +2 more
doaj