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Focal myositis

Skeletal Radiology, 1998
Focal myositis is a pseudotumor of soft tissue that typically occurs in the deep soft tissue of the extremities, and is a relatively rare lesion. There is a wide clinical spectrum, with approximately one-third of patients with focal myositis subsequently developing polymyositis, and clinical symptoms of generalized weakness, fever, myalgia, and weight ...
M J, Kransdorf, H T, Temple, D E, Sweet
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Focal myositis

Australasian Radiology, 2001
SUMMARYFocal myositis is a rare, benign focal inflammation of muscle. The lesion often presents as a mass that may be mistaken for a soft tissue sarcoma. This report describes the MRI and histopathological features of a case and illustrates how the diagnosis may be suspected on the basis of the MR findings.
H R, Galloway   +2 more
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Focal myositis

Cancer, 1977
Focal myositis, a new distinct clinicopathologic entity, is a benign inflammatory pseudotumor of skeletal muscle. Based on a study of 16 cases, the disease which affects both children and adults typically evolves over a period of several weeks as a localized painful swelling within the soft tissue of an extremity.
R R, Heffner   +2 more
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Oculomotor focal dystonia

Movement Disorders, 2001
In vivo imaging of the dopamine transporter, a protein on the terminals of dopaminergic projections from the substantia nigra to the striatum, provides an excellent marker of the dopaminergic system in patients with parkinsonism.1–8 Previous studies have demonstrated that SPECT and [123I] b-CIT (2bcarboxymethoxy- 3b-(4-iodophenyl)tropane), an agent ...
G. Galardi   +5 more
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Focal lipoatrophy

Muscle & Nerve, 1994
AbstractFocal atrophy of a limb is usually caused by loss of muscle due to nerve or muscle disease. However, focal atrophy of subcutaneous tissues, an uncommon but well described entity, can mimic neuromuscular disease by producing a similar appearance of the limb.
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Focal dermal hypoplasia without focal dermal hypoplasia

American Journal of Medical Genetics Part A, 2013
Focal dermal hypoplasia (FDH; Goltz–Gorlin syndrome) is an X‐linked dominant disorder affecting mainly tissues of ectodermal and mesodermal origin. The phenotype is characterized by hypoplastic linear skin lesions, eye malformations, hair and teeth anomalies, and multiple limbs malformations. The disorder is caused by PORCN mutations.
Contreras-Capetillo, Silvina N.   +3 more
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Focal Choroidal Excavation Associated with Focal Retinochoroiditis

Optometry and Vision Science, 2015
To describe detailed spectral-domain optical coherence tomography (OCT) findings for two patients with focal choroidal excavation (FCE) associated with focal retinochoroiditis.Three eyes from two patients with FCE associated with focal retinochoroiditis were evaluated by funduscopy, fluorescence angiography, indocyanine green angiography, and spectral ...
Tetsutaro, Ohki   +2 more
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