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Measures of Patellofemoral Morphology Predict the Risk of Local Cartilage Damage Progression: Letter to the Editor. [PDF]
Am J Sports MedDaungsupawong H, Wiwanitkit V.
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Re-examining the Disc-Centric Interpretation of Chronic Low Back Pain: A Narrative Review. [PDF]
CureusSawaf A.
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Dasatinib and quercetin senolytic treatment delays early onset intervertebral disc degeneration in SM/J mice. [PDF]
Bone ResNovais EJ +5 more
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Expert Opinion on Pharmacotherapy, 2003
The spinocerebellar ataxias (SCA) are a large group of inherited disorders affecting the cerebellum and its afferent and efferent pathways. Their hallmark symptom is slowly progressive, symmetrical, midline, and appendicular ataxia. Some may also have associated hyperkinetic movements (chorea, dystonia, myoclonus, postural/action tremor, restless legs,
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The spinocerebellar ataxias (SCA) are a large group of inherited disorders affecting the cerebellum and its afferent and efferent pathways. Their hallmark symptom is slowly progressive, symmetrical, midline, and appendicular ataxia. Some may also have associated hyperkinetic movements (chorea, dystonia, myoclonus, postural/action tremor, restless legs,
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Continuum, 2010
Frontotemporal degeneration (FTD), one of the most prevalent causes of presenile dementia, includes three subtypes: (1) behavioral variant FTD (bvFTD), (2) semantic variant (SV), and (3) progressive nonfluent aphasia (PNFA). Corticobasal degeneration, progressive supranuclear palsy, and FTD-ALS are linked clinically and pathologically to FTD.
Görsev G, Yener +2 more
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Frontotemporal degeneration (FTD), one of the most prevalent causes of presenile dementia, includes three subtypes: (1) behavioral variant FTD (bvFTD), (2) semantic variant (SV), and (3) progressive nonfluent aphasia (PNFA). Corticobasal degeneration, progressive supranuclear palsy, and FTD-ALS are linked clinically and pathologically to FTD.
Görsev G, Yener +2 more
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Brain, 1989
Three patients with clinical and pathological features of corticobasal degeneration are described. They presented with a progressive disease bearing some clinical resemblance to Steele-Richardson-Olszewski syndrome and displaying some pathological features of Pick's disease.
W R, Gibb, P J, Luthert, C D, Marsden
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Three patients with clinical and pathological features of corticobasal degeneration are described. They presented with a progressive disease bearing some clinical resemblance to Steele-Richardson-Olszewski syndrome and displaying some pathological features of Pick's disease.
W R, Gibb, P J, Luthert, C D, Marsden
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Seminars in Neurology, 2001
Corticobasal degeneration (CBG) is an increasingly recognized neurodegenerative disease with both motor and cognitive dysfunction. The diagnosis is probably underestimated because of the heterogeneity of clinical features, overlap with symptoms, and pathologic findings of other neurodegenerative diseases.
N P, Stover, R L, Watts
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Corticobasal degeneration (CBG) is an increasingly recognized neurodegenerative disease with both motor and cognitive dysfunction. The diagnosis is probably underestimated because of the heterogeneity of clinical features, overlap with symptoms, and pathologic findings of other neurodegenerative diseases.
N P, Stover, R L, Watts
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Degenerate equations and a degenerating parameter
Ukrainian Mathematical Journal, 1987Consider the nondegenerate systems in \(L^ 2:\) \[ (1)\quad A(t,\epsilon)x'=B(t,\epsilon)+f(t,\epsilon) \] where A, B are \(m\times m\)-matrices; \(x,f\in R^ m\), and the degenerate system \[ (2)\quad (\hat A(t)x)'=(\hat A'(t)+\hat B(t))x+\hat f(t). \] The author studies the convergence of the family of the solutions of the system (1) to the solution ...
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