SPG4 and Dementia: Expanding the Clinical Spectrum
ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
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Colonoscopy outcomes and clinical factors associated with significant findings in patients with positive fecal occult blood tests: A retrospective cohort study. [PDF]
Gönüllü ME +3 more
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Pathology and Genetics in a Global Cohort of Parkinsonian Disorders.
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A novel hierarchical framework elucidating regional differences in α-synuclein and tau co-pathology in military veterans with parkinsonism. [PDF]
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Configuring large language models to deliver patient-facing explanations of pathology reports. [PDF]
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CTE has multiple pathologic variants that might relate to different clinical symptom presentation. [PDF]
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Answer to Clinical Pathology Case, Summer 2010
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