Publications by authors named "H Fudaba"

The neural mechanisms underlying gross and fine motor dysfunction after subarachnoid hemorrhage (SAH) remain unknown. The γ-aminobutyric acid (GABA) deficit hypothesis proposes that reduced neuronal GABA concentrations and the subsequent lack of GABA-mediated inhibition cause motor impairment after SAH. This study aimed to explore the correlation between GABA levels and a behavioral measure of motor performance in patients with SAH.

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A stable, reliable, non-invasive, quantitative assessment of swallowing function remains to be established. Transcranial magnetic stimulation (TMS) is commonly used to aid in the diagnosis of dysphagia. Most diagnostic applications involve single-pulse TMS and motor evoked potential (MEP) recordings, the use of which is not clinically suitable in patients with severe dysphagia given the large variability in MEPs measured from the muscles involved in swallowing.

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Introduction: Multidrug chemoimmunotherapy with rituximab, high-dose methotrexate, procarbazine and vincristine (R-MPV) is a standard therapy for younger patients with primary central nervous system lymphoma (PCNSL); however, prospective data regarding its use in elderly patients are lacking. This multi-institutional, non-randomised, phase II trial will assess the efficacy and safety of R-MPV and high-dose cytarabine (HD-AraC) for geriatric patients with newly diagnosed PCNSL.

Methods And Analysis: Forty-five elderly patients will be included.

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Article Synopsis
  • Pineal parenchymal tumors of intermediate differentiation (PPTIDs) are rare brain tumors, making up less than 1% of CNS tumors, which creates challenges for diagnosis and treatment.* -
  • A study across 11 institutions identified 28 patients with PPTID, with findings showing a median age of 49, a predominance of females, and a gross total resection success rate of 46%.* -
  • The study concluded that female sex and gross total resection are important factors for better patient outcomes, with a high occurrence of leptomeningeal recurrences and KBTBD4 mutations present in most patients.*
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