169 results match your criteria: "University Health Network and The University of Toronto[Affiliation]"

Differences in progressive supranuclear palsy in patients of Asian ancestry?

Parkinsonism Relat Disord

January 2025

Edmond J. Safra Program in Parkinson's Disease, Rossy Program for PSP Research and the Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital, Toronto, ON, Canada; Tanz Centre for Research in Neurodegenerative Disease, University of Toronto, Toronto, Ontario, Canada; Department of Medicine, Division of Neurology, University Health Network and the University of Toronto, Toronto, Ontario, Canada.

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Squamous cell carcinoma (SCC) is one of the most common malignancies involving the parotid gland, but it has been recognized that the vast majority of parotid SCC represents metastases, especially from the ipsilateral facial skin. Bona fide primary SCC of the parotid is so rare that it is unclear whether it truly exists at all. We sought to molecularly characterize cases diagnosed as primary parotid gland SCC to see if they possess a unique genetic makeup.

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CSF α-Synuclein Seed Amplification Assay in Patients With Atypical Parkinsonian Disorders.

Neurology

September 2024

From the Tanz Centre for Research in Neurodegenerative Diseases (C.A., I.M.-V., A.V., S.T., M.H., F.T., C. Sato, D.M., C.J.A., K.M., A.E.L., E.R., G.G.K., M.C.T.); Krembil Brain Institute (I.M.-V., A.M.-R., B.C., D.F.T.-W., A.E.L., S.H.F., G.G.K., M.C.T.); The Edmond J. Safra Program in Parkinson's Disease and Morton and Gloria Shulman Movement Disorders Clinic (I.M.-V., A.M.-R., B.C., A.E.L., S.H.F., G.G.K., M.C.T.); Rossy Progressive Supranuclear Palsy Centre (I.M.-V., A.M.-R., A.E.L., G.G.K., M.C.T.), University Health Network and the University of Toronto; and University Health Network Memory Clinic (D.M.-F., C. Salvo, D.F.T.-W.), Toronto, Ontario, Canada.

Background And Objectives: There is no disease-modifying treatment of corticobasal syndrome (CBS) and progressive supranuclear palsy (PSP), 2 disorders characterized by their striking phenotypic, and, in CBS, pathologic heterogeneity. Seed amplification assays (SAAs) could enable the detection of neuropathologic processes, such as α-synuclein (αSyn) copathology, that affect the success of future disease-modifying treatment strategies. The primary objective was to assess possible αSyn copathology in CBS and PSP, as detected in CSF using an αSyn SAA (αSyn-SAA).

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Severe Acute Motor Exacerbations (SAME) across Metabolic, Developmental and Genetic Disorders.

Mov Disord

September 2024

Edmond J. Safra Program in Parkinson's Disease, Rossy PSP Centre and the Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital, Toronto, Ontario, Canada.

Acute presentation of severe motor disorders is a diagnostic and management challenge. We define severe acute motor exacerbations (SAME) as acute/subacute motor symptoms that persist for hours-to-days with a severity that compromise vital signs (temperature, breath, and heart rate) and bulbar function (swallowing/dysphagia). Phenomenology includes dystonia, choreoathetosis, combined movement disorders, weakness, and hemiplegic attacks.

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Clonic Perseveration in Neurodegenerative Parkinsonism.

Mov Disord Clin Pract

September 2024

Edmond J. Safra Program in Parkinson's Disease, Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital, University Health Network, Toronto, Ontario, Canada.

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Intratumoral heterogeneity is common in cancer, particularly in sarcomas like undifferentiated pleomorphic sarcoma (UPS), where individual cells demonstrate a high degree of cytogenic diversity. Previous studies showed that a small subset of cells within UPS, known as the metastatic clone (MC), as responsible for metastasis. Using a CRISPR-based genomic screen , we identified the COMPASS complex member as a key regulator maintaining the metastatic phenotype of the MC in murine UPS.

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Article Synopsis
  • Multiple system atrophy (MSA) is a neurodegenerative disease characterized by abnormal protein aggregation, resulting in symptoms like dysautonomia, parkinsonism, and ataxia.
  • This study aimed to assess the accuracy of diagnostic criteria for MSA, emphasizing the role of new MRI markers in diagnosis.
  • Results showed that while the criteria had high specificity (99-100%), their sensitivity was low initially but improved over time; excluding MRI features from the criteria significantly increased sensitivity without affecting specificity.
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Ethnic background and distribution of clinical phenotypes in patients with probable progressive supranuclear palsy.

Parkinsonism Relat Disord

June 2024

Edmond J. Safra Program in Parkinson's Disease, Rossy Program for PSP Research and the Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital, Toronto, ON, Canada; Tanz Centre for Research in Neurodegenerative Disease, University of Toronto, Toronto, Ontario, Canada; Department of Medicine, Division of Neurology, University Health Network and the University of Toronto, Toronto, Ontario, Canada. Electronic address:

Background: Progressive Supranuclear Palsy (PSP) is a sporadic neurodegenerative disease without a clear geographic prevalence. Cohorts studied in the UK and India showed no higher prevalence of atypical parkinsonism in South Asian patients. We describe the ethnic and racial background of PSP patients in the Greater Toronto Area (GTA), Canada.

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Objectives: To evaluate the effect of Alzheimer's disease (AD) -related biomarker change on clinical features, brain atrophy and functional connectivity of patients with corticobasal syndrome (CBS) and progressive supranuclear palsy (PSP).

Methods: Data from patients with a clinical diagnosis of CBS, PSP, and AD and healthy controls were obtained from the 4-R-Tauopathy Neuroimaging Initiative 1 and 2, the Alzheimer's Disease Neuroimaging Initiative, and a local cohort from the Toronto Western Hospital. Patients with CBS and PSP were divided into AD-positive (CBS/PSP-AD) and AD-negative (CBS/PSP-noAD) groups based on fluid biomarkers and amyloid PET scans.

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Purpose: Once the COVID-19 pandemic was declared, clinicians were redeployed to prepare for increased hospitalizations. This disruption necessitated rapid continuing professional development (CPD) resources for health care providers. This mixed-method study explored the experiences of occupational therapists and physiotherapists who accessed a CPD Web site that provided educational resources related to the pandemic to refresh their clinical knowledge and skills.

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Article Synopsis
  • Open retroperitoneal lymph node dissection (O-RPLND) is the traditional method for treating retroperitoneal nodal disease in testis cancer, while robotic RPLND (R-RPLND) is gaining popularity for benefits like less blood loss and quicker recovery.
  • A propensity score matching analysis compared the outcomes of O-RPLND and R-RPLND using data from 178 patients over a 32-year period.
  • Results showed that R-RPLND had shorter hospital stays and less estimated blood loss but longer surgery times, with similar relapse rates between the two methods.
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Background: The delivery of cardiothoracic health care is complex, and despite best efforts, adverse patient outcomes do occur. There is significant heterogeneity in morbidity and mortality rounds within and between institutions as well as undertones of a "blame and shame" culture prohibitive to meaningful quality assessment and improvement of patient care. The Quality Improvement and Patient Safety (QIPS) program was designed to address these issues.

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Keratocystoma is a rare salivary gland lesion that has been reported primarily in children and young adults. Because of a scarcity of reported cases, very little is known about it, including its molecular underpinnings, biological potential, and histologic spectrum. Purported to be a benign neoplasm, keratocystoma bears a striking histologic resemblance to benign lesions like metaplastic Warthin tumor on one end of the spectrum and squamous cell carcinoma on the other end.

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Background: The impact of age of onset on the presentation of progressive supranuclear palsy phenotypes is not well studied. We hypothesized that there is difference in presentation and phenotype between young- and late-onset PSP.

Objectives: Our aim was to compare phenotypes and rate of change in disability between young-onset PSP (YOPSP) and late-onset PSP (LOPSP).

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Future directions on aortic valve-sparing operations.

Ann Cardiothorac Surg

July 2023

Department of Cardiovascular & Thoracic Surgery, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain (UCL), Brussels, Belgium.

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The Removal of Uremic Solutes by Peritoneal Dialysis.

J Am Soc Nephrol

December 2023

Division of Nephrology and Department of Medicine, University Health Network and the University of Toronto, Canada.

Peritoneal dialysis (PD) is now commonly prescribed to achieve target clearances for urea or creatinine. The International Society for Peritoneal Dialysis has proposed however that such targets should no longer be imposed. The Society's new guidelines suggest rather that the PD prescription should be adjusted to achieve well-being in individual patients.

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Article Synopsis
  • Adenocarcinoma, NOS is a complex group of salivary gland tumors that includes tumors not yet well-defined, with some cases being reclassed into new categories like secretory carcinoma and microsecretory adenocarcinoma.
  • A study identified nine cases of a new salivary gland tumor type, predominantly affecting older women, particularly arising in the sublingual gland.
  • The tumors exhibited a unique biphasic structure with specific cell characteristics and immunohistochemical profiles, but no significant genetic mutations were found, and all were surgically removed.
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Background: Aortic valve sparing operations were introduced three decades ago but controversy remains regarding its appropriateness, reproducibility and durability. This article describes the long-term outcomes of patients who had reimplantation of the aortic valve.

Methods: All patients who had reimplantation of a tricuspid aortic valve at Toronto General Hospital from 1989 through 2019 were selected for this study.

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Article Synopsis
  • A study was conducted to determine how common true venous infarction is in patients with cerebral venous thrombosis (CVT) and to measure related conditions like diffusion abnormalities and hemorrhage.
  • Out of 73 initial patients studied, 59 were included after exclusions, revealing that only 12% had venous infarction, with a small fraction exhibiting significant infarct volume.
  • The research also found that 8% of patients showed transient diffusion abnormalities without actual infarction, contributing important insights to the management and prognosis of CVT.
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Article Synopsis
  • Functional neurological disorder (FND) is a common and serious condition that many doctors don’t fully understand.
  • It has been recognized for over 100 years but people with FND still face unfair treatment and discrimination.
  • The text argues that FND is a feminist issue because it often affects women and highlights the need for better education and healthcare for those affected by this disorder.
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