Search Results - "Laakso, Sini M."
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Early clinical features of new-onset refractory status epilepticus (NORSE) in adults
Published in BMC neurology (20-12-2022)“…The aim of this study was to identify early clinical features of patients with new-onset refractory status epilepticus (NORSE) that could direct the treatment…”
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Complete remission of central nervous system manifestations of IgG4-related disease with rituximab – a case report
Published in Therapeutic advances in neurological disorders (01-01-2023)“…IgG4-related disease (IgG4-RD) is an emerging immune-mediated chronic fibrotic disease characterized by tumour-like mass formation. Reports of brain…”
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Hemophagocytic lymphohistiocytosis in an adult patient with super‐refractory status epilepticus
Published in Epilepsia open (01-10-2024)“…This case report presents a 38‐year‐old male patient who, after a febrile infection, developed super‐refractory status epilepticus and multiorgan failure, and…”
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Effects of a Digital Care Pathway for Multiple Sclerosis: Observational Study
Published in JMIR human factors (07-08-2024)“…Helsinki University Hospital has developed a digital care pathway (DCP) for people with multiple sclerosis (MS) to improve the care quality. DCP was designed…”
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Intensive care due to myasthenia gravis: Risk factors and prognosis
Published in European journal of neurology (01-12-2024)“…Background and purpose Exacerbation of myasthenia gravis (MG) with respiratory failure requires intensive care. We aimed to study the risk factors for…”
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Comorbidities worsen the prognosis of generalized myasthenia gravis post-thymectomy
Published in Journal of the neurological sciences (15-08-2021)“…The effect of comorbidities on the prognosis of myasthenia gravis (MG) remains unclear. In particular, the role of other autoimmune diseases (AD) is…”
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Trigeminal neuralgia in multiple sclerosis: Prevalence and association with demyelination
Published in Acta neurologica Scandinavica (01-08-2020)“…Objectives The association of trigeminal neuralgia (TN) with multiple sclerosis (MS) is still widely unaddressed in larger, systematical clinical series. In…”
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Ectopic germinal centers in the thymus accurately predict prognosis of myasthenia gravis after thymectomy
Published in Modern pathology (01-09-2022)“…The ability of thymic histopathology to predict the long-term impact of thymectomy in non-thymomatous myasthenia gravis (NTMG) is mainly uncharted. We applied…”
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Exploring JC Polyomavirus Sequences and Human Gene Expression in Brain Tissue of Patients With Progressive Multifocal Leukoencephalopathy
Published in The Journal of infectious diseases (23-09-2024)“…Abstract Progressive multifocal leukoencephalopathy (PML) is a rare neurological condition associated with reactivation of dormant JC polyomavirus (JCPyV). In…”
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Incidental demyelination in magnetic resonance imaging and 10‐year risk of multiple sclerosis: A data lake cohort study
Published in European journal of neurology (01-08-2023)“…Background and purpose There is an absence of data from large population‐based cohort studies on the incidence of radiologically isolated syndrome (RIS). The…”
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A skewed ratio of free light chains is more common in patients with late-onset than early-onset myasthenia gravis
Published in Immunology letters (01-08-2023)“…•The κ/λ ratio is significantly elevated in patients with late-onset myasthenia gravis (LOMG).•Detected even after a decade of follow-up, these results suggest…”
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12
Cervical lymph node diameter reflects disease progression in multiple sclerosis
Published in Multiple sclerosis and related disorders (01-04-2024)“…•Cervical lymph nodes can be measured from multiple sclerosis follow-up head MRIs.•Smaller lymph node diameter predicts disease progression during…”
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13
High Epstein-Barr virus capsid antigen IgG level associates with the carriership of CD8+ T cell somatic mutations in the STAT3 SH2 domain
Published in Clinical immunology (Orlando, Fla.) (01-10-2023)“…High carrier prevalence of STAT3 SH2 domain somatic mutations was recently discovered in CD8+ T cells. We found these low-allele-fraction clones in 26% of…”
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Multiple sclerosis in Finland 2018—Data from the national register
Published in Acta neurologica Scandinavica (01-11-2019)“…Objectives Finland is a high‐risk multiple sclerosis (MS) region, but a national MS register has not existed until 2014. In this paper, we present the Finnish…”
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Clinically relevant increases in serum neurofilament light chain and glial fibrillary acidic protein in patients with Susac syndrome
Published in European journal of neurology (01-10-2023)“…Serum levels of neurofilament light chain (sNfL) and glial fibrillary acidic protein (sGFAP) are promising neuro-axonal damage and astrocytic activation…”
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Epstein-Barr Virus in the Cerebrospinal Fluid and Blood Compartments of Patients With Multiple Sclerosis and Controls
Published in Neurology : neuroimmunology & neuroinflammation (01-05-2024)“…Epstein-Barr virus (EBV) infection is a major risk factor of multiple sclerosis (MS). We examined the presence of EBV DNA in the CSF and blood of patients with…”
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17
Regulatory T cell defect in APECED patients is associated with loss of naive FOXP3+ precursors and impaired activated population
Published in Journal of autoimmunity (01-12-2010)“…Abstract The pathogenetic mechanisms of organ-specific autoimmune diseases remain obscured by the complexity of the genetic and environmental factors…”
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Expanded CD4+ Effector/Memory T Cell Subset in APECED Produces Predominantly Interferon Gamma
Published in Journal of clinical immunology (01-08-2016)“…Purpose Autoimmune polyendocrinopathy–candidiasis–ectodermal dystrophy (APECED) is a rare human autoimmune disorder caused by mutations in the AIRE (autoimmune…”
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IL-7 dysregulation and loss of CD8+ T cell homeostasis in the monogenic human disease autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy
Published in The Journal of immunology (1950) (15-08-2011)“…Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) is a monogenic autoimmune disease that is caused by mutations in the AIRE gene. Murine…”
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In vivo analysis of helper T cell responses in patients with autoimmune polyendocrinopathy - candidiasis - ectodermal dystrophy provides evidence in support of an IL-22 defect
Published in Autoimmunity (Chur, Switzerland) (01-12-2014)“…Abstract Autoimmune polyendocrinopathy - candidiasis - ectodermal dystrophy (APECED) is caused by mutations in the Autoimmune regulator (AIRE) gene and is…”
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