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1.
Dementia and Neurocognitive Disorders ; : 45-58, 2022.
Article Dans Anglais | WPRIM | ID: wpr-924899

Résumé

Recently, aducanumab, a beta amyloid targeted immunotherapy, has been approved by the US Food and Drug Administration for the treatment of Alzheimer’s dementia (AD). Although many questions need to be answered, this approval provides a promising hope for the development of AD drugs that could be supported by new biomarkers such as blood-based ones and composite neuropsychological tests that can confirm pathologic changes in early stages of AD. It is important to elucidate the complexity of AD which is known to be associated with other factors such as vascular etiologies and neuro-inflammation. Through the second international conference of the Korean Dementia Association (KDA), researchers from all over the world have participated in the exchange of opinions with KDA members on the most up-to-date topics. The Academic Committee of the KDA summarizes lectures to provide the depth of the conference as well as discussions. This will be an important milestone to widen the latest knowledge in the research of AD’s diagnosis, therapeutics, pathogenesis that can lead to the establishment of future directions.

2.
Journal of the Korean Neurological Association ; : 136-137, 2018.
Article Dans Coréen | WPRIM | ID: wpr-766636

Résumé

No abstract available.


Sujets)
Encéphalopathies , Métronidazole
3.
Dementia and Neurocognitive Disorders ; : 66-70, 2018.
Article Dans Anglais | WPRIM | ID: wpr-715324

Résumé

No abstract available.


Sujets)
Maladie d'Alzheimer , Aphasie progressive primaire
4.
Dementia and Neurocognitive Disorders ; : 32-36, 2018.
Article Dans Anglais | WPRIM | ID: wpr-713160

Résumé

BACKGROUND: Normal pressure hydrocephalus (NPH) is an etiology of dementia that is reversible following cerebrospinal fluid shunt placement, however, surgical intervention not always clinically effective and the respons to shunt therapy is poorly understood. Furthermore, NPH is a source of comorbidity in diseases with neurodegenerative pathology, such as Alzheimer's disease (AD). CASE REPORT: A 61-year-old woman presented to the neurology clinic with progressive gait difficulties and cognitive impairment over five years. Nine years after ventriculoperitoneal (VP) shunt treatment, the patient began to experience frequent falls. There was no improvement in clinical symptoms after the alteration of valve pressure on the VP shunt. An 18F-florbetaben amyloid positron emission tomography scan showed increased diffusion uptake over the bilateral cortices, precuneus, and posterior cingulate cortex. CONCLUSIONS: The patient of NPH was unresponsive to shunt therapy due to the development of AD.


Sujets)
Femelle , Humains , Adulte d'âge moyen , Chutes accidentelles , Maladie d'Alzheimer , Amyloïde , Dérivations du liquide céphalorachidien , Troubles de la cognition , Comorbidité , Démence , Diffusion , Démarche , Gyrus du cingulum , Hydrocéphalie , Hydrocéphalie chronique de l'adulte , Neurologie , Lobe pariétal , Anatomopathologie , Tomographie par émission de positons
5.
Journal of Clinical Neurology ; : 435-436, 2017.
Article Dans Anglais | WPRIM | ID: wpr-31738

Résumé

No abstract available.


Sujets)
Amnésie globale transitoire , Incidence , Corée , Saisons
6.
Dementia and Neurocognitive Disorders ; : 170-173, 2016.
Article Dans Anglais | WPRIM | ID: wpr-111894

Résumé

BACKGROUND: As rapidly progressive dementia (RPD), general paresis and Creutzfeldt-Jakob disease (CJD) may have overlapping clinical presentation due to a wide variety of clinical manifestations. CASE REPORT: A 57-year-old man presented with rapid progressive cognitive decline, behavioral change, ataxic gait, tremor and pyramidal signs for 3 months. In addition to these multiple systemic involvements, positive result for the cerebrospinal fluid (CSF) 14-3-3 protein tentatively diagnosed him as probable CJD. However, due to increased serum rapid plasma reagin, venereal disease research laboratory, and fluorescent treponemal antibody-absorption reactivity in CSF, the final diagnosis was changed to general paresis. CONCLUSIONS: A patient with RPD needs to be carefully considered for differential diagnosis, among a long list of diseases. It is important to rule out CJD, which is the most frequent in RPD and is a fatal disease with no cure. Diagnostic criteria or marker of CJD, such as 14-3-3 protein, may be inconclusive, and a typical pattern in diffusion-weighted imaging is important to rule out other reversible diseases.


Sujets)
Humains , Adulte d'âge moyen , Protéines 14-3-3 , Liquide cérébrospinal , Maladie de Creutzfeldt-Jakob , Démence , Diagnostic , Diagnostic différentiel , Démarche , Neurosyphilis , Plasma sanguin , Maladies sexuellement transmissibles , Tremblement
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