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stuttering/atrofie

Odkaz je uložen do schránky
ČlánkyKlinické testyPatenty
Strana 1 z 33 Výsledek

Deep brain stimulation of the subthalamic nucleus reversibly deteriorates stuttering in advanced Parkinson's disease.

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
The etiology of developmental stuttering is still unknown. In some patients, stuttering re-emerges or is aggravated with the onset of Parkinson's disease (PD). We here report on a patient with PD treated by deep brain stimulation of the subthalamic nucleus and severe deterioration of stuttering

A case of multiple system atrophy-parkinsonian type with stuttering- and palilalia-like dysfluencies and putaminal atrophy.

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
Both developmental and acquired stuttering are related to the function of the basal ganglia-thalamocortical loop, which includes the putamen. Here, we present a case of stuttering- and palilalia-like dysfluencies that manifested as an early symptom of multiple system atrophy-parkinsonian type

[A case of transient acute stuttering in cerebral atrophy].

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace

Early onset of deafening-induced song deterioration and differential requirements of the pallial-basal ganglia vocal pathway.

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
Similar to humans, songbirds rely on auditory feedback to maintain the acoustic and sequence structure of adult learned vocalizations. When songbirds are deafened, the learned features of song, such as syllable structure and sequencing, eventually deteriorate. However, the time-course and initial

[Palilalia and acquired stuttering in a case of Parkinson's disease].

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
We report palilalia and acquired stuttering in a 60-year-old Japanese male with Parkinson's disease. At the age of 54, he presented with resting tremor in the hand and foot on the left, and gradual slowness in voluntary movements. Two years later, resting tremor involved the right foot, and an

[Acquired stuttering as an early symptom in a patient with progressive supranuclear palsy].

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
We report a 57-year-old man with progressive supranuclear palsy (PSP) showing acquired stuttering (AS) as an early symptom. He had noticed micrographia at age 48, and thereafter he began to suffer from progressive speech disturbance at age 49. Neurological examination at age 57 revealed prominent
Background: Despite initial underreporting of language dysfunctions in corticobasal syndrome (CBS), aphasia is now recognized as a frequent feature of this disease. Aphasia in CBS seems clinically overlying to a non-fluent/agrammatic

An investigation into the personal financial costs associated with stuttering.

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
Stuttering has been found to deteriorate quality of life in psychological, emotional and social functioning domains. It is reasonable to assume then that stuttering would also be associated with economic consequences that may also challenge quality of life. Remarkably, the personal financial costs

Communicative and cognitive deterioration in dialysis dementia: two case studies.

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
We studied the cognitive and communicative deterioration of two patients who were treated by maintenance dialysis and developed a fatal progressive encephalopathy, "dialysis dementia." Detailed language, speech, and psychological evaluations support the contention that this neurologic syndrome is in

Olanzapine- and clozapine-induced stuttering. A case series.

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
Drug-induced stuttering has been described in association with several drugs, in particular antidepressants and low-potency neuroleptics. Here we describe a case series of stuttering induced by the atypical neuroleptics olanzapine and clozapine. Patients receiving neuroleptic treatment were

Acute intermittent porphyria presenting as progressive muscular atrophy in a young black man.

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
Acute intermittent porphyria, the most common porphyria affecting the nervous system, typically presents with neurovisceral crises followed by a motor neuropathy. We describe a 23-year-old black South African man presenting with a progressive stuttering, lower motor neuron syndrome developing over

[A case of hereditary sensory and autonomic neuropathy type 1E with frontal lobe dysfunction as an initial symptom].

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
A 49-year-old man had developed gradually personality change, gait disturbance, and hearing loss for five years. On admission, he presented with frontal release signs, stuttering, vertical gaze palsy, sensorineural deafness, muscle rigidity, ataxia, and sensory disturbance with areflexia in the

Speech, language, and cognitive dysfunction in children with focal epileptiform activity: A follow-up study.

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
We reviewed the medical history, EEG recordings, and developmental milestones of 19 children with speech and language dysfunction and focal epileptiform activity. Speech, language, and neuropsychological assessments and EEG recordings were performed at follow-up, and prognostic indicators were

Primary progressive aphasia and Pick complex.

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
Ten autopsied patients from a prospectively followed, clinically defined, neuropsychologically and radiologically documented cohort with primary progressive aphasia were histologically characterized. All were variants of frontotemporal degeneration (Pick complex): Pick body dementia, n=3,

Tourette syndrome and complex partial epilepsy--a case report.

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
Controversy exists over the pathophysiology of Tourette syndrome (TS). The case reported is a 37-year-old unmarried man suffering from both TS and complex partial epilepsy (CPE). He began to have seizures at 2-3 months of age. The CPE featured dark vision, dizziness, followed by unresponsiveness, a
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