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Spinal muscular atrophy with oculomotor palsy, epilepsy, and cerebellar hypoperfusion.
Oka A, Matsushita Y, Sakakihara Y, Momose T, Yanaginasawa M. Oka A, et al. Pediatr Neurol. 1995 May;12(4):365-9. doi: 10.1016/0887-8994(95)00058-n. Pediatr Neurol. 1995. PMID: 7546013
We report a boy with spinal muscular atrophy (SMA) type 1, who developed novel clinical and neuroradiologic features, indicating the broad spectrum of this degenerative disease. ...
We report a boy with spinal muscular atrophy (SMA) type 1, who developed novel clinical and neuroradiologic features, indicating the …
New ocular movement detector system as a communication tool in ventilator-assisted Werdnig-Hoffmann disease.
Kubota M, Sakakihara Y, Uchiyama Y, Nara A, Nagata T, Nitta H, Ishimoto K, Oka A, Horio K, Yanagisawa M. Kubota M, et al. Among authors: oka a. Dev Med Child Neurol. 2000 Jan;42(1):61-4. doi: 10.1017/s0012162200000116. Dev Med Child Neurol. 2000. PMID: 10665977
A non-contact communication system was developed for a ventilator-assisted patient with Werdnig-Hoffmann disease who had lost all voluntary movements except for those of the eye. The system detects the extraocular movements and converts them to either a 'yes'
A non-contact communication system was developed for a ventilator-assisted patient with Werdnig-Hoffmann disease who had lost
Communicating hydrocephalus in a patient with Gaucher's disease type 3.
Shiihara T, Oka A, Suzaki I, Ida H, Takeshita K. Shiihara T, et al. Among authors: oka a. Pediatr Neurol. 2000 Mar;22(3):234-6. doi: 10.1016/s0887-8994(99)00140-x. Pediatr Neurol. 2000. PMID: 10734257
The case of a 3-year-old male with type 3 Gaucher's disease, whose genotype for the beta-glucosidase gene was D409H/unknown mutation, is presented. After the onset of visceral and neurologic signs during infancy, a radiologic investigation at 3 years of age revealed …
The case of a 3-year-old male with type 3 Gaucher's disease, whose genotype for the beta-glucosidase gene was D409H/unknown mutation, …
Rapid immunologic diagnosis of classic late infantile neuronal ceroid lipofuscinosis.
Kurachi Y, Oka A, Mizuguchi M, Ohkoshi Y, Sasaki M, Itoh M, Hayashi M, Goto Y, Takashima S. Kurachi Y, et al. Among authors: oka a. Neurology. 2000 Apr 25;54(8):1676-80. doi: 10.1212/wnl.54.8.1676. Neurology. 2000. PMID: 10762513
OBJECTIVE: To establish a new method for rapid diagnosis of late infantile neuronal ceroid lipofuscinosis (LINCL, CLN2) using specific polyclonal antibodies against the CLN2 gene product. ...This relatively simple, specific, and cost-effective method is a promising …
OBJECTIVE: To establish a new method for rapid diagnosis of late infantile neuronal ceroid lipofuscinosis (LINCL, CLN2) using specifi …
Generators of rolandic discharges identified by magnetoencephalography.
Kubota M, Oka A, Kin S, Sakakihara Y. Kubota M, et al. Among authors: oka a. Electroencephalogr Clin Neurophysiol Suppl. 1996;47:393-401. Electroencephalogr Clin Neurophysiol Suppl. 1996. PMID: 9336001 Clinical Trial. No abstract available.
Current source localization of EEG paroxysms in a patient with congenital mirror movement.
Kubota M, Oka A, Kin S, Sakakihara Y. Kubota M, et al. Among authors: oka a. Electroencephalogr Clin Neurophysiol Suppl. 1996;47:357-62. Electroencephalogr Clin Neurophysiol Suppl. 1996. PMID: 9335998 No abstract available.
[Acute necrotizing encephalopathy with horizontal gaze palsy].
Kurachi Y, Kawahara H, Hatakeyama K, Yazawa K, Kubota M, Oka A, Kin S, Sakakihara Y, Yanagisawa M. Kurachi Y, et al. Among authors: oka a. No To Shinkei. 1997 Aug;49(8):753-8. No To Shinkei. 1997. PMID: 9282370 Japanese.
Acute necrotizing encephalopathy (ANE) of childhood is a newly proposed disease entity characterized by symmetrically distributed necrotic brain lesions in the thalamus, cerebral white matter, brainstem, and cerebellum. ...In addition to severe psychomotor delay, the patie …
Acute necrotizing encephalopathy (ANE) of childhood is a newly proposed disease entity characterized by symmetrically distributed nec …
Transcranial magnetic stimulation in an adrenoleukodystrophy patient.
Nezu A, Kimura S, Kobayashi T, Sekiguchi H, Ikuta K, Matsuyama S, Oka A, Sakakihara Y. Nezu A, et al. Among authors: oka a. Brain Dev. 1996 Jul-Aug;18(4):327-9. doi: 10.1016/0387-7604(96)00011-3. Brain Dev. 1996. PMID: 8879655
On TMS delivered through a circular coil, MEPs recorded from the relaxed first dorsal interosseous muscle showed that only the duration was significantly prolonged, which may be due to temporal dispersion of descending volleys in the pyramidal tracts, while the latency was …
On TMS delivered through a circular coil, MEPs recorded from the relaxed first dorsal interosseous muscle showed that only the durati …
Temporary improvement of neurological symptoms with gammaglobulin therapy in a boy with adrenoleukodystrophy.
Oka A, Saito M, Kubota M, Sakakihara Y, Yanagisawa M. Oka A, et al. Brain Dev. 1996 Mar-Apr;18(2):119-21. doi: 10.1016/0387-7604(95)00106-9. Brain Dev. 1996. PMID: 8733902
A 10-year-old boy with adrenoleukodystrophy was treated with gammaglobulin in conjunction with a mixture of glyceryl trioleate and glyceryl trierucate. With a high dose of gammaglobulin, clinical improvement, including the reduction of visual field defects, w
A 10-year-old boy with adrenoleukodystrophy was treated with gammaglobulin in conjunction with a mixture of glyceryl trioleate
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