Search Results - "Nishida, Yoshihiko"
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1
Clinicopathologic features of autosomal recessive amyotrophic lateral sclerosis associated with optineurin mutation
Published in Neuropathology (01-02-2014)“…We performed clinicopathological analyses of two amyotrophic lateral sclerosis (ALS) patients with homozygous Q398X optineurin (OPTN) mutation. Clinically,…”
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2
Phosphatidylinositol-4,5-bisphosphate is enriched in granulovacuolar degeneration bodies and neurofibrillary tangles
Published in Neuropathology and applied neurobiology (01-06-2014)“…Aims Among the pathological findings in Alzheimer's disease (AD), the temporal and spatial profiles of granulovacuolar degeneration (GVD) bodies are…”
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3
Distinct Incidence of Takotsubo Syndrome Between Amyotrophic Lateral Sclerosis and Synucleinopathies: A Cohort Study
Published in Frontiers in neurology (13-12-2018)“…Takotsubo syndrome (TTS) is an acute cardiac syndrome characterized by regional left ventricular dysfunction with a peculiar circumferential pattern, which…”
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4
Late-onset myasthenia gravis is predisposed to become generalized in the elderly
Published in eNeurologicalSci (01-03-2016)“…The continuous increase in the number of patients presenting with late-onset myasthenia gravis (LOMG) underscores the need for a better understanding of the…”
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5
Dysphagia in Parkinson's disease
Published in Rinsho shinkeigaku = Clinical neurology (31-08-2016)“…Although dysphagia is an important symptom associated with prognosis in patients with Parkinson's disease (PD), dysphagia tends to be overlooked until…”
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6
Hyperexcitability as a potential cause for diffuse lower motor neuron loss in Isaacs’ syndrome
Published in Neurology and clinical neuroscience (01-09-2013)“…We present a patient who initially developed diffuse painful muscle cramps who had elevated antibodies against voltage‐gated potassium channel (VGKC) complex…”
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7
Case of neuromyelitis optica spectrum disorder associated with central pontine and extrapontine myelinolysis preceded by syndrome of inappropriate antidiuretic hormone secretion
Published in Rinsho shinkeigaku = Clinical neurology (2014)“…A 36-year-old woman complained of general malaise. She presented with hyponatremia and plasma osmotic pressure was lower than urinary osmotic pressure. In…”
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8
Intravenous immunoglobulin for maintenance treatment of chronic inflammatory demyelinating polyneuropathy: a multicentre, open-label, 52-week phase III trial
Published in Journal of neurology, neurosurgery and psychiatry (01-10-2017)“…ObjectiveShort-term efficacy of induction therapy with intravenous immunoglobulin (Ig) in patients with chronic inflammatory demyelinating polyneuropathy…”
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9
Increased replication of HTLV-I in HTLV-I-associated myelopathy
Published in Annals of neurology (01-09-1989)“…To estimate the replication of the human T-cell leukemia virus type I (HTLV-I) in patients with HTLV-I-associated myelopathy (HAM), or tropical spastic…”
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10
Takotsubo syndrome complicated with amyotrophic lateral sclerosis (P4.056)
Published in Neurology (18-04-2017)“…Abstract only…”
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11
Randomized controlled trial of KW-6356 monotherapy in patients with early untreated Parkinson's disease
Published in Parkinsonism & related disorders (01-12-2023)“…KW-6356 is a novel selective adenosine A receptor antagonist/inverse agonist. We evaluated the efficacy and safety of KW-6356 as monotherapy in patients with…”
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12
Successful treatment of stiff person syndrome with sequential use of tacrolimus
Published in Journal of neurology, neurosurgery and psychiatry (01-10-2013)“…[...]intravenous Ig (400 mg/kg body weight/day) was administered for 5 days in case 1 ( figure 1 A), whereas the patient in case 2 underwent a course of three…”
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13
MFN2 transcripts escaping from nonsense-mediated mRNA decay pathway cause Charcot-Marie-Tooth disease type 2A2
Published in Journal of neurology, neurosurgery and psychiatry (01-11-2016)Get full text
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14
Late-onset spastic paraplegia: Aberrant SPG11 transcripts generated by a novel splice site donor mutation
Published in Journal of the neurological sciences (15-12-2015)“…Abstract We identified a novel homozygous mutation in the splice site donor (SSD) of intron 30 (c.5866 + 1G > A) in consanguineous Japanese SPG11 siblings…”
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15
Autopsy-Proven Amyotrophic Lateral Sclerosis Coexisted With Parkinson Disease: A Novel Association Of TDP-43 Proteinopathy And α-Synucleinopathy (P1.056)
Published in Neurology (08-04-2014)“…Abstract only…”
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16
Localization of myoglobin in human muscle cells by immunoelectron microscopy
Published in Muscle & nerve (01-02-1987)“…The localization of myoglobin in human skeletal muscle cell was studied by immunoelectron microscopy. The Fab'-horseradish peroxidase (HRP) conjugate was…”
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17
Missense and Nonsense Mutations in the Lysosomal α-Mannosidase Gene (MANB) in Severe and Mild Forms of α-Mannosidosis
Published in American journal of human genetics (01-10-1998)“…α-Mannosidosis is an autosomal recessive lysosomal-storage disorder caused by a deficiency of lysosomal α-mannosidase activity. This disease shows a wide range…”
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18
Cardiac dysfunction with Becker muscular dystrophy
Published in The American heart journal (01-09-1996)“…Cardiac function was examined in 21 patients with Becker muscular dystrophy (BMD) and compared with 43 patients with Duchenne muscular dystrophy (DMD) and 37…”
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19
Familial idiopathic basal ganglia calcification with dominant inheritance
Published in Nihon Naika Gakkai Zasshi (01-12-1988)Get full text
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20
Loss of postural reflexes in long-term occupational solvent exposure
Published in European neurology (01-01-2002)“…Inhalation of organic solvents has long been known to damage various nervous systems, including cerebellum, brainstem, and pyramidal tract. However, little is…”
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