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    • Neurology and clinical neuroscience Journal

    Papers
    A Case of Parkinson's Disease Following Autoimmune Autonomic Ganglionopathy
    Akihiko Mitsutake,Hideyuki Matsumo,Keiko Hatano,Osamu Higuchi,Shunya Nakane,Hideji Hashida
    Neurology And Clinical Neuroscience（2019）
    The patient is an 80‐year‐old man. At the age of 76, he presented with acute onset of severe orthostatic hypotension and diarrhea. Anti‐ganglionic acetylcholine receptor (anti‐gAChR) antibodies were positive, and prednisolone was effective. He was diagnosed with autoimmune autono...
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    Free-Floating Ball Thrombus In The Left Atrium: Percutaneous Transvenous Mitral Commissurotomy For Recurrence Prevention
    Masaru Seguchi,Masunari Shibata,Takeshi Takamura,Kota Maekawa,Takanori Sano,Kazuto Kobayashi,Fumitaka Miya
    Neurology And Clinical Neuroscience（2017）
    An 87-year-old female presented altered mental status and left hemiparesis. A cerebral angiogram showed abrupt cutoff of the right internal carotid artery. Mechanical thrombectomy was performed. Postoperative transthoracic echocardiography revealed a free-floating ball thrombus (...
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    Antibodies to a Brain‐type Creatine Kinase Associated with Paraneoplastic Neurological Syndromes
    Syuichi Tetsuka,Hideaki Yamasawa,Kunihiko Ikeguchi,Ken-ichi Fujimoto
    Neurology And Clinical Neuroscience（2015）
    Previously, we identified a brain‐type creatine kinase antibody to be associated with paraneoplastic cerebellar degeneration using a proteomic approach. Immunohistochemistry showed that this antibody reacted with both mouse cerebellar neurons and bladder cancer tissues. Furthermo...
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    An Autopsy Case of MM1‐type Sporadic Creutzfeldt–Jakob Disease with Long Survival of 7 Years
    Aya Kawanami,Akira Arakawa,Tomoyasu Matsubara, Masanobu Miyashita, Yuichi Miyagi,Kazuko Hasegawa,Shigeo Murayama,Saburo Yagishita,Yuko Saito
    Neurology And Clinical Neuroscience（2024）
    We report the first autopsy case of MM1-type sporadic Creutzfeldt-Jakob disease (sCJD) who survived 80 months after long-term artificial ventilatory support. The cerebral cortex and white matter exhibited severe atrophy, sparing the hippocampus. The prion protein aggregates of 10...
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    A Patient with Neuronal Intranuclear Inclusion Disease Developed Encephalitis‐like Symptoms after Cerebral Angiography
    Shin Koide,Shintaro Tsuboguchi,Shingo Koide,Itaru Ninomiya,Taiki Saito,Takanobu Ishiguro,Etsuji Saji,Yo Higuchi,Takeshi Ikeuchi,Makoto Oishi,Masato Kanazawa,Osamu Onodera
    Neurology And Clinical Neuroscience（2024）
    Patients with neuronal intranuclear inclusion disease (NIID) can present with encephalitis‐like symptoms such as recurrent paroxysmal fever and unconsciousness. To date, no specific triggers for these symptoms have been reported. In our case, an 78‐year‐old woman became unconscio...
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    Successful Treatment of Anti‐gad Antibody‐associated Autoimmune Cerebellar Ataxia with Combined Immunotherapies
    Yoshio Omote,Chika Matsuoka,Ryo Sasaki,Nozomi Hishikawa,Yuko Kawahara,Emi Nomura,Namiko Matsumoto,Yuki Taira,Mami Takemoto,Ryuta Morihara,Toru Yamashita,Koji Abe
    Neurology And Clinical Neuroscience（2021）
    Anti‐glutamic acid decarboxylase (GAD) antibody (Ab)‐associated autoimmune cerebellar ataxia (CA) is a rare neurological disorder, and a standardized therapy has not been established. Here, we report on a 58 year‐old man with type 1 diabetes mellitus, who developed progressive CA...
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    Negative Predictors of Clinical Response to Amitriptyline in Japanese Patients with Migraine
    Yuika Naito,Masakazu Ishii,Masaaki Ishibashi,Hideyo Kasai,Hirotaka Katoh
    Neurology And Clinical Neuroscience（2018）
    Migraine is the most common neurological disease. Recently, there is a wide variety of prophylactic drugs, but their effects differ among individuals.
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    PEG‐J Tube Breakage in a Patient with Parkinson's Disease Receiving Levodopa–carbidopa Intestinal Gel Therapy
    Temma Soga,Naoto Sugeno,Toru Baba,Xiaoyi Jin,Tomoyuki Koike,Takafumi Hasegawa,Masashi Aoki
    Neurology And Clinical Neuroscience（2018）
    Complications of levodopa–carbidopa intestinal gel (LCIG) therapy are relatively common, presenting in 40–96% of patients. Here, we report an unusual, accidental tube breakage in a patient with Parkinson’s disease (PD) under LCIG therapy. An 80-year-old man of PD with mild cognit...
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    A Japanese Patient with a VCP Mutation C.290g > A (p.g97e) Presenting a Rapid Progressive Respiratory Failure
    Emi Nomura,Yasuyuki Ohta,Kota Sato,Yuko Kawahara,Mami Takemoto,Yoshiaki Takahashi,Namiko Matsumoto,Taijun Yunoki,Toru Yamashita,Nozomi Hishikawa,Ichizo Nishino,Koji Abe
    Neurology And Clinical Neuroscience（2019）
    Inclusion body myopathy with Paget's disease of bone and frontotemporal dementia (IBMPFD) is an autosomal dominant disorder caused by mutations in the valosin‐containing protein (VCP) gene. IBMPFD usually presents progressive limb muscle weakness resulting in wheelchaired after m...
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    Pseudomeningocele As A Result of Traumatic Nerve Root Avulsion
    Joe James,James Jose
    Neurology And Clinical Neuroscience（2016）
    A 23-year-old man presented with weakness of shoulder abduction and elbow flexion on the right side, with numbness of the index finger and thumb, after a bike accident. On examination, he had grade II/V power of the deltoid and biceps, with absent biceps jerk and sensory impairme...
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    Comparative Study of Non‐parkinsonian and Parkinsonian Motor Symptoms in View of Brain Activities Monitored During Thalamotomy
    Nobuo Miyashita,Yohsuke Narabayashi,Tomokazu Oshima
    Neurology And Clinical Neuroscience（2015）
    Background: We treat non-parkinsonian motor disorders by thalamotomy, assuming their pathophysiological similarity to Parkinson's disease (PD).Aim: We compared the non-parkinsonian and parkinsonian brain activities to clarify their similarity and difference.Methods: We examined p...
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    Successful Switching of Anticoagulants in a Patient with Superficial Siderosis and Atrial Fibrillation
    Yuichiro Inatomi,Makoto Nakajima,Toshiro Yonehara,Yukio Ando
    Neurology And Clinical Neuroscience（2016）
    A 78‐year‐old man with atrial fibrillation treated with warfarin experienced acute headache, deafness, cerebellar ataxia and dysuria. Superficial siderosis was diagnosed on brain imaging; however, no bleeding sources were detected. His neurological deficits and bloody cerebrospin...
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    Tumefactive Demyelinating Disease Mimicking Malignant Tumor in Positron Emission Tomography with 11C‐methionine
    Kosuke Matsuzono,Kentaro Deguchi,Nozomi Hishikawa,Toru Yamashita,Tomotsugu Ichikawa,Isao Date,Koji Abe
    Neurology And Clinical Neuroscience（2015）
    Tumefactive demyelination is sometimes difficult differentiate from malignant tumors. Positron emission tomography with C-11-methionine is useful for diagnosing cerebral malignant tumors, but there are previous reports for tumefactive demyelination. We experienced a 32-year-old m...
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    Transient Myoclonic State with Asterixis Presenting As Persistent Hyperperfusion on Single‐photon Emission Computed Tomography: A Case Report
    Atsushi Umemura,Tomoko Oeda,Hideyuki Sawada
    Neurology And Clinical Neuroscience（2015）
    Transient myoclonic state with asterixis is characterized by sudden onset generalized myoclonus and asterixis without consciousness impairment. Electrophysiological studies have shown that myoclonus correlates with cortical hyperexcitability localized in the primary motor cortex ...
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