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81
Malignant Transformation Six Months after Removal of Intracranial Epidermoid Cyst: A Case Report
Published 2011-01-01“…A 52-year-old man presented with left facial paralysis and cerebellar ataxia. He had undergone total removal of a benign epidermoid cyst six months previously. …”
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82
Marchiafava-Bignami Disease in a Nonalcoholic Diabetic Patient
Published 2013-01-01“…Neurologic examination showed dysarthria, dysmetria, and ataxia but, otherwise, normal cranial nerves, motor and sensory functions, and tendon reflexes. …”
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83
Ramsay Hunt Syndrome Associated with Central Nervous System Involvement in an Adult
Published 2016-01-01“…We describe a 55-year-old diabetic female who presented with gait ataxia, right peripheral facial palsy, and painful vesicular lesions involving her right ear. …”
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84
Legionnaires' Disease with Facial Nerve Palsy
Published 2011-01-01“…After the two weeks, his respiratory symptoms, gait ataxia and dysarthria resolved. We report the first case of Legionnaires' disease with cerebellar dysfunction and seventh nerve palsy. …”
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85
Hemiataxia: A Novel Presentation of Anti-NMDA Receptor Antibody Mediated Encephalitis in an Adolescent
Published 2017-01-01“…Although orofacial dyskinesias were initially identified as a characteristic movement phenomenon in this type of encephalitis, an expanded range of abnormalities has recently been reported, including isolated ataxia. We report a case of isolated hemiataxia in a young adult with mild initial psychiatric manifestations. …”
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86
Brainstem and Cerebellar Involvement in Ramsay Hunt Syndrome
Published 2019-01-01“…This presented as left facial paralysis, left sixth nerve palsy, horizontal diplopia to the left lateral gaze, profound truncal ataxia, and left-sided dysmetria. Clinical awareness that Ramsay Hunt syndrome may also involve the brainstem and cerebellum is critical in evaluating the clinical neurologic findings and expanding the diagnostic workup to include brain magnetic resonance imaging and cerebrospinal fluid analysis, including varicella zoster polymerase chain reaction. …”
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87
Rare Association of Anti-Hu Antibody Positive Paraneoplastic Neurological Syndrome and Transitional Cell Bladder Carcinoma
Published 2012-01-01“…Central nervous system symptoms included cognitive problems, personality change, and truncal ataxia. Case notes and the literature were reviewed. …”
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88
Involvement of Coenzyme Q10 in Various Neurodegenerative and Psychiatric Diseases
Published 2023-01-01“…This agent has shown its efficacy in preventing and treating neurological diseases such as migraine, Parkinson’s disease, Alzheimer’s disease, Huntington’s disease, amyotrophic lateral sclerosis, and Friedreich’s ataxia. This study reviews the literature to highlight this agent’s potential therapeutic effects in the mentioned neurological disorders.…”
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89
Intravenous Immunoglobulin and Mycophenolate Mofetil for Long-Standing Sensory Neuronopathy in Sjögren's Syndrome
Published 2012-01-01“…In a few months, she developed ataxia with increased hypoanaesthesia. Electrodiagnostic tests revealed undetectable distal and proximal sensory nerve action potential in upper and lower limbs. …”
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90
Progress on neuromodulation for treatment of rare movement disorders
Published 2025-01-01“…This review systematically summarizes the application and efficacy of both invasived and non⁃invasived neuromodulation techniques in treating various rare movement disorders, including spinocerebellar ataxia (SCA), Huntington's disease (HD), and neuroacanthocytosis (NA), etc.. …”
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91
Severe Neurotoxicity due to Atropa belladonna Poisoning: A Case Report and Literature Review
Published 2024-01-01“…These manifestations may include flushing, mydriasis, tachycardia, ataxia, agitation, delirium, and urinary retention. …”
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92
Cyclooxygenase Inhibitor Associated with Carboplatin in Treatment of Metastatic Nasal Carcinoma in Dog
Published 2014-01-01“…After 7 months the treatment started, the animal presented with ataxia, vocalization, hyperesthesia, and anorexia. …”
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93
Familial Case of Pelizaeus-Merzbacher Disorder Detected by Oligoarray Comparative Genomic Hybridization: Genotype-to-Phenotype Diagnosis
Published 2017-01-01“…Pelizaeus-Merzbacher disease (PMD) is an X-linked recessive hypomyelinating leukodystrophy characterized by nystagmus, spastic quadriplegia, ataxia, and developmental delay. It is caused by mutation in the PLP1 gene. …”
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94
Encefalopatía de Wernicke en paciente no alcohólica. A propósito de un caso
Published 2019-12-01“…Luego de su recuperación, se ingresa nuevamente 11 días después con cuadro de ataxia, desviación del ojo derecho hacia ángulo nasal por parálisis del VI par craneal y confusión mental. …”
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95
Xeroderma Pigmentosum with Severe Neurological Manifestations/De Sanctis–Cacchione Syndrome and a Novel XPC Mutation
Published 2017-01-01“…He also displayed severe neurologic abnormalities (intellectual disability, ataxia, altered speech, and hyperreflexia), short stature, and microcephaly, which are features associated with DSC. …”
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96
Amelioration of Behavioural, Biochemical, and Neurophysiological Deficits by Combination of Monosodium Glutamate with Resveratrol/Alpha-Lipoic Acid/Coenzyme Q10 in Rat Model of Cis...
Published 2013-01-01“…Cisplatin or cis-diamminedichloroplatinum (II) (CDDP) is a cytotoxic chemotherapeutic agent with dose-dependent peripheral neuropathy as a foremost side effect characterised by ataxia, pain, and sensory impairment. Cumulative drug therapy of CDDP is known to produce severe oxidative damage. …”
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97
Pain in Neurodegenerative Disease: Current Knowledge and Future Perspectives
Published 2016-01-01“…The management of neurodegenerative diseases such as Alzheimer’s disease (AD) and other dementias, Parkinson’s disease (PD) and PD related disorders, motor neuron diseases (MND), Huntington’s disease (HD), spinocerebellar ataxia (SCA), and spinal muscular atrophy (SMA), is mainly addressed to motor and cognitive impairment, with special care to vital functions as breathing and feeding. …”
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98
Transient, Recurrent Central Nervous System Clinical Manifestations of X-Linked Charcot-Marie-Tooth Disease Presenting with Very Long Latency Periods between Episodes: Is Prolonged...
Published 2020-01-01“…Transient acute and recurrent or chronic central nervous system manifestations, predominantly, dysarthria, dysphagia, motor weakness, and ataxia, have been recognized as a feature of the X-linked type 1 of CMT (CMTX1). …”
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99
Prion Diseases and the Gastrointestinal Tract
Published 2006-01-01“…They are uniformly fatal neurological diseases, which are characterized by ataxia and vacuolation in the central nervous system. …”
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100
Paraneoplastic Neurological Syndromes: Severe Neurological Symptoms Resulting from Relatively Benign or Occult Tumours—Two Case Reports
Published 2013-01-01“…A 69-year-old female was admitted with a subacute onset of dysarthria, ataxia, and cerebellar signs. Workup revealed a relatively benign Non-Hodgkin’s Lymphoma. …”
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