Showing 81 - 100 results of 180 for search '"ataxia"', query time: 0.04s Refine Results
  1. 81

    Facial Involuntary Movements and Respiratory Failure in CANOMAD, Responsive to IVIG Therapy by Kate Johnson, Ashish Malkan, Mohamed Shaffi

    Published 2015-01-01
    “…CANOMAD is a rare chronic neuropathy, characterized by chronic sensory ataxia and intermittent brain stem symptoms due to antidisialosyl antibodies. …”
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    Article
  2. 82

    Extrapontine Myelinolysis following Extreme Hypernatremia and Hyperosmolarity by Jan-Niclas Schwade, Lior Haftel, Lars Rühe, Matthias Endmann

    Published 2019-01-01
    “…On the fourth day of hospitalization, the patient developed tremor, ataxia, and rigor. Cranial magnetic resonance imaging (cMRI) was performed and (mis)interpreted for meningoencephalitis, with corresponding diagnostic and therapeutic implications. …”
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  3. 83

    Thiazide-Associated Hyponatremia and Mortality Risk: A Cohort Study by Steven G. Achinger, Juan Carlos Ayus, Ambuj Kumar, Athanasios Tsalatsanis

    Published 2025-02-01
    “…Secondary outcomes include development of sepsis, pneumonia, urinary tract infection, cellulitis, myocardial infarction, stroke, congestive heart failure, ataxia, fall, and hip fracture. Analytical Approach: The design is a retrospective cohort study, propensity score matched. …”
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    Article
  4. 84

    Understanding the Pathogenesis of Angelman Syndrome through Animal Models by Nihar Ranjan Jana

    Published 2012-01-01
    “…Angelman syndrome (AS) is a neurodevelopmental disorder characterized by severe mental retardation, lack of speech, ataxia, susceptibility to seizures, and unique behavioral features such as easily provoked smiling and laughter and autistic features. …”
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    Article
  5. 85

    Enteric Fever as an Antecedent to Development of Miller-Fisher Syndrome and Possible Role of COVID-19 Vaccination by Tayyaba Binte Saleem, Muhammad Ibrahim, Faizan Fazal, Mohammad Ebad Ur Rehman, Ali Ahmad Ijaz, Humera Nasim

    Published 2023-12-01
    “…It is characterized by findings of ophthalmoplegia, ataxia, and areflexia. Here we present the case of Miller-Fisher Syndrome following an episode of typhoidal diarrhea. …”
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    Article
  6. 86

    Quantification of the usage of symptomatic treatment in patients suffering from multiple sclerosis. by Erélido Hernández Valero, Mikhail Benet Rodríguez

    Published 2007-08-01
    “…<strong><br />Results:</strong> High percentages of patients with clinical manifestations and without the proper treatment for rigidity, weakness, ataxia, urinary retention and incontinence, sexual dysfunction, constipation, fatigue, pain and depression were found. …”
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  7. 87

    Treatment of Ethylene Glycol Poisoning with Oral Ethyl Alcohol by B. Achappa, D. Madi, T. Kanchan, N. K. Kishanlal

    Published 2019-01-01
    “…A 70-year-old female presented to our hospital with ataxia after ingestion of ethylene glycol. The reported case describes the management of ethylene glycol poisoning using oral ethyl alcohol as an alternative to the recommended intravenous ethyl alcohol and fomepizole that are not available for use in India. …”
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    Article
  8. 88

    Isolated Bilateral Ptosis as an Early Sign of Guillain-Barré Syndrome by Yahia Z. Imam, Dirk Deleu

    Published 2013-01-01
    “…Our paper highlights the importance of recognizing GBS as a potential etiology in a patient presenting with isolated ptosis, particularly since the course of GBS can be more dramatic than in the anti-GBQ1b syndromes such as ophthalmoparesis without ataxia and Miller Fisher syndrome or ocular myasthenia. …”
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    Article
  9. 89

    Сlinical case of funicular myelosis in combination with a concomitant genetic predisposition to folate cycle disorder by O.D. Shulga, E.A. Popko, A.S. Chabanova, O.G. Kotsiuba, Q. Hussain

    Published 2024-06-01
    “…The disease is usually characterized by the presence of paresthesias, the development of sensitive ataxia, and impaired gait. The aim of the work was to demon­strate a clinical case of funicular myelosis in a young patient in order to improve the diagnostic process, paying attention to the genetic profile and identifying a concomitant predisposition to folate cycle disorder. …”
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    Article
  10. 90

    Clinical features of early multiple sclerosis by I. Čelpačenko, R. Stankevičiūtė, M. Malciūtė, R. Balnytė

    Published 2021-06-01
    “…Positive Babinski’s reflex, decreased muscle strength, ataxia, and diminished sense of vibration and proprioception were more frequent in patients older than 50 years compared with younger patients. …”
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    Article
  11. 91

    Magnetic Resonance Imaging Lesions in the Central Nervous System of a Dog with Canine Monocytic Ehrlichiosis by Linda G. Lang, John F. Griffin, Jonathan M. Levine, Edward B. Breitschwerdt

    Published 2011-01-01
    “…A ten-year-old neutered male dog was examined for tetraparesis, vestibular dysfunction, ataxia, and vertebral column hyperesthesia of 10 days duration. …”
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  12. 92

    Leukoreduction in a dog with acute leukemia by Brenna Hanratty, Anna Hauck, Amanda Foskett, J. D. Foster

    Published 2025-01-01
    “…Abstract A 9‐year‐old male castrated golden retriever cross was evaluated for an acute onset of ataxia. A complete blood count revealed marked leukocytosis, anemia, and thrombocytopenia. …”
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  13. 93

    Clinical characteristics of the Ala21Val variant in the myelin proteolipid protein 1 (PLP1) gene associated with Pelizaeus-Merzbacher disease in a Brazilian male patient by Pedro Manzke, Pedro Renato P. Brandão, Talita Balieiro, Diógenes Diego de Carvalho Bispo, Maria Joana Osório, Gustavo Barcelos Barra

    Published 2025-01-01
    “…He presented with developmental delays, nystagmus, spastic paraparesis, optic atrophy, dysphagia, appendicular ataxia, and progressive head tremor. Brain MRI revealed hypomyelination, diffuse white matter hyperintensity, and atrophy of the corpus callosum and cerebellum, expanding the known clinical spectrum of PMD.…”
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  14. 94

    D-Lactic Acidosis: An Underrecognized Complication of Short Bowel Syndrome by N. Gurukripa Kowlgi, Lovely Chhabra

    Published 2015-01-01
    “…D-lactic acid accumulation in the blood can cause neurologic symptoms such as delirium, ataxia, and slurred speech. Diagnosis is made by a combination of clinical and laboratory data including special assays for D-lactate. …”
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  15. 95

    Potential Adverse Consequences of Combination Therapy with Gabapentin and Pregabalin by Muhammad Nabeel Ghayur

    Published 2021-01-01
    “…We describe here a case of a female patient with a history of diabetes, diabetic neuropathy, and hypertension being prescribed both gabapentin and pregabalin concomitantly which led to adverse effects like drowsiness, dizziness, fatigue, and ataxia. Once the patient medication profile was revisited, the pharmacy staff was able to identify the therapeutic duplications (gabapentin and pregabalin). …”
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  16. 96

    Hsp104 suppresses polyglutamine-induced degeneration post onset in a drosophila MJD/SCA3 model. by Mimi Cushman-Nick, Nancy M Bonini, James Shorter

    Published 2013-01-01
    “…There are no effective therapeutics that antagonize or reverse the protein-misfolding events underpinning polyglutamine (PolyQ) disorders, including Spinocerebellar Ataxia Type-3 (SCA3). Here, we augment the proteostasis network of Drosophila SCA3 models with Hsp104, a powerful protein disaggregase from yeast, which is bafflingly absent from metazoa. …”
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  17. 97

    Olfactory dysfunction as a diagnostic and prognostic marker for movement disorders by Aliasghar Peyvandi, Shahrokh Khoshsirat, Narges Bazgir, Amirreza Zaker, Azin Tahvildari, Somayeh Niknazar, Sara Mohammadi, Mehri Salari

    Published 2024-12-01
    “…A systemic search strategy incorporating key terms such as movement disorders, dystonic disorders, tic disorders, parkinsonian disorders, parkinsonism, ataxia, essential tremors, drug-induced akathisia, and olfaction disorders was employed to query databases including Embase, Scopus, and PubMed. …”
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  18. 98

    Physiotherapy and Rehabilitation in a Child with Joubert Syndrome by Özge İpek, Özge Akyolcu, Banu Bayar

    Published 2017-01-01
    “…Joubert syndrome (JS) is a rare autosomal recessive genetic disorder characterized by brain malformation, hypotonia, breathing abnormalities, ataxia, oculomotor apraxia, and developmental delay. …”
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  19. 99

    Opsoclonus-myoclonus syndrome in the course of teratoma: a case report by Mateusz Szczupak, Jacek Kobak, Anna Wiśniewska, Justyna Kosydar-Bochenek, Arkadiusz Jamro, Sabina Krupa-Nurcek

    Published 2025-01-01
    “…It is manifested by the occurrence of opsoclonus, myoclonus, ataxia, as well as behavioral and sleep disorders. …”
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  20. 100

    The Big Yawning: Pathological Yawning as a Symptom of Neuromyelitis Optica Spectrum Disorders by Veronika Spahlinger, Annette Niessen, Sebastian Rauer, Stefan Krämer, Matthias Reinhard

    Published 2019-01-01
    “…A 67-year-old woman was admitted with a seven-day progressive hemisyndrome with left-sided limb ataxia and hypesthesia. The patient yawned with a high frequency, partially in salve-like episodes. …”
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