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893 search results for:

Ophthalmoparesis 

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  1. 07-02-2023 | COVID-19 | OriginalPaper

    Ophthalmoparesis from cranial nerve palsy in a patient with an acute COVID-19 infection

    A 40-year-old female patient, with a history of chronic allergic rhinosinusitis, presented to the emergency department with a 1-day history of a painless horizontal binocular diplopia on left-sided gaze. Neurological examination revealed an …

  2. 01-06-2008 | OriginalPaper

    Spinocerebellar ataxia type 28: A novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis

    We have recently mapped the spinocerebellar ataxia type 28 (SCA28) locus on chromosome 18p11.22 in a four-generation Italian family. The clinical phenotype in affected individuals of this family was characterized by juvenile onset, slowly …

  3. 01-04-2009 | OriginalPaper

    Amyloid myopathy with external ophthalmoparesis

  4. 01-08-1997 | OriginalPaper

    Recurrent external ophthalmoparesis during hormonal therapy after thyroid ablation. Case report

    We here report the case of a patient who had undergone total thyroid ablation for Graves' disease. After the beginning of oral therapy with 1-thyroxine, she developed a left external ophthalmoparesis that remitted with the discontinuation of the …

  5. 01-06-2013 | Letter

    Topographic diagnosis of internuclear ophthalmoparesis: evidence from a lesion-behavior mapping study

  6. 01-08-2000 | OriginalPaper

    Unilateral ophthalmoparesis and limb ataxia associated with anti-GQ1b IgG antibody

  7. 13-05-2024 | Giant Cell Arteritis | Online First

    Temporal arteritis presenting as third nerve palsy - a case report and review of literature

    Giant Cell Arteritis (GCA), also known as Temporal Arteritis, is a type of large vessel vasculitis primarily affecting the elderly population. It typically manifests with headaches, visual impairment, and jaw claudication. Although third nerve …

  8. Open Access 01-12-2022 | Diseases of the neuromuscular synapses and muscles | OriginalPaper

    NOTCH2NLC-related oculopharyngodistal myopathy type 3 complicated with focal segmental glomerular sclerosis: a case report

    Oculopharyngodistal myopathy (OPDM) is a rare, clinicopathologically distinct muscular disease. The typical clinical manifestations are insidiously progressive ptosis, ophthalmoparesis, facial and masseter weakness, dysphagia, and distal limb …

  9. 14-07-2023 | Ophthalmoparesis | Letter

    Before an abducens palsy can be attributed to a congenital vitamin-B12 deficiency, alternative causes must be ruled out

  10. Open Access 01-12-2024 | Ptosis | OriginalPaper

    COLQ-Congenital myasthenic syndrome in an Iranian cohort: the clinical and genetics spectrum

    Congenital myasthenic syndrome (CMS; OMIM #603,034) refers to a heterogeneous group of rare inherited disorders affecting neuromuscular transmission [ 1 ]. These syndromes are categorized into presynaptic, synaptic, and postsynaptic disorders based …

  11. 01-04-2024 | Cefazolin | News

    Multiple drugs

    Intestinal dysbiosis
  12. Open Access 01-12-2024 | Thrombectomy | OriginalPaper

    Orbital infarction syndrome following mechanical thrombectomy in internal carotid artery occlusion: a case report

    Orbital ischemic syndrome (OIS) is the ischemia of all intraorbital and intraocular structures, including the optic nerve, extraocular muscles, and orbital [ 1 ]. It was first described by Vergez in 1959 [ 2 ], who noted that patients suffering …

  13. 15-04-2024 | Guillain-Barré Syndrome | Online First

    Acute ataxic neuropathy due to Bartonella infection: a rare variant for a rare association

  14. 27-02-2024 | Salbutamol | Online First

    Congenital myasthenia syndrome with demyelinating sensorimotor neuropathy responsive to salbutamol monotherapy: a novel clinical phenotype of CHRNE mutation

  15. Open Access 25-01-2024 | Guillain-Barré Syndrome | BriefCommunication

    Only anti-GM4 antibody positivity in a Chinese girl with overlapping MFS/GBS: a case report

    Miller-Fisher syndrome (MFS), a clinical variant of Guillain-Barré syndrome (GBS) with a frequency that varies from 5 to 35%, is characterized by ophthalmoplegia, ataxia, and areflexia.

  16. 12-03-2024 | Lymphoma | Online First

    Neurolymphomatosis as primary presentation of extra-nodal NK/T-cell lymphoma, nasal type

    Neurolymphomatosis (NL) describes an infiltration of cranial and peripheral nerves by lymphoma cells, most frequently in non-Hodgkin B-cell lymphoma. This clinical entity is rare and poses a challenging diagnosis. We describe a case of a …

  17. 31-10-2023 | Abstract

    Abstracts of the 53 Annual Conference of the Italian Society of Neurology

  18. 31-03-2023 | Gaze-Evoked Nystagmus | ReviewPaper

    A Review of Ocular Movement Abnormalities in Hereditary Cerebellar Ataxias

    Cerebellar ataxias are a wide heterogeneous group of disorders that may present with fine motor deficits as well as gait and balance disturbances that have a significant influence on everyday activities. To review the ocular movements in …

  19. 01-12-2024 | Schwannoma | OriginalPaper

    Preservation of cranial nerve function in large and giant trigeminal schwannoma resection: a case series

    Trigeminal schwannomas (TSs) are rare (0.07–0.3%) intracranial tumors that arise from Schwann cells of the trigeminal nerve sheath [ 4 , 8 , 24 ]. They usually originate within the Gasserian ganglion in Meckel’s cave, in the cavernous sinus, or …

  20. Open Access 08-02-2024 | Polyneuropathy | Letter

    Inflammatory neuropathy with evidence of anti-GQ1b antibodies in angioimmunoblastic T cell lymphoma (AITL): a case report

    A 66-year-old male patient suspected of having Guillain-Barré syndrome (GBS) was referred to us by the internal medicine department of a peripheral hospital. The patient had developed rapidly progressive tetraparesis, in particular with leg …

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