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Year Number of Results
1990 2
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1995 1
1997 1
2000 1
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2005 1
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2012 2
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2014 3
2015 1
2019 1
2023 0

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Page 1
Peripheral nerve hyperexcitability.
Katirji B. Katirji B. Handb Clin Neurol. 2019;161:281-290. doi: 10.1016/B978-0-444-64142-7.00054-0. Handb Clin Neurol. 2019. PMID: 31307606 Review.
Central nervous system symptomatology is more common in Morvan syndrome, which also overlaps with limbic encephalitis. Cramp-fasciculation syndrome, a more common syndrome, may represent a milder form of peripheral nerve hyperexcitability. ...
Central nervous system symptomatology is more common in Morvan syndrome, which also overlaps with limbic encephalitis. Cramp-fasciculatio …
Cerebellar ataxia with neuropathy and vestibular areflexia syndrome (CANVAS) - a case report and review of literature.
Figura M, Gaweł M, Kolasa A, Janik P. Figura M, et al. Neurol Neurochir Pol. 2014;48(5):368-72. doi: 10.1016/j.pjnns.2014.08.003. Epub 2014 Sep 6. Neurol Neurochir Pol. 2014. PMID: 25440017 Review.
CANVAS (cerebellar ataxia with neuropathy and vestibular areflexia syndrome) is a rare neurological syndrome of unknown etiology. ...We present a case of 58-year-old male patient who has demonstrated gait disturbance, imbalance and paresthesia of feet for 2 years. On exami …
CANVAS (cerebellar ataxia with neuropathy and vestibular areflexia syndrome) is a rare neurological syndrome of unknown etiology. ... …
Fasciculations in human hereditary disease.
Finsterer J, Aliyev R. Finsterer J, et al. Acta Neurol Belg. 2015 Jun;115(2):91-5. doi: 10.1007/s13760-014-0335-6. Epub 2014 Jul 30. Acta Neurol Belg. 2015. PMID: 25073774 Review.
Among the non-hereditary diseases, fasciculations occur most frequently in peripheral nerve hyperexcitability syndromes (Isaac's syndrome, voltage-gated potassium channelopathy, cramp fasciculation syndrome, Morvan syndrome). ...Additionally, fasciculations h …
Among the non-hereditary diseases, fasciculations occur most frequently in peripheral nerve hyperexcitability syndromes (Isaac's synd …
Myokymia and neuromyotonia in veterinary medicine: a comparison with peripheral nerve hyperexcitability syndrome in humans.
Vanhaesebrouck AE, Bhatti SF, Franklin RJ, Van Ham L. Vanhaesebrouck AE, et al. Vet J. 2013 Aug;197(2):153-62. doi: 10.1016/j.tvjl.2013.03.002. Epub 2013 Apr 11. Vet J. 2013. PMID: 23583699 Review.
Hyperexcitability of the peripheral motor nerve can result into five different phenotypic main variants, i.e. fasciculations, myokymia, neuromyotonia, cramps and tetany, each with their own clinical and electromyographic characteristics. ...
Hyperexcitability of the peripheral motor nerve can result into five different phenotypic main variants, i.e. fasciculations, myokymi …
Central ocular motor disorders, including gaze palsy and nystagmus.
Strupp M, Kremmyda O, Adamczyk C, Böttcher N, Muth C, Yip CW, Bremova T. Strupp M, et al. J Neurol. 2014 Sep;261 Suppl 2(Suppl 2):S542-58. doi: 10.1007/s00415-014-7385-9. J Neurol. 2014. PMID: 25145891 Free PMC article. Review.
Gaze-evoked nystagmus (GEN) in all directions indicates a cerebellar dysfunction and can have multiple causes such as drugs, in particular antiepileptics, chronic alcohol abuse, neurodegenerative cerebellar disorders or cerebellar ataxias; purely vertical GEN is due to a m …
Gaze-evoked nystagmus (GEN) in all directions indicates a cerebellar dysfunction and can have multiple causes such as drugs, in particular a …
[Spinocerebellar ataxia type 36 (nicknamed Asidan)].
Abe K, Ikeda Y. Abe K, et al. Brain Nerve. 2012 Aug;64(8):937-41. Brain Nerve. 2012. PMID: 22868885 Review. Japanese.
We report the phenotype of spinocerebellar ataxia type 36 (SCA36), which is a novel type of dominant cerebellar ataxia nicknamed as "Asidan," caused by the expansion of a hexanucleotide GGCCTG repeat in intron 1 of the nucleolar protein 56 (NOP56) gene. Age at the o …
We report the phenotype of spinocerebellar ataxia type 36 (SCA36), which is a novel type of dominant cerebellar ataxia nicknam …
Machado-Joseph disease.
Sudarsky L, Coutinho P. Sudarsky L, et al. Clin Neurosci. 1995;3(1):17-22. Clin Neurosci. 1995. PMID: 7614089 Review.
Average age of onset is 35 to 40. Core features include progressive ataxia, dysarthria, postural instability, nystagmus, eyelid retraction, and facial fasciculations. ...The relationship between MJD and the other dominant inherited ataxias is discussed....
Average age of onset is 35 to 40. Core features include progressive ataxia, dysarthria, postural instability, nystagmus, eyelid retra …
Poisoning due to chlorophenoxy herbicides.
Bradberry SM, Proudfoot AT, Vale JA. Bradberry SM, et al. Toxicol Rev. 2004;23(2):65-73. doi: 10.2165/00139709-200423020-00001. Toxicol Rev. 2004. PMID: 15578861 Review.
Hypotension, which is common, is due predominantly to intravascular volume loss, although vasodilation and direct myocardial toxicity may also contribute. Coma, hypertonia, hyperreflexia, ataxia, nystagmus, miosis, hallucinations, convulsions, fasciculation and para …
Hypotension, which is common, is due predominantly to intravascular volume loss, although vasodilation and direct myocardial toxicity may al …
[Molecular genetics of inherited neuropathies].
Takashima H. Takashima H. Rinsho Shinkeigaku. 2006 Jan;46(1):1-18. Rinsho Shinkeigaku. 2006. PMID: 16541790 Review. Japanese.
HMSN-P is characterized by late onset, proximal dominant severe muscle weakness, fasciculations, muscle cramp and sensory involvement. HMSN-P is a primary neuronopathy. ...Clinical phenotypes of patients with TDP1, APTX, or SETX mutations share common clinical findings, na …
HMSN-P is characterized by late onset, proximal dominant severe muscle weakness, fasciculations, muscle cramp and sensory involvement …
Superficial siderosis should be included in the differential diagnosis of motor neuron disease.
Kumar N, Fogelson JL, Morris JM, Pichelmann MA. Kumar N, et al. Neurologist. 2012 May;18(3):139-45. doi: 10.1097/NRL.0b013e318251e6d6. Neurologist. 2012. PMID: 22549355 Review.
Following repair of the dural defect the patient noted an improvement in balance and strength and resolution of the fasciculations. A cervical and thoracic spine MRI showed resolution of the intraspinal fluid-filled collection, and a CSF study showed no red blood cells or …
Following repair of the dural defect the patient noted an improvement in balance and strength and resolution of the fasciculations. A …
20 results