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2000 4
2001 3
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Page 1
Multifocal motor neuropathy.
Biessels GJ, Franssen H, van den Berg LH, Gibson A, Kappelle LJ, Venables GS, Wokke JH. Biessels GJ, et al. J Neurol. 1997 Mar;244(3):143-52. doi: 10.1007/s004150050065. J Neurol. 1997. PMID: 9050954 Review.
Clinically, MMN is characterised by slowly progressive asymmetrical limb weakness, usually most prominent in the forearms. Weakness may be associated with muscle wasting, fasciculations and decreased tendon reflexes. ...
Clinically, MMN is characterised by slowly progressive asymmetrical limb weakness, usually most prominent in the forearms. Weakness m …
Neuromuscular Ultrasound: Indications in the Electrodiagnostic Laboratory.
Jorgensen SP, Cartwright MS, Norbury J. Jorgensen SP, et al. Am J Phys Med Rehabil. 2022 Jan 1;101(1):78-88. doi: 10.1097/PHM.0000000000001790. Am J Phys Med Rehabil. 2022. PMID: 33990480 Review.
Neuromuscular ultrasound can identify the causes of focal mononeuropathies, which can change treatment in specific cases. It is sensitive at identifying fasciculations and providing complementary evidence of autoimmune demyelinating polyneuropathies. ...
Neuromuscular ultrasound can identify the causes of focal mononeuropathies, which can change treatment in specific cases. It is sensitive at …
From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
Pennuto M, Rinaldi C. Pennuto M, et al. Mol Cell Endocrinol. 2018 Apr 15;465:113-121. doi: 10.1016/j.mce.2017.07.005. Epub 2017 Jul 5. Mol Cell Endocrinol. 2018. PMID: 28688959 Review.
The disease is transmitted in an X-linked fashion and is clinically characterized by weakness, atrophy and fasciculations of the limb and bulbar muscles as a result of a toxic gain-of-function of the mutant protein. ...
The disease is transmitted in an X-linked fashion and is clinically characterized by weakness, atrophy and fasciculations of the l
Facial onset sensory and motor neuronopathy.
Zheng Q, Chu L, Tan L, Zhang H. Zheng Q, et al. Neurol Sci. 2016 Dec;37(12):1905-1909. doi: 10.1007/s10072-016-2686-7. Epub 2016 Jul 29. Neurol Sci. 2016. PMID: 27473302 Review.
It is characterized by facial onset sensory abnormalities which may spread to the scalp, neck, upper trunk and extremities, followed by lower motor neuron deficits. Bulbar symptoms, such as dysarthria and dysphagia, muscle weakness, cramps and fasciculations, can pr …
It is characterized by facial onset sensory abnormalities which may spread to the scalp, neck, upper trunk and extremities, followed …
Post-polio syndrome. Cases report and review of literature.
Pastuszak Ż, Stępień A, Tomczykiewicz K, Piusińska-Macoch R, Galbarczyk D, Rolewska A. Pastuszak Ż, et al. Neurol Neurochir Pol. 2017 Mar-Apr;51(2):140-145. doi: 10.1016/j.pjnns.2017.01.009. Epub 2017 Feb 3. Neurol Neurochir Pol. 2017. PMID: 28209439 Review.
Electrophysiological abnormalities are seen in clinically affected and unaffected muscles. The most frequent are fasciculations and fibrillations during rest activity, extension of motor unit area, time duration and amplitude. ...
Electrophysiological abnormalities are seen in clinically affected and unaffected muscles. The most frequent are fasciculations and f …
Spinal and bulbar muscular atrophy: pathogenesis and clinical management.
Grunseich C, Rinaldi C, Fischbeck KH. Grunseich C, et al. Oral Dis. 2014 Jan;20(1):6-9. doi: 10.1111/odi.12121. Epub 2013 May 9. Oral Dis. 2014. PMID: 23656576 Free PMC article. Review.
Spinal and bulbar muscular atrophy, or Kennedy's disease, is an X-linked motor neuron disease caused by polyglutamine repeat expansion in the androgen receptor. The disease is characterised by weakness, atrophy and fasciculations in the limb and bulbar muscles. Affe …
Spinal and bulbar muscular atrophy, or Kennedy's disease, is an X-linked motor neuron disease caused by polyglutamine repeat expansion in th …
Beyond motor neurons: expanding the clinical spectrum in Kennedy's disease.
Manzano R, Sorarú G, Grunseich C, Fratta P, Zuccaro E, Pennuto M, Rinaldi C. Manzano R, et al. J Neurol Neurosurg Psychiatry. 2018 Aug;89(8):808-812. doi: 10.1136/jnnp-2017-316961. Epub 2018 Jan 20. J Neurol Neurosurg Psychiatry. 2018. PMID: 29353237 Free PMC article. Review.
Kennedy's disease, or spinal and bulbar muscular atrophy (SBMA), is an X-linked neuromuscular condition clinically characterised by weakness, atrophy and fasciculations of the limb and bulbar muscles, as a result of lower motor neuron degeneration. ...
Kennedy's disease, or spinal and bulbar muscular atrophy (SBMA), is an X-linked neuromuscular condition clinically characterised by weakness …
Diagnosis and management of motor neurone disease.
Orrell RW. Orrell RW. Practitioner. 2016 Sep;260(1796):17-21. Practitioner. 2016. PMID: 29116729 Review.
Key clinical presentations include bulbar (slurred or difficult speech, problems swallowing, tongue fasciculation), limb (typically in one limb with weakness and muscle wasting), respiratory (breathlessness, chest muscle fasciculation) and cognitive fe …
Key clinical presentations include bulbar (slurred or difficult speech, problems swallowing, tongue fasciculation), limb (typi …
[Myokymia].
Kaji M, Shoji H. Kaji M, et al. Nihon Rinsho. 1993 Nov;51(11):2866-70. Nihon Rinsho. 1993. PMID: 8277563 Review. Japanese.
Myokymia is caused by various diseases, such as, multiple sclerosis, hypothyroidism, Guillan-Barre syndrome and so on. Generally myokymia is classified into two types, i.e. limb myokymia and facial myokymia according to the site. On the other hand, myokymia with hyperhidro …
Myokymia is caused by various diseases, such as, multiple sclerosis, hypothyroidism, Guillan-Barre syndrome and so on. Generally myokymia is …
Hereditary spastic paraplegia: More than an upper motor neuron disease.
Parodi L, Fenu S, Stevanin G, Durr A. Parodi L, et al. Rev Neurol (Paris). 2017 May;173(5):352-360. doi: 10.1016/j.neurol.2017.03.034. Epub 2017 Apr 24. Rev Neurol (Paris). 2017. PMID: 28449883 Review.
Based on symptoms, HSPs can be divided into pure forms, presenting with pyramidal signs leading to lower-limb spasticity, and complex forms, when additional neurological or extraneurological symptoms are detected. ...The pathogenic mutations of SPGs primarily lead to progr …
Based on symptoms, HSPs can be divided into pure forms, presenting with pyramidal signs leading to lower-limb spasticity, and complex …
45 results