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Year Number of Results
1984 1
1989 1
2000 1
2004 1
2008 1
2011 2
2014 1
2015 2
2018 2
2024 0

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12 results

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Page 1
Cerebellar motor syndrome from children to the elderly.
Manto M. Manto M. Handb Clin Neurol. 2018;154:151-166. doi: 10.1016/B978-0-444-63956-1.00009-6. Handb Clin Neurol. 2018. PMID: 29903437 Review.
Symptoms and motor signs consist of speech deficits, impairments of limb movements, and abnormalities of posture/gait. Ataxic dysarthria has a typical scanning (explosive with staccato) feature, voice has a nasal character, and speech is slurred. ...Handwriting is irregula …
Symptoms and motor signs consist of speech deficits, impairments of limb movements, and abnormalities of posture/gait. Ataxic dysarth …
Acrophobia impairs visual exploration and balance during standing and walking.
Brandt T, Kugler G, Schniepp R, Wuehr M, Huppert D. Brandt T, et al. Ann N Y Acad Sci. 2015 Apr;1343:37-48. doi: 10.1111/nyas.12692. Epub 2015 Feb 26. Ann N Y Acad Sci. 2015. PMID: 25722015 Review.
Body posture is characterized by a stiffening of the musculoskeletal system with increased open-loop diffusion activity of body sway, a lowered sensory feedback threshold for closed-loop balance control, and increased co-contraction of antigravity leg and neck muscles. Walking is …
Body posture is characterized by a stiffening of the musculoskeletal system with increased open-loop diffusion activity of body sway, a lowe …
Progressive supranuclear palsy. Clinical and pharmacologic update.
Jankovic J. Jankovic J. Neurol Clin. 1984 Aug;2(3):473-86. Neurol Clin. 1984. PMID: 6398402 Review.
The other distinguishing clinical features of PSP include axial distribution of rigidity and broad-based gait with early postural instability. Furthermore, pseudobulbar palsy is an early feature, while profound dementia usually occurs late in the course of th …
The other distinguishing clinical features of PSP include axial distribution of rigidity and broad-based gait with earl …
[Vascular or "lower body Parkinsonism": rise and fall of a diagnosis].
Szirmai I. Szirmai I. Ideggyogy Sz. 2011 Nov 30;64(11-12):385-93. Ideggyogy Sz. 2011. PMID: 22611616 Review. Hungarian.
The "arteriosclerotic parkinsonism", which is called vascular parkinsonism (VP), was first described by Critchley'. The broad based slow gait, reduced stride lenght, start hesitation, freezing and paratonia was mentioned as "lower body parkinsonism" (LBP) whi …
The "arteriosclerotic parkinsonism", which is called vascular parkinsonism (VP), was first described by Critchley'. The broad base
[Gait disturbance in idiopathic normal pressure hydrocephalus].
Mori E. Mori E. Brain Nerve. 2008 Mar;60(3):219-24. Brain Nerve. 2008. PMID: 18402068 Review. Japanese.
This paper reviews the nature, differential diagnosis, pathophysiology, and evaluation of iNPH gait. Broad-based, short-step, magnetic gait with start hesitation and increased instability on turning, which is often expressed as apraxic/ataxic gait
This paper reviews the nature, differential diagnosis, pathophysiology, and evaluation of iNPH gait. Broad-based, short …
Acute cerebellitis in varicella: a ten year case series and systematic review of the literature.
Bozzola E, Bozzola M, Tozzi AE, Calcaterra V, Longo D, Krzystofiak A, Villani A. Bozzola E, et al. Ital J Pediatr. 2014 Jun 19;40:57. doi: 10.1186/1824-7288-40-57. Ital J Pediatr. 2014. PMID: 24942129 Free PMC article. Review.
The highest frequency of AC was observed in children from 1 to 5 years of age (60.9%). The most characteristic symptom of AC was a broad-based gait disturbance that progressed gradually over the course of a few days (95.8%). ...
The highest frequency of AC was observed in children from 1 to 5 years of age (60.9%). The most characteristic symptom of AC was a broad
Frontal lobe dysfunction in sporadic hyperekplexia--case study and literature review.
Gaitatzis A, Kartsounis LD, Gacinovic S, Costa DC, Harvey K, Harvey RJ, de Silva RN. Gaitatzis A, et al. J Neurol. 2004 Jan;251(1):91-8. doi: 10.1007/s00415-004-0288-4. J Neurol. 2004. PMID: 14999495 Review.
She was initially diagnosed with epilepsy and started on phenytoin with no resolution of her symptoms. Clinical examination revealed hyperreflexia and an insecure broad-based gait but no other abnormalities. Routine comprehensive neuropsychological assessment …
She was initially diagnosed with epilepsy and started on phenytoin with no resolution of her symptoms. Clinical examination revealed hyperre …
Partial MEF2C deletion in a Cypriot patient with severe intellectual disability and a jugular fossa malformation: review of the literature.
Tanteles GA, Alexandrou A, Evangelidou P, Gavatha M, Anastasiadou V, Sismani C. Tanteles GA, et al. Am J Med Genet A. 2015 Mar;167A(3):664-9. doi: 10.1002/ajmg.a.36945. Am J Med Genet A. 2015. PMID: 25691421 Review.
Deletions or intragenic mutations involving the MEF2C gene on chromosome 5q14.3 have generally been associated with a relatively uniform phenotype characterized by severe developmental delay, absent speech, stereotypies, absent or limited gait abilities, lack of a typical …
Deletions or intragenic mutations involving the MEF2C gene on chromosome 5q14.3 have generally been associated with a relatively uniform phe …
[A case of neurosarcoidosis with recurrent brainstem infarction, obstructive hydrocephalus and brainstem atrophy].
Kimura H, Takeuchi J, Tsutada T, Ohata K, Osawa M, Itoh Y. Kimura H, et al. Rinsho Shinkeigaku. 2018 Jul 27;58(7):445-450. doi: 10.5692/clinicalneurol.cn-001155. Epub 2018 Jun 30. Rinsho Shinkeigaku. 2018. PMID: 29962442 Review. Japanese.
We report the case of a 42-year-old female with neurosarcoidosis who was hospitalized in year 2017 for gait disturbance. In 2011, she suddenly had vertigo that lasted for a few days. ...Upon neurological examination, she presented with down beat nystagmus, muscle weakness …
We report the case of a 42-year-old female with neurosarcoidosis who was hospitalized in year 2017 for gait disturbance. In 2011, she …
A distinctive phenotype associated with an interstitial deletion 6q14 contained within a de novo pericentric inversion 6 (p11.2q15).
Passarge E. Passarge E. Cytogenet Cell Genet. 2000;91(1-4):192-8. doi: 10.1159/000056843. Cytogenet Cell Genet. 2000. PMID: 11173855 Review.
A striking, non-progressive deficit of motor control is manifest in an inability to use her hands properly and a broad-based slow-motion-like gait. Although severely deficient in abstract mental abilities and speech development, she is well adapted to family …
A striking, non-progressive deficit of motor control is manifest in an inability to use her hands properly and a broad-based s …
12 results