Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1982 2
1995 1
2002 1
2007 1
2008 1
2009 1
2012 3
2013 3
2014 1
2021 1
2022 1
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

14 results

Results by year

Filters applied: . Clear all
Proximity search should include two or more words. Proximity operator ignored :~0
Page 1
Treatment of cerebellar ataxia.
Jones TM, Shaw JD, Sullivan K, Zesiewicz TA. Jones TM, et al. Neurodegener Dis Manag. 2014;4(5):379-92. doi: 10.2217/nmt.14.27. Neurodegener Dis Manag. 2014. PMID: 25405651 Review.
Symptoms of cerebellar degeneration include ataxia or wide-based gait, visual and speech dysfunction, dysmetria, and dyscoordination. The etiology of cerebellar degeneration is vast and often complex, and requires neuroimaging, lab assessments, and a thorough family histor …
Symptoms of cerebellar degeneration include ataxia or wide-based gait, visual and speech dysfunction, dysmetria, and dyscoordination. …
Treatment and Management of Autosomal Recessive Cerebellar Ataxias: Current Advances and Future Perspectives.
Salem IH, Beaudin M, Klein CJ, Dupré N. Salem IH, et al. CNS Neurol Disord Drug Targets. 2023;22(5):678-697. doi: 10.2174/1871527321666220418114846. CNS Neurol Disord Drug Targets. 2023. PMID: 35440322 Review.
Furthermore, recent progress in gene and molecular targeting therapies is rapidly expanding and holds promise for repairing defective genes. Neurotransplantation of grafted stem cells, which is still at the experimental preclinical stage, has opened new therapeutic …
Furthermore, recent progress in gene and molecular targeting therapies is rapidly expanding and holds promise for repairing defective …
Recommendations for the diagnosis and management of Niemann-Pick disease type C: an update.
Patterson MC, Hendriksz CJ, Walterfang M, Sedel F, Vanier MT, Wijburg F; NP-C Guidelines Working Group. Patterson MC, et al. Mol Genet Metab. 2012 Jul;106(3):330-44. doi: 10.1016/j.ymgme.2012.03.012. Epub 2012 May 8. Mol Genet Metab. 2012. PMID: 22572546
Characteristic neurological manifestations of NP-C include saccadic eye movement (SEM) abnormalities or vertical supranuclear gaze palsy (VSGP), cerebellar signs (ataxia, dystonia/dysmetria, dysarthria and dysphagia) and gelastic cataplexy. Epileptic seizures are also comm …
Characteristic neurological manifestations of NP-C include saccadic eye movement (SEM) abnormalities or vertical supranuclear gaze palsy (VS …
Postural sway and neurocognition in individuals meeting criteria for a clinical high-risk syndrome.
Osborne KJ, Mittal VA. Osborne KJ, et al. Eur Arch Psychiatry Clin Neurosci. 2022 Feb;272(1):155-160. doi: 10.1007/s00406-021-01234-2. Epub 2021 Feb 19. Eur Arch Psychiatry Clin Neurosci. 2022. PMID: 33606092 Free PMC article.
Poorer working memory and processing speed were associated with less postural control. Consistent with the cognitive dysmetria theory of schizophrenia, neurocognitive deficits are associated with cerebellar dysfunction in this critical population....
Poorer working memory and processing speed were associated with less postural control. Consistent with the cognitive dysmetria theory …
Spinocerebellar ataxia type 7: clinical course, phenotype-genotype correlations, and neuropathology.
Horton LC, Frosch MP, Vangel MG, Weigel-DiFranco C, Berson EL, Schmahmann JD. Horton LC, et al. Cerebellum. 2013 Apr;12(2):176-93. doi: 10.1007/s12311-012-0412-4. Cerebellum. 2013. PMID: 22915085 Free PMC article.
Electroretinograms correlated with Brief Ataxia Rating Scale score and were a biomarker of disease onset and progression. All symptomatic patients developed gait ataxia, extremity dysmetria, dysarthria, dysrhythmia, and oculomotor abnormalities. Funduscopy revealed pale op …
Electroretinograms correlated with Brief Ataxia Rating Scale score and were a biomarker of disease onset and progression. All symptomatic pa …
Diagnosis and treatment of Parkes Weber syndrome: a review of 10 consecutive patients.
Girón-Vallejo O, López-Gutiérrez JC, Fernández-Pineda I. Girón-Vallejo O, et al. Ann Vasc Surg. 2013 Aug;27(6):820-5. doi: 10.1016/j.avsg.2013.01.001. Ann Vasc Surg. 2013. PMID: 23880459
Severe tricuspid insufficiency was observed in 1 patient. The median dysmetria between both lower extremities was 2.19 cm. Four patients are being treated successfully with compression garment therapy. ...
Severe tricuspid insufficiency was observed in 1 patient. The median dysmetria between both lower extremities was 2.19 cm. Four patie …
Idiopathic aneurysms of distal cerebellar arteries: endovascular treatment after rupture.
Mitsos AP, Corkill RA, Lalloo S, Kuker W, Byrne JV. Mitsos AP, et al. Neuroradiology. 2008 Feb;50(2):161-70. doi: 10.1007/s00234-007-0315-0. Epub 2007 Oct 23. Neuroradiology. 2008. PMID: 17955231 Review.
INTRODUCTION: Idiopathic ruptured aneurysms of distal cerebellar arteries (DCAAs) are rare, and their endovascular therapy (EVT) has as yet not been extensively reported. They are usually assumed to result from local arterial wall disruption rather than infection, unlike d …
INTRODUCTION: Idiopathic ruptured aneurysms of distal cerebellar arteries (DCAAs) are rare, and their endovascular therapy (EVT) has …
Spinocerebellar ataxias: genotype-phenotype correlations in 104 Brazilian families.
Teive HA, Munhoz RP, Arruda WO, Lopes-Cendes I, Raskin S, Werneck LC, Ashizawa T. Teive HA, et al. Clinics (Sao Paulo). 2012;67(5):443-9. doi: 10.6061/clinics/2012(05)07. Clinics (Sao Paulo). 2012. PMID: 22666787 Free PMC article.
In patients with spinocerebellar ataxia 10, the phenotype was also rather distinct and consisted of pure cerebellar ataxia and abnormal saccadic eye movement as well as ocular dysmetria. Patients with spinocerebellar ataxias 2 and 7 presented highly suggestive features of …
In patients with spinocerebellar ataxia 10, the phenotype was also rather distinct and consisted of pure cerebellar ataxia and abnormal sacc …
Movement disturbances in the differential diagnosis of Creutzfeldt-Jakob disease.
Edler J, Mollenhauer B, Heinemann U, Varges D, Werner C, Zerr I, Schulz-Schaeffer WJ. Edler J, et al. Mov Disord. 2009 Feb 15;24(3):350-6. doi: 10.1002/mds.22253. Mov Disord. 2009. PMID: 19053051
All patients had been referred with the differential diagnosis of prion disease. Ataxia and dysmetria were significantly more frequent in CJD than in AD or DLB patients, whereas hypokinesia was up to five times more frequent in AD or DLB (P < 0.05). ...
All patients had been referred with the differential diagnosis of prion disease. Ataxia and dysmetria were significantly more frequen …
Progressive neuromuscular disease in children with chronic cholestasis and vitamin E deficiency: clinical and muscle biopsy findings and treatment with alpha-tocopherol.
Guggenheim MA, Ringel SP, Silverman A, Grabert BE, Neville HE. Guggenheim MA, et al. Ann N Y Acad Sci. 1982;393:84-95. doi: 10.1111/j.1749-6632.1982.tb31235.x. Ann N Y Acad Sci. 1982. PMID: 6959572
We have studied four children (ages 6 to 17 years) with chronic cholestasis who developed a slowly progressive neuromuscular disease characterized by ataxia, dysmetria, areflexia, loss of vibratory sensation, and a variable ophthalmoplegia. ...
We have studied four children (ages 6 to 17 years) with chronic cholestasis who developed a slowly progressive neuromuscular disease charact …
14 results