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

Year Number of Results
1977 1
1981 2
1989 1
1991 1
1992 1
1993 1
1994 1
1995 1
1996 1
1997 1
1998 1
1999 1
2000 1
2001 2
2002 2
2003 3
2004 3
2005 2
2006 4
2008 6
2009 3
2010 1
2011 3
2012 2
2013 5
2014 5
2015 3
2016 3
2017 8
2018 4
2019 3
2020 2
2021 7
2022 2
2024 1

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83 results

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Page 1
Clinical and imaging clues to the diagnosis and follow-up of ptosis and ophthalmoparesis.
Keene KR, Kan HE, van der Meeren S, Verbist BM, Tannemaat MR, Beenakker JM, Verschuuren JJGM. Keene KR, et al. J Cachexia Sarcopenia Muscle. 2022 Dec;13(6):2820-2834. doi: 10.1002/jcsm.13089. Epub 2022 Sep 29. J Cachexia Sarcopenia Muscle. 2022. PMID: 36172973 Free PMC article. Review.
Ophthalmoparesis and ptosis can be caused by a wide range of rare or more prevalent diseases, several of which can be successfully treated. ...Lastly, orbital imaging can aid in the diagnosis. Fat replacement of the EOM is commonly observed in hereditary myopathic d …
Ophthalmoparesis and ptosis can be caused by a wide range of rare or more prevalent diseases, several of which can be successfully tr …
Clinical and Molecular Features of POLG-Related Sensory Ataxic Neuropathy with Dysarthria and Ophthalmoparesis.
Li LX, Jiang LT, Pan YG, Zhang XL, Pan LZ, Nie ZY, Chen YH, Jin LJ. Li LX, et al. J Mol Neurosci. 2021 Dec;71(12):2462-2467. doi: 10.1007/s12031-021-01831-9. Epub 2021 Apr 1. J Mol Neurosci. 2021. PMID: 33791913
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis (SANDO) is a rare mitochondrial disorder associated with mutations in the POLG gene, which encodes the DNA polymerase gamma catalytic subunit. ...The clinical spectrum of SANDO is heterogeneous. No clear correlati …
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis (SANDO) is a rare mitochondrial disorder associated with mutations in the …
The Spectrum of Vestibular and Ocular Motor Abnormalities in Thiamine Deficiency.
Kattah JC. Kattah JC. Curr Neurol Neurosci Rep. 2017 May;17(5):40. doi: 10.1007/s11910-017-0747-9. Curr Neurol Neurosci Rep. 2017. PMID: 28365885 Review.
Involvement of the vestibular and abducens nuclei may precede encephalopathy. Studies have shown mild ophthalmoparesis and bilateral symmetric vestibular loss in thiamine deficiency. ...Future studies in larger populations at risk are needed to confirm the results of these …
Involvement of the vestibular and abducens nuclei may precede encephalopathy. Studies have shown mild ophthalmoparesis and bilateral …
Spinocerebellar ataxia type 28.
Mariotti C, Bella DD, Di Donato S, Taroni F. Mariotti C, et al. Handb Clin Neurol. 2012;103:575-9. doi: 10.1016/B978-0-444-51892-7.00039-5. Handb Clin Neurol. 2012. PMID: 21827917
The clinical phenotype in affected individuals of this family was characterized by juvenile onset, slowly progressive gait and limb ataxia, dysarthria, hyperreflexia at lower limbs, nystagmus, and ophthalmoparesis. The mean age at onset was 19.5 years, and no evidence of a …
The clinical phenotype in affected individuals of this family was characterized by juvenile onset, slowly progressive gait and limb ataxia, …
Clinical and histologic findings in autosomal centronuclear myopathy.
Jeannet PY, Bassez G, Eymard B, Laforêt P, Urtizberea JA, Rouche A, Guicheney P, Fardeau M, Romero NB. Jeannet PY, et al. Neurology. 2004 May 11;62(9):1484-90. doi: 10.1212/01.wnl.0000124388.67003.56. Neurology. 2004. PMID: 15136669 Review.
Two presumed AR families and seven sporadic patients were analyzed together, and three subgroups were identified: 1) an early-onset form with ophthalmoparesis; 2) an early-onset form without ophthalmoparesis; and 3) a late-onset form without ophthalmoparesis. …
Two presumed AR families and seven sporadic patients were analyzed together, and three subgroups were identified: 1) an early-onset form wit …
Clinical Features and Brain MRI Findings in Korean Patients with AGel Amyloidosis.
Cheong EN, Paik W, Choi YC, Lim YM, Kim H, Shim WH, Park HJ. Cheong EN, et al. Yonsei Med J. 2021 May;62(5):431-438. doi: 10.3349/ymj.2021.62.5.431. Yonsei Med J. 2021. PMID: 33908214 Free PMC article.
The median age at dysarthria onset was 66 (interquartile range: 63.5-70) years. Ophthalmoparesis was observed in three patients. No patient presented with muscle weakness of the limbs. ...
The median age at dysarthria onset was 66 (interquartile range: 63.5-70) years. Ophthalmoparesis was observed in three patient …
Prediction of disease progression in Miller Fisher and overlap syndromes.
Verboon C, van Berghem H, van Doorn PA, Ruts L, Jacobs BC. Verboon C, et al. J Peripher Nerv Syst. 2017 Dec;22(4):446-450. doi: 10.1111/jns.12238. Epub 2017 Nov 15. J Peripher Nerv Syst. 2017. PMID: 29065229
Patients with Miller Fisher syndrome (MFS) may have a relatively mild clinical course or progress to Guillain-Barre syndrome (GBS) with limb weakness (MFS-GBS overlap syndrome). Other variants in this spectrum are GBS with ophthalmoparesis and Bickerstaff's Brainstem encep …
Patients with Miller Fisher syndrome (MFS) may have a relatively mild clinical course or progress to Guillain-Barre syndrome (GBS) with limb …
Predictors of Outcome Following Cerebral Aqueductoplasty: An Individual Participant Data Meta-analysis.
Fallah A, Wang AC, Weil AG, Ibrahim GM, Mansouri A, Bhatia S. Fallah A, et al. Neurosurgery. 2016 Feb;78(2):285-96. doi: 10.1227/NEU.0000000000001024. Neurosurgery. 2016. PMID: 26397447 Review.
In multivariate analysis, older age at surgery (hazard ratio [HR], 0.43; 95% CI, 0.21-0.88; P = .020), congenital etiology (HR, 0.18; 95% CI, 0.04-0.85; P = .030), and use of stent (HR, 0.30; 95% CI, 0.13-0.70; P = .006) were independent predictors of good outcome. Morbidi …
In multivariate analysis, older age at surgery (hazard ratio [HR], 0.43; 95% CI, 0.21-0.88; P = .020), congenital etiology (HR, 0.18; 95% CI …
Rod bipolar cell dysfunction in POLG retinopathy.
Sanderson KG, Millar E, Tumber A, Klatt R, Sondheimer N, Vincent A. Sanderson KG, et al. Doc Ophthalmol. 2021 Feb;142(1):111-118. doi: 10.1007/s10633-020-09777-w. Epub 2020 Jun 21. Doc Ophthalmol. 2021. PMID: 32567010
OBJECTIVE: To report the clinical and novel electrophysiological features in a child with POLG-related sensory ataxic neuropathy, dysarthria and ophthalmoparesis (SANDO). METHODS: The proband, a male child of Indian descent, underwent serial systemic and ophthalmological e …
OBJECTIVE: To report the clinical and novel electrophysiological features in a child with POLG-related sensory ataxic neuropathy, dysarthria …
Clinical Characteristics and Treatment Response of Chronic Inflammatory Demyelinating Polyradiculoneuropathy.
Suanprasert N, Hanchaiphiboolkul S. Suanprasert N, et al. J Med Assoc Thai. 2017 Mar;100(3):262-9. J Med Assoc Thai. 2017. PMID: 29911781
Autonomic symptoms, respiratory failure, bulbar involvement, ophthalmoparesis, ptosis, and muscle atrophy were rarely presented. The treatment response was generally favorable. ...CONCLUSION: Clinical characteristics, phenotypes, electrophysiological findings, and treatmen …
Autonomic symptoms, respiratory failure, bulbar involvement, ophthalmoparesis, ptosis, and muscle atrophy were rarely presented. The …
83 results