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

Year Number of Results
1963 1
1964 2
1965 1
1966 2
1967 4
1968 3
1969 7
1970 5
1971 9
1972 6
1973 1
1974 8
1975 5
1976 4
1977 7
1978 11
1979 1
1980 7
1981 5
1982 8
1983 10
1984 13
1985 8
1986 10
1987 9
1988 25
1989 40
1990 35
1991 27
1992 24
1993 38
1994 42
1995 31
1996 37
1997 33
1998 23
1999 35
2000 31
2001 45
2002 38
2003 39
2004 42
2005 45
2006 24
2007 35
2008 35
2009 31
2010 45
2011 42
2012 42
2013 46
2014 37
2015 49
2016 52
2017 50
2018 58
2019 51
2020 54
2021 47
2022 46
2023 50
2024 15

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1,478 results

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Page 1
Progressive external ophthalmoplegia.
Hirano M, Pitceathly RDS. Hirano M, et al. Handb Clin Neurol. 2023;194:9-21. doi: 10.1016/B978-0-12-821751-1.00018-X. Handb Clin Neurol. 2023. PMID: 36813323 Free PMC article. Review.
Progressive external ophthalmoplegia (PEO), characterized by ptosis and impaired eye movements, is a clinical syndrome with an expanding number of etiologically distinct subtypes. ...Since then, multiple point variants of mtDNA and nuclear genes have been identified …
Progressive external ophthalmoplegia (PEO), characterized by ptosis and impaired eye movements, is a clinical syndrome with an …
Mitochondrial Disorder: Kearns-Sayre Syndrome.
Tsang SH, Aycinena ARP, Sharma T. Tsang SH, et al. Adv Exp Med Biol. 2018;1085:161-162. doi: 10.1007/978-3-319-95046-4_30. Adv Exp Med Biol. 2018. PMID: 30578503 Review.
The fundus shows pigmentary retinopathy, with a salt-and-pepper appearance (Fig. 30.1), but vision remains good in most patients. Systemic involvement includes chronic progressive external ophthalmoplegia (CPEO), with ptosis being the most common complaint, and card …
The fundus shows pigmentary retinopathy, with a salt-and-pepper appearance (Fig. 30.1), but vision remains good in most patients. Systemic i …
Update: the Miller Fisher variants of Guillain-Barré syndrome.
Al Othman B, Raabe J, Kini A, Lee AG. Al Othman B, et al. Curr Opin Ophthalmol. 2019 Nov;30(6):462-466. doi: 10.1097/ICU.0000000000000611. Curr Opin Ophthalmol. 2019. PMID: 31567467 Review.
SUMMARY: GBS is characterized by an acute, ascending polyneuropathy, ataxia, areflexia, and CSF albuminocytologic dissociation. The MFV of GBS is associated with ophthalmoplegia. Clinicians should have high index of suspicion for MFV of GBS in patients with acute ophtha
SUMMARY: GBS is characterized by an acute, ascending polyneuropathy, ataxia, areflexia, and CSF albuminocytologic dissociation. The MFV of G …
Progressive supranuclear palsy.
Giagkou N, Höglinger GU, Stamelou M. Giagkou N, et al. Int Rev Neurobiol. 2019;149:49-86. doi: 10.1016/bs.irn.2019.10.013. Epub 2019 Nov 21. Int Rev Neurobiol. 2019. PMID: 31779824 Review.
Progressive External Ophthalmoplegia.
McClelland C, Manousakis G, Lee MS. McClelland C, et al. Curr Neurol Neurosci Rep. 2016 Jun;16(6):53. doi: 10.1007/s11910-016-0652-7. Curr Neurol Neurosci Rep. 2016. PMID: 27072953 Review.
Progressive external ophthalmoplegia (PEO), marked by progressive bilateral ptosis and diffuse reduction in ocular motility, represents a finding of mitochondrial myopathy rather than a true diagnosis. ...
Progressive external ophthalmoplegia (PEO), marked by progressive bilateral ptosis and diffuse reduction in ocular motility, r …
Hereditary inclusion-body myopathies.
Broccolini A, Mirabella M. Broccolini A, et al. Biochim Biophys Acta. 2015 Apr;1852(4):644-50. doi: 10.1016/j.bbadis.2014.08.007. Epub 2014 Aug 19. Biochim Biophys Acta. 2015. PMID: 25149037 Free article. Review.
IBMPFD probably represents a disorder of abnormal cellular trafficking of proteins and maturation of the autophagosome. HIBM with congenital joint contractures and external ophthalmoplegia is due to mutations of the Myosin Heavy Chain IIa gene that exerts a pathogen …
IBMPFD probably represents a disorder of abnormal cellular trafficking of proteins and maturation of the autophagosome. HIBM with congenital …
The neuro-ophthalmology of inherited myopathies.
Watson E, Ahmad K, Fraser CL. Watson E, et al. Curr Opin Ophthalmol. 2019 Nov;30(6):476-483. doi: 10.1097/ICU.0000000000000610. Curr Opin Ophthalmol. 2019. PMID: 31436541 Review.
This review, focusing especially on mitochondrial myopathies, provides updates on clinical features, diagnosis and recent therapeutic developments. RECENT FINDINGS: Ptosis and/or ophthalmoplegia is present in over half of patients with mitochondrial disease, and associated …
This review, focusing especially on mitochondrial myopathies, provides updates on clinical features, diagnosis and recent therapeutic develo …
Neuroradiological and clinical features in ophthalmoplegia.
Weidauer S, Hofmann C, Wagner M, Hattingen E. Weidauer S, et al. Neuroradiology. 2019 Apr;61(4):365-387. doi: 10.1007/s00234-019-02183-3. Epub 2019 Feb 12. Neuroradiology. 2019. PMID: 30747268 Review.
PURPOSE: Especially in acute onset of ophthalmoplegia, efficient neuroradiological evaluation is necessary to assist differential diagnosis, clinical course, and treatment options. METHODS: Different manifestations of ophthalmoplegia are explained and illustrated by …
PURPOSE: Especially in acute onset of ophthalmoplegia, efficient neuroradiological evaluation is necessary to assist differential dia …
MtDNA-maintenance defects: syndromes and genes.
Viscomi C, Zeviani M. Viscomi C, et al. J Inherit Metab Dis. 2017 Jul;40(4):587-599. doi: 10.1007/s10545-017-0027-5. Epub 2017 Mar 21. J Inherit Metab Dis. 2017. PMID: 28324239 Free PMC article. Review.
A large group of mitochondrial disorders, ranging from early-onset pediatric encephalopathic syndromes to late-onset myopathy with chronic progressive external ophthalmoplegia (CPEOs), are inherited as Mendelian disorders characterized by disturbed mitochondrial DNA …
A large group of mitochondrial disorders, ranging from early-onset pediatric encephalopathic syndromes to late-onset myopathy with chronic p …
1,478 results