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

Year Number of Results
1975 1
1977 1
1978 1
1979 1
1980 1
1981 1
1982 1
1983 1
1984 1
1985 2
1987 2
1989 1
1991 2
1992 3
1993 2
1996 1
1997 5
1998 3
1999 4
2000 3
2001 7
2002 2
2003 3
2004 9
2005 6
2006 11
2007 3
2008 8
2009 3
2010 11
2011 10
2012 7
2013 9
2014 11
2015 11
2016 8
2017 11
2018 11
2019 10
2020 14
2021 19
2022 10
2023 8
2024 2

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223 results

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Page 1
Parkinson's disease: clinical features and diagnosis.
Jankovic J. Jankovic J. J Neurol Neurosurg Psychiatry. 2008 Apr;79(4):368-76. doi: 10.1136/jnnp.2007.131045. J Neurol Neurosurg Psychiatry. 2008. PMID: 18344392 Review.
Absence of rest tremor, early occurrence of gait difficulty, postural instability, dementia, hallucinations, and the presence of dysautonomia, ophthalmoparesis, ataxia and other atypical features, coupled with poor or no response to levodopa, suggest diagnoses other than P …
Absence of rest tremor, early occurrence of gait difficulty, postural instability, dementia, hallucinations, and the presence of dysautonomi …
Mitochondrial Disorders.
Klopstock T, Priglinger C, Yilmaz A, Kornblum C, Distelmaier F, Prokisch H. Klopstock T, et al. Dtsch Arztebl Int. 2021 Nov 5;118(44):741-748. doi: 10.3238/arztebl.m2021.0251. Dtsch Arztebl Int. 2021. PMID: 34158150 Free PMC article. Review.
Typical manifestations include epileptic seizures, stroke-like episodes, hearing loss, retinopathy, external ophthalmoparesis, exercise intolerance, and diabetes mellitus. More than two manifestations of these types should arouse suspicion of a disease of energy metabolism …
Typical manifestations include epileptic seizures, stroke-like episodes, hearing loss, retinopathy, external ophthalmoparesis, exerci …
Guillain-Barré and Miller Fisher syndromes--new diagnostic classification.
Wakerley BR, Uncini A, Yuki N; GBS Classification Group; GBS Classification Group. Wakerley BR, et al. Nat Rev Neurol. 2014 Sep;10(9):537-44. doi: 10.1038/nrneurol.2014.138. Epub 2014 Jul 29. Nat Rev Neurol. 2014. PMID: 25072194 Review.
GBS is subclassified into classic and localized forms (for example, pharyngeal-cervical-brachial weakness and bifacial weakness with paraesthesias), and MFS is divided into incomplete (for example, acute ophthalmoparesis, acute ataxic neuropathy) and CNS subtypes (Bickerst …
GBS is subclassified into classic and localized forms (for example, pharyngeal-cervical-brachial weakness and bifacial weakness with paraest …
Miller Fisher's syndrome.
Teener JW. Teener JW. Semin Neurol. 2012 Nov;32(5):512-6. doi: 10.1055/s-0033-1334470. Epub 2013 May 15. Semin Neurol. 2012. PMID: 23677659 Review.
Miller Fisher's syndrome is a rare variant of Guillain-Barre's syndrome characterized by the acute development of ataxia, ophthalmoparesis, and areflexia. Most patients have a measureable antibody in serum directed against the GQ1b ganglioside. ...
Miller Fisher's syndrome is a rare variant of Guillain-Barre's syndrome characterized by the acute development of ataxia, ophthalmoparesi …
Bickerstaff brainstem encephalitis and Fisher syndrome: anti-GQ1b antibody syndrome.
Shahrizaila N, Yuki N. Shahrizaila N, et al. J Neurol Neurosurg Psychiatry. 2013 May;84(5):576-83. doi: 10.1136/jnnp-2012-302824. Epub 2012 Sep 15. J Neurol Neurosurg Psychiatry. 2013. PMID: 22984203 Review.
Following this, other neurological presentations that share anti-GQ1b antibodies emerged in the literature. These include acute ophthalmoparesis and acute ataxic neuropathy, which represent the less extensive spectrum of the disease whereas pharyngeal-cervical-brachial wea …
Following this, other neurological presentations that share anti-GQ1b antibodies emerged in the literature. These include acute ophthalmo …
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. ...Each pattern was linked to anatomical locations and either hereditary or acquired diseases. Hereditary muscle diseases often lead …
Ophthalmoparesis and ptosis can be caused by a wide range of rare or more prevalent diseases, several of which can be successfully tr …
What did he eat?
Rodrigo-Rey S, Gutiérrez-Ortiz C, Muñoz S, Ortiz-Castillo JV, Siatkowski RM. Rodrigo-Rey S, et al. Surv Ophthalmol. 2021 Sep-Oct;66(5):892-896. doi: 10.1016/j.survophthal.2020.09.007. Epub 2020 Sep 30. Surv Ophthalmol. 2021. PMID: 33010288 Free PMC article.
Ten days before these symptoms he suffered from a gastrointestinal infection. Ophthalmological examination revealed bilateral ophthalmoparesis and diffuse hyporeflexia. Magnetic resonance imaging of the brain was normal. ...Miller Fisher syndrome and its atypical variants …
Ten days before these symptoms he suffered from a gastrointestinal infection. Ophthalmological examination revealed bilateral ophthalmopa …
A shotgun wedding.
Ekeh L, Dermarkarian CR, Foroozan R, Bhatti MT. Ekeh L, et al. Surv Ophthalmol. 2021 Jul-Aug;66(4):668-673. doi: 10.1016/j.survophthal.2020.06.007. Epub 2020 Jul 4. Surv Ophthalmol. 2021. PMID: 32628947
Initially, the patient had mild visual symptoms, but later on developed prominent features of CCF including chemosis, proptosis, ophthalmoparesis and conjunctival injection . The fistula was embolized via an intravascular coiling procedure. ...
Initially, the patient had mild visual symptoms, but later on developed prominent features of CCF including chemosis, proptosis, ophthalm …
Acute muscular weakness in children.
Torricelli RPJE. Torricelli RPJE. Arq Neuropsiquiatr. 2017 Apr;75(4):248-254. doi: 10.1590/0004-282X20170026. Arq Neuropsiquiatr. 2017. PMID: 28489146 Free article. Review.
Early detection of hyperCKemia may lead to a myositis diagnosis, and hypokalemia points to the diagnosis of periodic paralysis. Ophthalmoparesis, ptosis and bulbar signs are suggestive of myasthenia gravis or botulism. ...
Early detection of hyperCKemia may lead to a myositis diagnosis, and hypokalemia points to the diagnosis of periodic paralysis. Ophthalmo …
Paralytic strabismus.
LaRoche GR. LaRoche GR. Curr Opin Ophthalmol. 1999 Oct;10(5):310-3. doi: 10.1097/00055735-199910000-00005. Curr Opin Ophthalmol. 1999. PMID: 10621543 Review.
Advances in genetics are now helping us further understand complex entities such as progressive external ophthalmoparesis and congenital fibrosis syndrome. At the other end of the spectrum, colleagues are reporting clinical findings to help specify the diagnosis of conditi …
Advances in genetics are now helping us further understand complex entities such as progressive external ophthalmoparesis and congeni …
223 results