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Acute vestibular syndrome associated with anti-GQ1b antibody.
Lee SU, Kim HJ, Choi JY, Kim JK, Kim JS. Lee SU, et al. Neurology. 2019 Sep 10;93(11):e1085-e1092. doi: 10.1212/WNL.0000000000008107. Epub 2019 Aug 9. Neurology. 2019. PMID: 31399495
RESULTS: Patients with AVS showed various ocular motor findings that included head-shaking nystagmus (n = 6), spontaneous nystagmus (n = 5), gaze-evoked nystagmus (n = 5), central positional nystagmus (n = 3), canal paresis (n = 2), and abnormal head-impulse tests (n = 1) without …
RESULTS: Patients with AVS showed various ocular motor findings that included head-shaking nystagmus (n = 6), spontaneous nystagmus (n = 5), …
Synthetic lethal mutants in Escherichia coli define pathways necessary for survival with RNase H deficiency.
Das S, Forrest J, Kuzminov A. Das S, et al. J Bacteriol. 2023 Oct 26;205(10):e0028023. doi: 10.1128/jb.00280-23. Epub 2023 Oct 11. J Bacteriol. 2023. PMID: 37819120 Free PMC article.
RNase H deficiency leads to complications in bacteria, yeast, and mouse, and diseases like progressive external ophthalmoplegia (mitochondrial defects in RNASEH1) and Aicardi-Goutieres syndrome (defects in RNASEH2) in humans. ...
RNase H deficiency leads to complications in bacteria, yeast, and mouse, and diseases like progressive external ophthalmoplegia …
Visual prognosis in compressive optic neuropathy secondary to sphenoid sinus mucocele: A systematic review.
Li E, Howard MA, Vining EM, Becker RD, Silbert J, Lesser RL. Li E, et al. Orbit. 2018 Aug;37(4):280-286. doi: 10.1080/01676830.2017.1423087. Epub 2018 Jan 5. Orbit. 2018. PMID: 29303386 Review.
Sphenoid sinus mucoceles (SSMs) are rare, benign lesions that can expand, often presenting with ocular symptoms-decreased vision, diplopia, visual field defects, proptosis, and external ophthalmoplegia. Reported cases are few, visual compromise varies, and factors a …
Sphenoid sinus mucoceles (SSMs) are rare, benign lesions that can expand, often presenting with ocular symptoms-decreased vision, diplopia, …
Systematic review of cardiac electrical disease in Kearns-Sayre syndrome and mitochondrial cytopathy.
Kabunga P, Lau AK, Phan K, Puranik R, Liang C, Davis RL, Sue CM, Sy RW. Kabunga P, et al. Int J Cardiol. 2015 Feb 15;181:303-10. doi: 10.1016/j.ijcard.2014.12.038. Epub 2014 Dec 13. Int J Cardiol. 2015. PMID: 25540845 Review.
Kearns-Sayre syndrome (KSS) is a mitochondrial disorder characterised by onset before the age of 20years, progressive external ophthalmoplegia, and pigmentary retinopathy, accompanied by either cardiac conduction defects, elevated cerebrospinal fluid protein or cere …
Kearns-Sayre syndrome (KSS) is a mitochondrial disorder characterised by onset before the age of 20years, progressive external oph …