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Quoted phrase not found in phrase index: "Cranial nerve motor loss"
Page 1
Neuro-ophthalmic manifestations of tuberculosis.
Dhiman R, Lakra S, Panda PK, Hemachandran N, Sharma S, Saxena R. Dhiman R, et al. Eye (Lond). 2022 Jan;36(1):15-28. doi: 10.1038/s41433-021-01619-6. Epub 2021 Jun 14. Eye (Lond). 2022. PMID: 34127839 Free PMC article. Review.
They are mostly the result of the visual pathway and/or ocular motor and other cranial nerve involvement. Furthermore, toxic optic neuropathy and paradoxical response to anti-tubercular drugs (ATT) are also not uncommon. ...The presence of neuro-ophthalmic fe …
They are mostly the result of the visual pathway and/or ocular motor and other cranial nerve involvement. Furthermore, …
Brown-Vialetto-Van Laere syndrome.
Sathasivam S. Sathasivam S. Orphanet J Rare Dis. 2008 Apr 17;3:9. doi: 10.1186/1750-1172-3-9. Orphanet J Rare Dis. 2008. PMID: 18416855 Free PMC article. Review.
The syndrome most frequently presents with sensorineural deafness, which is usually progressive and severe. Lower cranial nerve involvement and lower and upper motor neuron limb signs are common neurological features. ...The differential diagnoses include the …
The syndrome most frequently presents with sensorineural deafness, which is usually progressive and severe. Lower cranial nerve
Neurological and Ophthalmological Manifestations of Varicella Zoster Virus.
Kedar S, Jayagopal LN, Berger JR. Kedar S, et al. J Neuroophthalmol. 2019 Jun;39(2):220-231. doi: 10.1097/WNO.0000000000000721. J Neuroophthalmol. 2019. PMID: 30188405 Review.
Postherpetic neuralgia, a debilitating pain syndrome occurs in 30% HZ, whereas 50% HZO develop ophthalmic complications. Diplopia from cranial nerve palsy occurs in less than 30% HZO, whereas optic neuropathy is seen in less than 1% HZO. ...Patients with neurologica …
Postherpetic neuralgia, a debilitating pain syndrome occurs in 30% HZ, whereas 50% HZO develop ophthalmic complications. Diplopia from cr
Mandibular nerve entrapment in the infratemporal fossa.
Piagkou MN, Demesticha T, Piagkos G, Androutsos G, Skandalakis P. Piagkou MN, et al. Surg Radiol Anat. 2011 May;33(4):291-9. doi: 10.1007/s00276-010-0706-5. Epub 2010 Aug 10. Surg Radiol Anat. 2011. PMID: 20697711 Review.
The posterior trunk of the mandibular nerve (V(3)) comprises of three main branches. Various anatomic structures may entrap and potentially compress the mandibular nerve branches. ...The entrapment of the MN motor branches can lead to paresis or weakness in t …
The posterior trunk of the mandibular nerve (V(3)) comprises of three main branches. Various anatomic structures may entrap and poten …
Extra- and intramuscular innervation of the masseter: Implications for facial reanimation.
Bikey D, Agur AMR, Fattah AY. Bikey D, et al. J Plast Reconstr Aesthet Surg. 2023 Oct;85:508-514. doi: 10.1016/j.bjps.2023.07.003. Epub 2023 Jul 17. J Plast Reconstr Aesthet Surg. 2023. PMID: 37633253
PURPOSE: Irreversible facial paralysis results in significant functional impairment. The motor nerve to the masseter is a reconstructive option, but despite its clinical importance, there are few parametric anatomic studies of the masseteric nerve. ...RESULTS …
PURPOSE: Irreversible facial paralysis results in significant functional impairment. The motor nerve to the masseter is a reco …
Visual outcomes after treatment of pituitary adenomas.
Fraser CL, Biousse V, Newman NJ. Fraser CL, et al. Neurosurg Clin N Am. 2012 Oct;23(4):607-19. doi: 10.1016/j.nec.2012.06.004. Epub 2012 Aug 28. Neurosurg Clin N Am. 2012. PMID: 23040747 Review.
The location of the pituitary gland makes involvement of both the visual pathways and the ocular motor cranial nerves likely when there is adenomatous expansion. A sudden expression of visual loss or diplopia commonly accompanies pituitary apoplexy. Several p …
The location of the pituitary gland makes involvement of both the visual pathways and the ocular motor cranial nerves l …
Clinical and electrophysiological aspects of Charcot-Marie-Tooth disease.
Pareyson D, Scaioli V, Laurà M. Pareyson D, et al. Neuromolecular Med. 2006;8(1-2):3-22. doi: 10.1385/nmm:8:1-2:3. Neuromolecular Med. 2006. PMID: 16775364 Review.
The demyelinating recessive forms, termed CMT4, usually have early onset and run a more severe course than the dominant types. Pure motor CMT types are now classified as distal hereditary motor neuronopathy. ...Late onset, prominent or peculiar sensory manife …
The demyelinating recessive forms, termed CMT4, usually have early onset and run a more severe course than the dominant types. Pure …
Clinical, electrophysiological findings and evaluation of prognosis of patients with Guillain-Barre syndrome.
Kılıç B, Güngör S, Özgör B. Kılıç B, et al. Turk J Pediatr. 2019;61(2):200-208. doi: 10.24953/turkjped.2019.02.008. Turk J Pediatr. 2019. PMID: 32077646 Free article.
All of the patients had muscle weakness on examination; in addition to that hyperesthesia (31%), autonomic symptoms (13.3%), sensory loss (11.1%), ataxia (11.1%), bilateral facial nerve palsy (6.6%), oculomotor nerve palsy (2.2%), and multiple cranial nerv
All of the patients had muscle weakness on examination; in addition to that hyperesthesia (31%), autonomic symptoms (13.3%), sensory loss (1 …
Transcondylar Approach for Resection of Medullary Cavernous Malformation: 2-Dimensional Operative Video.
Erkmen K, Al-Mefty O. Erkmen K, et al. Oper Neurosurg (Hagerstown). 2021 Aug 16;21(3):E233-E234. doi: 10.1093/ons/opab220. Oper Neurosurg (Hagerstown). 2021. PMID: 34192765
Cavernous malformations located within the brainstem present with a high rate of neurological symptoms and carry a more aggressive course in both pediatric and adult populations.1,2 Cavernomas within the medulla are the rarest form, representing only 5% of all brainstem le …
Cavernous malformations located within the brainstem present with a high rate of neurological symptoms and carry a more aggressive course
Progressive neurodegeneration following spinal cord injury: Implications for clinical trials.
Ziegler G, Grabher P, Thompson A, Altmann D, Hupp M, Ashburner J, Friston K, Weiskopf N, Curt A, Freund P. Ziegler G, et al. Neurology. 2018 Apr 3;90(14):e1257-e1266. doi: 10.1212/WNL.0000000000005258. Epub 2018 Mar 7. Neurology. 2018. PMID: 29514946 Free PMC article.
As atrophy progressed in the thalamus, sustained iron accumulation was evident. Smaller cord and cranial corticospinal tract atrophy, and myelin changes within the sensorimotor cortices, by 6 months predicted recovery in lower extremity motor score at 2 years …
As atrophy progressed in the thalamus, sustained iron accumulation was evident. Smaller cord and cranial corticospinal tract atrophy, …
71 results