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Facial Nerves

The facial nerves are a pair of cranial nerves that control the muscles of the face, enabling expressions and facial movements.
These nerves originate in the brainstem and innervate the muscles responsible for blinking, smiling, frowning, and other facial gestures.
Disordrs affecting the facial nerves, such as facial paralysis or Bell's palsy, can have a significant impact on an individual's ability to communicate and express emotions.
Resaerchers can utilize PubCompare.ai's AI-powered platform to optimizie research protocols for studying the facial nerves, easily locating relevant literature and leveraging comparative analysis to identify the best approaches and products for their needs.
Ths innovative solution can take your facial nerve research to the next level.

Most cited protocols related to «Facial Nerves»

The process used to automatically identify the labyrinth, ossicles, and external auditory canal relies on atlas-based registration, a common technique in the field of medical imaging. The principle of atlas-based registration is that an image of a known subject can be transformed automatically such that the anatomical structures of the known subject are made to overlap with the corresponding structures in the image of an unknown subject. Given a perfect registration, transformed labels from the known atlas exactly identify the location of the structures in the unknown image. Figure 1 shows an example of atlas-based registration as is typically used in neurosurgical applications. The underlying assumption of this method is that the images of different subjects are topologically similar such that a one-to-one mapping between all corresponding anatomical structures can be established via a smooth transformation. For patients with normal anatomy, this assumption is valid in the anatomical regions surrounding the labyrinth, ossicles, and external auditory canal. Using atlas-based registration methods described previously [6 ,7 ,8 ] and an atlas constructed with a CT of a “normal” subject, we created a registration approach to allow labeling of these structures on temporal bone CT’s.
For the anatomical region surrounding the facial nerve and chorda tympani, topological similarity between images cannot be assumed due to the highly variable pneumatized bone. Therefore, the facial nerve and chorda tympani are identified using another approach, the navigated optimal medial axis and deformable-model algorithm (NOMAD) [8 ]. NOMAD is a general framework for localizing tubular structures. Statistical a-priori intensity and shape information about the structure is stored in a model. Atlas-based registration is used to roughly align this model information to an unknown CT. Using the model information, the optimal axis of the structure is identified. The full structure is then identified by expanding this centerline using deformable-model (ballooning) techniques.
To validate our process, we quantified automated identification error as follows: (1) The temporal bone structures were manually identified in all CT scans by a student rater then verified and corrected by an experienced surgeon. (2) Binary volumes were generated from the manual delineations, with a value of 1 indicating an internal voxel and 0 being an external voxel. (3) Surface voxels were identified in both the automatic and manually generated volumes. (4) For each voxel on the automatic surface, the distance to the closest manual surface voxel was computed. We call this the false positive error distance (FP). Similarly, for each voxel on the manual surface, the distance to the closest automatic surface voxel was computed, which we call the false negative error distance (FN) (See Figure 2). We compute both FP and FN errors because, as shown in Figure 2, the FP and FN errors are not necessarily the same for a given point. In fact, to properly characterize identification errors, computing both distances is necessary.
Publication 2009
Body Regions Bones Epistropheus External Auditory Canals Facial Nerves Labyrinth Patients Student Surgeons Temporal Bone Tympani Nerves, Chorda X-Ray Computed Tomography

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Publication 2018
Acoustics Anisotropy Brain Brain Stem Cell Nucleus Cerebellum Corpus Callosum Corticobulbar Tracts Cranium Facial Nerves Fibrosis Joints Microdissection Neural Pathways Neurons Radiation Sense of Smell Somatosensory Cortex Spinothalamic Tracts Thalamus White Matter

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Publication 2012
Animals Arteries Body Temperature Catheters Dissection Ear Electron Microscopy External Auditory Canals Facial Nerves Injections, Intraperitoneal Injuries Ketamine Microscopy Muscle Tissue Needles Obstetric Delivery Operative Surgical Procedures Oxide, Ethylene Phocidae Polyethylenes Skin Stapedius Temporal Bone Tissue Adhesives Xylazine
Male B57BL/6 mice (postnatal 8-week-old) were used in the present study. All anesthetic, surgical, and postsurgical procedures used in this study, as well as animal care, were approved by the Institutional Animal Care Committee of Seoul National University of Korea (IACUC No. 15-0204-C2A4). The mice were divided into three groups: control, SSD-4-week, and SSD-8-week. The control group (postnatal 8-week-old, n = 9) mice were subjected to MEMRI immediately. The SSD-4-week group underwent left-side cochlear ablation surgery and recovered for 4 more weeks until MEMRI study (postnatal 12-week-old, n = 11). The SSD-8-week group recovered for 8 weeks after left cochlear ablation surgery before MEMRI study (postnatal 16-week-old, n = 11) (Figure 1).
The mice were anesthetized with an intraperitoneal injection of a mixture of Zoletil (30 mg/kg) and xylazine (5 mg/kg). All cochlear ablation surgeries were conducted unilaterally on the left ear. After the fur was shaved behind the left ear, a postauricular incision was made. The otic bulla was dissected with care to preserve the facial nerve. A small opening was made in the otic bulla, and the cochlea was visualized. The cochlea was punctured with a 26-gauge needle and was irrigated with kanamycin through the perforation three times. Then, the opening in the cochlea was closed with glue, and a subcutaneous 4.0 Vicryl suture was added. Hearing levels were confirmed before MEMRI acquisitions in all mice groups using the auditory brainstem response (ABR) (SmartEP, Intelligent Hearing Systems, Miami, FL, USA) as described previously [5 (link)]. The ABR results are presented in Table 1. The average ABR thresholds of the deaf side were 81.36 (standard deviation (SD) = 10.02) dB SPL and 80.00 (SD = 10.00) dB SPL for SSD-4-week and SSD-8-week groups, respectively.
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Publication 2018
Anesthetics Animal Care Committees Animals Auditory Brainstem Responses Brain Stem Cochlea Ear Facial Nerves Hearing Impaired Persons Injections, Intraperitoneal Institutional Animal Care and Use Committees Kanamycin Males Mice, House Needles Operative Surgical Procedures Sutures Vicryl Xylazine Zoletil
The injections of virus (PRSx8-hChR2 (H134R)-mCherry or PRSx8-Allato-EGFP) were made while the rats (Sprague-Dawley, males, weight: 219–282gm) were anaesthetized with a mixture of ketamine (75mg/kg), xylazine (5mg/kg) and acepromazine (1mg/kg) administered i.m. Surgery used standard aseptic methods, and after surgery, the rats were treated with the antibiotic ampicillin (100mg/kg, i.m.) and the analgesic ketorolac (0.6mg/kg, i.p.). The lentivirus was delivered into the RTN by controlled pressure injection (60 PSI, 3–8 ms pulses) using glass pipettes pulled to an external tip diameter of 25μm. These pipettes (resistance: 6–12Ω) allowed the recording of antidromic field potentials that were elicited by stimulating the mandibular branch of the facial nerve and were used to direct the electrode tip to the desired sites under the caudal pole of the facial nucleus. Injections were made unilaterally at 2 and, more rarely 3 different rostro-caudally aligned sites separated by 200 (3 injections) or 300μm (2 injections) for a total volume of 400 nl. In a subset of animals (n=5), we also injected anti-dopamine-β-hydroxylase conjugated to saporin (antiDβH-sap; Advanced Targeting Systems, San Diego, CA) at 0.22 μg per μl bilaterally (4 sites total, 100nl per site) into the region of the lateral horn of the second thoracic segment (1.0–1.2mm lateral of midline, 1mm below lateral sulcus) in order to destroy the C1 neurons that project to the spinal cord. Animals were maintained for no less than 3 weeks before they were used in physiological experiments. The surgical procedures and virus injections produced no observable behavioral or respiratory effects and these rats gained weight normally.
Publication 2009
Acepromazine Ampicillin Analgesics Animals Antibiotics Asepsis Chest Dopamine beta Monooxygenase Face Facial Nerves Facial Nucleus Horns Ketamine Ketorolac Lentivirus Males Mandible Mandibular Nerves Neurons Operative Surgical Procedures physiology Pressure Pulses Rattus Respiratory Rate Saporins Spinal Cord Virus Xylazine

Most recents protocols related to «Facial Nerves»

Institutional abbreviations follow [57 (link)].
Anatomical abbreviations are as follows: abc: condyle for the anterior pelvic basal; abv: anterior pelvic basal; aoc: antorbital cartilage; ap: apopyle; ax: axial cartilage; bp: basipterygium; bp: basipterygium; bse: barrel-shaped elements; btp: basitrabecular process; buVII: buccopharyngeal branch of facial nerve; b1: first intermediate segment; b2: second intermediate segment; cbp: condyle for the basipterygium; cg: clasper groove; cnab: fleshy core; co: coracoid bar; df: diazonal foramen; ec: ethmoidal canal of ophthalmicus superficialis nerve; elf: endolymphatic foramen; ep: epiphysial pit; fopp: profundus canal for the ophthalmicus profundus nerve; fpb: facet for the basipterygium; fpr: facet for propterygium; fvn: foramen for ventral fin nerve; hp: hypopyle; lpp: lateral prepelvic process; lra: lateral rostral appendage; mes: mesopterygium; mnl: medial nasal lobe supported by cartilage; mp: mesial process; mra: medial rostral appendage; mrp: median rostral prominence; msc: mesocondyle; mtc: metacondyle; mtp: metapterygium; nab: nasal barbel; nc: nasal capsule; oc: otic capsule; pc: procondyle; pcf: pectoral fin; pcr: pectoral fin radials; pep: preorbital process; plf: perilymphatic foramen; plp: posterior-lateral process; poc: preorbital canal of superficial ophthalmic nerve; pop: postorbital process; pro: propterygium; ptp: posterior triangular process; pub: puboischiadic bar; p2: pelvic fin; r: rostrum; rd: dorsal marginal cartilage; rh: rhipidion; rl: pelvic radials; rk: rostral keel; rv: ventral marginal cartilage; scl: scapula; snf: subnasal fenestra; scp: scapular process; sec: subethmoid chamber; sep: supraethmoidal process; snf: subnasal fenestra; td: dorsal terminal cartilage; td2: dorsal terminal 2 cartilage; tv: ventral terminal cartilage; tv2: ventral terminal 2 cartilage; t3: accessory terminal 3 cartilage; β: beta cartilage.
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Publication 2023
Capsule Cartilage Condyle Endolymph Epiphyses Facial Nerves Labyrinths, Bony Nervousness Nose Ophthalmic Nerve Pelvis Perilymph Pulp Canals Scapula Spinal Canal
First, a literature search was performed on Pubmed to identify associated symptoms of congenital FNP. The search was limited to English literature that also provided an abstract. The following keywords were used: “congenital facial nerve palsy”, “asymmetric crying facies”, “Goldenhar syndrome and facial palsy”, “hemifacial macrosomia and facial palsy” and “CHARGE syndrome and facial palsy”. With these keywords, 840 publications were found on 03/03/2022. After reading the title, a first selection could already be excluded for our purpose. After reading the abstract and searching through footnotes, 57 articles were withheld for further reading (Figure 1). After thorough reading, not all articles had additional information on associated symptoms. In the end, 40 articles were identified that describe associated symptoms of congenital FNP.
Hereafter, we conducted a retrospective, single center study with approval of the medical ethical committee of UZ Brussel (B.U.N. 143201627518). The electronic medical records of all children with congenital FNP presenting at ENT-department of University Hospital Brussel (UZ Brussel) between 1992 and 2022 were screened. Moreover, an e-Health platform allowed even to consult electronic medical files from other hospitals in Belgium when parents gave informed consent. The e-Health platform is a nationwide network for hospitals in Belgium, where all actors of healthcare can exchange medical information, with permission and respect for the patient's privacy (21 ). In Belgium, patients have a free choice which doctor or specialist they consult. Accessing e-Health allowed collecting information on comorbidities that might have been treated outside our hospital.
The identified characteristics of congenital FNP from our literature were enumerated and analyzed with attention to all comorbidities in our population. Demographic data were studied. All available audiological tests and diagnostic imaging studies (MRI and/or CT) were also assessed. Specific CT-scans of the temporal bone were studied for anomalies using dedicated planning software (OTOPLAN®, CAScination AG, Bern, Switzerland) allowing to estimate cochlear duct lengths and even facial nerve anomalies. Although surgical treatment is beyond the scope of our study, also this information was gathered for our series and reported.
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Publication 2023
Asymmetric crying facies Attention CHARGE Syndrome Child Duct, Cochlear Facial Nerves Goldenhar Syndrome Operative Surgical Procedures Paralysis, Facial Parent Patients Physicians Temporal Bone Tests, Diagnostic X-Ray Computed Tomography
The primary GLM analysis consists of fitting four model regressors (referred to as covariates) to the recorded data. For each 30 s block, there are 15 s of task, either movie viewing or face viewing (depending upon the condition), and 15 s of rest. During the 15 s task epochs, visual stimuli were presented to both participants: the Movie Watcher viewed movie clips on a small LCD monitor (figure 1c), and the smart glass was transparent so the Face Watcher could observe the face of the Movie Watcher. For each type of movie, the onsets and durations were used to construct the square wave block design model. The three movie types served as the first three covariates. The fourth model covariate (referred to as Intensity) was a modulated block design created to specifically interrogate the neural responses of the Face Watcher's brain by either the affective ratings or the facial AUs of the Movie Watcher.
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Publication 2023
Brain Clip EPOCH protocol Face Facial Nerves

Injury to middle ear ossicles, Facial nerve, Tegmen injury, Chorda tympani injury.

Patient may at risk of developing loss of hearing, Loss of taste sensation in the anterior 2/3rd of the tongue, Facial palsy and CSF otorrhea.

Alternatively—Endoscopic Ear Drill / Curette can be used which also have the same complications.
Dimensions of Instrument: Straight instruments of size 1 mm, 2 mm Chisel and Mallet.
Publication 2023
Ageusia Drill Endoscopy Facial Nerves Injuries Middle Ear Ossicle, Auditory Paralysis, Facial Patients Tegmentum Mesencephali Tongue Tympani Nerves, Chorda
3D volumetric temporal bone models, with segmented internal structures, taken from the VR simulator were prepared for printing using Meshmixer (Autodesk, San Rafael, Calif, USA) and FlashPrint (FlashForge 3D Printer, Jinhua City, China). Polylactic acid (PLA) was selected as the material to print the models, as a previous study showed it to have a similar appearance and physical likeness to human bone.13 (link) The models were printed in 2 colors using a Flashforge Dreamer 3D printer (FlashForge 3D Printer): white for the bone and pink for anatomical landmarks (dura, sigmoid sinus, facial nerve, and ossicles). When operating on 3D printed temporal bone (PTB) models, study participants were provided with a handheld surgical drill, irrigation, and a surgical microscope.
Publication 2023
Anatomic Landmarks Bones Drill Dura Mater Facial Nerves Homo sapiens Microscopy Operative Surgical Procedures Physical Examination poly(lactic acid) Sigmoid Colon Sinuses, Nasal Temporal Bone

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More about "Facial Nerves"

Facial nerves, also known as the nervus facialis or seventh cranial nerve, are a crucial component of the human nervous system.
These nerves originate in the brainstem and are responsible for controlling the muscles of the face, enabling a wide range of facial expressions and gestures.
Disorders affecting the facial nerves, such as facial paralysis or Bell's palsy, can have a significant impact on an individual's ability to communicate and express emotions.
Researchers can utilize advanced tools like PubCompare.ai's AI-powered platform to optimize their research protocols for studying the facial nerves.
This innovative solution can help researchers easily locate relevant literature, including journal articles, pre-prints, and patents, and leverage comparative analysis to identify the best approaches and products for their needs.
The platform's AI-driven capabilities can take facial nerve research to the next level, providing researchers with powerful insights and facilitating the development of more effective treatments and interventions.
Key topics related to facial nerves include innervation of the muscles responsible for blinking, smiling, frowning, and other facial movements, as well as the impact of conditions like facial paralysis and Bell's palsy.
Researchers may also utilize specialized tools and techniques, such as dissecting fluorescent microscopes, Rh-Dx, SiControl, NeuroTrace 530/615, Zoletil, SAS version 9.4, and Artis Pheno, to study the facial nerves and develop new therapies.
By leveraging the power of AI and the wealth of available literature, researchers can optimize their protocols and drive breakthroughs in the field of facial nerve research.