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Ophthalmic Plastic and Reconstructive Surgery, ISSN 0740-9303, 2017, Volume 33, Issue 6, pp. 419 - 425
Journal Article
Journal of the American Academy of Dermatology, ISSN 0190-9622, 2014, Volume 71, Issue 4, pp. 760 - 763
Journal Article
European Archives of Oto-Rhino-Laryngology, ISSN 0937-4477, 9/2015, Volume 272, Issue 9, pp. 2445 - 2450
Journal Article
European Archives of Oto-Rhino-Laryngology, ISSN 0937-4477, 12/2017, Volume 274, Issue 12, pp. 4217 - 4223
The objective of this paper is to assess synkinesis associated with post paretic voluntary facial movements using the objective OSCAR method and to investigate... 
Subjective scaling of synkinesis | Objective scaling of synkinesis | Medicine & Public Health | House–Brackmann | Head and Neck Surgery | Otorhinolaryngology | Neurosurgery | Synkinesis | Facial nerve palsy | OSCAR | Fisch grading | House-Brackmann | SYSTEM | MOTION | OTORHINOLARYNGOLOGY | FACE | Real property | Paralysis | Valuation | Analysis | Index Medicus
Journal Article
Annals of Plastic Surgery, ISSN 0148-7043, 03/2013, Volume 70, Issue 3, pp. 313 - 316
Journal Article
Laryngoscope, ISSN 0023-852X, 2018
To determine the intrarater, interrater, and retest reliability of facial nerve grading of patients with facial palsy (FP) using standardized videos recorded... 
assessment | intrarater reliability | outcome measure | interrater reliability | Facial nerve | facial paralysis | facial grading
Journal Article
JAMA Facial Plastic Surgery, ISSN 2168-6076, 07/2016, Volume 18, Issue 4, pp. 292 - 299
Journal Article
Muscle & Nerve, ISSN 0148-639X, 05/2016, Volume 53, Issue 5, pp. 762 - 769
IntroductionHereditary gelsolin amyloidosis (GA) is a rare condition caused by the gelsolin gene mutation. The diagnostic triad includes corneal lattice... 
cranial neuropathy | amyloidosis | gelsolin | bilateral facial paresis | facial paresis grading | Facial paresis grading | Amyloidosis | Gelsolin | Cranial neuropathy | Bilateral facial paresis | GSN GENE | NEUROSCIENCES | FINNISH TYPE FAF | POLYNEUROPATHY TYPE-IV | CLINICAL NEUROLOGY | LATTICE CORNEAL-DYSTROPHY | HEARING-LOSS | NEUROPATHY | FAMILIAL AMYLOIDOSIS | MERETOJAS SYNDROME | HEREDITARY AMYLOIDOSIS | MUTATION | Vestibulocochlear Nerve Diseases - physiopathology | Cutis Laxa - etiology | Humans | Middle Aged | Vestibulocochlear Nerve Diseases - etiology | Oculomotor Nerve Diseases - etiology | Male | Amyloid Neuropathies, Familial - physiopathology | Facial Nerve Diseases - etiology | Hypoglossal Nerve Diseases - physiopathology | Corneal Dystrophies, Hereditary - physiopathology | Facial Paralysis - physiopathology | Aged, 80 and over | Adult | Female | Electromyography | Amyloidosis - complications | Cranial Nerve Diseases - physiopathology | Hypoglossal Nerve Diseases - etiology | Trigeminal Nerve Diseases - physiopathology | Trigeminal Nerve Diseases - etiology | Amyloid Neuropathies, Familial - complications | Amyloidosis - physiopathology | Neural Conduction | Facial Nerve Diseases - physiopathology | Oculomotor Nerve Diseases - physiopathology | Facial Muscles - physiopathology | Cranial Nerve Diseases - etiology | Corneal Dystrophies, Hereditary - complications | Aged | Facial Paralysis - etiology | Development and progression | Paralysis, Facial | Gene mutations | Wood products | Workshops | Index Medicus
Journal Article
Journal of Drugs in Dermatology, ISSN 1545-9616, 08/2015, Volume 14, Issue 8, pp. 841 - 844
Journal Article