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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 Article
Acta Neurochirurgica, ISSN 0001-6268, 12/2011, Volume 153, Issue 12, pp. 2365 - 2375
The aim of this study was to evaluate the anatomy of the central myelin portion and the central myelin-peripheral myelin transitional zone of the trigeminal,... 
Cranial nerve vascular compression syndromes | Hemifacial spasm | Neurosurgery | Vago-glossopharyngeal neuralgia | Anatomy | Neuroradiology | Neurology | Surgical Orthopedics | Trigeminal neuralgia | Medicine & Public Health | Minimally Invasive Surgery | Cranial nerves | Interventional Radiology | SURGERY | NEURALGIA | ROOT | DISABLING POSITIONAL VERTIGO | MICROVASCULAR DECOMPRESSION | SELECTION CRITERIA | CLINICAL NEUROLOGY | SEVERE TINNITUS | COCHLEAR NERVE | NEUROVASCULAR CONFLICT | SUPERIOR OBLIQUE MYOKYMIA | Glossopharyngeal Nerve Diseases - epidemiology | Vagus Nerve Diseases - epidemiology | Humans | Glossopharyngeal Nerve - physiology | Male | Vagus Nerve Diseases - physiopathology | Facial Nerve - physiology | Glossopharyngeal Nerve - cytology | Vagus Nerve - pathology | Rhombencephalon - cytology | Cranial Nerves - physiology | Radiculopathy - pathology | Glossopharyngeal Nerve Diseases - pathology | Nerve Fibers, Myelinated - pathology | Nerve Fibers, Myelinated - physiology | Aged, 80 and over | Radiculopathy - physiopathology | Female | Cranial Nerve Diseases - epidemiology | Cranial Nerve Diseases - physiopathology | Cranial Nerves - cytology | Radiculopathy - epidemiology | Vertebrobasilar Insufficiency - epidemiology | Glossopharyngeal Nerve Diseases - physiopathology | Trigeminal Neuralgia - epidemiology | Facial Nerve Diseases - epidemiology | Trigeminal Nerve - pathology | Trigeminal Neuralgia - physiopathology | Vertebrobasilar Insufficiency - complications | Facial Nerve Diseases - physiopathology | Vagus Nerve Diseases - pathology | Rhombencephalon - physiology | Syndrome | Vagus Nerve - physiology | Trigeminal Nerve - physiology | Facial Nerve Diseases - pathology | Cranial Nerves - physiopathology | Rhombencephalon - physiopathology | Trigeminal Neuralgia - pathology | Causality | Facial Nerve - pathology | Cranial Nerve Diseases - pathology | Medicine, Experimental | Comparative analysis | Medical research | Index Medicus | Compression | Brain stem | Myelin | Facial nerve | Trigeminal nerve | Cadavers | Glossopharyngeal nerve | Skull | Neuralgia | Vagus nerve
Journal Article
Clinical Medicine, Journal of the Royal College of Physicians of London, ISSN 1470-2118, 12/2017, Volume 17, Issue 6, pp. 575 - 577
In this case study, we summarise the inpatient investigations and management of a 68-year-old woman with Takotsubo cardiomyopathy secondary to a Varicella... 
Cranial mononeuropathy | Encephalitis | Cranial nerve neuropathies | Takotsubo cardiomyopathy | Troponin rise | Varicella zoster | MEDICINE, GENERAL & INTERNAL | encephalitis | cranial nerve neuropathies | CARDIOMYOPATHY | troponin rise | ACUTE MYOCARDIAL-INFARCTION | TAKO-TSUBO | APICAL BALLOONING SYNDROME | Acyclovir - therapeutic use | Humans | Vagus Nerve Diseases - physiopathology | Atrial Fibrillation - physiopathology | Encephalitis, Varicella Zoster - complications | Facial Nerve Diseases - etiology | Facial Paralysis - physiopathology | Electrocardiography | Troponin - blood | Female | Atrial Fibrillation - diagnosis | Cranial Nerve Diseases - physiopathology | Encephalitis, Varicella Zoster - diagnosis | Vagus Nerve Diseases - etiology | Antiviral Agents - therapeutic use | Takotsubo Cardiomyopathy - blood | Takotsubo Cardiomyopathy - diagnosis | Encephalitis, Varicella Zoster - drug therapy | Facial Nerve Diseases - physiopathology | Cranial Nerve Diseases - etiology | Takotsubo Cardiomyopathy - etiology | Takotsubo Cardiomyopathy - physiopathology | Encephalitis, Varicella Zoster - physiopathology | Hearing Loss, Sensorineural - etiology | Atrial Fibrillation - etiology | Aged | Facial Paralysis - etiology | Hearing Loss, Sensorineural - physiopathology | Cardiac arrhythmia | Heart attacks | Nuclear magnetic resonance--NMR | Medical imaging | Cardiomyopathy | Chicken pox | Cardiovascular disease | Systematic review | Family medical history | Hearing impairment | Patients | Case studies | Ultrasonic imaging | Coronary vessels | Sepsis | Acute coronary syndromes | Neurological disorders | Acute Medical Care
Journal Article
Muscle and Nerve, ISSN 0148-639X, 05/2010, Volume 41, Issue 5, pp. 679 - 684
Hereditary amyloidosis of the Finnish type (HAF, or familial amyloid polyneuropathy type IV) is an autosomal dominant disease that has been described most... 
Corneal lattice dystrophy | Familial amyloid neuropathy | Gelsolin | Facial palsy | Hereditary amyloidosis | facial palsy | SUBSTITUTION | POLYNEUROPATHY | LIVER-TRANSPLANTATION | GELSOLIN AMYLOIDOSIS | gelsolin | familial amyloid neuropathy | corneal lattice dystrophy | FAF | NEUROSCIENCES | CLINICAL NEUROLOGY | GENE | MUTATION | hereditary amyloidosis | EXPERIENCE | Peripheral Nervous System Diseases - diagnosis | Genetic Testing | Cranial Nerve Diseases - genetics | Humans | Middle Aged | Facial Nerve Diseases - metabolism | Male | Peripheral Nervous System Diseases - physiopathology | Amyloid Neuropathies, Familial - physiopathology | Young Adult | Electrodiagnosis | Hypoglossal Nerve Diseases - physiopathology | Corneal Dystrophies, Hereditary - physiopathology | DNA Mutational Analysis | Inheritance Patterns - genetics | Adult | Female | Peripheral Nerves - metabolism | Peripheral Nervous System Diseases - genetics | Cranial Nerve Diseases - physiopathology | Disability Evaluation | Amyloid Neuropathies, Familial - genetics | Cranial Nerves - metabolism | Genotype | Oculomotor Nerve Diseases - diagnosis | Corneal Dystrophies, Hereditary - diagnosis | Facial Nerve Diseases - physiopathology | Corneal Dystrophies, Hereditary - metabolism | Hypoglossal Nerve Diseases - metabolism | Mutation - genetics | Oculomotor Nerve Diseases - physiopathology | Cranial Nerve Diseases - diagnosis | Peripheral Nerves - physiopathology | Neurologic Examination | Genetic Markers - genetics | Adolescent | Finland | Cranial Nerves - physiopathology | Aged | Gelsolin - genetics | Germany | Oculomotor Nerve Diseases - metabolism | Amyloid Neuropathies, Familial - diagnosis | Index Medicus
Journal Article
Neurology, ISSN 0028-3878, 02/2015, Volume 84, Issue 7, pp. e46 - e47
Journal Article
Current Eye Research, ISSN 0271-3683, 02/2016, Volume 41, Issue 2, pp. 179 - 185
Purpose: To investigate the relationship between meibomian gland dysfunction (MGD) and incomplete blinking caused by cranial nerve seven (CN VII) palsy.... 
meibomian gland dysfunction | cranial nerve seven palsy | Blinking | Prospective Studies | Tears - chemistry | Humans | Middle Aged | Male | Facial Nerve Diseases - physiopathology | Fluorophotometry | Blinking - physiology | Meibomian Glands - physiopathology | Adult | Female | Aged | Eyelid Diseases - physiopathology | Index Medicus
Journal Article