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Annals of Otology, Rhinology & Laryngology, ISSN 0003-4894, 12/2016, Volume 125, Issue 12, pp. 1010 - 1014
Objective: Imaging plays a critical role in the evaluation of patients presenting with unilateral vocal fold paresis or paralysis of unknown etiology. In those... 
imaging | occult etiology | idiopathic vocal fold paralysis | ETIOLOGY | MANAGEMENT | OTORHINOLARYNGOLOGY | IMMOBILITY | COMPUTED-TOMOGRAPHY | CORD PARALYSIS | Aftercare - methods | Humans | Middle Aged | Thyroid Neoplasms - diagnostic imaging | Carcinoma, Acinar Cell - complications | Thyroid Neoplasms - complications | Laryngeal Neoplasms - diagnostic imaging | Male | Paraganglioma - complications | Tomography, X-Ray Computed | Carcinoma, Squamous Cell - diagnostic imaging | Carcinoma - diagnostic imaging | Mediastinal Diseases - complications | Squamous Cell Carcinoma of Head and Neck | Carcinoma - complications | Time Factors | Nerve Sheath Neoplasms - complications | Pyriform Sinus - diagnostic imaging | Adult | Female | Retrospective Studies | Sarcoidosis - diagnostic imaging | Vocal Cord Paralysis - diagnostic imaging | Skull Base Neoplasms - diagnostic imaging | Mediastinal Diseases - diagnostic imaging | Carcinoma, Acinar Cell - diagnostic imaging | Head and Neck Neoplasms - diagnostic imaging | Tracheal Neoplasms - diagnostic imaging | Kaplan-Meier Estimate | Vagus Nerve Diseases - diagnostic imaging | Skull Base Neoplasms - complications | Vagus Nerve Diseases - complications | Thyroid Cancer, Papillary | Positron Emission Tomography Computed Tomography | Magnetic Resonance Imaging | Paraganglioma - diagnostic imaging | Sarcoidosis - complications | Tracheal Neoplasms - complications | Carcinoma, Papillary | Carcinoma, Squamous Cell - complications | Head and Neck Neoplasms - complications | Aged | Vocal Cord Paralysis - etiology | Hypopharyngeal Neoplasms - complications | Nerve Sheath Neoplasms - diagnostic imaging | Hypopharyngeal Neoplasms - diagnostic imaging | Laryngeal Neoplasms - complications
Journal Article
Neurosurgery, ISSN 0148-396X, 03/2005, Volume 56, Issue 3, pp. 510 - 515
OBJECTIVE: Spinal nerve sheath tumors arise from the spinal nerve root and grow along it. There are two sites at which the growth of a tumor is restricted: the... 
Extramedullary tumor | Myelopathy | Neuroma | Radiculopathy | Dumbbell tumor | Neurofibroma | SURGERY | neuroma | MANAGEMENT | SERIES | RESECTION | extramedullary tumor | SCHWANNOMA | neurofibroma | radiculopathy | CLINICAL NEUROLOGY | myelopathy | CERVICAL-SPINE | ROOTS | NEUROMAS | NEUROLOGICAL DEFICIT | NEURINOMAS | Japan - epidemiology | Spinal Nerves - pathology | Neurofibromatosis 1 - epidemiology | Peripheral Nervous System Neoplasms - surgery | Humans | Middle Aged | Spinal Nerves - surgery | Male | Laminectomy | Paresthesia - etiology | Neurofibroma - pathology | Neurofibromatosis 2 - epidemiology | Nerve Sheath Neoplasms - complications | Nerve Sheath Neoplasms - pathology | Pain - etiology | Spinal Cord Neoplasms - surgery | Adult | Female | Peripheral Nervous System Neoplasms - complications | Retrospective Studies | Peripheral Nervous System Neoplasms - epidemiology | Peripheral Nervous System Neoplasms - pathology | Muscle Weakness - etiology | Nerve Sheath Neoplasms - epidemiology | Neuroma - pathology | Neurofibroma - surgery | Dura Mater - pathology | Neuroma - epidemiology | Treatment Outcome | Neurofibroma - epidemiology | Neuroma - surgery | Spinal Cord Neoplasms - complications | Magnetic Resonance Imaging | Nerve Sheath Neoplasms - surgery | Adolescent | Spinal Cord Neoplasms - pathology | Aged | Spinal Nerve Roots - pathology | Spinal Cord Neoplasms - epidemiology
Journal Article
Cancer, ISSN 0008-543X, 04/2007, Volume 109, Issue 7, pp. 1406 - 1412
BACKGROUND Patients affected by neurofibromatosis type 1 (NF1) are at higher risk of developing soft‐tissue sarcomas (STS) than the general population. The... 
pediatric soft tissue sarcomas | neurofibromatosis | malignant peripheral nerve sheath tumor | rhabdomyosarcoma | Pediatric soft tissue sarcomas | Neurofibromatosis | Malignant peripheral nerve sheath tumor | Rhabdomyosarcoma | NF1 PATIENTS | SURVIVAL | MULTIPLE NEUROFIBROMATOSIS | VONRECKLINGHAUSEN NEUROFIBROMATOSIS | INTERGROUP RHABDOMYOSARCOMA | CHILDHOOD | MALIGNANT SCHWANNOMA | ONCOLOGY | EMBRYONAL RHABDOMYOSARCOMA | SINGLE-INSTITUTION | NERVE SHEATH TUMORS | Sarcoma - complications | Prognosis | Prospective Studies | Humans | Child, Preschool | Infant | Male | Neurofibrosarcoma - diagnosis | Peripheral Nervous System Neoplasms - therapy | Sarcoma - therapy | Neurofibromatosis 1 - therapy | Neoplasms, Second Primary - complications | Neoplasms, Second Primary - therapy | Nerve Sheath Neoplasms - complications | Female | Peripheral Nervous System Neoplasms - complications | Sarcoma - diagnosis | Child | Neurofibrosarcoma - therapy | Rhabdomyosarcoma - complications | Rhabdomyosarcoma - diagnosis | Risk Factors | Nerve Sheath Neoplasms - diagnosis | Neurofibromatosis 1 - diagnosis | Peripheral Nervous System Neoplasms - diagnosis | Survival Rate | Combined Modality Therapy | Neoplasms, Second Primary - diagnosis | Neurofibrosarcoma - complications | Adolescent | Neurofibromatosis 1 - complications | Nerve Sheath Neoplasms - therapy | Rhabdomyosarcoma - therapy | Research | Sarcoma | Demographic aspects | Cancer in children
Journal Article
British Journal of Oral and Maxillofacial Surgery, ISSN 0266-4356, 2017, Volume 55, Issue 7, pp. e35 - e37
Abstract Repeated haemorrhages in peripheral nerve sheath tumours of the salivary glands are rare. We report the case of a patient with neurofibromatosis type... 
Surgery | Salivary gland | Neurofibromatosis type 1 | Peripheral nerve sheath tumours | SURGERY | NEUROFIBROMA | DENTISTRY, ORAL SURGERY & MEDICINE | Recurrence | Cheek - injuries | Salivary Gland Neoplasms - complications | Nerve Sheath Neoplasms - complications | Hemorrhage - etiology | Humans | Adolescent | Neurofibromatosis 1 - complications | Male | Tumors
Journal Article
Journal of Neuropathology & Experimental Neurology, ISSN 0022-3069, 04/2015, Volume 74, Issue 4, pp. 288 - 292
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 06/2014, Volume 164, Issue 6, pp. 1431 - 1437
Journal Article