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City Kaiser-Kupfer / Manchester / Philadelphia / Springfield / Edinburgh / / Company Central Manchester Foundation Trust / NF2 / Regional Genetics Service / Menon AG / Faryniarz AG / Bayer / LG / Hanemann CO / National Molecular Genetics Reference Laboratory / Creative Commons / BioMed Central Ltd. / / Country United Kingdom / Finland / United States / / / Event FDA Phase / / Facility St Mary's Hospital / laboratory Type / Hall BD / / IndustryTerm protein product / magnetic resonance imaging / non-functional protein product / clinical management / Clinic equipment / gene product / / MedicalCondition asymmetric disease / von Recklinghausen disease / ependymomas / synonyms Definition Neurofibromatosis / Rare Diseases / inherited tumour prone disorders / retinoblastoma / Intracranial astrocytoma / seizures / deep-seated subcutaneous nodular tumours / also occasional intracutaneous tumours / multi-tumour disease die / main tumours / nerve tumour / autosomal dominant disease / bilateral schwannoma involvement / polyneuropathy / Rare Diseases BioMed Central Open Access Review Neurofibromatosis / Intracranial meningiomas / particularly aggressive tumours / severe disease / hausen disease / neurofibroma / classical neurofibromatosis / generalised symptomtatic severe polyneuropathy / tumor / constitutional neurofibromatosis / Tumors / bilateral acoustic neuroma / occasional definite neurofibromas / peripheral neurofibromatosis / optic nerve sheath tumours / optic nerve meningiomas / symptomatic cranial and spinal tumours / Neurofibromatosis / cranial meningiomas / vomiting / vestibular schwannoma / Vestibular schwannomas / dominantly inherited tumour predisposition syndrome / intracranial meningioma / deficiency / dizziness / NA Ependymoma / tinnitus / tumours / Genes Chromosomes Cancer / Abstract Neurofibromatosis / associated facial nerve schwannomas / meningioma / non cranial schwannomas / headaches / human acoustic neuroma / sporadic meningiomas / von Recklinghausen neurofibromatosis / bilateral eighth nerve tumours / glioma / Multiple meningioma / Nausea / particularly cranial meningiomas / muscle weakness / meningiomas / gliomas / Central neurofibromatosis / acoustic neurofibromatosis / deafness / neurofibromas / dominantly inherited tumour prone disorder / late-stage disease / Bell's-like palsy / late stage disease / bilateral 8th nerve tumours / tumour-prone disorder / bilateral vestibular schwannomas / schwannoma / hearing loss / separate genetic and clinical diseases / blindness / skin tumours / sporadic meningioma / Spinal tumours / sporadic disease / mosaic disease / cataracts / Disease / mononeuropathy / extensive retinal hamartomas / tumour / neurofibromatosis-associated meningiomas / sporadic schwannomas / pain / milder disease / schwannomas / schwannoma growing / sporadic vestibular schwannomas / poliolike illness / severe multi-tumour disease / Nervous System Tumors / NA Cataract / tumour prone disorders / true vertigo / cataract / syndrome / / MedicalTreatment microsurgery / radiotherapy / Surgery / radiation / radiosurgery / radiation therapy / radiation treatments / cochlear implants / counselling / radiation treatment / cochlear implant / drug therapies / / MusicGroup Nausea / / Organization National Institute of Health / St Mary's Hospital / / Person Arch Dis / Gareth R Evans / Arch Neurol / Ramesh V / Charles C. Thomas / Harvey Cushing / Blair V / Otolaryngologist / / / Position Conneally PM / Permanent clinic staff Neurosurgeon / physician / Short PM / author / peripheral nerve surgeon / plastic surgeon / Ramsden RT / King / hearing therapist / physiotherapist / Short MP / Rubio MP / clinic nurse/patient link worker and a dedicated clinic secretary / WB / neurologist / Duyao MP / physiotherapist / paediatrician / plastic surgeon / neurologist / / Product avastin / NF2 / PI3 / / ProvinceOrState Maine / Illinois / / Region North West England / / Technology radiation / Screening protocol / magnetic resonance imaging / genotype / recombination / Gel Electrophoresis / gene analysis / MRI / / URL http / SocialTag 
Orphanet Journal of Rare Diseases BioMed Central Open Access