Results 191 to 200 of about 47,993 (230)

Quality of life and neurological symptoms in patients with neurofibromatosis type 2: a national database study in Japan. [PDF]

Environ Health Prev Med
Yamauchi T, Suka M.
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Audiological Outcome of the Simultaneous Tumor Resection and Cochlear Implantation in Two Cases of Sporadic and Two Cases of Neurofibromatosis Type 2-Associated Intracochlear Schwannoma. [PDF]

J Clin Med
AlMutawah AA, Kim T, Chung JW.
europepmc   +1 more source

Recent advances in bone and soft tissue tumors: lipomatous tumors [PDF]

, 2012
Creytens, David
core   +1 more source

Neurofibromatosis type 2

, 2010
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Neurofibromatosis Type 2

2011
Neurofibromatosis type 2 (NF2) is an autosomal-dominant inherited tumour predisposition syndrome caused by mutations in the NF2 gene on chromosome 22. Affected individuals develop schwannomas characteristically affecting both vestibular nerves leading to hearing loss and eventual deafness.
Evans, GR, Lloyd, SK, Ramsden, RT
  +8 more sources