Results 141 to 150 of about 2,776 (190)

Selective subperineurial dissection in vestibular schwannoma surgery: how I do it. [PDF]

Acta Neurochir (Wien)
Sayanagi T, Tamura R, Ohira T, Toda M.
europepmc   +1 more source

SMARCB1-related schwannomatosis and other SMARCB1-associated phenotypes: clinical spectrum and molecular pathogenesis. [PDF]

Fam Cancer
Kehrer-Sawatzki H, Cooper DN.
europepmc   +1 more source

Rare case of schwannomatosis presenting with cauda equina syndrome: a case report. [PDF]

Ann Med Surg (Lond)
Khan A, Zahoor N, Riaz AA, Siddique H, Malik A, Ahmed R, Poombal F, Antar M.   +7 more
europepmc   +1 more source

A systematic review and meta-analysis of outcomes following active surveillance, surgery and radiotherapy of meningiomas in NF2-related schwannomatosis. [PDF]

Neurooncol Adv
Sheppard J, Kannan S, Halliday J, Rutherford S, Lavin T, Forde C, Smith MJ, Evans G, King AT, Islim AI, Pathmanaban ON.   +10 more
europepmc   +1 more source

The comparable tumour microenvironment in sporadic and NF2-related schwannomatosis vestibular schwannoma.

Brain Communications, 2023
Bilateral vestibular schwannoma is the hallmark of NF2-related schwannomatosis, a rare tumour predisposition syndrome associated with a lifetime of surgical interventions, radiotherapy and off-label use of the anti-angiogenic drug bevacizumab. Unilateral
Grace E Gregory
exaly   +2 more sources

Frequency of SMARCB1 mutations in familial and sporadic schwannomatosis

Neurogenetics, 2012
Mutations of the SMARCB1 gene have been implicated in several human tumour predisposing syndromes. They have recently been identified as an underlying cause of the tumour suppressor syndrome schwannomatosis.
Cecilie F Rustad, Miriam J Smith, Gareth Evans   +2 more
exaly   +2 more sources