MeSH Review:
Brachial Plexus Neuritis
Kuhlenbäumer,
Hannibal,
Nelis,
Schirmacher,
Verpoorten,
Meuleman,
Watts,
De Vriendt,
Young,
Stögbauer,
Halfter,
Irobi,
Goossens,
Del-Favero,
Betz,
Hor,
Kurlemann,
Bird,
Airaksinen,
Mononen,
Serradell,
Prats,
Van Broeckhoven,
De Jonghe,
Timmerman,
Ringelstein,
Chance,
van Alfen,
van Engelen,
Ørstavik,
Skard Heier,
Young,
Stögbauer,
- Mutations in SEPT9 cause hereditary neuralgic amyotrophy. Kuhlenbäumer, G., Hannibal, M.C., Nelis, E., Schirmacher, A., Verpoorten, N., Meuleman, J., Watts, G.D., De Vriendt, E., Young, P., Stögbauer, F., Halfter, H., Irobi, J., Goossens, D., Del-Favero, J., Betz, B.G., Hor, H., Kurlemann, G., Bird, T.D., Airaksinen, E., Mononen, T., Serradell, A.P., Prats, J.M., Van Broeckhoven, C., De Jonghe, P., Timmerman, V., Ringelstein, E.B., Chance, P.F. Nat. Genet. (2005)
- Brachial plexus involvement as the only expression of hereditary neuropathy with liability to pressure palsies. Ørstavik, K., Skard Heier, M., Young, P., Stögbauer, F. Muscle Nerve (2001)
- Mutation analysis of a putative sialyltransferase gene, the SFRS2 splicing factor gene and the c-myb ET-locus in two families with hereditary neuralgic amyotrophy (HNA). Kuhlenbaeumer, G., Meuleman, J., Schirmacher, A., Stoegbauer, F., Ringelstein, E.B., Wehnert, M., Hoeltzenbein, M., Broeckhoven, C.V., Timmerman, V. Ann. Hum. Genet. (1998)
- Cervical root compression by a loop of the vertebral artery: case report. Duthel, R., Tudor, C., Motuo-Fotso, M.J., Brunon, J. Neurosurgery (1994)
- The clinical spectrum of neuralgic amyotrophy in 246 cases. van Alfen, N., van Engelen, B.G. Brain (2006)
