Hereditary neuropathy with a tendency to pressure palsy
Wulff, C.H.
Tidsskrift for den Norske Laegeforening Tidsskrift for Praktisk Medicin Ny Raekke 102(23): 1153-1155
1982
ISSN/ISBN: 0029-2001 PMID: 6963030 Document Number: 187049
Document emailed within 1 workday
Related Documents
György, I.; Bíró, A.; Mechler, F.; Molnár, Mária.Judit. 2008: Hereditary neuropathy with liability to pressure palsy in childhood Ideggyogyaszati Szemle 61(11-12): 423-425Traccis, S.; Pirisi, A.; Mutani, R. 1982: Unusual manifestation of hereditary neuropathy with liability to pressure palsy Acta Neurologica 4(3): 168-173
Cavallari, V.; Di Pasquale, M.R.; Scuderi, D. 1981: Hereditary neuropathy with a tendency to compression paralysis. Electrophysiological, morphometric and ultrastructural study of 2 familial cases Acta Neurologica 3(1): 187-196
Partanen, J.; Falck, B.; Kilpeläinen, H.; Kangasniemi, P.; Riekkinen, P. 1981: Hereditary pressure-sensitive neuropathy Duodecim; Laaketieteellinen Aikakauskirja 97(21): 1761-1767
Liedholm, L.J. 1998: Recurrent palsies--consider hereditary pressure neuropathy! Lakartidningen 95(14): 1527-1531
Chua, S.Y.; Lim, Y.W.; Lam, K.S.; Low, C.O. 2006: Hereditary neuropathy with liablity to pressure palsies Singapore Medical Journal 47(7): 625-626
Kramer, M.; Ly, A.; Li, J. 2016: Phenotype HNPP (Hereditary Neuropathy With Liability to Pressure Palsies) Induced by Medical Procedures American Journal of Orthopedics 45(1): E27-E28
Moszyńska, I.; Kabzińska, D.; Sinkiewicz-Darol, E.; Kochański, A. 2009: A newly identified Thr99fsX110 mutation in the PMP22 gene associated with an atypical phenotype of the hereditary neuropathy with liability to pressure palsies Acta Biochimica Polonica 56(4): 627-630
Minauchi, Y.; Kohka, M.; Igata, A.; Ohkatsu, Y. 1982: A familial case with hereditary pressure-sensitive neuropathy, with "tomacula"--the first case in Japan Rinsho Shinkeigaku 22(10): 918-925
Serena, M.; Bardin, P.G. 1988: Hereditary neuropathy with recurrent mononeuropathy (tomaculous neuropathy) Rivista di Neurologia 58(3): 97-105
Brunner, W.; Hartmann, G. 1985: Hereditary antithrombin III deficiency as a cause of an increased tendency to thrombosis. Case report Schweizerische Medizinische Wochenschrift 115(10): 343-345
Kaeser, H.E. 1992: Polyneuropathies with an abnormal tendency for pressure-induced paralysis Schweizerische Rundschau für Medizin Praxis 81(42): 1250-1253
Nakagawa, M.; Takashima, H. 2004: Update on hereditary neuropathy Rinsho Shinkeigaku 44(11): 991-994
Kira, J.; Kuroiwa, Y.; Onishi, A. 1982: Polyneuropathy: hereditary neuropathy Nihon Rinsho. Japanese Journal of Clinical Medicine 40(7): 1475-1481
Axelsson, G.; Liedholm, L.J. 2002: Multifocal motor neuropathy--unusual cause of hypoglossal palsy Lakartidningen 99(13): 1448-1450
Mosin, I.M. 2001: Leber's hereditary optic neuropathy Vestnik Oftalmologii 117(2): 48-51
Puri, V.; Anjaneyulu, A. 1996: Hereditary sensory neuropathy type Ii Neurology India 44(4): 229-230
Letchavanakul, A.; Dechphongsaphilas, W.; Dhamcharee, V. 1999: Leber's hereditary optic neuropathy Journal of the Medical Association of Thailand 82(10): 1051-1055
Shagina, O.A.; Dadali, E.L.; Fedotov, V.P.; Tiburkova, T.B.; Poliakov, A.V. 2010: Hereditary motor and sensory neuropathy type 4A Zhurnal Nevrologii i Psikhiatrii Imeni S.S. Korsakova 110(5 Part 1): 13-16
Van den Neucker, K.; Vanderstraeten, G. 1990: Hereditary compression neuropathy. Report of a family Electromyography and Clinical Neurophysiology 30(8): 509-512