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olivopontocerebellar atrophy with slow eye movement相关文献:
A variety of olivopontocerebellar atrophy distinguished by slow eye movements and peripheral neuropathy.
Wadia NH.
Adv Neurol. 1984;41:149-77.
PMID:6093483
Neuropathological background of oculomotor disturbances in olivopontocerebellar atrophy with special reference to slow saccade.
Mizutani T, Satoh J, Morimatsu Y.
Clin Neuropathol. 1988 Mar-Apr;7(2):53-61.
PMID:3164663
Selective, circuit-wide sparing of floccular connections in hereditary olivopontine cerebellar atrophy with slow saccades.
Ying SH, Horn AK, Geiner S, Wadia NH, Büttner-Ennever JA.
Prog Brain Res. 2008;171:583-6. doi: 10.1016/S0079-6123(08)00684-5.
PMID:18718358
An autopsy case of an aged patient with spinocerebellar ataxia type 2.
Ishida C, Komai K, Yonezawa K, Sakajiri K, Nitta E, Kawashima A, Yamada M.
Neuropathology. 2011 Oct;31(5):510-8. doi: 10.1111/j.1440-1789.2010.01176.x. Epub 2010 Dec 6.
PMID:21134000
Menzel's hereditary ataxia with slow eye movements and myoclonus. A clinico-pathological study.
Rondot P, De Recondo J, Davous P, Vedrenne C.
J Neurol Sci. 1983 Sep;61(1):65-80. doi: 10.1016/0022-510x(83)90055-2.
PMID:6631453
Oculomotor testing in the differential diagnosis of degenerative ataxic disorders.
Wessel K, Moschner C, Wandinger KP, Kömpf D, Heide W.
Arch Neurol. 1998 Jul;55(7):949-56. doi: 10.1001/archneur.55.7.949.
PMID:9678312
Saccade velocity in idiopathic and autosomal dominant cerebellar ataxia.
Bürk K, Fetter M, Skalej M, Laccone F, Stevanin G, Dichgans J, Klockgether T.
J Neurol Neurosurg Psychiatry. 1997 Jun;62(6):662-4. doi: 10.1136/jnnp.62.6.662.
PMID:9219762
Autosomal recessive ataxia, slow eye movements and psychomotor retardation.
Najim al-Din AS, al-Kurdi A, Dasouki M, Wriekat AL, al-Khateeb M, Mubaidin A, al-Hiari M.
J Neurol Sci. 1994 Jun;124(1):61-6. doi: 10.1016/0022-510x(94)90011-6.
PMID:7931423
Ultralow vestibuloocular reflex time constants.
Baloh RW, Beykirch K, Tauchi P, Yee RD, Honrubia V.
Ann Neurol. 1988 Jan;23(1):32-7. doi: 10.1002/ana.410230107.
PMID:3422799
[Clinical study of gene locus heterogeneity in hereditary olivopontocerebellar atrophy (OPCA)--report of 2 pedigrees affected with non SCA1 type OPCA].
Sasaki H, Wakisaka A, Tashiro K, Hamada T, Shima K.
Rinsho Shinkeigaku. 1991 Nov;31(11):1170-6.
PMID:1813183
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