Journal articles on the topic 'Spinocerebellar Degenerations'

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1

SOBUE, Itsuro. "Spinocerebellar Degenerations." Japanese Journal of Medicine 24, no. 1 (1985): 62–67. http://dx.doi.org/10.2169/internalmedicine1962.24.62.

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2

Teive, Hélio A. G. "Spinocerebellar Degenerations in Japan." Neuroepidemiology 32, no. 3 (2009): 184–85. http://dx.doi.org/10.1159/000195687.

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3

Perlman, Susan L. "Spinocerebellar degenerations: An update." Current Neurology and Neuroscience Reports 2, no. 4 (July 2002): 331–41. http://dx.doi.org/10.1007/s11910-002-0009-2.

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4

Cedarbaum, Jesse M., and John P. Blass. "Mitochondrial dysfunction and spinocerebellar degenerations." Neurochemical Pathology 4, no. 1 (February 1986): 43–63. http://dx.doi.org/10.1007/bf02834298.

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5

Mizuno, Masahiro, Masaaki Yamane, and Ryuichi Osanai. "Visual suppression test in spinocerebellar degenerations." Practica Oto-Rhino-Laryngologica 81, no. 2 (1988): 165–71. http://dx.doi.org/10.5631/jibirin.81.165.

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6

SRIDHARAN, R., K. RADHAKRISHNAN, P. P. ASHOK, and M. E. MOUSA. "PREVALENCE AND PATTERN OF SPINOCEREBELLAR DEGENERATIONS IN NORTHEASTERN LIBYA." Brain 108, no. 4 (1985): 831–43. http://dx.doi.org/10.1093/brain/108.4.831.

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7

Shibata-Hamaguchi, Ayumi, Chiho Ishida, Kazuo Iwasa, and Masahito Yamada. "Prevalence of Spinocerebellar Degenerations in the Hokuriku District in Japan." Neuroepidemiology 32, no. 3 (2009): 176–83. http://dx.doi.org/10.1159/000195686.

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8

Hirayama, K., T. Takayanagi, R. Nakamura, N. Yanagisawa, T. Hattori, K. Kita, S. Yanagimoto, et al. "Spinocerebellar degenerations in Japan: a nationwide epidemiological and clinical study." Acta Neurologica Scandinavica 89, S153 (April 1994): 1–22. http://dx.doi.org/10.1111/j.1600-0404.1994.tb05401.x.

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9

KOSAKA, Kenji, Ryuichi NAKAMURA, Masaaki FUJITA, Banri AMAKUSA, and Toru HOSOKAWA. "Application of an Extended ADL Scale to Patients with Spinocerebellar Degenerations." Japanese Journal of Rehabilitation Medicine 32, no. 1 (1995): 59–62. http://dx.doi.org/10.2490/jjrm1963.32.59.

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10

Uzunov, N., M. Kutchoukov, and Chr Kolchev. "CT scan and threshold vibrometry in the diagnosis of spinocerebellar degenerations." Italian Journal of Neurological Sciences 12, no. 2 (April 1991): 175–79. http://dx.doi.org/10.1007/bf02337030.

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11

Mizuno, Masahiro, Masaaki Yamane, and Ryuichi Osanai. "Visual suppression test in spinocerebellar degenerations - In association with neurotological examinations." Practica Oto-Rhino-Laryngologica 82, no. 5 (1989): 647–52. http://dx.doi.org/10.5631/jibirin.82.647.

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12

EMOTO, Kouji, Masayoshi UENO, Toshifumi KANAIZUMI, Shiho SUGIMORI, Masami YAGI, Hideaki SHIMOMURA, and Hiroshige NAKANO. "A CASE OF EXOGASTRIC GIANT LEIOMYOMA IN A PATIENT WITH SPINOCEREBELLAR DEGENERATIONS." Journal of the Japanese Practical Surgeon Society 57, no. 12 (1996): 3014–18. http://dx.doi.org/10.3919/ringe1963.57.3014.

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13

FUJITA, MASAAKI, and RYUICHI NAKAMURA. "Characteristics of the fastest isometric knee extension in patients with spinocerebellar degenerations." Tohoku Journal of Experimental Medicine 157, no. 1 (1989): 13–17. http://dx.doi.org/10.1620/tjem.157.13.

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14

Ito, Kenji, Chigumi Ohtsuka, Kunihiro Yoshioka, Tetsuya Maeda, Suguru Yokosawa, Futoshi Mori, Tsuyoshi Matsuda, Yasuo Terayama, and Makoto Sasaki. "Differentiation Between Multiple System Atrophy and Other Spinocerebellar Degenerations Using Diffusion Kurtosis Imaging." Academic Radiology 26, no. 11 (November 2019): e333-e339. http://dx.doi.org/10.1016/j.acra.2018.12.015.

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15

YOSHIDA, MOTOAKI, TAKAO NAKANISHI, and YOSHINARI KOMATSU. "Acute and chronic effects of thyrotropin-releasing hormone (TRH) on stabilogram in spinocerebellar degenerations." Tohoku Journal of Experimental Medicine 148, no. 3 (1986): 327–31. http://dx.doi.org/10.1620/tjem.148.327.

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16

Shimoda, Kotaro, Chikanori Hikasa, Seiho Nishikawa, and Kazuro Takahashi. "Relation between monoamine metabolites in cerebrospinal fluid and severity of symptoms in spinocerebellar degenerations." Journal of the Autonomic Nervous System 21, no. 2-3 (December 1987): 251–52. http://dx.doi.org/10.1016/0165-1838(87)90042-7.

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17

De Michele, G., P. P. Mainenti, A. Soricelli, F. Di Salle, E. Salvatore, M. R. Longobardi, A. Postiglione, M. Salvatore, and A. Filla. "Cerebral blood flow in spinocerebellar degenerations: a single photon emission tomography study in 28 patients." Journal of Neurology 245, no. 9 (August 20, 1998): 603–8. http://dx.doi.org/10.1007/s004150050253.

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18

Teräväinen, H., M. Hietanen, J. Stoessl, and D. B. Calne. "Dementia in Movement Disorders." Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 13, S4 (November 1986): 546–58. http://dx.doi.org/10.1017/s031716710003729x.

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Abstract:Of all the movement disorders, Huntington's disease has been most consistently associated with dementia, while it is only over the last decade that intellectual and cognitive decline have been recognized as common features of Parkinson's disease. It is now known that the pathology in these two conditions reflects differential involvement of the striatum. The Huntington lesion is primarily in the caudate, while the Parkinson lesion preferentially affects the putamen. Both conditions have more diffuse pathology, and dementia may also occur in a wide range of other extrapyramidal diseases, such as progressive supranuclear palsy, the parkinsonism-dementia complex of Guam, and certain spinocerebellar degenerations. Clinicopathological correlations will be reviewed in these disorders of primarily subcortical pathology, and comparisons will be made with Alzheimer's disease, a disorder of predominantly cortical pathology.
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19

Gonçalves, A., C. Oliveira, M. A. Ferro, M. Dinis, and L. Cunha. "Glutamate Dehydrogenase Deficiency in Machado-Joseph Disease." Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 20, no. 2 (May 1993): 147–50. http://dx.doi.org/10.1017/s0317167100047727.

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ABSTRACT:We studied the activity of glutamate dehydrogenase (GDH) in leukocytes from 23 patients with domi-nantly inherited ataxia. All the patients were assessed with a rating scale for ataxias and met the clinical criteria for the diagnosis of Machado-Joseph disease. The mean age of onset of symptoms was 37.8, SD 13.4 years and the duration of the disease was 7.4, SD 4.9. Leukocyte GDH activity was significantly decreased (p < 0.001) when compared to 20 normal controls. These data extend previous reports indicating that a GDH deficiency is present in peripheral tissues from some patients with spinocerebellar degenerations. Furthermore, this study suggests that a genetic deficiency of GDH may underlie some forms of dominant ataxias; this deficiency may be marked in patients with Machado-Joseph disease and is not specific for any type of multiple system atrophy.
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20

Yamamoto, H., S. Saito, and I. Sobue. "Bedside and electro-oculographic analysis of abnormal ocular movements in spinocerebellar degenerations: Effects of thyrotropin-releasing hormone." Neurology 38, no. 1 (January 1, 1988): 110. http://dx.doi.org/10.1212/wnl.38.1.110.

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21

FUJITA, Masaaki. "Electromyographic Reaction Time of the Biceps Brachii Muscle during Passive Elbow Movements in Patients with Parkinson's Disease and Those with Spinocerebellar Degenerations." Japanese Journal of Rehabilitation Medicine 30, no. 6 (1993): 391–98. http://dx.doi.org/10.2490/jjrm1963.30.391.

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22

FUJITTA, Masaaki, Tomiyoshi CHIDA, and Ryuichi NAKAMURA. "Relation of Maximum Walking Speed to Isokinetic Strength for Knee Extension and Stability of Station in Patients with Spinocerebellar Degenerations. Effect of Intensive Physical Therapy." Japanese Journal of Rehabilitation Medicine 29, no. 3 (1992): 211–15. http://dx.doi.org/10.2490/jjrm1963.29.211.

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23

Millichap, J. Gordon. "Spinocerebellar Degeneration." Pediatric Neurology Briefs 1, no. 4 (September 1, 1987): 26. http://dx.doi.org/10.15844/pedneurbriefs-1-4-5.

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24

Nabatame, Hidehiko, Hidenao Fukuyama, Ichiro Akiguchi, Masakuni Kameyama, Kazumasa Nishimura, and Yoshihisa Nakano. "Spinocerebellar Degeneration." Journal of Computer Assisted Tomography 12, no. 2 (March 1988): 298–303. http://dx.doi.org/10.1097/00004728-198803000-00020.

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25

Perlman, Susan L. "Spinocerebellar degeneration." Expert Opinion on Pharmacotherapy 4, no. 10 (October 2003): 1637–41. http://dx.doi.org/10.1517/14656566.4.10.1637.

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26

Takeichi, Norihito. "Spinocerebellar degeneration (SCD)." Equilibrium Research 73, no. 2 (2014): 47–54. http://dx.doi.org/10.3757/jser.73.47.

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27

Takeichi, Norihito. "Spinocerebellar degeneration (SCD)." Equilibrium Research 74, no. 3 (2015): 159–65. http://dx.doi.org/10.3757/jser.74.159.

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28

Miyai, Ichiro. "Neurorehabilitation for spinocerebellar degeneration." Rinsho Shinkeigaku 53, no. 11 (2013): 931–33. http://dx.doi.org/10.5692/clinicalneurol.53.931.

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29

MATSUOKA, Yukihiko, and Nobuo SAKURAI. "Spinocerebellar degeneration and neuropeptides." Japanese Journal of Medicine 28, no. 6 (1989): 791–93. http://dx.doi.org/10.2169/internalmedicine1962.28.791.

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30

Harding, A. "TRH and Spinocerebellar Degeneration." Journal of Neurology, Neurosurgery & Psychiatry 50, no. 7 (July 1, 1987): 955–56. http://dx.doi.org/10.1136/jnnp.50.7.955-a.

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31

Harding, A. "TRH and Spinocerebellar Degeneration." Journal of Neurology, Neurosurgery & Psychiatry 50, no. 9 (September 1, 1987): 1252. http://dx.doi.org/10.1136/jnnp.50.9.1252.

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32

Fujimoto, Hiroaki, and Ichiro Miyai. "Neurorehabilitation Therapy for Spinocerebellar Degeneration." Japanese Journal of Rehabilitation Medicine 58, no. 5 (May 18, 2021): 536–43. http://dx.doi.org/10.2490/jjrmc.58.536.

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33

Sasaki, Hidenao. "4. Spinocerebellar Degeneration: Recent Progress." Nihon Naika Gakkai Zasshi 102, Suppl (2013): 129b. http://dx.doi.org/10.2169/naika.102.129b.

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34

Kawai, Y., M. Suenaga, H. Watanabe, and G. Sobue. "Cognitive Impairment in Spinocerebellar Degeneration." European Neurology 61, no. 5 (2009): 257–68. http://dx.doi.org/10.1159/000206850.

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35

Abel, L. A. "Saccadic deterioration in spinocerebellar degeneration." Neuro-Ophthalmology 5, no. 3 (January 1985): 145–53. http://dx.doi.org/10.3109/01658108509079656.

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36

Nakazato, Taizo, Takeshi Sato, Toshiki Nakamura, Shoji Tsuji, and Hirotaro Narabayashi. "Adrenoleukodystrophy Presenting as Spinocerebellar Degeneration." European Neurology 29, no. 4 (1989): 229–34. http://dx.doi.org/10.1159/000116417.

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37

Hirono, N., A. Yamadori, M. Kameyama, T. Mezaki, and K. Abe. "Spinocerebellar degeneration (SCD): cognitive disturbances." Acta Neurologica Scandinavica 84, no. 3 (September 1991): 226–30. http://dx.doi.org/10.1111/j.1600-0404.1991.tb04943.x.

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38

Ben Hamida, M., F. Letaief, F. Hentati, and C. Ben Hamida. "Hypertrophic neuropathy in spinocerebellar degeneration." Acta Neuropathologica 75, no. 1 (January 1987): 51–61. http://dx.doi.org/10.1007/bf00686793.

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39

Yoshii, Fumihito, Hitoshi Tomiyasu, Ryo Watanabe, and Masafuchi Ryo. "MRI Signal Abnormalities of the Inferior Olivary Nuclei in Spinocerebellar Ataxia Type 2." Case Reports in Neurology 9, no. 3 (November 10, 2017): 267–71. http://dx.doi.org/10.1159/000481303.

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Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant spinocerebellar degeneration, associated with extended repeats of the trinucleotide CAG in the ATXN2 gene on the long arm of chromosome 12. Magnetic resonance imaging (MRI) of SCA2 showed significant atrophies of the brainstem, middle cerebellar peduncles, and cerebellum. We report two genetically proven SCA2 patients who showed hypertrophy of the inferior olivary nuclei on proton density- and T2-weighted MRI. This pattern has never been reported in patients with SCA1, SCA3, or SCA6, and may make it possible to differentiate SCA2 from other hereditary spinocerebellar ataxias.
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40

Ramnarayan, R., and Simon Herculus. "Intrathecal baclofen pump in spinocerebellar degeneration." Neurology India 64, no. 6 (2016): 1354. http://dx.doi.org/10.4103/0028-3886.193789.

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41

IKEUCHI, TAKESHI. "Gene diagnosis of inheritance spinocerebellar degeneration." Nihon Naika Gakkai Zasshi 83, no. 11 (1994): 2000–2006. http://dx.doi.org/10.2169/naika.83.2000.

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42

Ishibashi, Yasuko, Rie Naito, Yuki Matsui, Keiko Sugasawa, and Toshihisa Murofushi. "Nystagmus-sensation Dissociation in Spinocerebellar Degeneration." Acta Oto-Laryngologica 123, no. 8 (August 2003): 928–31. http://dx.doi.org/10.1080/00016480310005084.

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43

Mier, A., C. Brophy, C. W. Havard, and M. Green. "Severe diaphragm weakness in spinocerebellar degeneration." Thorax 43, no. 1 (January 1, 1988): 78–79. http://dx.doi.org/10.1136/thx.43.1.78.

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44

Sakakibara, Ryuji, Takamichi Hattori, Masaki Tojo, Tomonori Yamanishi, Kosaku Yasuda, and Keizo Hirayama. "Micturitional disturbance in hereditory spinocerebellar degeneration." Journal of the Autonomic Nervous System 50, no. 3 (January 1995): 363. http://dx.doi.org/10.1016/s0165-1838(95)90086-1.

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45

Kaloustian, Vazken M. Der, Nabil I. Jarudi, Muin J. Khoury, Adel K. Afifi, Nadia B. Bahuth, Mary E. Deeb, John Shammas, Muhammad A. Mikati, John M. Opitz, and James F. Reynolds. "Familial spinocerebellar degeneration with corneal dystrophy." American Journal of Medical Genetics 20, no. 2 (February 1985): 325–39. http://dx.doi.org/10.1002/ajmg.1320200216.

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46

Munoz, D. G., E. S. Emery, and R. A. Highland. "Mitochondrial hydroxyapatite deposits in spinocerebellar degeneration." Annals of Neurology 22, no. 2 (August 1987): 258–63. http://dx.doi.org/10.1002/ana.410220211.

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47

Kajiyama, K., S. Ueno, T. Tatsumi, S. Yorifuji, M. Takahashi, and S. Tarui. "Decreased glutamate dehydrogenase protein in spinocerebellar degeneration." Journal of Neurology, Neurosurgery & Psychiatry 51, no. 8 (August 1, 1988): 1078–80. http://dx.doi.org/10.1136/jnnp.51.8.1078.

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48

Durr, Alexandra, and Alexis Brice. "Clinical and genetic aspects of spinocerebellar degeneration." Current Opinion in Neurology 13, no. 4 (August 2000): 407–13. http://dx.doi.org/10.1097/00019052-200008000-00007.

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49

Nakazawa, Toru, Toshiaki Abe, Takefumi Hasegawa, and Makoto Tamai. "Optic Disc Edema Associated with Spinocerebellar Degeneration." Ophthalmologica 212, no. 4 (1998): 281–83. http://dx.doi.org/10.1159/000027308.

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50

Wood, N. "DS1.2 Spinocerebellar degeneration: Genetic and clinical aspects." Clinical Neurophysiology 117 (September 2006): 19. http://dx.doi.org/10.1016/j.clinph.2006.07.050.

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