Results 71 to 80 of about 2,684 (177)

Hereditary spastic paraparesis and other hereditary myelopathies [PDF]

, 2018
Bunn, L, Denton, A, Marsden, J, Padmakumari Sivaraman Nair, K   +3 more
core   +1 more source

Systematic review of autosomal recessive ataxias and proposal for a classification [PDF]

, 2017
Christopher J. Klein, Guy A. Rouleau, Marie Beaudin, Nicolas Dupré   +3 more
core   +1 more source

Spinocerebellar Degeneration [PDF]

Proceedings of the Royal Society of Medicine, 1950
openaire   +1 more source

The carboxy-terminal fragment of α1A calcium channel preferentially aggregates in the cytoplasm of human spinocerebellar ataxia type 6 Purkinje cells [PDF]

, 2009
Taro Ishiguro, Kinya Ishikawa, Makoto Takahashi, Masato Obayashi, Takeshi Amino, Nozomu Sato, Masaki Sakamoto, Hiroto Fujigasaki, Fuminori Tsuruta, Ricardo Dolmetsch, Takao Arai, Hidenao Sasaki, Kazuro Nagashima, Takeo Kato, Mitsunori Yamada, Hitoshi Takahashi, Yoshio Hashizume, Hidehiro Mizusawa, WA Catterall, KS Jongh De, ML Duennwald, CF Fletcher, M Frontali, K Gierga, N Gomez-Ospina, CM Gomez, S Gunawardena, N Hazeki, JW Hell, JT Hulme, JT Hulme, T Ikeuchi, K Ishikawa, K Ishikawa, K Ishikawa, K Ishikawa, C Jodice, J Kitano, HB Kordasiewicz, HB Kordasiewicz, S Koyano, T Kubodera, K Kuroiwa, A Lunkes, B Marqueze-Pouey, Z Matsuyama, A McCampbell, Y Mori, Y Nagai, K Nozaki, RA Ophoff, MF Peters, ES Piedras-Renteria, S Restituito, H Saegusa, T Sakurai, H Sasaki, E Scherzinger, T Shimohata, A Stea, H Takahashi, H Takahashi, T Takahashi, H Takano, O Tanaka, V Tarlac, S Toru, Y Trottier, T Tsunemi, T Tsunemi, T Uchihara, H Vacher, D Walker, K Watase, RE Westenbroek, RE Westenbroek, AJ Williams, I Yabe, M Yamada, M Yamada, Q Yue, O Zhuchenko   +81 more
core   +1 more source

Spinocerebellar degeneration and neuropeptides.

Japanese Journal of Medicine, 1989
Y, Matsuoka, N, Sakurai
openaire   +4 more sources

Spinocerebellar degenerations.

Nihon Naika Gakkai Zasshi, 1984
openaire   +3 more sources

Spinocerebellar degeneration (SCD)

Equilibrium Research, 2014
openaire   +3 more sources

Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations. [PDF]

Eur J Hum Genet
Yahia A, Hamed AAA, Mohamed IN, Elseed MA, Salih MA, El-Sadig SM, Siddig HE, Nasreldien AEM, Abdullah MA, Elzubair M, Omer FY, Bakhiet AM, Abubaker R, Abozar F, Adil R, Emad S, Musallam MA, Eltazi IZM, Omer Z, Malik H, Mohamed MOE, Elhassan AA, Mohamed EOE, Ahmed AKMA, Ahmed EAA, Eltaraifee E, Hussein BK, Abd Allah ASI, Salah L, Nimir M, Tag Elseed OM, Elhassan TEA, Elbashier A, Alfadul ESA, Fadul M, Ali KF, Taha SOMA, Bushara EE, Amin M, Koko M, Ibrahim ME, Ahmed AE, Elsayed LEO, Stevanin G.   +43 more
europepmc   +1 more source

Identification of a Novel <i>CLPX</i> Variant in a Mixed-Breed Dog with Anemia and Spinocerebellar Ataxia. [PDF]

Genes (Basel)
de Cecco BS, Blake JM, Kim NJ, Coffey MC, Johnston AN, Miller AD, Ekenstedt KJ, Lee J.   +7 more
europepmc   +1 more source

Two Cases of Autosomal Recessive Spinocerebellar Ataxia-8 Showing Two Novel Variants of SYNE1 in Japanese Families. [PDF]

Intern Med
Yunoki T, Matsuoka C, Osakada Y, Fukui Y, Takemoto M, Morihara R, Yamashita T, Ishiura H.   +7 more
europepmc   +1 more source