Screening for spinocerebellar ataxia type 36 (SCA36) in the Greek population von Katsimpouris, D., Kartanou, C., Breza, M., Panas, M., Koutsis, G., Karadima, G.

Volltext

Repeat expansions in NOP56 are a cause of spinocerebellar ataxia Type 36 in the British population von Lam, Tanya, Rocca, Clarissa, Ibanez, Kristina, Dalmia, Anupriya, Tallman, Samuel, Hadjivassiliou, Marios, Hensiek, Anke, Nemeth, Andrea, Facchini, Stefano, Wood, Nicholas, Cortese, Andrea, Houlden, Henry, Tucci, Arianna

Volltext

Screening for the FMR1 premutation in Greek patients with late-onset movement disorders von Kartanou, Chrisoula, Seferiadi, Maria, Pomoni, Stella, Potagas, Constantin, Sofocleous, Chrystalena, Traeger-Synodinos, Joanne, Stefanis, Leonidas, Panas, Marios, Koutsis, Georgios, Karadima, Georgia

Volltext

Screening for SCA27B, CANVAS and other repeat expansion disorders in Greek patients with late-onset cerebellar ataxia suggests a need to update current diagnostic algorithms von Koutsis, Georgios, Kartanou, Chrisoula, Kontogeorgiou, Zoi, Koniari, Chrysoula, Mitrousias, Alexandros, Pellerin, David, Dicaire, Marie-Jose, Iruzubieta, Pablo, Danzi, Matt C., Athanassopoulos, Konstantinos, Ragazos, Nikolaos, Stamelou, Maria, Rentzos, Michail, Anagnostou, Evangelos, Zuchner, Stephan, Brais, Bernard, Houlden, Henry, Panas, Marios, Stefanis, Leonidas, Karadima, Georgia

Volltext

Incidence of different pressure patterns of spinal cerebellar ataxia (SCA) and analysis of imaging and genetic diagnosis von Peng, Yufen, Tu, Qi, Han, Yao, Gao, Liang, Fu, Jianjun

Volltext

Genetic Movement Disorders Commonly Seen in Asians von Jagota, Priya, Lim, Shen‐Yang, Pal, Pramod Kumar, Lee, Jee‐Young, Kukkle, Prashanth Lingappa, Fujioka, Shinsuke, Shang, Huifang, Phokaewvarangkul, Onanong, Bhidayasiri, Roongroj, Mohamed Ibrahim, Norlinah, Ugawa, Yoshikazu, Aldaajani, Zakiyah, Jeon, Beomseok, Diesta, Cid, Shambetova, Cholpon, Lin, Chin‐Hsien

Volltext