Imaging of dopamine transporters in Parkinson disease: a meta‐analysis of (18)F/(123)I‐FP‐CIT studies

por Kong, Yanyan, Zhang, Chencheng, Liu, Kawai, Wagle Shukla, Aparna, Sun, Bomin, Guan, Yihui
Publicado 2020

Associations of sleep characteristics with alpha‐synuclein in cerebrospinal fluid in older adults

por Wang, Xiao‐Tong, Liu, Feng‐Tao, Bi, Yan‐Lin, Shen, Xue‐Ning, Xu, Wei, Wang, Jian, Tan, Lan, Yu, Jin‐Tai
Publicado 2020

Re‐defining the clinicopathological spectrum of neuronal intranuclear inclusion disease

por Chen, Hao, Lu, Likui, Wang, Bin, Cui, Guiyun, Wang, Xingqi, Wang, Yujing, Raza, Hafiz Khuram, Min, Yan, Li, Keke, Cui, Yingying, Miao, Zhigang, Wan, Bo, Sun, Miao, Xu, Xingshun
Publicado 2020

Association of rare variants in neurodegenerative genes with familial Alzheimer’s disease

por Zhang, Weiwei, Jiao, Bin, Xiao, Tingting, Liu, Xixi, Liao, Xinxin, Xiao, Xuewen, Guo, Lina, Yuan, Zhenhua, Yan, Xinxiang, Tang, Beisha, Shen, Lu
Publicado 2020

Does including machine learning predictions in ALS clinical trial analysis improve statistical power?

por Zhou, Nina, Manser, Paul
Publicado 2020

Promoting identification of amyotrophic lateral sclerosis based on label‐free plasma spectroscopy

por Zhang, Qi‐Jie, Chen, Yang, Zou, Xiao‐Huan, Hu, Wei, Ye, Min‐Lu, Guo, Qi‐Fu, Lin, Xue‐Liang, Feng, Shang‐Yuan, Wang, Ning
Publicado 2020

LAMA2‐related muscular dystrophy: Natural history of a large pediatric cohort

por Zambon, Alberto A., Ridout, Deborah, Main, Marion, Mein, Rachael, Phadke, Rahul, Muntoni, Francesco, Sarkozy, Anna
Publicado 2020

Association of serum Apolipoprotein B with cerebrospinal fluid biomarkers of Alzheimer’s pathology

por Hu, Hao, Tan, Lan, Bi, Yan‐Lin, Xu, Wei, Tan, Lin, Shen, Xue‐Ning, Hou, Xiao‐He, Ma, Ya‐Hui, Dong, Qiang, Yu, Jin‐Tai
Publicado 2020

Discordant Alzheimer's neurodegenerative biomarkers and their clinical outcomes

por Guo, Yu, Li, Hong‐Qi, Tan, Lin, Chen, Shi‐Dong, Yang, Yu‐Xiang, Ma, Ya‐Hui, Zuo, Chuan‐Tao, Dong, Qiang, Tan, Lan, Yu, Jin‐Tai
Publicado 2020

Neurodegeneration trajectory in pediatric and adult/late DM1: A follow‐up MRI study across a decade

por Labayru, Garazi, Jimenez‐Marin, Antonio, Fernández, Esther, Villanua, Jorge, Zulaica, Miren, Cortes, Jesus M., Díez, Ibai, Sepulcre, Jorge, López de Munain, Adolfo, Sistiaga, Andone
Publicado 2020

Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia

por Lai, Lu‐Lu, Chen, Yi‐Jun, Li, Yun‐Lu, Lin, Xiao‐Hong, Wang, Meng‐Wen, Dong, En‐Lin, Wang, Ning, Chen, Wan‐Jin, Lin, Xiang
Publicado 2020

Association of genetic variants in migraineurs with and without restless legs syndrome

por Lin, Guan‐Yu, Lin, Yu‐Kai, Liang, Chih‐Sung, Lee, Jiunn‐Tay, Tsai, Chia‐Lin, Hung, Kuo‐Sheng, Luo, Wen‐Jie, Tsai, Chia‐Kuang, Hsu, Yu‐Wei, Ho, Tsung‐Han, Yang, Fu‐Chi
Publicado 2020

Dominant mutations in ITPR3 cause Charcot‐Marie‐Tooth disease

por Rönkkö, Julius, Molchanova, Svetlana, Revah‐Politi, Anya, Pereira, Elaine M., Auranen, Mari, Toppila, Jussi, Kvist, Jouni, Ludwig, Anastasia, Neumann, Julika, Bultynck, Geert, Humblet‐Baron, Stéphanie, Liston, Adrian, Paetau, Anders, Rivera, Claudio, Harms, Matthew B., Tyynismaa, Henna, Ylikallio, Emil
Publicado 2020

Plasma proteome in multiple sclerosis disease progression

por Malekzadeh, Arjan, Leurs, Cyra, van Wieringen, Wessel, Steenwijk, Martijn D., Schoonheim, Menno M., Amann, Michael, Naegelin, Yvonne, Kuhle, Jens, Killestein, Joep, Teunissen, Charlotte E.
Publicado 2019

Ring trial of 2nd generation RT‐QuIC diagnostic tests for sporadic CJD

por Orrú, Christina D., Groveman, Bradley R., Foutz, Aaron, Bongianni, Matilde, Cardone, Franco, McKenzie, Neil, Culeux, Audrey, Poleggi, Anna, Grznarova, Katarina, Perra, Daniela, Fiorini, Michele, Liu, Xiaoqin, Ladogana, Anna, Sbriccoli, Marco, Hughson, Andrew G., Haïk, Stéphane, Green, Alison J., Geschwind, Michael D., Pocchiari, Maurizio, Safar, Jiri G., Zanusso, Gianluigi, Caughey, Byron
Publicado 2020

Optic, trigeminal, and facial neuropathy related to anti‐neurofascin 155 antibody

por Ogata, Hidenori, Zhang, Xu, Inamizu, Saeko, Yamashita, Ken‐ichiro, Yamasaki, Ryo, Matsushita, Takuya, Isobe, Noriko, Hiwatashi, Akio, Tobimatsu, Shozo, Kira, Jun‐ichi
Publicado 2020

Genetic factors for susceptibility to and manifestations of neuromyelitis optica

por Matsushita, Takuya, Masaki, Katsuhisa, Isobe, Noriko, Sato, Shinya, Yamamoto, Ken, Nakamura, Yuri, Watanabe, Mitsuru, Suenaga, Toshihiko, Kira, Jun‐ichi
Publicado 2020

The presence of leukoaraiosis enhances the association between sTWEAK and hemorrhagic transformation

por da Silva‐Candal, Andrés, Pérez‐Mato, María, Rodríguez‐Yáñez, Manuel, López‐Dequidt, Iria, Pumar, José M., Ávila‐Gómez, Paulo, Sobrino, Tomás, Campos, Francisco, Castillo, José, Hervella, Pablo, Iglesias‐Rey, Ramón
Publicado 2020

Plasma NfL and GFAP as biomarkers of spinal cord degeneration in adrenoleukodystrophy

por van Ballegoij, Wouter J. C., van de Stadt, Stephanie I.W., Huffnagel, Irene C., Kemp, Stephan, Willemse, Eline A. J., Teunissen, Charlotte E., Engelen, Marc
Publicado 2020

Viltolarsen in Japanese Duchenne muscular dystrophy patients: A phase 1/2 study

por Komaki, Hirofumi, Takeshima, Yasuhiro, Matsumura, Tsuyoshi, Ozasa, Shiro, Funato, Michinori, Takeshita, Eri, Iwata, Yasuyuki, Yajima, Hiroyuki, Egawa, Yoichi, Toramoto, Takuya, Tajima, Masaya, Takeda, Shinichi
Publicado 2020