Works matching IS 16602854 AND DT 2018 AND VI 18 AND IP 2/3

Results: 15

Front & Back Matter.

Published in:: Neurodegenerative Diseases, 2018, v. 18, n. 2/3, p. N.PAG, doi. 10.1159/000492956
Publication type:: Article

Erratum.

Published in:

2018

By:

Seo, Han Gil

Publication type:

Correction Notice

Novel <bold>ABCD1</bold> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum.

Published in:

Neurodegenerative Diseases, 2018, v. 18, n. 2/3, p. 156, doi. 10.1159/000490248

By:

Qiu, Yusen;
Xin, Ling;
Wang, Yuyao;
Yu, Yanyan;
Zou, Keji;
Zhou, Qian;
Chen, Yunqing;
Chen, Shuyun;
Zhu, Min;
Hong, Daojun

Publication type:

Article

Interferon Lambda Family along with HTLV-1 Proviral Load, Tax, and HBZ Implicated in the Pathogenesis of Myelopathy/Tropical Spastic Paraparesis.

Published in:

Neurodegenerative Diseases, 2018, v. 18, n. 2/3, p. 150, doi. 10.1159/000490058

By:

Mozhgani, Sayed-Hamidreza;
Jahantigh, Hamid Reza;
Rafatpanah, Houshang;
Valizadeh, Narges;
Mohammadi, Asadollah;
Basharkhah, Samira;
Rezaee, Seyed Abdolrahim

Publication type:

Article

Association between White Matter Lesions and Non-Motor Symptoms in Parkinson Disease.

Published in:

Neurodegenerative Diseases, 2018, v. 18, n. 2/3, p. 127, doi. 10.1159/000489311

By:

Lee, Jeong-Yoon;
Kim, Ji Sun;
Jang, Wooyoung;
Park, Jinse;
Oh, Eungseok;
Youn, Jinyoung;
Park, Suyeon;
Cho, Jin Whan

Publication type:

Article

Education-Adjusted Normality Thresholds for FDG-PET in the Diagnosis of Alzheimer Disease.

Published in:

Neurodegenerative Diseases, 2018, v. 18, n. 2/3, p. 120, doi. 10.1159/000488915

By:

Mainta, Ismini C.;
Trombella, Sara;
Morbelli, Silvia;
Frisoni, Giovanni B.;
Garibotto, Valentina

Publication type:

Article

Neurofilament Subunit L Levels in the Cerebrospinal Fluid and Serum of Patients with Amyotrophic Lateral Sclerosis.

Published in:

Neurodegenerative Diseases, 2018, v. 18, n. 2/3, p. 165, doi. 10.1159/000488681

By:

Gong, Zhong-Ying;
Lv, Gao-Peng;
Gao, Li-Na;
Lu, Yi;
Guo, Jie;
Zang, Da-Wei

Publication type:

Article

Distinctive Olfactory Pattern in Parkinson’s Disease and Non-Neurodegenerative Causes of Hyposmia.

Published in:

Neurodegenerative Diseases, 2018, v. 18, n. 2/3, p. 143, doi. 10.1159/000488680

By:

Crespo Cuevas, Ane Miren;
Ispierto, Lourdes;
Vilas, Dolores;
Planas, Anna;
Planas, Albert;
Isern, Irina;
Sanchez, Josep;
De Haro, Josep;
Alvarez, Ramiro

Publication type:

Article

Feasibility of Smartphone-Based Testing of Interference in Parkinson’s Disease.

Published in:

Neurodegenerative Diseases, 2018, v. 18, n. 2/3, p. 133, doi. 10.1159/000488593

By:

Lee, Will;
Williams, David R.;
Evans, Andrew

Publication type:

Article

Gradual Phenotype Development in Huntington Disease Transgenic Minipig Model at 24 Months of Age.

Published in:

Neurodegenerative Diseases, 2018, v. 18, n. 2/3, p. 107, doi. 10.1159/000488592

By:

Vidinská, Daniela;
Vochozková, Petra;
Šmatlíková, Petra;
Ardan, Taras;
Klíma, Jiří;
Juhás, Štefan;
Juhásová, Jana;
Bohuslavová, Božena;
Baxa, Monika;
Valeková, Ivona;
Motlík, Jan;
Ellederová, Zdenka

Publication type:

Article

Combinations of Multiple Neuroimaging Markers using Logistic Regression for Auxiliary Diagnosis of Alzheimer Disease and Mild Cognitive Impairment.

Published in:

Neurodegenerative Diseases, 2018, v. 18, n. 2/3, p. 91, doi. 10.1159/000487801

By:

Mao, Nini;
Liu, Yunting;
Chen, Kewei;
Yao, Li;
Wu, Xia

Publication type:

Article

Characteristics of Early Oropharyngeal Dysphagia in Patients with Multiple System Atrophy.

Published in:

Neurodegenerative Diseases, 2018, v. 18, n. 2/3, p. 84, doi. 10.1159/000487800

By:

Lee, Hyun Haeng;
Seo, Han Gil;
Kim, Kwang-dong;
Lee, Seung Hak;
Lee, Woo Hyung;
Oh, Byung-Mo;
Lee, Woong-Woo;
Kim, Yoon;
Kim, Aryun;
Kim, Han-Joon;
Jeon, Beomseok;
Han, Tai Ryoon

Publication type:

Article

Cognitive Reserve Hypothesis in Frontotemporal Dementia: Evidence from a Brain SPECT Study in a Series of Greek Frontotemporal Dementia Patients.

Published in:

Neurodegenerative Diseases, 2018, v. 18, n. 2/3, p. 69, doi. 10.1159/000486621

By:

Maiovis, Pantelis;
Ioannidis, Panagiotis;
Gerasimou, Georgios;
Gotzamani- Psarrakou, Anna;
Karacostas, Dimitrios

Publication type:

Article

Phenotypic Variability in Autosomal Dominant Familial Alzheimer Disease due to the S170F Mutation of Presenilin-1.

Published in:

Neurodegenerative Diseases, 2018, v. 18, n. 2/3, p. 57, doi. 10.1159/000485899

By:

Tiedt, Hannes O.;
Benjamin, Beate;
Niedeggen, Michael;
Lueschow, andreas

Publication type:

Article

Whole-Genome Linkage Analysis with Whole-Exome Sequencing Identifies a Novel Frameshift Variant in <bold>NEFH</bold> in a Chinese Family with Charcot-Marie-Tooth 2: A Novel Variant in <bold>NEFH</bold> for Charcot-Marie-Tooth 2.

Published in:

Neurodegenerative Diseases, 2018, v. 18, n. 2/3, p. 74, doi. 10.1159/000487754

By:

Bian, Xianli;
Lin, Pengfei;
Li, Jiangxia;
Long, Feng;
Duan, Ruonan;
Yuan, Qianqian;
Li, Yan;
Gao, Fei;
Gao, Shang;
Wei, Shijun;
Li, Xi;
Sun, Wenjie;
Gong, Yaoqin;
Yan, Chuanzhu;
Liu, Qiji

Publication type:

Article