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:
- 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:
- 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:
- 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:
- 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:
- 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:
- 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:
- 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:
- 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
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- 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:
- 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:
- 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:
- 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:
- 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
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- Publication type:
- Article