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Rescue of lysosomal function as therapeutic strategy for SPG15 ...
“Ears of the Lynx” MRI Sign Is Associated with SPG11 and SPG15 ...
Lysosomal abnormalities in hereditary spastic paraplegia types SPG15 ...
Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent ...
(PDF) SPG15 is the second most common cause of hereditary spastic ...
Table 1 from SPG15 is the second most common cause of hereditary ...
(PDF) Identification of the SPG15 Gene, Encoding Spastizin, as a ...
MRI data from three SPG15 patients | Download Scientific Diagram
Frequency and phenotype of SPG11 and SPG15 in complicated hereditary ...
(PDF) Rescue of lysosomal function as therapeutic strategy for SPG15 ...
Comparison between SPG11 and SPG15 patients reported in the literature ...
(PDF) Frequency and phenotype of SPG11 and SPG15 in complicated spastic ...
a Forest plot of SPG15 mutation frequencies in HSP patients. The ...
Hallmarks of SPG15 pathology in fibroblasts. (A) Schematic of the ...
Effect of Drp1 knockdown in rescuing axonal defects in SPG15 and SPG48 ...
SPG15 KO neurons exhibit impaired axonal trafficking. Kymographs ...
SPG15 and SPG48 neurons have altered mitochondrial morphology. (A ...
Inhibiting mitochondrial fission improves neurite outgrowth in SPG15 ...
NfL Elevations Decrease with Disease Duration in SPG11 and SPG15
Reduced mitochondrial membrane potential in SPG15 and SPG48 neurons ...
Loss of SPG15 impairs lysosomal lipid metabolism. (A) 15 month old ...
Increased neurite swellings within SPG15 and SPG48 telencephalic ...
SPG15 and SPG48 neurons display impaired neurite outgrowth. (A ...
SPG15 truncating mutations identified in this study | Download ...
Interaction between AP-5 and the hereditary spastic paraplegia proteins ...
ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic ...
Spastic Paraplegia 15 | Hereditary Ocular Diseases
(PDF) Lysosomal abnormalities in hereditary spastic paraplegia types ...
Investigating Hereditary Spastic Paraplegia Axonal Degeneration by ...
Hereditary spastic paraplegia | PPSX
(PDF) Interaction Between AP-5 and the Hereditary Spastic Paraplegia ...
Schematic representation of the SPG15/ZFYVE26 gene and distribution of ...
Clinical and genetic study of hereditary spastic paraplegia in Canada ...
Kjellin syndrome: hereditary spastic paraplegia with pathognomonic ...
An integrated modelling methodology for estimating global incidence and ...
Figure 1 from Spastic paraplegia with thinning of the corpus callosum ...
Pluripotent Stem Cells as a Preclinical Cellular Model for Studying ...
(PDF) Overlapping phenotypes in complex spastic paraplegias SPG11 ...
Spastic Paraplegia Study Links Early Immune Activation | Technology ...
Frontiers | Case report: Hereditary spastic paraplegia with a novel ...
Defective autophagy in spastizin mutated patients with hereditary ...
Frontiers | Neuroimaging in Hereditary Spastic Paraplegias: Current Use ...
SPG35/FA2H and SPG48/AP5Z1 genetic variants identified in the study ...
Table 1 from A complex form of hereditary spastic paraplegia harboring ...
Figure 1 from A complex form of hereditary spastic paraplegia harboring ...
(PDF) Clinical features and management of hereditary spastic paraplegia
Frontiers | The therapeutic effects of physical treatment for patients ...
Hereditary Spastic Paraplegia with Mental Impairment, Thin Corpus ...
Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary ...
Starvation-enhanced recruitment of AP-5/SPG11/SPG15 to late ...
遺伝性痙性対麻痺 HSP: hereditary spastic paraplegia│医學事始 いがくことはじめ
Frontiers | Clinical analysis in patients with SPG11 hereditary spastic ...
Figure: MRI in SPG15, SPG11 and SPG4. | Download Scientific Diagram
Phenotypic Variability with Two Novel Variants in SPG15: Catching the ...
A Review of the Genetic Spectrum of Hereditary Spastic Paraplegias in ...
(PDF) Neuropsychology and MRI correlates of neurodegeneration in SPG11 ...
A review of the genetic spectrum of hereditary spastic paraplegias ...
Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
SPG15/ZFYVE26 novel genetic variants identified in nine Italian ...
Frontiers | Pharmacological rescue of mitochondrial and neuronal ...
RCSB PDB - 8YAD: structure of SPG11-SPG15 complex
HSP15 | Rare Diseases: Genetics and Metabolism
Frontiers | Clinical Features and Genetic Spectrum of Patients With ...
Immune Cells Drive Congenital Paralysis Disease
Immune Cells Drive Congenital Paralysis Disease — btc
