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The spastic paraplegia SPG10 locus: narrowing of critical region and ...
Clinical findings in patients with genetically confirmed SPG10 and ...
SPG10 is a rare cause of spastic paraplegia in European families ...
Pedigree of the SPG10 family. Arrow indicates the index patient. The ...
(PDF) The spastic paraplegia SPG10 locus: Narrowing of critical region ...
同軸歯車減速機 - SPG10 - Orbray Co., Ltd - 中実軸 / 0 - 0.1 Nm / コンパクト
Figure 1 from Late-onset spastic paraplegia type 10 (SPG10) family ...
Figure 2 from Role of Kinesin-1 in the Pathogenesis of SPG10, a Rare ...
Altered CSF levels of monoamines in hereditary spastic paraparesis 10 ...
Late-onset spastic paraplegia type 10 (SPG10) family presenting with ...
(PDF) Hereditary spastic paraplegia:A novel mutation and expansion of ...
Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia ...
Figure 4 from Human SPG11 cerebral organoids reveal cortical ...
Human SPG11 cerebral organoids reveal cortical neurogenesis impairment ...
Frontiers | Pharmacological rescue of mitochondrial and neuronal ...
Frontiers | Axon-Specific Mitochondrial Pathology in SPG11 Alpha Motor ...
The Diagnostic Landscape of Adult Neurogenetic Disorders
Abnormal Paraplegin Expression in Swollen Neurites, τ- and α-Synuclein ...
Frontiers | Clinical analysis in patients with SPG11 hereditary spastic ...
Pluripotent Stem Cells as a Preclinical Cellular Model for Studying ...
Application of a Clinical Workflow May Lead to Increased Diagnostic ...
Table 2 from Autosomal dominant hereditary spastic paraplegia: DHPLC ...
The foundation and architecture of precision medicine in neurology and ...
Neuroinflammatory disease signatures in SPG11-related hereditary ...
Brain tissue classification - Eureka | Patsnap
Progressive supranuclear palsy and multiple system atrophy | PPTX
A New Locus for Autosomal Dominant “Pure” Hereditary Spastic Paraplegia ...
Anantara Siam Bangkok Hotel... - Anantara Siam Bangkok Hotel
Figure 1 from Mutation analysis of the paraplegin gene (SPG7) in ...
Figure 1 from Dementia in SPG4 hereditary spastic paraplegia | Semantic ...
Frontiers | Genotype and phenotype spectrum of 10 children with STXBP1 ...
De novo variants in SP9 cause a novel form of interneuronopathy ...
USP10 in Neurological Disorders: Mechanistic Insights and Emerging ...
Pharmacological rescue of mitochondrial and neuronal defects in SPG7 ...
Neuroimaging patterns in paediatric onset hereditary spastic ...
Novel mutation of SPG4 gene in a Chinese family with hereditary spastic ...
Expanding the Phenotypic Spectrum of SPG7 Rare Damaging Variants ...
Table 2 from Dementia in SPG4 hereditary spastic paraplegia | Semantic ...
Novel genotype-phenotype and MRI correlations in a large cohort of ...
Figure 1 from The Diagnostic Landscape of Adult Neurogenetic Disorders ...
Morphology of SPG. A.1: Schematic showing the localization of SPG (dark ...
Table 1 from A clinical , genetic and biochemical study of SPG 7 ...
Clinical characteristics and genetic status of patients with sphenoid ...
Table 1 from Autosomal dominant hereditary spastic paraplegia: DHPLC ...
Multigeneration family with dominant SPG30 hereditary spastic ...
Figure I from Charting a Course for Genetic Discovery in Neurological ...
Table 1 from Neurotransmitter abnormalities and response to ...
Figure 2 from Annals of Rehabilitation Medicine Case Report ...
Genome-Scale Networks Link Neurodegenerative Disease Genes to α ...
Severe axonal neuropathy is a late manifestation of SPG11 - PMC
Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent ...
A Neurodevelopmental Phenotype Is Linked to SMG8 (A) Genomewide linkage ...
Clinical and neurophysiological summary characteristics of the SPG5 ...
Mutation analysis of the SPG4 gene in Italian patients with pure and ...
