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Brain and Nerve, ISSN 1881-6096, 10/2014, Volume 66, Issue 10, pp. 1210 - 1217
Journal Article
Brain and nerve = Shinkei kenkyu no shinpo, ISSN 1881-6096, 10/2014, Volume 66, Issue 10, p. 1210
Japan Spastic Paraplegia Research Consortium (JASPAC), a nationwide clinical and genetic survey of patients with hereditary spastic paraplegia (HSP), was... 
Paraplegia - epidemiology | Humans | Paraplegia - etiology | Databases, Factual
Journal Article
Clinical Neurology, ISSN 0009-918X, 2014, Volume 54, Issue 12, pp. 1009 - 1011
Journal Article
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, ISSN 1590-1874, 08/2019, pp. 1 - 2
Journal Article
Rinsho shinkeigaku = Clinical neurology, 2014, Volume 54, Issue 12, p. 1009
Hereditary spastic paraplegia (HSP) is a clinically and genetically heterogeneous group of neurodegenerative disorders that are clinically characterized by... 
Japan - epidemiology | Phenotype | Paraplegia - epidemiology | Peptide Termination Factors - genetics | Humans | Vesicular Transport Proteins - genetics | Paraplegia - genetics | Paraplegia - classification | Paraplegia - diagnosis | Mitochondrial Proteins - genetics | Mutation
Journal Article
The Cerebellum, ISSN 1473-4222, 2007, Volume 6, Issue 4, pp. 353 - 359
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) was originally found among inhabitants of the Charlevoix-Saguenay region of northeastern... 
genetic | Ataxia | gene | degenerative | recessive | Neurology | Neurosciences | Biomedicine | Neurobiology | Genetic | Degenerative | Gene | Recessive | POPULATION | PARAPLEGIA | NEUROSCIENCES | RECESSIVE SPASTIC ATAXIA | ONSET CEREBELLAR-ATAXIA | ataxia | CHARLEVOIX-SAGUENAY | NORTHEASTERN QUEBEC | ARSACS | MUTATIONS | RETAINED TENDON REFLEXES | Humans | Middle Aged | Tomography, Emission-Computed, Single-Photon | Male | Gait Disorders, Neurologic - genetics | Spinocerebellar Ataxias - congenital | Psychomotor Performance - physiology | Motor Neurons - pathology | Young Adult | Heat-Shock Proteins - genetics | Sural Nerve - pathology | Wheelchairs | Nerve Fibers, Myelinated - pathology | Gait Disorders, Neurologic - physiopathology | Adult | Female | Spinocerebellar Ataxias - genetics | Muscle Spasticity - epidemiology | Sensory Receptor Cells - pathology | Cerebellar Ataxia - epidemiology | Spinocerebellar Ataxias - epidemiology | Neural Conduction - physiology | Cerebellar Ataxia - pathology | Spinocerebellar Ataxias - pathology | Muscle Spasticity - pathology | Disease Progression | Magnetic Resonance Imaging | Cerebellar Ataxia - genetics | Biopsy | Adolescent | Age of Onset | Intellectual Disability - psychology | Retinal Neurons - pathology | Intellectual Disability - etiology | Muscle, Skeletal - pathology | Heat-Shock Proteins - physiology | Muscle Spasticity - genetics | Bacteriology | Mutation
Journal Article
Nature Genetics, ISSN 1061-4036, 04/2018, Volume 50, Issue 4, pp. 581 - 590
Journal Article
Neurology Research International, ISSN 2090-1852, 2012, Volume 2012, pp. 197438 - 7
Neuroferritinopathy is a neurodegenerative disease which demonstrates brain iron accumulation caused by the mutations in the ferritin light chain gene. On... 
Review
Journal Article
Journal Article
INTERNAL MEDICINE, ISSN 0918-2918, 2019, Volume 58, Issue 16, pp. 2397 - 2400
Journal Article
Neurological Sciences, ISSN 1590-1874, 02/2019, Volume 40, Issue 2, pp. 429 - 431
Journal Article
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