Ears of the Lynx Magnetic Resonance Imaging Sign
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
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SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
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A 28-year-old Woman with Lower Extremity Spasticity and Microcytic Anemia
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Degenerative Diseases of the Nervous System, Hereditary Spastic Paraplagia
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The Hereditary Spastic Paraplegias
Arch Neurol 60:1045-1049, Fink,J.K., 2003
Hereditary Spastic Paraplegia:Advances in Genetic Research
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Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
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X-Linked Pure Familial Spastic Paraparesis
Arch Neurol 52:665-669, Cambi,F.,et al, 1995
Progressive Spastic Paraparesis & Adrenal Insufficiency
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"Ears of the Lynx" MRI Sign is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia
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Hereditary Spastic Paraplegia
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Hereditary Spastic Paraparesis: A Review of New Developments
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MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
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Familial Spastic Paraparesis Syndrome Associated with HTLV-I Infection
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Hereditary Motor and Sensory Neuropathies and Hereditary Spastic Paraplegia:A Magnetic Stimulation Study
Ann Neurol 28:43-49, Claus,D.,et al, 1990
The Autosomal Dominant Form of"Pure"Familial Spastic Paraplegia:Clinical Findings & Linkage Analysis of a Pedigree
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Familial Spastic Paraparesis & Deafness, A New X-Linked Neurodegenerative Disorder
Arch Neurol 43:943-946, Wells,C.R.&Jankovic,J., 1986
Neurodegenerative Disease of Infancy & Childhood
Ann Neurol 13:351-364, Dyken,P.,et al, 1983
Familial Spastic Paraplegia, Mental Retardation, & Precocious Puberty
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Hereditary Ataxias
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