Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
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A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025
Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
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A 2-Year-Old Girl with Acute Encephalopathy After Febrile Systemic Illness
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Amyotrophic Lateral Sclerosis
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Spinal Muscular Atrophy
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
AJNR 39:1657-1661, Codjia, P.,et al, 2018
A Neonate with Micrognathia and Hypotonia
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Hydrocephalus in Children
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Non-Alzheimers Dementia 1 Frontotemporal Dementia
Lancet 386:1672-1682, Bang, Jee.,et al, 2015
Degenerative Diseases of the Nervous System, Werdnig-Hoffman Disease, Spinal Muscular Atrophy
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Degenerative Diseases of the Nervous System, Kugelberg-Welander Syndrome SMAIII
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Spinal Muscular Atrophy A Timely Review
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Genetics of Familial Amyotrophic Lateral Sclerosis
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Amyotrophic Lateral Sclerosis
Lancet 369:2031-2041, Mitchell,J.D. & Borasio,G.D., 2007
Hyperhomocysteinemia, Low Folate and Vitamin B12 Concentrations, and Methylene Tetrahydrofolate Reductase Mutation in Cerebral Venous Thrombosis
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Amyotrophic Lateral Sclerosis
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Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
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Distal Hereditary Upper Limb Muscular Atrophy
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Hereditary Form of Parkinsonism-Dementia
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Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
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Intrafamilial Heterogeneity in Hereditary Motor Neuron Disease
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Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
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Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
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Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
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Phenotypic Heterogeneity of Spinal Muscular Atrophy Mapping to Chromosome 5q11. 2-12. 3 (SMA5q)
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Joubert Syndrome:A Clinico-Radiological Study
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Computed Tomography and Magnetic Resonance Imaging in Adult-Onset Leukodystrophy
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The Molecular Genetic Revolution, Its Impact on Clinical Neurology
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Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
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Cerebral Ventricular Dilation in Congenital Myotonic Dystrophy
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Familial Recurrent Bell's Palsy with Ocular Motor Palsies
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Hereditary Neuropathy with Liability to Pressure Palsies
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Location of the Gene for X-Linked Spinal Muscular Atrophy
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Familial Occurrence of Idiopathic Normal-Pressure Hydrocephalus
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Familial Occurrence of Amyotrophic Lateral Sclerosis, Parkinsonism, & Dementia
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Congenital Hydrocephalus & Eye Abnormalities with Severe Developmental Brain Defects:Warburg's Syndrome
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Familial Porencephaly
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Clinicopathological Conference
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A Surgical Approach To The Treatment Of Fetal Hydrocephalus
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Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
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Progressive Pontobulbar Palsy With Deafness
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Familial Spastic Paraplg, Peroneal Neuropathy, & Crural Hypopig, A New Neurocut Synd
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Placement Of Ventriculo-Amniotic Shunt For Hydrocephalus In A Fetus
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Computed tomography in Hallervorden-Spatz disease
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