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Leukodystrophy
Adult Onset) an Information Sheet for the Person Who Has Been Diagnosed with a Leukodystrophy, Their Family, and Friends
Child Neurology: Hereditary Spastic Paraplegia in Children S.T
Hereditary Spastic Paraparesis: a Review of New Developments
Autosomal Dominant Leukodystrophy with Autonomic Symptoms
Hereditary Spastic Paraplegias
Blueprint Genetics Leukodystrophy and Leukoencephalopathy Panel
Acute Disseminated Encephalomyelitis: Treatment Guidelines
Childhood Neurological Conditions and Disorders
Late Onset Globoid Cell Leukodystrophy Patient's Late Onset (At Age 14
Leukodystrophies by Raphael Schiffmann MD (Dr
Late-Onset Leukodystrophy Mimicking Hereditary Spastic Paraplegia Without Diffuse Leukodystrophy on Neuroimaging
Migraine and Stroke
Adult Leukodystrophies: a Step- By-Step Diagnostic Approach
A Unique Familial Leukodystrophy with Adult Onset Dementia and Abnormal Glycolipid Storage: a New Lysosomal Disease?
The Significance of Elevated CSF Lactate S L Chow, Z J Rooney, M a Cleary, P T Clayton, J V Leonard
The Leukodystrophies
The Role of White Matter Dysfunction and Leukoencephalopathy
Genetic Types of HSP* Autosomal Dominant
Top View
A Case of Tuberculosis-Associated Acute Disseminated Encephalomyelitis in a Seven- Month-Old Infant
A Practical Approach to Diagnosing Adult Onset Leukodystrophies
Paediatric Multiple Sclerosis: What It Is and What It Is
Leukodystrophy and Progressive Myoclonic Epilepsy
A Novel POLR3A Genotype
A Child with Acute Onset of Neurological Signs
Clinical Association of Intrathecal and Mirrored Oligoclonal Bands in Paediatric Neurology
Developmental Disabilities Handbook
Case Report a Rare Young Case of Charcot-Marie-Tooth with Stroke-Like Presentation and Transient Leukodystrophy
Consensus Statement on Preventive and Symptomatic Care of Leukodystrophy Patients
Adult Onset Leukodystrophy with Neuroaxonal Spheroids: Clinical, Neuroimaging and Neuropathologic Observations
Differentiation of Hereditary Spastic Paraparesis from Primary Lateral Sclerosis in Sporadic Adult-Onset Upper Motor Neuron Syndromes
Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force
Metachromatic Leukodystrophy. Case Presentation
Hereditary Spastic Paraplegia: from Diagnosis to Emerging Therapeutic Approaches
The Emerging Role of the Lysosome in Parkinson's Disease
Monogenic Diseases Masquerading As Multiple Sclerosis
Leukodystrophy Fact Sheet
CSF1R-Related Leukoencephalopathy Caused by CSF1R P.Arg777trp and CSF1R P.Arg782cys Mutations: a Report of Four Cases in Sweden
Chapter 2.2 Abundant Extracellular Myelin in the Meninges of Patients
Leukodystrophy Overview Genereview Table 8 Authors: Vanderver A, Tonduti D, Schiffmann R, Schmidt J, Van Der Knaap M Date: February 2014
Practical Approach to the Diagnosis of Adult-Onset Leukodystrophies
Progressive Early-Onset Leukodystrophy Related to Biallelic Variants in the KARS Gene: the First Case Described in Latin America
Toward a Better Understanding of Brain Lesions During
Leukoencephalopathy with Calcifications and Cysts—The First
Metachromatic Leukodystrophy
A Case of Acute Disseminated Encephalomyelitis Mimicking Leukodystrophy